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· · COA & SDS disponible pour chaque produit · Expédition le jour même sur les articles en stock Chlorphénoxamine - ≥98% , Histamine H1 receptor antagonist, CAS No.77-38-3, Histamine H1 receptor antagonist
Synonyms
AS-76607 | Contristamine | p-Chlor-alpha-methyl-diphenhydramin [German] | 4-06-00-04717 (Beilstein Handbook Reference) | Clorfenossamina [DCIT] | 2-[1-(4-chlorophenyl)-1-phenyl-ethoxy]-N,N-dimethyl-ethanamine | 2-[1-(4-Chlorophenyl)-1-phenylethoxy]-N,N-di
Storage
A conserver entre 2 et 8°C
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping A conserver entre 2 et 8°C Ships Glace humide Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Vue d’ensemble La chlorphénoxamine est un antihistaminique et un anticholinergique utilisé comme agent antiprurigineux et antiparkinsonien
Specifications Synonymes
AS-76607 | Contristamine | p-Chlor-alpha-methyl-diphenhydramin [German] | 4-06-00-04717 (Beilstein Handbook Reference) | Clorfenossamina [DCIT] | 2-[1-(4-chlorophenyl)-1-phenyl-ethoxy]-N,N-dimethyl-ethanamine | 2-[1-(4-Chlorophenyl)-1-phenylethoxy]-N,N-di
Spécifications et pureté
≥98%
Conditions de stockage de stockage
A conserver entre 2 et 8°C
Mécanisme d'action
Histamine H1 receptor antagonist
Propriétés du produit Noms et identifiants Pubchem Sid 488180072 Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180072 Sourires canoniques CC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)OCCN(C)C IUPAC Name 2-[1-(4-chlorophenyl)-1-phenylethoxy]-N,N-dimethylethanamine InChIKey KKHPNPMTPORSQE-UHFFFAOYSA-N INCHI 1S/C18H22ClNO/c1-18(21-14-13-20(2)3,15-7-5-4-6-8-15)16-9-11-17(19)12-10-16/h4-12H,13-14H2,1-3H3 Isomères SMILES CC(C1=CC=CC=C1)(C2=CC=C(C=C2)Cl)OCCN(C)C Poids moléculaire 303.83 Reaxy-Rn 2057618 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2057618&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Benzenoids Classe Benzene and substituted derivatives Subclass Diphenylmethanes Intermediate Tree Nodes Not available Direct Parent Diphenylmethanes Alternative Parents Benzylethers Chlorobenzenes Aryl chlorides Trialkylamines Dialkyl ethers Organopnictogen compounds Organochlorides Hydrocarbon derivatives Molecular Framework Aromatic homomonocyclic compounds Substituents Diphenylmethane - Benzylether - Chlorobenzene - Halobenzene - Aryl chloride - Aryl halide - Tertiary aliphatic amine - Tertiary amine - Ether - Dialkyl ether - Organochloride - Organohalogen compound - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Structure 3D Cibles associées (humaines) Cibles associées (non humaines) Mécanismes d'action Certificats (CoA, COO, BSE/TSE et tableau d'analyse) Propriétés chimiques et physiques Solubilité DMSO : ≥ 48 mg/mL (157.98 mM) Poids moléculaire 303.800 g/mol XLogP3 4.100 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 6 Exact Mass 303.139 Da Monoisotopic Mass 303.139 Da Topological Polar Surface Area 12.500 Ų Heavy Atom Count 21 Formal Charge 0 Complexity 296.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 1 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 1
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