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Sodium cyclohexanecarboxylate, with the molecular formula C6H9NaO2, is a sodium salt of cyclohexanecarboxylic acid. It is a versatile chemical compound known for its buffering capabilities, pH stabilization, and potential anti-inflammatory and antimicrobial properties. This makes it a valuable ingredient in various industries, including pharmaceuticals, food, and cosmetics.

136-01-6

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136-01-6 Usage

Uses

Used in Pharmaceutical Formulations:
Sodium cyclohexanecarboxylate is used as a buffering agent to maintain stable pH levels in pharmaceutical products, ensuring their efficacy and safety.
Used in Food Industry:
As a food additive, sodium cyclohexanecarboxylate helps stabilize pH levels in various food products, enhancing their taste, texture, and shelf life.
Used in Skincare and Cosmetics:
Sodium cyclohexanecarboxylate is used as a key ingredient in skincare products and cosmetics for its ability to stabilize pH levels, providing a balanced and healthy environment for the skin.
Used in Chemistry and Material Science:
In the fields of chemistry and material science, sodium cyclohexanecarboxylate is utilized in various applications due to its unique properties, such as pH stabilization and potential anti-inflammatory and antimicrobial effects.
Used in Antimicrobial Applications:
Sodium cyclohexanecarboxylate has been studied for its potential antimicrobial properties, making it a valuable component in products that require microbial control.
Used in Anti-inflammatory Applications:
Due to its potential anti-inflammatory properties, sodium cyclohexanecarboxylate may be used in formulations that aim to reduce inflammation and provide relief from various conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 136-01-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136-01:
(5*1)+(4*3)+(3*6)+(2*0)+(1*1)=36
36 % 10 = 6
So 136-01-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2.Na/c8-7(9)6-4-2-1-3-5-6;/h6H,1-5H2,(H,8,9);/q;+1/p-1

136-01-6SDS

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 sodium,cyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names cyclohexanecarboxylic acid Na-salt

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:136-01-6 SDS

136-01-6Relevant academic research and scientific papers

ADENOSINE RECEPTOR ANTAGONISTS AND USES THEREOF

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Paragraph 00361; 00362, (2019/10/01)

Disclosed herein are compounds, compositions, formulations, and methods for modulating the A2B adenosine receptor.

Process for preparing 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid

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Page/Page column 4, (2008/12/06)

The present invention relates to a process for the preparation of 1-(2-ethyl-butyl)- cyclohexanecarboxylic acid which is useful as an intermediate in the preparation of pharmaceutical active compounds, wherein cyclohexanecarboxylic acid alkali metal salt reacts with an alkylating agent in the presence of a secondary amine and (C1-C6) alkyllithium, (C3-C6) cycloalkyllithium or phenyllithium.

Preparing carboxylic acids from glycidonitriles through enol acylates

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, (2008/06/13)

Process for preparing carboxylic acids by converting a glycidonitrile to the enol acylate via hydrohalogenation, acylation and dehydrohalogenation procedures, and conversion of the enol acylate to the carboxylate salt with a base and of the salt to the carboxylic acid with acid. Cyanide content in the mixture is destroyed by adding persulfate or hypochlorite salts. This process, can be used, e.g., to prepare 2-(4'-isobutylphenyl)propionic acid, now known generically as ibuprofen, a highly active anti-inflammatory drug, as well as a host of other useful carboxylic acids.

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