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BUTTPARK 153\57-05 is a chemical compound that consists of butylated hydroxytoluene (BHT) and propyl gallate. BHT is an antioxidant and preservative commonly used in food, pharmaceuticals, and cosmetics, while propyl gallate is another antioxidant commonly used in the food industry. The combination of the two chemicals in BUTTPARK 153\57-05 provides enhanced antioxidant properties, protecting products from oxidative degradation and extending their shelf life.
Used in Food Industry:
BUTTPARK 153\57-05 is used as an additive in the food industry to maintain product quality and prevent spoilage. The enhanced antioxidant properties of BUTTPARK 153\57-05 protect food products from oxidative degradation, thereby extending their shelf life.
Used in Pharmaceutical Industry:
BUTTPARK 153\57-05 is used as an antioxidant and preservative in the pharmaceutical industry. The enhanced antioxidant properties of BUTTPARK 153\57-05 protect pharmaceutical products from oxidative degradation, thereby extending their shelf life and maintaining their quality.
Used in Personal Care Products:
BUTTPARK 153\57-05 is used as an antioxidant and preservative in personal care products. The enhanced antioxidant properties of BUTTPARK 153\57-05 protect personal care products from oxidative degradation, thereby extending their shelf life and maintaining their quality.

76498-32-3

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76498-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76498-32-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,9 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76498-32:
(7*7)+(6*6)+(5*4)+(4*9)+(3*8)+(2*3)+(1*2)=173
173 % 10 = 3
So 76498-32-3 is a valid CAS Registry Number.

76498-32-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 6-chloro-2,5-dimethyl-pyrimidine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-chloro-2,5-dimethylpyrimidine-6-carboxylic acid,ethyl ester

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:76498-32-3 SDS

76498-32-3Relevant academic research and scientific papers

NEW CCR2 RECEPTOR ANTAGONISTS AND USES THEREOF

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Page/Page column 43, (2012/01/14)

The present invention relates to novel antagonists for CCR2 (CC chemokine receptor 2) and their use for providing medicaments for treating conditions and diseases, especially pulmonary diseases like asthma and COPD.

NEW SELECTIVE CCR2 ANTAGONISTS

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Page/Page column 89, (2013/02/28)

The present invention relates to novel and selective antagonists for CCR2 (CC chemokine receptor 2) and their use for providing medicaments for treating conditions and diseases, especially pulmonary diseases like asthma and COPD as well as pain.

Synthesis of benzoylpyrimidines as antagonists of the corticotropin- releasing factor-1 receptor

Webb, Thomas R.,Moran, Terry,Huang, Charles Q.,McCarthy, James R.,Grigoriadis, Dimitri E.,Chen, Chen

, p. 3869 - 3873 (2007/10/03)

A series of benzoylpyrimidines derived from the anilinepyrimidine CRF 1 antagonists were synthesized. Several synthetic routes were developed to explore the SAR of this series of compounds. Compounds such as 8d (Ki=15nM) exhibited high binding affinities at the human CRF 1 receptor.

Chemistry of 2-Substituted Pyrimidines. Studies Directed toward the Synthesis of the Pyrimidine Moiety of Bleomycin

Hagmann, William K.,Basha, Fatima Z.,Hashimoto, Mitsunori,Frye, Bruce R.,Kojo, Shosuke,Hecht, Sidney M.

, p. 1413 - 1423 (2007/10/02)

Synthetic approaches to 2-substituted pyrimidines have been studied in an effort to facilitate the preparation of the pyrimidine moiety of bleomycin (2).Ethyl 2,5-dimethyl-4-oxopyrimidine-6-carboxylate (4) has been utilized as starting material; its conve

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