Chlorpheniramine Related Compound C

USP/1123146 - United States Pharmacopeia (USP) Reference Standard

Synonym: 3-(4-Chlorophenyl)-N-methyl-3-(pyridin-2-yl)propan-1-amine maleate salt

CAS Number: 22630-25-7
Empirical Formula (Hill Notation): C₁₅H₁₇ClN₂ · C₄H₄O₄
Molecular Weight: 376.83
Linear Formula: C₁₅H₁₇ClN₂ · C₄H₄O₄
Product Type: Chemical

Catalog Number	PKG Qty.	Price	Quantity


45-1123146-10MG	10 mg	$2270.00 1/EA		Add To Favorites

Properties
Descriptions
Safety Info.
Basic Data

API family	chlorpheniramine
application(s)	pharmaceutical (small molecule)
format	neat
grade	pharmaceutical primary standard
InChI	1S/C15H17ClN2.C4H4O4/c1-17-11-9-14(15-4-2-3-10-18-15)12-5-7-13(16)8-6-12;5-3(6)1-2-4(7)8/h2-8,10,14,17H,9,11H2,1H3;1-2H,(H,5,6)(H,7,8)/b;2-1-
InChI key	MGNXGZAZRYTQMW-BTJKTKAUSA-N
manufacturer/tradename	USP
storage temp.	2-8°C

Analysis Note:	These products are for test and assay use only. They are not meant for administration to humans or animals and cannot be used to diagnose, treat, or cure diseases of any kind.
Application:	Central nervous system research: Chlorpheniramine Related Compound C is examined for its effects on the central nervous system, specifically regarding histamine-related responses, providing insights for antihistamine development and neurological research (Kamei, 2021 ). Virucidal research applications: The virucidal effects of Chlorpheniramine Related Compound C against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are studied, demonstrating potential applications in pandemic response and viral research (Westover et al., 2020 ). Bitter taste receptor research: Investigations into the effects of Chlorpheniramine Related Compound C on the expression of bitter taste receptor T2R7 and its signaling effectors in cellular models contribute to the understanding of taste perception and receptor activation mechanisms (Su et al., 2019 ). Synthesis and evaluation of antihistaminic agents: Chlorpheniramine Related Compound C plays a role in the design and synthesis of new chemical entities aiming for improved antihistaminic and antiasthmatic properties, enhancing pharmaceutical innovations and therapeutic strategies (Sirisha et al., 2014 ). Mast cell degranulation and histamine release: The compound′s involvement in studying the biological mechanisms of pain and edema induced by venom illustrates its utility in pharmacological and toxicological research, highlighting its role in elucidating histamine pathways (Liu et al., 2007 ).
General description:	This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia .
Other Notes:	Sales restrictions may apply.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point(F)	Not applicable
Flash Point(C)	Not applicable

Storage Temp.	2-8°C
UNSPSC	41116107

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