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CARBINOXAMINE MALEATE SALT

CAS No.
3505-38-2
Chemical Name:
CARBINOXAMINE MALEATE SALT
Synonyms
clistin;ciberon;lergefin;hislosine; Allergefon;Maleate clistinmaleate;clistinemaleate;allergefonmaleate;CarbinoxaMine 
CBNumber:
CB4183800
Molecular Formula:
C20H23ClN2O5
Molecular Weight:
406.86
MDL Number:
MFCD00082461
MOL File:
3505-38-2.mol
MSDS File:
SDS
Last updated:2023-09-07 16:59:03

CARBINOXAMINE MALEATE SALT Properties

Melting point 116-1180C
storage temp. Keep in dark place,Sealed in dry,Room Temperature
Water Solubility Completely soluble in water
solubility Chloroform: Slightly Soluble; Methanol: Slightly Soluble
color White to Almost white
Merck 14,1799
InChIKey GVNWHCVWDRNXAZ-BTJKTKAUSA-N
CAS DataBase Reference 3505-38-2(CAS DataBase Reference)
FDA UNII 02O55696WH
EPA Substance Registry System Ethanamine, 2-[(4-chlorophenyl)-2-pyridinylmethoxy]-N,N-dimethyl-, (2Z)-2-butenedioate (1:1) (3505-38-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301-H315-H319-H335
Precautionary statements  P301+P310+P330-P302+P352-P305+P351+P338
Hazard Codes  T
Risk Statements  25-36/37/38
Safety Statements  26-36/37/39-45
RIDADR  3249
WGK Germany  3
RTECS  US6350000
HazardClass  6.1(b)
PackingGroup  III
HS Code  2933399090
Toxicity LD50 in mice (mg/kg): 166 i.p. (Cahen)
NFPA 704
0
2 0

CARBINOXAMINE MALEATE SALT price More Price(23)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR2802 Carbinoxamine Maleate certified reference material, pharmaceutical secondary standard 3505-38-2 400MG $243 2024-03-01 Buy
Sigma-Aldrich 1096000 Carbinoxamine maleate United States Pharmacopeia (USP) Reference Standard 3505-38-2 200mg $174.4 2024-03-01 Buy
Sigma-Aldrich C8278 Carbinoxamine maleate salt analytical standard 3505-38-2 10g $158 2022-05-15 Buy
TCI Chemical C3057 Carbinoxamine Maleate >98.0%(HPLC)(T) 3505-38-2 5g $70 2024-03-01 Buy
TCI Chemical C3057 Carbinoxamine Maleate >98.0%(HPLC)(T) 3505-38-2 25g $230 2024-03-01 Buy
Product number Packaging Price Buy
PHR2802 400MG $243 Buy
1096000 200mg $174.4 Buy
C8278 10g $158 Buy
C3057 5g $70 Buy
C3057 25g $230 Buy

CARBINOXAMINE MALEATE SALT Chemical Properties,Uses,Production

Description

Carbinoxamine is a competitive histamine H1 receptor antagonist (Ki = 2.3 nM) and first generation antihistamine. It also competes with [3H]diltiazem, an L-type calcium channel blocker, for binding to the benzothiazepine site on rat cardiomyocytes (Ki = 1.08 nM). Carbinoxamine decreases negative inotropic activity in isolated guinea pig left atria by 76% (EC50 = 250 nM) and negative chronotropic activity in guinea pig spontaneously beating isolated right atria (EC50s = 250 and 480 nM, respectively) by 48% compared with control. Formulations containing carbinoxamine have been used in the treatment of allergic rhinitis.

Chemical Properties

Off-White Solid

Originator

Clistin,McNeil,US,1953

Uses

antihistaminic

Uses

Analgesic and anti-inflammatory compound

Definition

ChEBI: The maleic acid salt of carbinoxamine. An ethanolamine-type antihistamine, used for treating hay fever, as well as mild cases of Parkinson's disease.

Manufacturing Process

As described in US Patent 2,800,485 a solution of p-chlorophenylmagnesium bromide is prepared by adding dropwise a solution of 230 g (1.2 mols) of p-bromochlorobenzene in 900 cc of anhydrous ether to 26.7 g (1.1 g-atoms) of magnesium suspended in 100 cc of anhydrous ether containing a small crystal of iodine. To this solution, 107 g (1 mol) of 2-pyridinealdehyde are added slowly with stripping at a rate to maintain refluxing. The reaction mixture is then stirred for one hour at room temperature. The mixture is then poured onto an equal volume of crushed ice and water and acidified with concentrated hydrochloric acid. The ether layer is removed. The aqueous layer is made basic with ammonia and extracted with ether. The ether solution is evaporated and the residue dried by addition of benzene and removal by distillation to give 208 g (95%) of solid alpha-(p-chlorophenyl)-2-pyridinemethanol melting at 78° to 80°C. The p-chlorophenyl pyridinemethanol may alternatively be prepared from 4-chloroacetophenone, pyridine and granular aluminum as described in US Patent 2,606,195. In either case, the synthesis then proceeds as described in US Patent 2,800,485.
A solution of 219 g (1 mol) of α-(p-chlorophenyl)-2-pyridinemethanol in one liter of dry toluene is heated to 100°C with stirring. Twenty-three grams (1 g-atom) of sodium are then added in portions. After all the sodium has reacted, a dried solution of 2-dimethylaminoethyl chloride in benzene is added. This benzene solution is prepared by dissolving 173 g (1.2 mols) of 2- dimethylaminoethyl chloride hydrochloride in the minimum amount of water, adding 500 cc of benzene followed by 300 g of sodium carbonate decahydrate, stirring, separating the benzene layer and drying.
The mixture is refluxed with stirring for ten hours, cooled and filtered. The filtrate is extracted three times with 200 cc portions of 6 N acetic acid. The aqueous acetic acid solution is then made strongly basic with 10% sodium hydroxide solution, and extracted three times with 200 cc portions of ether. The ether extract is dried with anhydrous sodium sulfate, stirred with 5 g of activated carbon and filtered to provide 2-[p-chloro-α(2-dimethylaminoethoxy) benzyl]pyridine in solution. Addition of a solution of 116 g (1 mol) of maleic acid in 1,500 cc of ether gives 323 g (79%) of solid which, on recrystallization from ethyl acetate, gives white solid 2-[p-chloro-α(2-dimethylaminoethoxy) benzyl]pyridine maleate melting at 117° to 119°C.

brand name

Clistin (Ortho- McNeil).

Therapeutic Function

Antihistaminic

General Description

Carbinoxamine is availableas a bitter bimaleate salt, (d, l)-2-[p-chloro- -[2-(dimethylamino)ethoxy]benzyl]pyridine bimaleate (Clistin), which isa white crystalline powder that is very soluble in water andfreely soluble in alcohol and in chloroform. The pH of a 1%solution is between 4.6 and 5.1.
Carbinoxamine is a potent antihistaminic and is availableas the racemic mixture. It differs structurally from chlorpheniramineonly in having an oxygen atom separate theasymmetric carbon atom from the aminoethyl side chain. Themore active levo isomer of carbinoxamine has the (S) absoluteconfiguration and can be superimposed on the moreactive dextro isomer (S configuration) of chlorpheniramine.

CARBINOXAMINE MALEATE SALT Preparation Products And Raw materials

Global( 199)Suppliers
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Anhui Ruihan Technology Co., Ltd
+8617756083858 daisy@anhuiruihan.com China 994 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
career henan chemical co
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Shaanxi Dideu Medichem Co. Ltd
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+8618530059196 sale04@alfachem.cn China 12477 58
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0551-65418671 sales@tnjchem.com China 34572 58
ANHUI WITOP BIOTECH CO., LTD
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Xi'an MC Biotech, Co., Ltd.
029-89275612 +8618991951683 mcbio_sales@163.com China 2255 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9409 58

View Lastest Price from CARBINOXAMINE MALEATE SALT manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Carbinoxamine maleate pictures 2023-09-08 Carbinoxamine maleate
3505-38-2
US $0.00 / KG Ton 1KG Ton USP43 98%+ 2 tons/month Zhuhai Hairuide Bioscience and Technology Co., Ltd
Carbinoxamine maleate salt pictures 2023-09-07 Carbinoxamine maleate salt
3505-38-2
US $30.00 / kg 1kg 99% 1000t/year Anhui Ruihan Technology Co., Ltd
Carbinoxamine Maleates pictures 2021-07-20 Carbinoxamine Maleates
3505-38-2
US $1.00-1.00 / KG 1g 99% 50tons Shaanxi Dideu Medichem Co. Ltd
  • Carbinoxamine maleate pictures
  • Carbinoxamine maleate
    3505-38-2
  • US $0.00 / KG Ton
  • USP43 98%+
  • Zhuhai Hairuide Bioscience and Technology Co., Ltd
2-((4-chlorophenyl)-2-pyridinylmethoxy)-n,n-dimethyl-ethanamin(z)-2-bute 2-(p-chloro-alpha-(2-(dimethylamino)ethoxy)benzyl)pyridinebimaleate 2-(p-chloro-alpha-(2-(dimethylamino)ethoxy)benzyl)pyridinemaleate 2-(p-chloro-alpha-(2-(dimethylamino)ethoxy)benzyl)-pyridinmaleate(1:1) 2-[(4-chlorophenyl)-2-pyridinylmethoxy]-n,n-dimethyl-ethanamin(z)-2-butene allergefonmaleate ciberon clistin clistinemaleate clistinmaleate hislosine lergefin p-carbinoxaminemaleate carbinoxamine hydrogen maleate N-[2-[(4-Chlorophenyl)(2-pyridinyl)methoxy]ethyl]-N,N-dimethylamine maleate salt Carbinoxamine Meleate CarbinoxaMine Maleate Salt, USP Carbinoxamine Maleate (200 mg) CarbinoxaMine  Maleate  arbinoxaMine Maleate {2-[(4-chlorophenyl)(pyridin-2-yl)methoxy]ethyl}dimethylamine maleate CARBINOXAMINE MALEATE CARBINOXAMINE MALEATE SALT Allergefon 2-[(4-Clorophenyl)-2-pyridinylmethoxy]-N,N-dimethyl-ethanamine Maleate Salt 2-[(4-chlorophenyl)-(2-pyridyl)methoxy]ethyl-dimethyl-amine 2-[(4-chlorophenyl)-(2-pyridyl)methoxy]-N,N-dimethylethanamine 2-[(4-chlorophenyl)-(2-pyridyl)methoxy]-N,N-dimethyl-ethanamine 2-[(4-chlorophenyl)-pyridin-2-yl-methoxy]-N,N-dimethyl-ethanamine 2-[(4-chlorophenyl)-pyridin-2-ylmethoxy]-N,N-dimethylethanamine Ethanamine, 2-((4-chlorophenyl)-2-pyridinylmethoxy)-N,N-dimethyl-, (2Z)-2-butenedioate (1:1) Carbinoxamine Maleates Carbinoxamine Maleate > But-2-enedioic acid (2-[(4-chlorophenyl)(pyridin-2-yl)methoxy]ethyl)dimethylamine CARBINOXAMINE MALEATE SALT USP/EP/BP "(+/-)-Carbinoxamine D6 Maleate (N,N-dimethyl-d6)" Carbinoxamine Maleate (1096000) Carbinoxamine Maleate, ≥ 98.0% 3505-38-2 C16H19ClN2OC4H4O4 C17H22N2OC4H4O4 C20H23ClN2O5 CA - CG Analytical Chromatography Product Catalog Alphabetic Analytical Standards Intermediates & Fine Chemicals Pharmaceuticals Alphabetic C CA - CGForensic and Veterinary Standards Drugs&Metabolites Neat Compounds Aromatics Heterocycles CLISTIN