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Clofibrylglycine is a metabolite of the pharmaceutical drug clofibrate, which is used to treat high cholesterol levels. It is formed in the liver during the metabolism of clofibrate and is excreted in urine. Clofibrylglycine is a key marker for monitoring clofibrate therapy, as it indicates the effectiveness of the drug and helps in adjusting dosages. It is also used in research to study the pharmacokinetics and metabolism of clofibrate.

4896-55-3

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4896-55-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4896-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,9 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4896-55:
(6*4)+(5*8)+(4*9)+(3*6)+(2*5)+(1*5)=133
133 % 10 = 3
So 4896-55-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H14ClNO4/c1-12(2,11(17)14-7-10(15)16)18-9-5-3-8(13)4-6-9/h3-6H,7H2,1-2H3,(H,14,17)(H,15,16)

4896-55-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name clofibric acid glycinate

1.2 Other means of identification

Product number -
Other names [2-(4-Chloro-phenoxy)-2-methyl-propionylamino]-acetic 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:4896-55-3 SDS

4896-55-3Upstream product

4896-55-3Downstream Products

4896-55-3Relevant academic research and scientific papers

Pyridylmethyl esters of N-(phenoxyalkanoyl)peptide derivatives for therepeutic use

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, (2008/06/13)

Pyridylmethyl esters of N-(phenoxyalkanoyl)peptide derivatives are disclosed. The derivatives are characterized by having a phenoxyalkanoyl group and a pyridylmethyloxy group-joined together by a peptide group. They possess antihyperlipoproteinemic activi

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