NSC-7661
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    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H591575

CAS#: 90-41-5

Description: NSC-7661, also known as 2-Biphenylamine is a is a substrate for UGTs (UDP-glucuronosyltransferases), including UGT1A4, UGT2B13 and UGT2B16.


Chemical Structure

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NSC-7661
CAS# 90-41-5

Theoretical Analysis

Hodoodo Cat#: H591575
Name: NSC-7661
CAS#: 90-41-5
Chemical Formula: C12H11N
Exact Mass: 169.09
Molecular Weight: 169.227
Elemental Analysis: C, 85.17; H, 6.55; N, 8.28

Price and Availability

Size Price Availability Quantity
5g USD 250 2 Weeks
10g USD 350 2 Weeks
25g USD 450 2 Weeks
100g USD 850 2 Weeks
500g USD 1950 2 Weeks
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Synonym: 2-Biphenylamine; NSC 7661; NSC-7661; NSC7661; 2-Aminobiphenyl; 2-ABP;

IUPAC/Chemical Name: 2-Biphenylamine;

InChi Key: TWBPWBPGNQWFSJ-UHFFFAOYSA-N

InChi Code: InChI=1S/C12H11N/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H,13H2

SMILES Code: NC1=CC=CC=C1C2=CC=CC=C2

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 169.23 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Madawala H, Sabaragamuwe SG, Elangovan S, Kim J. In Situ Measuring Partition Coefficient at Intact Nanoemulsions: A New Application of Single-Entity Electrochemistry. Anal Chem. 2021 Jan 19;93(2):1154-1160. doi: 10.1021/acs.analchem.0c04205. Epub 2020 Dec 8. PMID: 33290054.


2: Sabaragamuwe SG, Madawala H, Puri SR, Kim J. Towards ultralow detection limits of aromatic toxicants in water using pluronic nanoemulsions and single- entity electrochemistry. Anal Chim Acta. 2020 Dec 1;1139:129-137. doi: 10.1016/j.aca.2020.09.053. Epub 2020 Sep 29. PMID: 33190695.


3: Fischer O, Hofmann J, Rampp H, Kaindl J, Pratsch G, Bartuschat A, Taudte RV, Fromm MF, Hübner H, Gmeiner P, Heinrich MR. Regiospecific Introduction of Halogens on the 2-Aminobiphenyl Subunit Leading to Highly Potent and Selective M3 Muscarinic Acetylcholine Receptor Antagonists and Weak Inverse Agonists. J Med Chem. 2020 Apr 23;63(8):4349-4369. doi: 10.1021/acs.jmedchem.0c00297. Epub 2020 Apr 9. PMID: 32202101.


4: Rama RJ, Maya C, Nicasio MC. Dialkylterphenyl Phosphine-Based Palladium Precatalysts for Efficient Aryl Amination of N-Nucleophiles. Chemistry. 2020 Jan 22;26(5):1064-1073. doi: 10.1002/chem.201903279. Epub 2020 Jan 16. PMID: 31743505.


5: Belai N, White SR. Determination of Unsulfonated Aromatic Amines in FD&C Yellow No. 5 and FD&C Yellow No. 6 by Liquid Chromatography-Triple Quadrupole Mass Spectrometry. J AOAC Int. 2019 Mar 1;102(2):580-589. doi: 10.5740/jaoacint.18-0165. Epub 2018 Oct 10. PMID: 30305202.


6: Mazumder S, Ahamed RA, McGahee E, Wang L, Seyler TH. A New Automated Method for the Analysis of Aromatic Amines in Human Urine by GC-MS/MS. J Anal Toxicol. 2019 Jan 1;43(1):25-35. doi: 10.1093/jat/bky045. PMID: 30010885; PMCID: PMC6330153.


7: Takekuma Y, Ishizaka H, Sumi M, Sato Y, Sugawara M. Difference in the Dissolution Behaviors of Tablets Containing Polyvinylpolypyrrolidone (PVPP) Depending on Pharmaceutical Formulation After Storage Under High Temperature and Humid Conditions. J Pharm Pharm Sci. 2016 Oct-Dec;19(4):511-519. doi: 10.18433/J3HW3Q. PMID: 28057169.


8: Khan S, Adhikari DK, Gupta S, Gupta N. High-level expression, purification and characterization of carbazole dioxygenase, a three components dioxygenase, of Pseudomonas GBS.5. Biotechnol Lett. 2015 Oct;37(10):1945-52. doi: 10.1007/s10529-015-1876-3. Epub 2015 Jul 5. PMID: 26142698.


9: Suzuki C, Hirano K, Satoh T, Miura M. Direct synthesis of N-H carbazoles via iridium(III)-catalyzed intramolecular C-H amination. Org Lett. 2015 Mar 20;17(6):1597-600. doi: 10.1021/acs.orglett.5b00502. Epub 2015 Mar 11. PMID: 25760543.


10: Weinstein AB, Stahl SS. Palladium Catalyzed Aryl C-H Amination with O2 via In Situ Formation of Peroxide-Based Oxidant(s) from Dioxane. Catal Sci Technol. 2014 Dec 1;4(12):4301-4307. doi: 10.1039/C4CY00764F. PMID: 25530837; PMCID: PMC4270377.


11: Hendron E, Wang X, Zhou Y, Cai X, Goto J, Mikoshiba K, Baba Y, Kurosaki T, Wang Y, Gill DL. Potent functional uncoupling between STIM1 and Orai1 by dimeric 2-aminodiphenyl borinate analogs. Cell Calcium. 2014 Dec;56(6):482-92. doi: 10.1016/j.ceca.2014.10.005. Epub 2014 Oct 23. PMID: 25459299; PMCID: PMC4314399.


12: Zhang HH, Dong J, Hu QS. tBu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complex As Precatalyst for Pd-Catalyzed Coupling Reactions of Aryl Halides with Polyfluoroarenes via C-H Activation Strategy. European J Org Chem. 2014 Feb 1;2014(6):1327-1332. doi: 10.1002/ejoc.201301272. PMID: 24778575; PMCID: PMC4000033.


13: Bruno NC, Niljianskul N, Buchwald SL. N-substituted 2-aminobiphenylpalladium methanesulfonate precatalysts and their use in C-C and C-N cross-couplings. J Org Chem. 2014 May 2;79(9):4161-6. doi: 10.1021/jo500355k. Epub 2014 Apr 18. PMID: 24724692; PMCID: PMC4017611.


14: Chen LC, Chueh TC, Tuan YF, Chen CC, Chien CC, Lee HY, Chen SC. Activation of MAPK pathways and downstream transcription factors in 2-aminobiphenyl-induced apoptosis. Environ Toxicol. 2015 Feb;30(2):205-11. doi: 10.1002/tox.21886. Epub 2013 Jul 8. PMID: 23836369.


15: Czerwinski CJ, Fetisov EO, Gloriozov IP, Oprunenko YF. DFT study of intramolecular interring η6,η6-haptotropic rearrangements in tricarbonylchromium complexes of 2-aminobiphenyl and 4-aminobiphenyl. Dalton Trans. 2013 Aug 7;42(29):10487-94. doi: 10.1039/c3dt50655j. PMID: 23752476.


16: Zhang HH, Xing CH, Tsemo GB, Hu QS. t-Bu3P-Coordinated 2-Phenylaniline-Based Palladacycle Complex as a Precatalyst for the Suzuki Cross-coupling Polymerization of Aryl Dibromides with Aryldiboronic Acids. ACS Macro Lett. 2013 Jan 15;2(1):10-13. doi: 10.1021/mz300479b. PMID: 23687619; PMCID: PMC3653593.


17: Bruno NC, Tudge MT, Buchwald SL. Design and Preparation of New Palladium Precatalysts for C-C and C-N Cross-Coupling Reactions. Chem Sci. 2013;4:916-920. doi: 10.1039/C2SC20903A. PMID: 23667737; PMCID: PMC3647481.


18: Pratsch G, Wallaschkowski T, Heinrich MR. The Gomberg-Bachmann reaction for the arylation of anilines with aryl diazotates. Chemistry. 2012 Sep 10;18(37):11555-9. doi: 10.1002/chem.201200430. Epub 2012 Aug 6. PMID: 22887751.


19: Chen CC, Cheng YY, Chen SC, Tuan YF, Chen YJ, Chen CY, Chen LC. Cyclooxygenase-2 expression is up-regulated by 2-aminobiphenyl in a ROS and MAPK-dependent signaling pathway in a bladder cancer cell line. Chem Res Toxicol. 2012 Mar 19;25(3):695-705. doi: 10.1021/tx2004689. Epub 2012 Feb 15. PMID: 22288910.


20: Czerwinski CJ, Guzei IA, Riggle KM, Schroeder JR, Spencer LC. Haptotropic rearrangement in tricarbonylchromium complexes of 2-aminobiphenyl and 4-aminobiphenyl. Dalton Trans. 2011 Oct 7;40(37):9439-46. doi: 10.1039/c1dt10994d. Epub 2011 Aug 16. PMID: 21847474.