Carbinoxamine maleate structure, CAS 3505-38-2

Carbinoxamine maleate

CAS Number3505-38-2

SynonymsCarbinoxamine maleate salt; CarbinoxamineMaleateSalt; MFCD00082461; (Z)-but-2-enedioic acid,2-[(4-chlorophenyl)-pyridin-2-ylmethoxy]-N,N-dimethylethanamine; Carbinoxamine Maleate; EINECS 222-498-0

Molecular FormulaC20H23ClN2O5

Molecular Weight406.86

Purity98.00%

Density

Boiling Point381.1ºC at 760 mmHg

Melting Point116-118ºC

Flash Point

Appearanceoff-white solid

EINECS

MSDSChineseEnglish

Symbol6.1(b)

Signal WordWarning

Cat. No.: 2A-9029880 Purity: 98.00%
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Quality Control of [ 3505-38-2 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number3505-38-2
Catalog No.2A-9029880
Chinese Name马来酸卡比沙明
SynonymsCarbinoxamine maleate salt; CarbinoxamineMaleateSalt; MFCD00082461; (Z)-but-2-enedioic acid,2-[(4-chlorophenyl)-pyridin-2-ylmethoxy]-N,N-dimethylethanamine; Carbinoxamine Maleate; EINECS 222-498-0
Molecular FormulaC20H23ClN2O5
Molecular Weight406.86
Purity98.00
Boiling Point381.1ºC at 760 mmHg
Melting Point116-118ºC
Appearanceoff-white solid
Water SolubilityWater solubility: completely soluble; easily solub
Storage ConditionThe warehouse is ventilated and dried at low tempe
PackagingIII
ApplicationCarbinoxamine maleate salt is an antagonist of histamine H1 receptors.
HTC2933399090
PubChem ID329749235
SMILESCN(C)CCOC(c1ccc(Cl)cc1)c1ccccn1.O=C(O)C=CC(=O)O
InChIInChI=1S/C16H19ClN2O.C4H4O4/c1-19(2)11-12-20-16(15-5-3-4-10-18-15)13-6-8-14(17)9-7-13;5-3(6)1-2-4(7)8/h3-10,16H,11-12H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1-
InChI KeyGVNWHCVWDRNXAZ-BTJKTKAUSA-N
Hazard Symbols6.1(b)
BioactivityCarbinoxamine maleate salt is a histamine H1 receptor antagonist. Related Catalog Signaling Pathways >> GPCR/G Protein >> Histamine Receptor Signaling Pathways >> Immunology/Inflammation >> Histamine Receptor Research Areas >> Neurological Disease Target histamine H1 receptor[1] References [1]. Harikrishnan A, et al. The cooperative effect of Lewis pairs in the Friedel-Crafts hydroxyalkylation reaction: a simple and effective route for the synthesis of (±)-carbinoxamine. Org Biomol Chem. 2015 Mar 28;13(12):3633-47. Chemical & Physical Properties Boiling Point 381.1ºC at 760 mmHg Melting Point 116-118ºC Molecular Formula C20H23ClN2O5 Molecular Weight 406.86000 Flash Point 184.3ºC Exact Mass 406.13000 PSA 99.96000 LogP 3.11440 InChIKey GVNWHCVWDRNXAZ-BTJKTKAUSA-N SMILES CN(C)CCOC(c1ccc(Cl)cc1)c1ccccn1.O=C(O)C=CC(=O)O
Use ofCarbinoxamine maleate salt is a histamine H1 receptor antagonist. Properties Articles17 Name carbinoxamine maleate Synonym More Synonyms Carbinoxamine maleate salt Biological Activity Description Carbinoxamine maleate salt is a histamine H1 receptor antagonist. Related Catalog Signaling Pathways >> GPCR/G Protein >> Histamine Receptor Signaling Pathways >> Immunology/Inflammation >> Histamine Receptor Research Areas >> Neurological Disease histamine H1 receptor[1] References [1]. Harikrishnan A, et al. The cooperative effect of Lewis pairs in the Friedel-Crafts hydroxyalkylation reaction: a simple and effective route for the synthesis of (±)-carbinoxamine. Org Biomol Chem. 2015 Mar 28;13(12):3633-47. Chemical & Physical Properties Exact Mass 406.13000 PSA 99.96000 LogP 3.11440 InChIKey GVNWHCVWDRNXAZ-BTJKTKAUSA-N
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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