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109882-26-0

109882-26-0

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  • 99% up by HPLC Bendamustine Impurity A 4-(6-((2-chloroethyl)(2-hydroxyethyl)amino)-3-methylbenzimidazolyl(2))butyric acid hydrochloride 109882-26-0

    Cas No: 109882-26-0

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109882-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109882-26-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,8,8 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109882-26:
(8*1)+(7*0)+(6*9)+(5*8)+(4*8)+(3*2)+(2*2)+(1*6)=150
150 % 10 = 0
So 109882-26-0 is a valid CAS Registry Number.

109882-26-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(6-((2-chloroethyl)(2-hydroxyethyl)amino)-3-methylbenzimidazolyl(2))butyric acid hydrochloride

1.2 Other means of identification

Product number -
Other names 4-{5-[(2-Chloro-ethyl)-(2-hydroxy-ethyl)-amino]-1-methyl-1H-benzoimidazol-2-yl}-butyric acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:109882-26-0 SDS

109882-26-0Upstream product

109882-26-0Downstream Products

109882-26-0Relevant articles and documents

Preparation method and applications of bendamustine hydrochloride dimer

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Paragraph 0023; 0024; 0025, (2016/10/31)

The present invention relates to a preparation method and applications of a bendamustine hydrochloride dimer represented by a formula III. The preparation method comprises that bendamustine hydrochloride reacts with monohydroxyphenyl bendamustine hydrochloride under the conditions of a catalyst and a condensation agent to obtain the bendamustine hydrochloride dimer (represented by the formula III). According to the present invention, the compound represented by the formula III can be adopted as the control substance for the bendamustine hydrochloride related substance detection, and can further be used for the purity control of the bendamustine hydrochloride raw material or bendamustine hydrochloride preparation.

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