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1132650-67-9

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1132650-67-9 Usage

Chemical Properties

Off-White Solid

Uses

Lisinopril Cyclohexyl Analogue (Lisinopril EP Impurity F) is a Lisinopril (L468985) impurity.

Check Digit Verification of cas no

The CAS Registry Mumber 1132650-67-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,2,6,5 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1132650-67:
(9*1)+(8*1)+(7*3)+(6*2)+(5*6)+(4*5)+(3*0)+(2*6)+(1*7)=119
119 % 10 = 9
So 1132650-67-9 is a valid CAS Registry Number.

1132650-67-9 Well-known Company Product Price

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  • Sigma-Aldrich

  • (Y0001234)  Lisinopril impurity F  European Pharmacopoeia (EP) Reference Standard

  • 1132650-67-9

  • Y0001234

  • 1,880.19CNY

  • Detail

1132650-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Lisinopril Cyclohexyl Analogue

1.2 Other means of identification

Product number -
Other names Lisinopril impurity F

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:1132650-67-9 SDS

1132650-67-9Upstream product

1132650-67-9Downstream Products

1132650-67-9Relevant articles and documents

Preparing method for cyclohexyl impurity of ACEI medicine

-

Paragraph 0022; 0023; 0024; 0025; 0026; 0027; 0028, (2017/01/31)

The invention discloses a preparing method for a cyclohexyl impurity of ACEI medicine. The preparing method comprises the following steps that firstly, raw ACEI medicine is dissolved in alcohol, then glacial acetic acid and a catalyst are added, and hydrogen is introduced after nitrogen displacement is carried out three times, wherein the pressure of hydrogen is controlled to be 10-50 psi, the reaction temperature ranges from 20 DEG C to 50 DEG C, and the reaction time ranges from 6 h to 48 h; secondly, a reaction solution obtained in the first step is filtered, filter liquor is subjected to vacuum concentration with the concentration temperature not higher than 35 DEG C, then concentrate is separated and purified with HPLC, purified substances continue to be concentrated and dried, and the cyclohexyl impurity of ACEI medicine is obtained. The preparing process is low in cost, operation is easy, and a qualified and cheap comparison product easy to obtain can be provided for quality control over ACEI medicine.

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