NSC19005 structure, CAS 5452-87-9

NSC19005

CAS Number5452-87-9

SynonymsN-methyl-2-pyridin-2-yl-N-(2-pyridin-2-ylethyl)ethanamine; NSC19005

Molecular FormulaC15H19N3

Molecular Weight241.33100

Purity98%%

Density1.067g/cm3

Boiling Point371.9ºC at 760mmHg

Melting Point

Flash Point

Appearancelight yellow solid

EINECS

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Symbol

Signal Word

Cat. No.: 2A-1170704 Purity: 98%%
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Quality Control of [ 5452-87-9 ] Purity: 98%% SDS Specification MoL

Chemical & Physical Properties
CAS Number5452-87-9
Catalog No.2A-1170704
Chinese NameN-甲基-N,N-双(2-吡啶基乙基)胺
SynonymsN-methyl-2-pyridin-2-yl-N-(2-pyridin-2-ylethyl)ethanamine; NSC19005
Molecular FormulaC15H19N3
Molecular Weight241.33100
Purity98%
Density1.067g/cm3
Boiling Point371.9ºC at 760mmHg
Appearancelight yellow solid
Storage Condition-20℃
ApplicationBetahistine EP Impurity C (NSC19005) is an impurity of Betahistine. Betahistine is an orally active histamine H1 receptor agonist and H3 receptor antagonist studied in rheumatoid arthritis (RA).
HTC2933399090
PubChem ID81958
SMILESCN(CCc1ccccn1)CCc1ccccn1
InChIInChI=1S/C15H19N3/c1-18(12-8-14-6-2-4-10-16-14)13-9-15-7-3-5-11-17-15/h2-7,10-11H,8-9,12-13H2,1H3
InChI KeyPQHKIDBZBKQYMR-UHFFFAOYSA-N
Use ofBetahistine EP Impurity C (NSC19005) is an impurity of Betahistine[1]. Betahistine is a potent, orally active and well-tolerated histamine H1 receptor agonist and H3 receptor antagonist used for the study of rheumatoid arthritis (RA)[2][3]. Properties Name N-Methyl-N,N-bis(2-pyridylethyl)amine Synonym More Synonyms Betahistine EP Impurity C Biological Activity Description Betahistine EP Impurity C (NSC19005) is an impurity of Betahistine[1]. Betahistine is a potent, orally active and well-tolerated histamine H1 receptor agonist and H3 receptor antagonist used for the study of rheumatoid arthritis (RA)[2][3]. Related Catalog Signaling Pathways >> Immunology/Inflammation >> Histamine Receptor Research Areas >> Inflammation/Immunology Signaling Pathways >> GPCR/G Protein >> Histamine Receptor In Vitro Betahistine (0-10 μM) inhibits [125I]iodoproxyfan binding to membranes of CHO (rH3(445)R) and CHO (hH3(445)R) cells with IC50 values of 1.9 μM and 3.3 μM, respectively. Lead to Ki values of 1.4 μM and 2.5 μM, respectively[3]. References [1]. Murilo B. M. de Mello, et al. Characterization and in silico Mutagenic Assessment of a New Betahistine Degradation Impurity. J. Braz. Chem. Soc. vol.30 no.7 São Paulo July 2019 Epub July 04, 2019 [2]. Poyurovsky M, et al. The effect of betahistine, a histamine H1 receptor agonist/H3 antagonist, on olanzapine-induced weight gain in first-episode schizophrenia patients. Int Clin Psychopharmacol. 2005 Mar;20(2):101-3. [3]. Betahistine EP Impurity C (NSC19005) is an impurity of Betahistine[1]. Betahistine is a potent, orally active and well-tolerated histamine H1 receptor agonist and H3 receptor antagonist used for the study of rheumatoid arthritis (RA)[2]. Chemical & Physical Properties Molecular Formula C15H19N3 Exact Mass 241.15800 PSA 29.02000 LogP 2.19360 Index of Refraction 1.568 InChIKey PQHKIDBZBKQYMR-UHFFFAOYSA-N Storage condition -20℃ Safety Information HS Code 2933399090
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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