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Mebeverine hydrochloride

CAS No.
2753-45-9
Chemical Name:
Mebeverine hydrochloride
Synonyms
MEBEVERINE;MEBEVERINE HCL;COLOFAC;csag-144;duspatalin;Colofac Hydrochloride;Duspatal Hydrochloride;MEBEVERINE HYDROCHLORIDE;Duspatalin Hydrochloride;Mebeverine HCL SR Pellets
CBNumber:
CB2444585
Molecular Formula:
C25H35NO5.ClH
Molecular Weight:
466.01
MDL Number:
MFCD00083411
MOL File:
2753-45-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-03 11:24:09
Product description Number Pack Size Price
Mebeverine hydrochloride European Pharmacopoeia (EP) Reference Standard Y0002079 10 mg $164
Mebeverine hydrochloride British Pharmacopoeia (BP) Reference Standard BP1271 100 mg $180
Mebeverine hydrochloride British Pharmacopoeia (BP) Reference Standard BP1271 1 unit $167
Mebeverine Hydrochloride FM25024 0.25g $389.4
Mebeverine Hydrochloride FM25024 0.5g $519.2
More product size

Mebeverine hydrochloride Properties

Melting point 105-107 C
storage temp. Inert atmosphere,2-8°C
solubility DMSO : ≥ 155 mg/mL (332.61 mM)
form Solid
pka pKa 9.07± 0.02(40% EtOH,t =25,) (Uncertain)
color White to off-white
Major Application pharmaceutical
InChI 1S/C25H35NO5.ClH/c1-6-26(19(2)17-20-9-12-22(28-3)13-10-20)15-7-8-16-31-25(27)21-11-14-23(29-4)24(18-21)30-5;/h9-14,18-19H,6-8,15-17H2,1-5H3;1H
InChIKey PLGQWYOULXPJRE-UHFFFAOYSA-N
SMILES Cl.CCN(CCCCOC(=O)c1ccc(OC)c(OC)c1)C(C)Cc2ccc(OC)cc2
CAS DataBase Reference 2753-45-9(CAS DataBase Reference)
FDA UNII 15VZ5AL4JN
ATC code A03AA04
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  36-26
WGK Germany  3
RTECS  YX5425000
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral

Mebeverine hydrochloride price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich Y0002079 Mebeverine hydrochloride European Pharmacopoeia (EP) Reference Standard 2753-45-9 10 mg $164 2026-04-30 Buy
Sigma-Aldrich BP1271 Mebeverine hydrochloride British Pharmacopoeia (BP) Reference Standard 2753-45-9 100 mg $180 2026-04-30 Buy
Sigma-Aldrich BP1271 Mebeverine hydrochloride British Pharmacopoeia (BP) Reference Standard 2753-45-9 1 unit $167 2025-07-31 Buy
Biosynth FM25024 Mebeverine Hydrochloride 2753-45-9 0.25g $389.4 2026-06-04 Buy
Biosynth FM25024 Mebeverine Hydrochloride 2753-45-9 0.5g $519.2 2026-06-04 Buy
Product number Packaging Price Buy
Y0002079 10 mg $164 Buy
BP1271 100 mg $180 Buy
BP1271 1 unit $167 Buy
FM25024 0.25g $389.4 Buy
FM25024 0.5g $519.2 Buy

Mebeverine hydrochloride Chemical Properties,Uses,Production

Chemical Properties

White Solid

Originator

Duspatalin,Duphar,France,1965

Uses

muscarinic ACh agonist, antiglaucoma

Uses

Smooth muscle relaxant. Antispasmodic.

Manufacturing Process

(A) Sodium-3,4-Dimethoxybenzoate: A solution of 91 g of 3,4- dimethoxybenzoic acid in 500 ml of boiling, absolute alcohol was added quickly to a solution of 11.5 g of sodium in 300 ml of absolute alcohol; after cooling to room temperature the resulting precipitate was filtered off and washed with 2 x 50 ml of absolute alcohol and 4 x 200 ml of ether and dried in air to constant weight; yield 92.5 g, MP about 265°C. The filtrate was bulked with the alcohol and ether washings, left to stand overnight, and a further precipitate then filtered off, washed with 3 x 100 ml of ether, and dried in air to constant weight. Yield 22.5 g, MP about 265°C. Total yield therefore 115 g (=113%).
(B) 4'-Chlorobutyl-3,4-Dimethoxybenzoate: 92 g of the sodium salt described under (A) (it contains at the most 81.5 g of sodium 3,4-dimethoxybenzoate) was boiled in 900 ml of tetramethylene dichloride for 90 hours; after cooling the mixture was filtered and the residue washed with 3 x 50 ml of ether. The filtrate was evaporated to dryness in vacuo and the residue (102 g) was distilled in vacuo. Fraction 1: 50° to 55°C/0.5 mm; 19 g (probably tetramethylene dichloride). Fraction 2: 175° to 184°C/0.5 mm; 77.5 g (=71%); Cl= 12.6% (calculated 13.0%). Remark: The second fraction partially solidified or became more viscous on standing, and even during the distillation.
(C) 4'-Iodobutyl-3,4-Dimethoxybenzoate: 32.5 g of 4'-chlorobutyl-3,4- dimethoxybenzoate and 19.5 g of sodium iodide (10% excess) were boiled in 150 ml of methyl ethyl ketone for 2.5 hours; after cooling and filtering off the sodium chloride produced, the reaction was found not to be entirely completed; boiling was then continued for another two hours; the reaction mixture was cooled, and the solid filtered off and washed with 2 x 100 ml of ether.
The filtrate was evaporated to dryness in vacuo and the residue was dissolved in 300 ml of ether and 100 ml of water; the layers were separated and the water layer was once again extracted with 100 ml of ether; then the ether layers were boiled and washed again with a solution of 3.5 g of sodium thiosulfate in 100 ml of water. The ether layer was dried over sodium sulfate. Finally the solution was filtered and the ether was evaporated; the residue was an almost colorless oil, which partially solidified or became more viscous after being left to stand for some time. Yield: 40 g (=92%), I=34.2% (calculated 34.9%).
(D) 4'-[N-Ethyl-1''-Methyl-2''-(4'''-Methoxyphenyl)Ethylamino]Butyl-3,4- Dimethoxybenzoate Hydrochloride: 10.3 g of 4'-iodobutyl-3,4- dimethoxybenzoate and 11.0 g of N-ethyl-p-methoxyphenylisopropylamine (obtained by catalytic reduction of an alcoholic solution of an excess quantity (60%) of p-methoxy-phenyl-acetone, to which was added a 33% (weight-for-weight) aqueous solution of ethylamine, with Pt as a catalyst), were boiled in 200 ml of methyl ethyl ketone for 20 hours, cooled and the iodine ion was determined; the reaction was found to be complete. Then the methyl ethyl ketone was evaporated in vacuo and the residue was dissolved in 300 ml of water and 30 ml of ether; the layers were separated and the water layer was extracted twice more with 20 ml portions of ether.

Therapeutic Function

Spasmolytic

Mebeverine hydrochloride Preparation Products And Raw materials

Global( 166)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Tianfu Chemical Co.,Ltd.
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career henan chemical co
+86-0371-86658258 sales@coreychem.com China 29766 58
CONIER CHEM AND PHARMA LIMITED
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TargetMol Chemicals Inc.
+1-781-999-5354; +1-00000000000 marketing@targetmol.com United States 32431 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-17392587031 1059@dideu.com China 9984 58
AFINE CHEMICALS LIMITED
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Finetech Industry Limited
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Dayang Chem (Hangzhou) Co.,Ltd.
+86-0571-88938639 17705817739 info@dycnchem.com China 52693 58
HANGZHOU LEAP CHEM CO., LTD.
+86-571-87711850 +8619957148339 market18@leapchem.com China 24569 58
TargetMol Chemicals Inc.
+1-781-999-5354; support@targetmol.com United States 38999 58

View Lastest Price from Mebeverine hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Mebeverine hydrochloride pictures 2026-06-02 Mebeverine hydrochloride
2753-45-9
$83.00 99.83% 10g TargetMol Chemicals Inc.
Mebeverine hydrochloride pictures 2026-06-02 Mebeverine hydrochloride
2753-45-9
$83.00 99.83% 10g TargetMol Chemicals Inc.
Mebeverine hydrochloride  pictures 2021-11-11 Mebeverine hydrochloride
2753-45-9
$10.00 1Kg/Bag 99% 20 Tons Hebei Zhanyao Biotechnology Co. Ltd

Mebeverine hydrochloride Spectrum

4-(ethyl(p-methoxy-alpha-methylphenethyl)amino)butylveratratehydrochloride 3,4-Dimethoxybenzoic acid 4-[ethyl[2-(4-methoxyphenyl)-1-methylethyl] amino]butyl ester HCl Benzoic acid,3,4-diMethoxy-, 4-[ethyl[2-(4-Methoxyphenyl)-1-Methylethyl]aMino]butyl ester,hydrochloride (1:1) 3,4-dimethoxybenzoic acid 4-[ethyl-[2- 4-[ethyl-[2-(4-methoxyphenyl)-1-methyl-ethyl]amino]butyl 3,4-dimethoxybenzoate 4-[ethyl-[2-(4-methoxyphenyl)-1-methyl-ethyl]amino]butyl 3,4-dimethoxybenzoate hydrochloride 4-{ethyl[2-(4-methoxyphenyl)-1-methylethyl]amino}butyl 3,4-dimethoxybenzoate hydrochloride 3,4-dimethoxybenzoic acid 4-[ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl ester hydrochloride csag-144 duspatalin veratricacid,4-(ethyl(p-methoxy-alpha-methylphenethyl)amino)butylester,hydr MEBEVERINE HYDROCHLORIDE COLOFAC 3,4-Dimethoxybenzoicacid4-ethyl2-(4-methoxyphenyl)-1-methylethylaminobutylesterhydrochloride 4-[Ethyl-[1-(4-methoxyphenyl)propan-2-yl]amino]butyl 3,4-dimethoxybenzoate hydrochloride Colofac Hydrochloride Duspatal Hydrochloride Duspatalin Hydrochloride Mebeverine hydrochloride USP/EP/BP Mebeverine hydrochloride (Y0002079)Q: What is Mebeverine hydrochloride (Y0002079) Q: What is the CAS Number of Mebeverine hydrochloride (Y0002079) Mebeverine HydrochlorideQ: What is Mebeverine Hydrochloride Q: What is the CAS Number of Mebeverine Hydrochloride Q: What is the storage condition of Mebeverine Hydrochloride Q: What are the applications of Mebeverine Hydrochloride 2753-45-9 Mebeverine hydrochloride Mebeverine hydrochloride salt MEBEVERINE HCL 20% TASTE MASK GRANULES Mebeverine HCL SR Pellets Mebeverine hydrochloride, 10 mM in DMSO Mebeverine impurity standard Mebeverine hydrochloride: 4-(1RS)-Ethyl2-(4-methoxyphenyl)-1-ethylethylaminobutyl 3,4-dimethoxybenzoate hydrochloride MEBEVERINE MEBEVERINE HCL 2753-45-9 C25H35NO5xHCl C25H35NO5 C25H36ClNO5 C25H35NO5HCl C25H35NO5ClH Alphabetic Analytical Chromatography Product Catalog Analytical Standards MEA - MES Intermediates of Mebeverine Amines Aromatics Intermediates & Fine Chemicals Pharmaceuticals GLAUCOSTAT