1.0g of Piprocaine (Citrate Salt)

This is an analog of "pipercaine", related to the parent compound of; cocaine / tropacocaine and to study in relation to; 1-methyl-3-propyl-4-(para-chlorophenyl)piperidine & the 3rd position substitution. It is likely higher nM binding affinity for the receptors of interest, relating to these compounds.

Not available where scheduled. Review the laws in your country before ordering.

SMILES: OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCC1CN(C)CCC1OC(=O)C1=CC=CC=C1

InChI=1/C16H23NO2.C6H8O7/c1-3-7-14-12-17(2)11-10-15(14)19-16(18)13-8-5-4-6-9-13;7-3(8)1-6(13,5(11)12)2-4(9)10/h4-6,8-9,14-15H,3,7,10-12H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

InChIKey=YRTCVCOGDFHGJL-UHFFFAOYNA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

Buy 10.0g of Piprocaine (Citrate Salt)

This is an analog of "pipercaine", related to the parent compound of; cocaine / tropacocaine and to study in relation to; 1-methyl-3-propyl-4-(para-chlorophenyl)piperidine & the 3rd position substitution. It is likely higher nM binding affinity for the receptors of interest, relating to these compounds.

Not available where scheduled. Review the laws in your country before ordering.

SMILES: OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCC1CN(C)CCC1OC(=O)C1=CC=CC=C1

InChI=1/C16H23NO2.C6H8O7/c1-3-7-14-12-17(2)11-10-15(14)19-16(18)13-8-5-4-6-9-13;7-3(8)1-6(13,5(11)12)2-4(9)10/h4-6,8-9,14-15H,3,7,10-12H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

InChIKey=YRTCVCOGDFHGJL-UHFFFAOYNA-N

This is an analog of "pipercaine", related to the parent compound of; cocaine / tropacocaine and to study in relation to; 1-methyl-3-propyl-4-(para-chlorophenyl)piperidine & the 3rd position substitution. It is likely higher nM binding affinity for the receptors of interest, relating to these compounds.

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

2.5g of Piprocaine (Citrate Salt)

Not available where scheduled. Review the laws in your country before ordering.

SMILES: OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCC1CN(C)CCC1OC(=O)C1=CC=CC=C1

InChI=1/C16H23NO2.C6H8O7/c1-3-7-14-12-17(2)11-10-15(14)19-16(18)13-8-5-4-6-9-13;7-3(8)1-6(13,5(11)12)2-4(9)10/h4-6,8-9,14-15H,3,7,10-12H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

InChIKey=YRTCVCOGDFHGJL-UHFFFAOYNA-N

This is an analog of "pipercaine", related to the parent compound of; cocaine / tropacocaine and to study in relation to; 1-methyl-3-propyl-4-(para-chlorophenyl)piperidine & the 3rd position substitution. It is likely higher nM binding affinity for the receptors of interest, relating to these compounds.

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

Buy piprocaine, related/cocaine analog - 5.0g of Piprocaine (Citrate Salt) - white powder, 98%+ purity

Not available where scheduled. Review the laws in your country before ordering.

SMILES: OC(=O)CC(O)(CC(O)=O)C(O)=O.CCCC1CN(C)CCC1OC(=O)C1=CC=CC=C1

InChI=1/C16H23NO2.C6H8O7/c1-3-7-14-12-17(2)11-10-15(14)19-16(18)13-8-5-4-6-9-13;7-3(8)1-6(13,5(11)12)2-4(9)10/h4-6,8-9,14-15H,3,7,10-12H2,1-2H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)

InChIKey=YRTCVCOGDFHGJL-UHFFFAOYNA-N

This is an analog of "pipercaine", related to the parent compound of; cocaine / tropacocaine and to study in relation to; 1-methyl-3-propyl-4-(para-chlorophenyl)piperidine & the 3rd position substitution. It is likely higher nM binding affinity for the receptors of interest, relating to these compounds.

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

Buy 5.0g (±)-1-phenyl-2-propanol

A aliphatic alcohol for subtitution and organic chemical lab work - if made a carbamate, it is a structural isomer of phenprobamate.

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

CC(CC1=CC=CC=C1)O

InChI=1S/C9H12O/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3

WYTRYIUQUDTGSX-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis;

MSDS:

Links:

http://www.chemspider.com/Chemical-Structure.84999.html?rid=f45915af-89dc-4c3c-942b-16f6ce82550d&page_num=0

https://pubchem.ncbi.nlm.nih.gov/compound/94185

50g (±)-1-phenyl-2-propanol

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

CC(CC1=CC=CC=C1)O

InChI=1S/C9H12O/c1-8(10)7-9-5-3-2-4-6-9/h2-6,8,10H,7H2,1H3

WYTRYIUQUDTGSX-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis;

MSDS:

Links:

http://www.chemspider.com/Chemical-Structure.84999.html?rid=f45915af-89dc-4c3c-942b-16f6ce82550d&page_num=0

https://pubchem.ncbi.nlm.nih.gov/compound/94185

Not available to countries where scheduled. Review the laws in your country before ordering.

SMILES; CC12CCC3C(C1CCC24C(=CC(=O)OC)OC(O4)(C)OC)CCC5=CC(=O)CCC35

InChI= 1S/C25H34O6/c1-23-11-9-18-17-8-6-16(26)13-15(17)5-7-19(18)20(23)10-12-25(23)21(14-22(27)28-3)30-24(2,29-4)31-25/h13-14,17-20H,5-12H2,1-4H3/b21-14+/t17-,18+,19+,20-,23-,24?,25-/m0/s1

InChI Key; KCQHQCDHFVGNMK-DEIKBOPOSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

MSDS; MSDS (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

Links:

https://pubchem.ncbi.nlm.nih.gov/compound/101524490#section=IUPAC-Name

InChI Key; KCQHQCDHFVGNMK-DEIKBOPOSA-N, White Powder, 98%+ purity.

Not available to countries where scheduled. Review the laws in your country before ordering.

SMILES; CC12CCC3C(C1CCC24C(=CC(=O)OC)OC(O4)(C)OC)CCC5=CC(=O)CCC35

InChI= 1S/C25H34O6/c1-23-11-9-18-17-8-6-16(26)13-15(17)5-7-19(18)20(23)10-12-25(23)21(14-22(27)28-3)30-24(2,29-4)31-25/h13-14,17-20H,5-12H2,1-4H3/b21-14+/t17-,18+,19+,20-,23-,24?,25-/m0/s1

InChI Key; KCQHQCDHFVGNMK-DEIKBOPOSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

MSDS; MSDS (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

Links:

https://pubchem.ncbi.nlm.nih.gov/compound/101524490#section=IUPAC-Name

Not available to countries where scheduled. Review the laws in your country before ordering.

SMILES; CC12CCC3C(C1CCC24C(=CC(=O)OC)OC(O4)(C)OC)CCC5=CC(=O)CCC35

InChI= 1S/C25H34O6/c1-23-11-9-18-17-8-6-16(26)13-15(17)5-7-19(18)20(23)10-12-25(23)21(14-22(27)28-3)30-24(2,29-4)31-25/h13-14,17-20H,5-12H2,1-4H3/b21-14+/t17-,18+,19+,20-,23-,24?,25-/m0/s1

InChI Key; KCQHQCDHFVGNMK-DEIKBOPOSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

MSDS;MSDS (17a,20E)-17,20-[(1-Methoxyethylidene)bis(oxy)]-3-oxo-19-norpregna- 4,20-diene-21-carboxylic Acid Methyl Ester

Links:

https://pubchem.ncbi.nlm.nih.gov/compound/101524490#section=IUPAC-Name

Review the laws in your country before ordering.

InChI=1S/C22H30N4O/c1-18(2)10-12-24-21-20(9-6-11-23-21)22(27)26-15-13-25(14-16-26)17-19-7-4-3-5-8-19/h3-9,11,18H,10,12-17H2,1-2H3,(H,23,24)

InChI Key;DYTOQURYRYYNOR-UHFFFAOYSA-N

For research purposes. Not for use in-vitro.

3rd Party Analysis; H-NMR (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone

MSDS; MSDS (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone

Further data on (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone:

http://www.chemspider.com/Chemical-Structure.32701740.html?rid=5c907e75-7a8f-4ae0-a491-7df4a9ba01de

https://pubchem.ncbi.nlm.nih.gov/compound/50922681

Buy NSI-189

Review the laws in your country before ordering.

InChI=1S/C22H30N4O/c1-18(2)10-12-24-21-20(9-6-11-23-21)22(27)26-15-13-25(14-16-26)17-19-7-4-3-5-8-19/h3-9,11,18H,10,12-17H2,1-2H3,(H,23,24)

InChI Key;DYTOQURYRYYNOR-UHFFFAOYSA-N

For research purposes. Not for use in-vitro.

3rd Party Analysis; H-NMR (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone

MSDS; MSDS (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone

Further data on (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone:

http://www.chemspider.com/Chemical-Structure.32701740.html?rid=5c907e75-7a8f-4ae0-a491-7df4a9ba01de

https://pubchem.ncbi.nlm.nih.gov/compound/50922681

Buy NSI-189

Review the laws in your country before ordering.

InChI=1S/C22H30N4O/c1-18(2)10-12-24-21-20(9-6-11-23-21)22(27)26-15-13-25(14-16-26)17-19-7-4-3-5-8-19/h3-9,11,18H,10,12-17H2,1-2H3,(H,23,24)

InChI Key;DYTOQURYRYYNOR-UHFFFAOYSA-N

For research purposes. Not for use in-vitro.

3rd Party Analysis; H-NMR (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone

MSDS; MSDS (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone

Further data on (4-Benzyl-1-piperazinyl){2-[(3-methylbutyl)amino]-3-pyridinyl}methanone:

http://www.chemspider.com/Chemical-Structure.32701740.html?rid=5c907e75-7a8f-4ae0-a491-7df4a9ba01de

https://pubchem.ncbi.nlm.nih.gov/compound/50922681

Buy NSI-189

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C12H18N2.ClH/c1-13-7-9-14(10-8-13)11-12-5-3-2-4-6-12;/h2-6H,7-11H2,1H3;1H

InChI Key NSKWYRZISOURNW-UHFFFAOYSA-N

SMILES CN1CCN(CC1)CC2=CC=CC=C2.Cl

For research purposes. Not for use in-vivo.

3rd Party Analysis; 1-Benzyl-4-methylpiperazine-HCl-2(1) 1-Benzyl-4-methylpiperazine-HCl-1(1)

MSDS; 1-benzyl-4-methylpiperazine HCl

Link:

https://pubchem.ncbi.nlm.nih.gov/compound/44181811

http://www.chemspider.com/Chemical-Structure.21241219.html?rid=c26f3a9c-87b4-4d31-bf67-b3891462cce1

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C12H18N2.ClH/c1-13-7-9-14(10-8-13)11-12-5-3-2-4-6-12;/h2-6H,7-11H2,1H3;1H

InChI Key NSKWYRZISOURNW-UHFFFAOYSA-N

SMILES CN1CCN(CC1)CC2=CC=CC=C2.Cl

For research purposes. Not for use in-vivo.

3rd Party Analysis; 1-Benzyl-4-methylpiperazine-HCl-2(1) 1-Benzyl-4-methylpiperazine-HCl-1(1)

MSDS; 1-benzyl-4-methylpiperazine HCl

Link:

https://pubchem.ncbi.nlm.nih.gov/compound/44181811

http://www.chemspider.com/Chemical-Structure.21241219.html?rid=c26f3a9c-87b4-4d31-bf67-b3891462cce1

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C12H18N2.ClH/c1-13-7-9-14(10-8-13)11-12-5-3-2-4-6-12;/h2-6H,7-11H2,1H3;1H

InChI Key NSKWYRZISOURNW-UHFFFAOYSA-N

SMILES CN1CCN(CC1)CC2=CC=CC=C2.Cl

For research purposes. Not for use in-vivo.

3rd Party Analysis; 1-Benzyl-4-methylpiperazine-HCl-2(1) 1-Benzyl-4-methylpiperazine-HCl-1(1)

MSDS; 1-benzyl-4-methylpiperazine HCl

Link:

https://pubchem.ncbi.nlm.nih.gov/compound/44181811

http://www.chemspider.com/Chemical-Structure.21241219.html?rid=c26f3a9c-87b4-4d31-bf67-b3891462cce1

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C12H18N2.ClH/c1-13-7-9-14(10-8-13)11-12-5-3-2-4-6-12;/h2-6H,7-11H2,1H3;1H

InChI Key NSKWYRZISOURNW-UHFFFAOYSA-N

SMILES CN1CCN(CC1)CC2=CC=CC=C2.Cl

For research purposes. Not for use in-vivo.

3rd Party Analysis; 1-Benzyl-4-methylpiperazine-HCl-2(1) 1-Benzyl-4-methylpiperazine-HCl-1(1)

MSDS; 1-benzyl-4-methylpiperazine HCl

Link:

https://pubchem.ncbi.nlm.nih.gov/compound/44181811

http://www.chemspider.com/Chemical-Structure.21241219.html?rid=c26f3a9c-87b4-4d31-bf67-b3891462cce1

| white powder, 98%+ Molecular weight; 408.385 g/mol - for research comparative studies.  Not for use in vivo.

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES: OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.CN1CCC(CC1)OC(=O)C1=CC=CC=C1

InChI=1S/C13H17NO2.C6H8O7/c1-14-9-7-12(8-10-14)16-13(15)11-5-3-2-4-6-11;7-3(8)1-6(13,5(11)12)2-4(9)10/h2-6,12H,7-10H2,1H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/p-3

InChIKey=IQRROIGKIMNDAP-UHFFFAOYSA-K

For research purposes. Not for use in-vivo.

Pipercaine / 1-methylpiperidin-4-yl benzoate, from researching it's in-vitro properties and of similar substituted analogs, has about 4 x less affinity than cocaine and also a sodium channel blocker like cocaine. It has a piperidine (cutting out a 2-carbon chain of the ring) instead of a tropane ring.

3rd Party Analysis; Pipercaine-3 Pipercaine-2 Pipercaine-1

MSDS; 1-methylpiperidin-4-yl benzoate CITRATE__pipercaine CITRATE

Links:

https://pubchem.ncbi.nlm.nih.gov/substance/preview/1279778533

http://www.chemspider.com/Chemical-Structure.189111.html?rid=c11ae1f9-a396-4c41-b25a-33305cd4452c

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES: OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.CN1CCC(CC1)OC(=O)C1=CC=CC=C1

InChI=1S/C13H17NO2.C6H8O7/c1-14-9-7-12(8-10-14)16-13(15)11-5-3-2-4-6-11;7-3(8)1-6(13,5(11)12)2-4(9)10/h2-6,12H,7-10H2,1H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/p-3

InChIKey=IQRROIGKIMNDAP-UHFFFAOYSA-K

For research purposes. Not for use in-vivo.

Pipercaine / 1-methylpiperidin-4-yl benzoate, from researching it's in-vitro properties and of similar substituted analogs, has about 4 x less affinity than cocaine and also a sodium channel blocker like cocaine. It has a piperidine (cutting out a 2-carbon chain of the ring) instead of a tropane ring.

3rd Party Analysis; Pipercaine-3 Pipercaine-2 Pipercaine-1

MSDS; 1-methylpiperidin-4-yl benzoate CITRATE__pipercaine CITRATE

Links:

https://pubchem.ncbi.nlm.nih.gov/substance/preview/1279778533

http://www.chemspider.com/Chemical-Structure.189111.html?rid=c11ae1f9-a396-4c41-b25a-33305cd4452c

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES: OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.CN1CCC(CC1)OC(=O)C1=CC=CC=C1

InChI=1S/C13H17NO2.C6H8O7/c1-14-9-7-12(8-10-14)16-13(15)11-5-3-2-4-6-11;7-3(8)1-6(13,5(11)12)2-4(9)10/h2-6,12H,7-10H2,1H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/p-3

InChIKey=IQRROIGKIMNDAP-UHFFFAOYSA-K

For research purposes. Not for use in-vivo.

Pipercaine / 1-methylpiperidin-4-yl benzoate, from researching it's in-vitro properties and of similar substituted analogs, has about 4 x less affinity than cocaine and also a sodium channel blocker like cocaine. It has a piperidine (cutting out a 2-carbon chain of the ring) instead of a tropane ring.

3rd Party Analysis; Pipercaine-3 Pipercaine-2 Pipercaine-1

MSDS; 1-methylpiperidin-4-yl benzoate CITRATE__pipercaine CITRATE

Links:

https://pubchem.ncbi.nlm.nih.gov/substance/preview/1279778533

http://www.chemspider.com/Chemical-Structure.189111.html?rid=c11ae1f9-a396-4c41-b25a-33305cd4452c

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES: CN1CCC(CC1)OC(=O)c2ccccc2

InChI=1S/C13H17NO2/c1-14-9-7-12(8-10-14)16-13(15)11-5-3-2-4-6-11/h2-6,12H,7-10H2,1H3

InChIKey=ITBIONVQXMUSAI-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

Pipercaine / 1-methylpiperidin-4-yl benzoate, from researching it's in-vitro properties and of similar substituted analogs, has about 4 x less affinity than cocaine and also a sodium channel blocker like cocaine. It has a piperidine (cutting out a 2-carbon chain of the ring) instead of a tropane ring.

3rd Party Analysis; HNMR of 1-methylpiperidin-4-yl benzoate hydrochloride__pipercaine HCl

MSDS; MSDS 1-methylpiperidin-4-yl benzoate hydrochloride__pipercaine HCl

Links:

http://www.chemspider.com/Chemical-Structure.189111.html?rid=c11ae1f9-a396-4c41-b25a-33305cd4452c

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES: CN1CCC(CC1)OC(=O)c2ccccc2

InChI=1S/C13H17NO2/c1-14-9-7-12(8-10-14)16-13(15)11-5-3-2-4-6-11/h2-6,12H,7-10H2,1H3

InChIKey=ITBIONVQXMUSAI-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

Pipercaine / 1-methylpiperidin-4-yl benzoate, from researching it's in-vitro properties and of similar substituted analogs, has about 4 x less affinity than cocaine and also a sodium channel blocker like cocaine. It has a piperidine (cutting out a 2-carbon chain of the ring) instead of a tropane ring.

3rd Party Analysis; HNMR of 1-methylpiperidin-4-yl benzoate hydrochloride__pipercaine HCl

MSDS; MSDS 1-methylpiperidin-4-yl benzoate hydrochloride__pipercaine HCl

Links:

http://www.chemspider.com/Chemical-Structure.189111.html?rid=c11ae1f9-a396-4c41-b25a-33305cd4452c

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES: CN1CCC(CC1)OC(=O)c2ccccc2

InChI=1S/C13H17NO2/c1-14-9-7-12(8-10-14)16-13(15)11-5-3-2-4-6-11/h2-6,12H,7-10H2,1H3

InChIKey=ITBIONVQXMUSAI-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

Pipercaine / 1-methylpiperidin-4-yl benzoate, from researching it's in-vitro properties and of similar substituted analogs, has about 4 x less affinity than cocaine and also a sodium channel blocker like cocaine. It has a piperidine (cutting out a 2-carbon chain of the ring) instead of a tropane ring.

3rd Party Analysis; HNMR of 1-methylpiperidin-4-yl benzoate hydrochloride__pipercaine HCl

MSDS; MSDS 1-methylpiperidin-4-yl benzoate hydrochloride__pipercaine HCl

Links:

http://www.chemspider.com/Chemical-Structure.189111.html?rid=c11ae1f9-a396-4c41-b25a-33305cd4452c

Buy Methamphproamine - 1.0g of 1-Phenyl-3-methylaminobutane HCl. 98%+ purity white powder | CAS#63957-19-7

Not available where scheduled. Review the laws in your country before ordering.

SMILES: CC(CCc1ccccc1)NC

InChI=1S/C11H17N/c1-10(12-2)8-9-11-6-4-3-5-7-11/h3-7,10,12H,8-9H2,1-2H3

InChIKey: PUAUJIPHHQUZGF-UHFFFAOYSA-N

1-Phenyl-3-methylaminobutane (methamphproamine) a specialty research chemical for study that is not directly related as an analog to methamphetamine or as a structural isomer as the central carbon chain of this new family of compounds is a butane with the amino on the 3rd position on the chain.

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

Links for more info. on this chemical:

https://pubchem.ncbi.nlm.nih.gov/compound/115420

http://www.chemspider.com/Chemical-Structure.103252.html

2.5g of 1-Phenyl-3-methylaminobutane HCl

Not available where scheduled. Review the laws in your country before ordering.

SMILES: CC(CCc1ccccc1)NC

InChI=1S/C11H17N/c1-10(12-2)8-9-11-6-4-3-5-7-11/h3-7,10,12H,8-9H2,1-2H3

InChIKey: PUAUJIPHHQUZGF-UHFFFAOYSA-N

1-Phenyl-3-methylaminobutane (methamphproamine) a specialty research chemical for study that is not directly related as an analog to methamphetamine or as a structural isomer as the central carbon chain of this new family of compounds is a butane with the amino on the 3rd position on the chain.

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

Links for more info. on this chemical:

https://pubchem.ncbi.nlm.nih.gov/compound/115420

http://www.chemspider.com/Chemical-Structure.103252.html

Buy Methamphproamine  - 5.0g of 1-Phenyl-3-methylaminobutane HCl

Not available where scheduled. Review the laws in your country before ordering.

SMILES: CC(CCc1ccccc1)NC

InChI=1S/C11H17N/c1-10(12-2)8-9-11-6-4-3-5-7-11/h3-7,10,12H,8-9H2,1-2H3

InChIKey: PUAUJIPHHQUZGF-UHFFFAOYSA-N

1-Phenyl-3-methylaminobutane (methamphproamine) a specialty research chemical for study that is not directly related as an analog to methamphetamine or as a structural isomer as the central carbon chain of this new family of compounds is a butane with the amino on the 3rd position on the chain.

For research purposes. Not for use in-vivo.

3rd Party Analysis:

MSDS:

Links for more info. on this chemical:

https://pubchem.ncbi.nlm.nih.gov/compound/115420

http://www.chemspider.com/Chemical-Structure.103252.html

Buy 10mg - L1P (N-1-propyl Lysergamide) / Lysergic Acid N-propyl amide

.LAMPA Analog for comparative for this lysergamide and others, for whatever the study is, from correlations of different length N-alkyl chains on the amide, cyclic groups of the same number of carbons, etc. This one is quite a special, relatively unstudied chemical for research.

OC(=O)\C=C\C(O)=O.CCCNC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

InChI=1/C19H23N3O.C4H4O4/c1-3-7-20-19(23)13-8-15-14-5-4-6-16-18(14)12(10-21-16)9-17(15)22(2)11-13;5-3(6)1-2-4(7)8/h4-6,8,10,13,17,21H,3,7,9,11H2,1-2H3,(H,20,23);1-2H,(H,5,6)(H,7,8)/b;2-1+

InChIKey=DIPLDPQMHFBDNW-WLHGVMLRNA-N

For research purposes only and not for use in vivo.

HNMR:

MSDS:

example /no other links found;
https://pubchem.ncbi.nlm.nih.gov/compound/139024833

Buy 10mg - LAMPA (N-methyl-N-propyl Lysergamide) CAS#40158-98-3

.

SMILES: CCCN(C)C(=O)[C@H]1CN([C@@H]2CC3=CNC4=CC=CC(=C34)C2=C1)C

InChI=1S/C20H25N3O/c1-4-8-22(2)20(24)14-9-16-15-6-5-7-17-19(15)13(11-21-17)10-18(16)23(3)12-14/h5-7,9,11,14,18,21H,4,8,10,12H2,1-3H3/t14-,18-/m1/s1

InChIKey=CZRJGQXHVRNZRZ-RDTXWAMCSA-N

For research purposes only and not for use in vivo.

HNMR:

MSDS:

https://pubchem.ncbi.nlm.nih.gov/compound/13932543
https://www.chemspider.com/Chemical-Structure.32675221.html

Buy 95%+ LSD-25-pyrrolidate / 10mg - N-pyrrolidinyl lysergamide (hemifumarate) (LDP-824/ LAPy)

..."The two ethyl groups were incorporated into ring structures such as the pyrrolidide, piperidide, and morpholide, shown above, but these also had reduced anti-serotonin and psychedelic effects (Cerletti and Doepfner 1958). Although the morpholide had less than one-tenth of the potency of LSD in blocking the action of serotonin, it did however have nearly 75% of the potency of LSD as a psychedelic (Gogerty and Dille 1957).

For lysergic acid amides where only one alkyl chain was attached (e.g. lysergic acid monoethylamide), relative antiserotonin activity was related to the length of the alkyl chain. Activity increased with chain length to a maximum of 75% of the potency of LSD with the n-pentylamide (five carbon atoms in a chain) (Cerletti and Doepfner 1958)."...

Ref.: Nichols, LSD and Its Lysergamide Cousins (https://www.heffter.org/wp-content/uploads/2020/04/chap6.pdf)

CN1CC(C=C2C1CC1=CNC3=C1C2=CC=C3)C(=O)N1CCCC1

InChI=1/C20H23N3O/c1-22-12-14(20(24)23-7-2-3-8-23)9-16-15-5-4-6-17-19(15)13(11-21-17)10-18(16)22/h4-6,9,11,14,18,21H,2-3,7-8,10,12H2,1H3

InChIKey=SETDYMMXQQXCRP-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: There is water in the DMSO-d6 used to dissolve the sample and pulling it in, it seemed to have made the water 3.3 peak quite large and the sample is dry. Where the peaks are, they are proportional and symmetrical and the compound identified/confirmed correct. Just a confirmatory analysis...we used our own custom synthesis procedure we developed that we became good at and consistent with.

MSDS:

LINKS:

https://pubchem.ncbi.nlm.nih.gov/compound/200628

Buy LSM-775 - 10mg N-morpholinyl lysergamide "LAMo" - 95%+ purity.

..."The two ethyl groups were incorporated into ring structures such as the pyrrolidide, piperidide, and morpholide, shown above, but these also had reduced anti-serotonin and psychedelic effects (Cerletti and Doepfner 1958). Although the morpholide had less than one-tenth of the potency of LSD in blocking the action of serotonin, it did however have nearly 75% of the potency of LSD as a psychedelic (Gogerty and Dille 1957).

For lysergic acid amides where only one alkyl chain was attached (e.g. lysergic acid monoethylamide), relative antiserotonin activity was related to the length of the alkyl chain. Activity increased with chain length to a maximum of 75% of the potency of LSD with the n-pentylamide (five carbon atoms in a chain) (Cerletti and Doepfner 1958)."...

Ref.: Nichols, LSD and Its Lysergamide Cousins (https://www.heffter.org/wp-content/uploads/2020/04/chap6.pdf)

CN1CC(C=C2C1CC1=CNC3=C1C2=CC=C3)C(=O)N1CCOCC1

InChI=1/C20H23N3O2/c1-22-12-14(20(24)23-5-7-25-8-6-23)9-16-15-3-2-4-17-19(15)13(11-21-17)10-18(16)22/h2-4,9,11,14,18,21H,5-8,10,12H2,1H3

InChIKey=OTQWCDNEJVKXKG-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: There is water in the DMSO-d6 used to dissolve the sample and pulling it in, it seemed to have made the water 3.3 peak quite large and the sample is dry. Where the peaks are, they are proportional and symmetrical and the compound identified/confirmed correct. Just a confirmatory analysis...we used our own custom synthesis procedure we developed that we became good at and consistent with.

MSDS:

LINKS:

https://pubchem.ncbi.nlm.nih.gov/compound/199507

Buy LSP lysergamide, an LSD analog - 10mg N-3-amyl lysergamide freebase as tan solid & good purity "L3A"

InChI=1S/C21H27N3O/c1-4-15(5-2)23-21(25)14-9-17-16-7-6-8-18-20(16)13(11-22-18)10-19(17)24(3)12-14/h6-9,11,14-15,19,22H,4-5,10,12H2,1-3H3,(H,23,25)

ZQONRMXCBQXYCK-UHFFFAOYSA-N

CCC(CC)NC(=O)C1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C

For research purposes only and not for use in vivo.

In the rotovap. drying as final product to be sold;

HNMR:

MSDS:

Links:

https://pubchem.ncbi.nlm.nih.gov/compound/10019984

http://www.chemspider.com/Chemical-Structure.8195557.html

Scheduled in USA, cannot sell this there without a permit to be shipped with shipping label.

Buy 10mg N-1-butyl lysergamide (Maleate) (L1B) - Grey powder. InChIKey=ZRKPZIJFZRINOR-WLHGVMLRNA-N

InChI=1/C20H25N3O.C4H4O4/c1-3-4-8-21-20(24)14-9-16-15-6-5-7-17-19(15)13(11-22-17)10-18(16)23(2)12-14;5-3(6)1-2-4(7)8/h5-7,9,11,14,18,22H,3-4,8,10,12H2,1-2H3,(H,21,24);1-2H,(H,5,6)(H,7,8)/b;2-1+

OC(=O)\C=C\C(O)=O.CCCCNC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

InChIKey=ZRKPZIJFZRINOR-WLHGVMLRNA-N

For research purposes only and not for use in vivo.

HNMR:

https://syntharise.com/wp-content/uploads/2024/08/N-1-butyl-lysergamide-1.pdf

MSDS:

https://syntharise.com/wp-content/uploads/2024/08/L1B-Maleate-1.pdf

LINKS:

https://pubchem.ncbi.nlm.nih.gov/substance/385635903

https://www.chemspider.com/Chemical-Structure.23157987.html

Buy LSP analog -  10mg N-1-pentyl Lysergamide (hemifumarate) (L1A)

..."For lysergic acid amides where only one alkyl chain was attached (e.g. lysergic acid monoethylamide), relative antiserotonin activity was related to the length of the alkyl chain. Activity increased with chain length to a maximum of 75% of the potency of LSD with the n-pentylamide (five carbon atoms in a chain) (Cerletti and Doepfner 1958)."...

Ref.: Nichols, LSD and Its Lysergamide Cousins (https://www.heffter.org/wp-content/uploads/2020/04/chap6.pdf)

CCCCCNC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

InChI=1/C21H27N3O/c1-3-4-5-9-22-21(25)15-10-17-16-7-6-8-18-20(16)14(12-23-18)11-19(17)24(2)13-15/h6-8,10,12,15,19,23H,3-5,9,11,13H2,1-2H3,(H,22,25)

InChIKey=ZWLCMQVCVMIVGG-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: There is water in the DMSO-d6 used to dissolve the sample and pulling it in, it seemed to have made the water 3.3 peak quite large and the sample is dry. Where the peaks are, they are proportional and symmetrical and the compound identified/confirmed correct. Just a confirmatory analysis...we used our own custom synthesis procedure we developed that we became good at and consistent with.

MSDS:

Buy rare lysergamides - 10mg N-2-amyl lysergamide, an LSD analog. grey powder & anhydrous.

InChI=1/C21H27N3O.C4H4O4/c1-4-6-13(2)23-21(25)15-9-17-16-7-5-8-18-20(16)14(11-22-18)10-19(17)24(3)12-15;5-3(6)1-2-4(7)8/h5,7-9,11,13,15,19,22H,4,6,10,12H2,1-3H3,(H,23,25);1-2H,(H,5,6)(H,7,8)/b;2-1+

InChIKey=HLXBHRSDSATZNL-WLHGVMLRNA-N

OC(=O)\C=C\C(O)=O.CCCC(C)NC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

For research purposes only and not for use in vivo.

HNMR: (water (the 3.33ppm area) added to DMSO-d6 as sample was dry to being static when sent and cannot be hygroscopic) Sample you will get is dry, to static forming from plastic, so dry and pure as stated!

MSDS:

Buy Lysergamides - 10mg N-2-amyl lysergamide tartrate - N-2-pentyl lysergamide / lysergic acid 2-pentyl amide (L2A/ LSP analog)

InChI=1/C21H27N3O.C4H6O6/c1-4-6-13(2)23-21(25)15-9-17-16-7-5-8-18-20(16)14(11-22-18)10-19(17)24(3)12-15;5-1(3(7)8)2(6)4(9)10/h5,7-9,11,13,15,19,22H,4,6,10,12H2,1-3H3,(H,23,25);1-2,5-6H,(H,7,8)(H,9,10)

OC(C(O)C(O)=O)C(O)=O.CCCC(C)NC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

InChIKey=FALOKDBCKOICBP-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: (very diluted sample and the peaks correlate from peak area)

MSDS:

Buy Cyclic substituted lysergamide - N-cyclopentyl - 95%+ purity grey powder

10mg Lysergic Acid Cyclopentylamide (hemifumarate) / LCyP

CN1CC(C=C2C1CC1=CNC3=C1C2=CC=C3)C(=O)NC1CCCC1

InChI=1/C21H25N3O/c1-24-12-14(21(25)23-15-5-2-3-6-15)9-17-16-7-4-8-18-20(16)13(11-22-18)10-19(17)24/h4,7-9,11,14-15,19,22H,2-3,5-6,10,12H2,1H3,(H,23,25)

InChIKey=GIUWLXABHBAKDK-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: There is water in the DMSO-d6 used to dissolve the sample and pulling it in, it seemed to have made the water 3.3 peak quite large and the sample is dry. Where the peaks are, they are proportional and symmetrical and the compound identified/confirmed correct. Just a confirmatory analysis...we used our own custom synthesis procedure we developed that we became good at and consistent with.

MSDS:

LINKS:

https://pubchem.ncbi.nlm.nih.gov/compound/71300677

Scheduled in USA, cannot sell this there without a permit to be shipped with shipping label.

InChI=1/C20H25N3O.C4H4O4/c1-4-12(2)22-20(24)14-8-16-15-6-5-7-17-19(15)13(10-21-17)9-18(16)23(3)11-14;5-3(6)1-2-4(7)8/h5-8,10,12,14,18,21H,4,9,11H2,1-3H3,(H,22,24);1-2H,(H,5,6)(H,7,8)/b;2-1+

InChIKey=ZTGNYXZGRAGIGW-WLHGVMLRNA-N

OC(=O)C=CC(O)=O.CCC(C)NC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

For research purposes only and not for use in vivo.

HNMR:

MSDS:

LSB FREEBASE

LINKS:

https://pubchem.ncbi.nlm.nih.gov/substance/385635903

https://www.chemspider.com/Chemical-Structure.23157987.html

Scheduled in USA, cannot sell this there without a permit to be shipped with shipping label.

Buy LSB, an LSD analog - 10mg N-2-butyl lysergamide (Maleate) (LSB) 95%+ grey solid/powder - good purity/freshly made

InChI=1/C20H25N3O.C4H4O4/c1-4-12(2)22-20(24)14-8-16-15-6-5-7-17-19(15)13(10-21-17)9-18(16)23(3)11-14;5-3(6)1-2-4(7)8/h5-8,10,12,14,18,21H,4,9,11H2,1-3H3,(H,22,24);1-2H,(H,5,6)(H,7,8)/b;2-1+

InChIKey=ZTGNYXZGRAGIGW-WLHGVMLRNA-N

OC(=O)\C=C\C(O)=O.CCC(C)NC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

For research purposes only and not for use in vivo.

HNMR: (water (the 3.33ppm area) added to DMSO-d6 (slightly wet) - sample was dry

https://syntharise.com/wp-content/uploads/2024/08/N-sec-butyl-lysergamide.pdf

MSDS:

https://syntharise.com/wp-content/uploads/2024/08/LSB-Maleate.pdf

LINKS:

https://pubchem.ncbi.nlm.nih.gov/substance/385635903

https://www.chemspider.com/Chemical-Structure.23157987.html

Buy LDP / lysergic acid N,N-dipropyl Amide (2:1) fumarate - grey powder

10mg N,N-dipropyl lysergamide (hemifumarate) - LDP

InChI=1/C22H29N3O.C4H4O4/c1-4-9-25(10-5-2)22(26)16-11-18-17-7-6-8-19-21(17)15(13-23-19)12-20(18)24(3)14-16;5-3(6)1-2-4(7)8/h6-8,11,13,16,20,23H,4-5,9-10,12,14H2,1-3H3;1-2H,(H,5,6)(H,7,8)/b;2-1+

InChIKey=IFFPLOCNQAATOZ-WLHGVMLRNA-N

OC(=O)C=CC(O)=O.CCCN(CCC)C(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

For research purposes only and not for use in vivo.

HNMR: (water (the 3.33ppm area) added to DMSO-d6 as sample was dry to being static when sent and cannot be hygroscopic) Sample you will get is dry, to static forming from plastic, so dry and pure as stated!

MSDS:

10mg N,N-dipropyl lysergamide (hemitartrate) - LDP

InChI=1/C22H29N3O.C4H6O6/c1-4-9-25(10-5-2)22(26)16-11-18-17-7-6-8-19-21(17)15(13-23-19)12-20(18)24(3)14-16;5-1(3(7)8)2(6)4(9)10/h6-8,11,13,16,20,23H,4-5,9-10,12,14H2,1-3H3;1-2,5-6H,(H,7,8)(H,9,10)

OC(C(O)C(O)=O)C(O)=O.CCCN(CCC)C(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

InChIKey=NLTOYQKTNNRXCZ-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: (very diluted sample and the peaks correlate from peak area)

MSDS:

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

For research purposes. Not for use in-vivo.

3rd Party Analysis; 

MSDS;

2-PEP_2-(1-phenylethyl)piperidine

https://pubchem.ncbi.nlm.nih.gov/compound/90915405

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

For research purposes. Not for use in-vivo.

3rd Party Analysis; 

MSDS;

2-PEP_2-(1-phenylethyl)piperidine

https://pubchem.ncbi.nlm.nih.gov/compound/90915405

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES:CCN(CC)CCOC(=O)c1ccccc1

InChI=1S/C13H19NO2/c1-3-14(4-2)10-11-16-13(15)12-8-6-5-7-9-12/h5-9H,3-4,10-11H2,1-2H3

InChIKey=GEVPHAFTDXTZHY-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis; HNMR of 2-(diethylamino)ethyl benzoate hydrochloride

MSDS; MSDS of 2-(diethylamino)ethyl benzoate hydrochloride PROCAINE ANALOG

Links:

http://www.chemspider.com/Chemical-Structure.16454.html?rid=02b8c48d-7ebc-494c-99b8-7f44405f1467

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES:CCN(CC)CCOC(=O)c1ccccc1

InChI=1S/C13H19NO2/c1-3-14(4-2)10-11-16-13(15)12-8-6-5-7-9-12/h5-9H,3-4,10-11H2,1-2H3

InChIKey=GEVPHAFTDXTZHY-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis; HNMR of 2-(diethylamino)ethyl benzoate hydrochloride

MSDS; MSDS of 2-(diethylamino)ethyl benzoate hydrochloride PROCAINE ANALOG

Links:

http://www.chemspider.com/Chemical-Structure.16454.html?rid=02b8c48d-7ebc-494c-99b8-7f44405f1467

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

SMILES:CCN(CC)CCOC(=O)c1ccccc1

InChI=1S/C13H19NO2/c1-3-14(4-2)10-11-16-13(15)12-8-6-5-7-9-12/h5-9H,3-4,10-11H2,1-2H3

InChIKey=GEVPHAFTDXTZHY-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis; HNMR of 2-(diethylamino)ethyl benzoate hydrochloride

MSDS; MSDS of 2-(diethylamino)ethyl benzoate hydrochloride PROCAINE ANALOG

Links:

http://www.chemspider.com/Chemical-Structure.16454.html?rid=02b8c48d-7ebc-494c-99b8-7f44405f1467

Review the laws in your country before ordering.

InChI=1S/C17H17N3O/c1-11-3-6-13(7-4-11)17-14(9-15(18)21)20-10-12(2)5-8-16(20)19-17/h3-8,10H,9H2,1-2H3,(H2,18,21)

InChIKey=FMSOBRRSCPBFCO-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR of 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide

MSDS: MSDS of 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide

Links for further data on 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide:

https://pubchem.ncbi.nlm.nih.gov/compound/20715215#section=Top

http://www.chemspider.com/Chemical-Structure.19513915.html?rid=82e7a875-9f68-407d-a340-cc9e580cefea

Review the laws in your country before ordering.

InChI=1S/C17H17N3O/c1-11-3-6-13(7-4-11)17-14(9-15(18)21)20-10-12(2)5-8-16(20)19-17/h3-8,10H,9H2,1-2H3,(H2,18,21)

InChIKey=FMSOBRRSCPBFCO-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR of 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide

MSDS: MSDS of 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide

Links for further data on 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide:

https://pubchem.ncbi.nlm.nih.gov/compound/20715215#section=Top

http://www.chemspider.com/Chemical-Structure.19513915.html?rid=82e7a875-9f68-407d-a340-cc9e580cefea

Review the laws in your country before ordering.

InChI=1S/C17H17N3O/c1-11-3-6-13(7-4-11)17-14(9-15(18)21)20-10-12(2)5-8-16(20)19-17/h3-8,10H,9H2,1-2H3,(H2,18,21)

InChIKey=FMSOBRRSCPBFCO-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR of 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide

MSDS: MSDS of 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide

Links for further data on 2-[6-methyl-2-(4-methylphenyl)imidazo[1,2-a]pyridin-3-yl]acetamide:

https://pubchem.ncbi.nlm.nih.gov/compound/20715215#section=Top

http://www.chemspider.com/Chemical-Structure.19513915.html?rid=82e7a875-9f68-407d-a340-cc9e580cefea

Review the laws in your country before ordering.

SMILES; Cc1c(ccc(c1Cl)C#N)N[C@@H](c2nnc(o2)c3ccc(cc3)C#N)[C@H](C)O

InChI=1S/C20H16ClN5O2/c1-11-16(8-7-15(10-23)17(11)21)24-18(12(2)27)20-26-25-19(28-20)14-5-3-13(9-22)4-6-14/h3-8,12,18,24,27H,1-2H3/t12-,18+/m0/s1

InChI Key; XMBUPPIEVAFYHO-KPZWWZAWSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: 2-Chloro-4-({1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile H-NMR

MSDS: 2-Chloro-4-({1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile MSDS

Links:

http://www.chemspider.com/Chemical-Structure.26387625.html?rid=a72cb7a1-5b9a-4042-a605-c27fd1d768e7

https://pubchem.ncbi.nlm.nih.gov/compound/44200882

Buy RAD140

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SMILES; Cc1c(ccc(c1Cl)C#N)N[C@@H](c2nnc(o2)c3ccc(cc3)C#N)[C@H](C)O

InChI=1S/C20H16ClN5O2/c1-11-16(8-7-15(10-23)17(11)21)24-18(12(2)27)20-26-25-19(28-20)14-5-3-13(9-22)4-6-14/h3-8,12,18,24,27H,1-2H3/t12-,18+/m0/s1

InChI Key; XMBUPPIEVAFYHO-KPZWWZAWSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: 2-Chloro-4-({1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile H-NMR

MSDS: 2-Chloro-4-({1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile MSDS

Links:

http://www.chemspider.com/Chemical-Structure.26387625.html?rid=a72cb7a1-5b9a-4042-a605-c27fd1d768e7

https://pubchem.ncbi.nlm.nih.gov/compound/44200882

Buy RAD140

Review the laws in your country before ordering.

SMILES; Cc1c(ccc(c1Cl)C#N)N[C@@H](c2nnc(o2)c3ccc(cc3)C#N)[C@H](C)O

InChI=1S/C20H16ClN5O2/c1-11-16(8-7-15(10-23)17(11)21)24-18(12(2)27)20-26-25-19(28-20)14-5-3-13(9-22)4-6-14/h3-8,12,18,24,27H,1-2H3/t12-,18+/m0/s1

InChI Key; XMBUPPIEVAFYHO-KPZWWZAWSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: 2-Chloro-4-({1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile H-NMR

MSDS: 2-Chloro-4-({1-[5-(4-cyanophenyl)-1,3,4-oxadiazol-2-yl]-2-hydroxypropyl}amino)-3-methylbenzonitrile MSDS

Links:

http://www.chemspider.com/Chemical-Structure.26387625.html?rid=a72cb7a1-5b9a-4042-a605-c27fd1d768e7

https://pubchem.ncbi.nlm.nih.gov/compound/44200882

Buy Obeticholic Acid, Online Canadian Research Chemical Supplier,

Review the laws in your country before ordering.

SMILES: Cc1c(c(ccc1N2[C@H]3C[C@@](C[C@H]2CC3)(O)C)C#N)Cl

InChI=1S/C16H19ClN2O/c1-10-14(6-3-11(9-18)15(10)17)19-12-4-5-13(19)8-16(2,20)7-12/h3,6,12-13,20H,4-5,7-8H2,1-2H3/t12-,13-/m1/s1

OUEODVPKPRQETQ-CHWSQXEVSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR 2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methylbenzonitrile

MSDS; MSDS 2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methylbenzonitrile

Links:

http://www.chemspider.com/Chemical-Structure.24633808.html?rid=fa8ddef3-81a6-4b2a-bdbd-d3931f985d02

Review the laws in your country before ordering.

SMILES: Cc1c(c(ccc1N2[C@H]3C[C@@](C[C@H]2CC3)(O)C)C#N)Cl

InChI=1S/C16H19ClN2O/c1-10-14(6-3-11(9-18)15(10)17)19-12-4-5-13(19)8-16(2,20)7-12/h3,6,12-13,20H,4-5,7-8H2,1-2H3/t12-,13-/m1/s1

OUEODVPKPRQETQ-CHWSQXEVSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR 2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methylbenzonitrile

MSDS; MSDS 2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methylbenzonitrile

Links:

http://www.chemspider.com/Chemical-Structure.24633808.html?rid=fa8ddef3-81a6-4b2a-bdbd-d3931f985d02

Review the laws in your country before ordering.

SMILES: Cc1c(c(ccc1N2[C@H]3C[C@@](C[C@H]2CC3)(O)C)C#N)Cl

InChI=1S/C16H19ClN2O/c1-10-14(6-3-11(9-18)15(10)17)19-12-4-5-13(19)8-16(2,20)7-12/h3,6,12-13,20H,4-5,7-8H2,1-2H3/t12-,13-/m1/s1

OUEODVPKPRQETQ-CHWSQXEVSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis: H-NMR 2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methylbenzonitrile

MSDS; MSDS 2-Chloro-4-[(1R,5R)-3-hydroxy-3-methyl-8-azabicyclo[3.2.1]oct-8-yl]-3-methylbenzonitrile

Links:

http://www.chemspider.com/Chemical-Structure.24633808.html?rid=fa8ddef3-81a6-4b2a-bdbd-d3931f985d02

Not available to US customers and other countries where scheduled. Review the laws in your country before ordering.

InChI=1S/C16H14N2O/c1-2-15-17-14-11-7-6-10-13(14)16(19)18(15)12-8-4-3-5-9-12/h3-11H,2H2,1H3

InChI Key; FDLSIWMJFKVWIC-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis;2-Ethyl-3-phenyl-4(3H)-quinazolinone H-NMR (ephinazone)

MSDS;MSDS 2-Ethyl-3-phenyl-4(3H)-quinazolinone

Links for further data on 2-Ethyl-3-phenyl-4(3H)-quinazolinone;

http://www.chemspider.com/Chemical-Structure.628426.html?rid=57e79491-e8e7-43b2-ac86-722a8b45291b

Buy 2-ethyl-3-phenyl-4(3H)-quinazolinone

Not available to US customers and other countries where scheduled. Review the laws in your country before ordering.

InChI=1S/C16H14N2O/c1-2-15-17-14-11-7-6-10-13(14)16(19)18(15)12-8-4-3-5-9-12/h3-11H,2H2,1H3

InChI Key; FDLSIWMJFKVWIC-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis;2-Ethyl-3-phenyl-4(3H)-quinazolinone H-NMR (ephinazone)

MSDS;MSDS 2-Ethyl-3-phenyl-4(3H)-quinazolinone

Links for further data on 2-Ethyl-3-phenyl-4(3H)-quinazolinone;

http://www.chemspider.com/Chemical-Structure.628426.html?rid=57e79491-e8e7-43b2-ac86-722a8b45291b

Buy 2-ethyl-3-phenyl-4(3H)-quinazolinones

Not available to US customers and other countries where scheduled. Review the laws in your country before ordering.

InChI=1S/C16H14N2O/c1-2-15-17-14-11-7-6-10-13(14)16(19)18(15)12-8-4-3-5-9-12/h3-11H,2H2,1H3

InChI Key; FDLSIWMJFKVWIC-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis;2-Ethyl-3-phenyl-4(3H)-quinazolinone H-NMR (ephinazone)

MSDS;MSDS 2-Ethyl-3-phenyl-4(3H)-quinazolinone

Links for further data on 2-Ethyl-3-phenyl-4(3H)-quinazolinone;

http://www.chemspider.com/Chemical-Structure.628426.html?rid=57e79491-e8e7-43b2-ac86-722a8b45291b

Buy 2-ethyl-3-phenyl-4(3H)-quinazolinone

Related to substitution position on the phenyl ring as the 2-Hydroxy on; Salicylmethylecgonine, (2′-Hydroxycocaine) where it increases binding affinity 10 fold. 2-Fluoropipercaine would also have increased binding affinity in relation.  This a Pipercaine (1-methylpiperidin-4-yl benzoate) analog, with similar DAT properties to cocaine in-vitro and also a sodium channel blocker like cocaine. It has a N-methyl-piperidine instead of a tropane ring and the 2-fluoro on the phenyl group.

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C13H16FNO2.ClH/c1-15-8-6-10(7-9-15)17-13(16)11-4-2-3-5-12(11)14;/h2-5,10H,6-9H2,1H3;1H

InChIKey=JBILONPCIZFRJM-UHFFFAOYSA-N

Cl.CN1CCC(CC1)OC(=O)C1=CC=CC=C1F

For research purposes. Not for use in-vivo.

3rd Party Analysis;

MSDS; 2-FluoroPIPERCAINE HCl

2-fluoropipercaine HCl Link:

https://pubchem.ncbi.nlm.nih.gov/compound/12437909

Related to substitution position on the phenyl ring as the 2-Hydroxy on; Salicylmethylecgonine, (2′-Hydroxycocaine) where it increases binding affinity 10 fold. 2-Fluoropipercaine would also have increased binding affinity in relation.  This a Pipercaine (1-methylpiperidin-4-yl benzoate) analog, with similar DAT properties to cocaine in-vitro and also a sodium channel blocker like cocaine. It has a N-methyl-piperidine instead of a tropane ring and the 2-fluoro on the phenyl group.

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C13H16FNO2.ClH/c1-15-8-6-10(7-9-15)17-13(16)11-4-2-3-5-12(11)14;/h2-5,10H,6-9H2,1H3;1H

InChIKey=JBILONPCIZFRJM-UHFFFAOYSA-N

Cl.CN1CCC(CC1)OC(=O)C1=CC=CC=C1F

For research purposes. Not for use in-vivo.

3rd Party Analysis;

MSDS; 2-FluoroPIPERCAINE HCl

2-fluoropipercaine HCl Link:

https://pubchem.ncbi.nlm.nih.gov/compound/12437909

Related to substitution position on the phenyl ring as the 2-Hydroxy on; Salicylmethylecgonine, (2′-Hydroxycocaine) where it increases binding affinity 10 fold. 2-Fluoropipercaine would also have increased binding affinity in relation.  This a Pipercaine (1-methylpiperidin-4-yl benzoate) analog, with similar DAT properties to cocaine in-vitro and also a sodium channel blocker like cocaine. It has a N-methyl-piperidine instead of a tropane ring and the 2-fluoro on the phenyl group.

Not available where scheduled unless permit is provided. Review the laws in your country before ordering.

InChI=1S/C13H16FNO2.ClH/c1-15-8-6-10(7-9-15)17-13(16)11-4-2-3-5-12(11)14;/h2-5,10H,6-9H2,1H3;1H

InChIKey=JBILONPCIZFRJM-UHFFFAOYSA-N

Cl.CN1CCC(CC1)OC(=O)C1=CC=CC=C1F

For research purposes. Not for use in-vivo.

3rd Party Analysis;

MSDS; 2-FluoroPIPERCAINE HCl

2-fluoropipercaine HCl Link:

https://pubchem.ncbi.nlm.nih.gov/compound/12437909

Review the laws in your country before ordering.

SMILES; CCC(C)(C)OC(=O)N

InChI=1S/C6H13NO2/c1-4-6(2,3)9-5(7)8/h4H2,1-3H3,(H2,7,8)

InChI Key; AUQKXXDHDKEBEY-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis:(2-methylbutan-2-yl)carbamate

MSDS;MSDS (2-methylbutan-2-yl) carbamate

Links for further data on 2-Methyl-2-butanyl carbamate;

http://www.chemspider.com/Chemical-Structure.61808.html?rid=8f376c14-1c61-4034-b141-3eacaf7a1d8a

https://pubchem.ncbi.nlm.nih.gov/compound/68533

Review the laws in your country before ordering.

SMILES; CCC(C)(C)OC(=O)N

InChI=1S/C6H13NO2/c1-4-6(2,3)9-5(7)8/h4H2,1-3H3,(H2,7,8)

InChI Key; AUQKXXDHDKEBEY-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis:(2-methylbutan-2-yl)carbamate

MSDS;MSDS (2-methylbutan-2-yl) carbamate

Links for further data on 2-Methyl-2-butanyl carbamate;

http://www.chemspider.com/Chemical-Structure.61808.html?rid=8f376c14-1c61-4034-b141-3eacaf7a1d8a

https://pubchem.ncbi.nlm.nih.gov/compound/68533

Review the laws in your country before ordering.

SMILES; CCC(C)(C)OC(=O)N

InChI=1S/C6H13NO2/c1-4-6(2,3)9-5(7)8/h4H2,1-3H3,(H2,7,8)

InChI Key; AUQKXXDHDKEBEY-UHFFFAOYSA-N

For research purposes. Not for use in-vivo.

3rd Party Analysis:(2-methylbutan-2-yl)carbamate

MSDS;MSDS (2-methylbutan-2-yl) carbamate

Links for further data on 2-Methyl-2-butanyl carbamate;

http://www.chemspider.com/Chemical-Structure.61808.html?rid=8f376c14-1c61-4034-b141-3eacaf7a1d8a

https://pubchem.ncbi.nlm.nih.gov/compound/68533

10.0g of 2-Methyl-2-propyl-1,3-propanediol

Not available where scheduled. Review the laws in your country before ordering.

InChI=1S/C7H16O2/c1-3-4-7(2,5-8)6-9/h8-9H,3-6H2,1-2H3
InChIKey: JVZZUPJFERSVRN-UHFFFAOYSA-N
SMILES: CCCC(C)(CO)CO

Research chemical for study that is the alcohol that is used to make the carbamates; Meprobamate & Carisoprodol. A very nice addition for versatile use in synthesis and other laboratory research uses/studies.

For research purposes. Not for use in-vivo.

MSDS:

LINK:

https://pubchem.ncbi.nlm.nih.gov/compound/66220

Buy lysergamides - 40mg - L1P (N-1-propyl Lysergamide)

.LAMPA Analog for comparative for this lysergamide and others, for whatever the study is, from correlations of different length N-alkyl chains on the amide, cyclic groups of the same number of carbons, etc. This one is quite a special, relatively unstudied chemical for research.

OC(=O)C=CC(O)=O.CCCNC(=O)C1CN(C)C2CC3=CNC4=C3C(=CC=C4)C2=C1

InChI=1/C19H23N3O.C4H4O4/c1-3-7-20-19(23)13-8-15-14-5-4-6-16-18(14)12(10-21-16)9-17(15)22(2)11-13;5-3(6)1-2-4(7)8/h4-6,8,10,13,17,21H,3,7,9,11H2,1-2H3,(H,20,23);1-2H,(H,5,6)(H,7,8)/b;2-1+

InChIKey=DIPLDPQMHFBDNW-WLHGVMLRNA-N

For research purposes only and not for use in vivo.

HNMR:

MSDS:

example /no other links found;
https://pubchem.ncbi.nlm.nih.gov/compound/139024833

40mg - LAMPA (N-methyl-N-propyl Lysergamide)

SMILES: CCCN(C)C(=O)[C@H]1CN([C@@H]2CC3=CNC4=CC=CC(=C34)C2=C1)C

InChI=1S/C20H25N3O/c1-4-8-22(2)20(24)14-9-16-15-6-5-7-17-19(15)13(11-21-17)10-18(16)23(3)12-14/h5-7,9,11,14,18,21H,4,8,10,12H2,1-3H3/t14-,18-/m1/s1

InChIKey=CZRJGQXHVRNZRZ-RDTXWAMCSA-N

For research purposes only and not for use in vivo.

HNMR:

MSDS:

https://pubchem.ncbi.nlm.nih.gov/compound/13932543
https://www.chemspider.com/Chemical-Structure.32675221.html

40mg N-pyrrolidinyl lysergamide (hemifumarate) (LDP-824/ LSD-25-pyrrolidate/ LAPy)

..."The two ethyl groups were incorporated into ring structures such as the pyrrolidide, piperidide, and morpholide, shown above, but these also had reduced anti-serotonin and psychedelic effects (Cerletti and Doepfner 1958). Although the morpholide had less than one-tenth of the potency of LSD in blocking the action of serotonin, it did however have nearly 75% of the potency of LSD as a psychedelic (Gogerty and Dille 1957).

For lysergic acid amides where only one alkyl chain was attached (e.g. lysergic acid monoethylamide), relative antiserotonin activity was related to the length of the alkyl chain. Activity increased with chain length to a maximum of 75% of the potency of LSD with the n-pentylamide (five carbon atoms in a chain) (Cerletti and Doepfner 1958)."...

Ref.: Nichols, LSD and Its Lysergamide Cousins (https://www.heffter.org/wp-content/uploads/2020/04/chap6.pdf)

CN1CC(C=C2C1CC1=CNC3=C1C2=CC=C3)C(=O)N1CCCC1

InChI=1/C20H23N3O/c1-22-12-14(20(24)23-7-2-3-8-23)9-16-15-5-4-6-17-19(15)13(11-21-17)10-18(16)22/h4-6,9,11,14,18,21H,2-3,7-8,10,12H2,1H3

InChIKey=SETDYMMXQQXCRP-UHFFFAOYNA-N

For research purposes only and not for use in vivo.

HNMR: There is water in the DMSO-d6 used to dissolve the sample and pulling it in, it seemed to have made the water 3.3 peak quite large and the sample is dry. Where the peaks are, they are proportional and symmetrical and the compound identified/confirmed correct. Just a confirmatory analysis...we used our own custom synthesis procedure we developed that we became good at and consistent with.

MSDS:

LINKS:

https://pubchem.ncbi.nlm.nih.gov/compound/200628

Buy 40mg of LSP / N-3-amyl lysergamide freebase, as tan solid/powder - pure Lysergamide, H-NMR tested and approved

InChI=1S/C21H27N3O/c1-4-15(5-2)23-21(25)14-9-17-16-7-6-8-18-20(16)13(11-22-18)10-19(17)24(3)12-14/h6-9,11,14-15,19,22H,4-5,10,12H2,1-3H3,(H,23,25)

ZQONRMXCBQXYCK-UHFFFAOYSA-N

CCC(CC)NC(=O)C1CN(C2CC3=CNC4=CC=CC(=C34)C2=C1)C

For research purposes only and not for use in vivo.

In the rotovap. drying as final product to be sold;

HNMR:

MSDS:

Links:

https://pubchem.ncbi.nlm.nih.gov/compound/10019984

http://www.chemspider.com/Chemical-Structure.8195557.html