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Dexchlorpheniramine Maleate

Dexchlorpheniramine Maleate Structure
CAS No.
2438-32-6
Chemical Name:
Dexchlorpheniramine Maleate
Synonyms
Polamin;Phenamin;Sensidyn;polaramin;Polaramine;d-Form maleate;poraminemaleate;polaraminemaleate;D-CHLORPHENIRAMINE MALEATE;Chlorpheniramine d-maleate
CBNumber:
CB8392741
Molecular Formula:
C20H23ClN2O4
Molecular Weight:
390.86
MOL File:
2438-32-6.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:32

Dexchlorpheniramine Maleate Properties

Melting point 112-115 °C(lit.)
alpha D25 +44.3° (c = 1 in dimethylformamide)
storage temp. 2-8°C
solubility Very soluble in water, freely soluble in ethanol (96 per cent), in methanol and in methylene chloride.
form Solid
color White to off-white
PH pH(10g/l, 25℃) : 4.0~5.0
Merck 13,2198

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H301
Precautionary statements  P301+P330+P331+P310
Hazard Codes  T
Risk Statements  25
Safety Statements  36/37/39-45
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  US6504000
HS Code  2933399090
NFPA 704
0
2 0

Dexchlorpheniramine Maleate price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) C4915 S-(+)-Chlorpheniramine maleate salt 2438-32-6 1G ₹9082.18 2022-06-14 Buy
Sigma-Aldrich(India) PHR2803 Dexchlorpheniramine Maleate 2438-32-6 500MG ₹15360.68 2022-06-14 Buy
Sigma-Aldrich(India) C4915 S-(+)-Chlorpheniramine maleate salt 2438-32-6 5G ₹35538.48 2022-06-14 Buy
Product number Packaging Price Buy
C4915 1G ₹9082.18 Buy
PHR2803 500MG ₹15360.68 Buy
C4915 5G ₹35538.48 Buy

Dexchlorpheniramine Maleate Chemical Properties,Uses,Production

Description

Dexchlorpheniramine Maleate is the maleate salt form of dexchlorpheniramine, an alkylamine, and first-generation histamine antagonist with anti-allergic activity. Dexchlorpheniramine maleate competitively blocks H1 receptors, thereby preventing the actions of histamine on bronchial smooth muscle, capillaries and gastrointestinal (GI) smooth muscle. This prevents histamine-induced bronchoconstriction, vasodilation, increased capillary permeability, and GI smooth muscle spasms.

Chemical Properties

Dexchlorpheniramine maleate is a white, odourless, crystalline powder which in aqueous solution has a pH of between 4 and 5. It is freely soluble in water, soluble in alcohol and in chloroform, but only slightly soluble in benzene or ether.

Uses

Dexchlorpheniramine is an antihistamine used to relieve symptoms of allergy, hay fever, and the common cold. Polaramine (dexchlorpheniramine maleate) is the dextro-isomer of chlorpheniramine maleate and the S-enantiomer of Chlorpheniramine. It is an antihistamine with anticholinergic properties. S-(+)-Chlorpheniramine maleate salt has been used to study the anticholinergic effect of Achillea millefolium and Portulaca olerace on muscarinic receptors of guinea pig tracheal smooth muscle.

General Description

Dexchlorpheniramine(Polaramine) is the dextrorotatory enantiomer of chlorpheniramine.In vitro and in vivo studies of the enantiomers ofchlorpheniramine showed that the antihistaminic activity existspredominantly in the dextro isomer. As mentioned previously,the dextro isomer has the (S) configuration, which issuperimposable on the (S) configuration of the more activelevorotatory enantiomer of carbinoxamine.

Mode of action

Dexchlorpheniramine, the d-isomer of the racemic compound chlorpheniramine, is two times more active than chlorpheniramine. Dexchlorpheniramine does not prevent the release of histamine, but rather, competes with free histamine for binding at the H1-receptor sites, and competitively antagonizes the effects of histamine on H1- receptors in the GI tract, uterus, large blood vessels, and bronchial muscle. Blockade of H1-receptors also suppresses the formation of oedema, flare, and pruritus that result from histaminic activity. Since dexchlorpheniramine binds to central and peripheral H1-receptors, sedative effects are likely to occur. H1- antagonists are structurally similar to anticholinergic agents and therefore possess the potential to exhibit anticholinergic properties of varying degrees. They also have antipruritic effects. Dexchlorpheniramine has high antihistaminic activity, moderate anticholinergic effects and minimal sedative effects. The medicine does not possess antiemetic properties.

References

[1] P. E. CHAVES. Assessment of cytotoxicity, genotoxicity, and mutagenicity of the dexchlorpheniramine reference standard and pharmaceutical formula in human peripheral blood mononuclear cells[J]. Brazilian Journal of Pharmaceutical Sciences, 2022, 18 1. DOI:10.1590/s2175-97902022e20096.
[2] GUSTAVO FACCHINI MSC. Ultraviolet A photosensitivity profile of dexchlorpheniramine maleate and promethazine-based creams: Anti-inflammatory, antihistaminic, and skin barrier protection properties[J]. Journal of Cosmetic Dermatology, 2017, 16 4: e59-e67. DOI:10.1111/jocd.12349.
[3] MASAAKI TAGAWA. Neuroimaging of histamine H1-receptor occupancy in human brain by positron emission tomography (PET): a comparative study of ebastine, a second-generation antihistamine, and (+)-chlorpheniramine, a classical antihistamine.[J]. British journal of clinical pharmacology, 2001, 52 5 1: 501-509. DOI:10.1046/J.1365-2125.2001.01471.X.
[4] DONG LIANG. Identification of anthelmintic parbendazole as a therapeutic molecule for HNSCC through connectivity map-based drug repositioning[J]. Acta Pharmaceutica Sinica B, 2022, 12 5: Pages 2429-2442. DOI:10.1016/j.apsb.2021.12.005.

Dexchlorpheniramine Maleate Preparation Products And Raw materials

Raw materials

Preparation Products

Dexchlorpheniramine Maleate Suppliers

Global( 141)Suppliers
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Halcyon Labs Pvt. Ltd +919833750169 Mumbai, India 17 58 Inquiry
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Mahrshee Laboratories Pvt Ltd +91-9824100314 +91-9227402952 Gujarat, India 63 58 Inquiry
(+)-CHLORPHENIRAMINE MALEATE SALT DEXCHLOROPHENIRAMINE MALEATE DEXCHLORPHENIRAMINE MALEATE D-CHLORPHENIRAMINE MALEATE GAMMA-[4-CHLOROPHENYL]-N,N-DIMETHYL-2-PYRIDINEPROPANAMINE MALEATE SALT (+)-2-(p-chloro-alpha-(2-(dimethylamino)ethyl)benzyl)pyridinemaleate (Z)-but-2-enedioic acid,(3S)-3-(4-chlorophenyl)-N,N-dimethyl-3-pyridin-2-ylpropan-1-amine (s)-(+)-chlorpheniraminemaleate dextrochlorpheniraminemaleate g-(4-chlorophenyl)-N,N-dimethyl-2-pyridinepropanaminemaleate polaramin polaraminemaleate poraminemaleate pyridine,2-(p-chloro-alpha-(2-(dimethylamino)ethyl)benzyl)-,maleate(1:1),(+ γ-(4-Chlorophenyl)-N,N-dimethyl-2-pyridinepropanamine d-Form maleate s-(+)-chlorpheniraminemaleate [gamma-(4-chlorophenyl)-pyridine-2-propyl](dimethyl)ammonium hydrogen (Z)-maleate DexchlorpheniramineMaleate-Bp/Ep/Usp 2-Pyridinepropanamine, .gamma.-(4-chlorophenyl)-N,N-dimethyl-, (.gamma.S)-, (2Z)-2-butenedioate (1:1) (s)-γ-(4-chlorophenyl)-n,n-dimethyl-2-pyridinepropanamine maleate salt s-(+)-chlorpheniramine maleate salt DEXCHLORPHENIRAMINEMALEATE,USP 2-Pyridinepropanamine, γ-(4-chlorophenyl)-N,N-dimethyl-, (S)-, (Z)-2-butenedioate (1:1) 2-Pyridinepropanamine, γ-(4-chlorophenyl)-N,N-dimethyl-, (γS)-, (2Z)-2-butenedioate (1:1) d-2-[p-Chloro-α-(2-dimethylaminoethyl)benzyl]pyridine bimaleate Dexchlorpheniramine hydrogen maleate Phenamin Polamin Polaramine Pyridine, 2-[p-chloro-α-[2-(dimethylamino)ethyl]benzyl]-, maleate (1:1), (S)- (8CI) Sensidyn γ-(4-Chlorophenyl)-N,N-dimethyl-2-pyridinepropanamine, (+)-Chlorpheniramine maleate salt Chlorpheniramine d-maleate d-Chlorpheniramine·maleic acid (+)-Chloropromazine Maleate Dexchlorpheniramine Maleate (300 mg) (γS)-γ-(4-Chlorophenyl)-N,N-diMethyl-2-pyridinepropanaMine (2Z)-2-Butenedioate 2-[p-Chloro-α-[2-(diMethylaMino)ethyl]benzyl]pyridine Maleate Dexchlorpheniramine maleate CRS (S)-Chlorpheniramine Maleate(Dexchlorpheniramine Maleate) DEXCHLORPHENIRAMINE MALEATE USP/EP/BP Dexchlorpheniramine maleateQ: What is Dexchlorpheniramine maleate Q: What is the CAS Number of Dexchlorpheniramine maleate Q: What is the storage condition of Dexchlorpheniramine maleate Dexchlorpheniramine Maleate (1179005) [3-(11,12-Dihydro-6H-dibenzo[b,f]azocin-5-yl)-propyl]-dimethyl-amine (S)-3-(4-chlorophenyl)-N,N-dimethyl-3-(pyridin-2-yl)propan-1-amine maleate Histamine Receptor,Dexchlorpheniramine Maleate,Dexchlorpheniramine,inhibit,Inhibitor Brompheniramine Maleate Impurity B as Maleate Brompheniramine Maleate EP Impurity B as Maleate 2438-32-6 C20H23ClN2O4 39086 H1 histamine receptor antagonist; active isomer. DIDRONEL Amines Chiral Reagents Heterocycles Intermediates & Fine Chemicals