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Dichlorostearic acid is a chemical compound with the formula C18H34O2Cl2, characterized by the presence of two chlorine atoms attached to a stearic acid molecule. Stearic acid, a saturated fatty acid, is commonly found in various animal and vegetable fats and oils. The dichlorination of stearic acid results in the formation of dichloro derivatives, which possess unique properties compared to the parent compound. Dichlorostearic acid has potential applications in the synthesis of various chemicals, such as surfactants, lubricants, and plasticizers, due to its altered physical and chemical properties. However, it is essential to consider the potential environmental and health impacts associated with the use of chlorinated compounds, as they can be persistent and bioaccumulative in the environment.

5829-48-1

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5829-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5829-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5829-48:
(6*5)+(5*8)+(4*2)+(3*9)+(2*4)+(1*8)=121
121 % 10 = 1
So 5829-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C18H34Cl2O2/c1-2-3-4-5-7-10-13-16(19)17(20)14-11-8-6-9-12-15-18(21)22/h16-17H,2-15H2,1H3,(H,21,22)

5829-48-1SDS

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 DICHLOROSTEARIC ACID

1.2 Other means of identification

Product number -
Other names RARECHEM AL BE 0644

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:5829-48-1 SDS

5829-48-1Relevant academic research and scientific papers

Catalysis of phosphorus(V)-mediated transformations: Dichlorination reactions of epoxides under appel conditions

Denton, Ross M.,Tang, Xiaoping,Przeslak, Adam

supporting information; experimental part, p. 4678 - 4681 (2010/12/24)

A stereospecific triphenylphosphine oxide-catalyzed 1,2-dichlorination reaction of epoxides has been developed. The reaction is effective for a range of terminal and internal epoxides. In contrast to the classical Appel-type dichlorination of epoxides, oxalyl chloride is used as a stoichiometric reagent to generate the chlorophosphonium salt responsible for dichlorination from catalytic triphenylphosphine oxide.

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