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D-Sulfophenylacetic acid, also known as 2-(4-Sulfophenyl)acetic acid, is a chemical compound characterized by the molecular formula C8H8O4S. It presents as a white crystalline powder that exhibits solubility in water and ethanol. This versatile compound is recognized for its utility as an intermediate in the synthesis of pharmaceuticals, dyes, and other organic compounds, as well as serving as a chemical reagent in a variety of chemical processes.

39925-38-7

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39925-38-7 Usage

Uses

Used in Pharmaceutical Industry:
D-Sulfophenylacetic acid is utilized as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicines. Its role in this industry is pivotal for creating active pharmaceutical ingredients and facilitating advancements in medicinal chemistry.
Used in Dye Industry:
In the dye industry, D-Sulfophenylacetic acid serves as a crucial intermediate, playing a significant part in the production of different types of dyes. Its chemical properties allow for the creation of colorants used in textiles, printing inks, and other applications requiring coloration.
Used in Chemical Processes:
As a chemical reagent, D-Sulfophenylacetic acid is employed in a range of chemical processes. Its reactivity and solubility properties make it suitable for use in various reactions, contributing to the synthesis of a wide array of chemical products.
Used in Surfactant Production:
D-Sulfophenylacetic acid finds application as a component in the production of surfactants. Surfactants are essential in industries such as cosmetics, detergents, and cleaning products, where they reduce surface tension and enable the mixing of substances that do not normally dissolve in each other.
Used in Plastics Manufacturing:
In the plastics industry, D-Sulfophenylacetic acid is used in the manufacturing of certain types of plastics. Its incorporation can influence the properties of the final plastic products, such as their flexibility, durability, or chemical resistance, depending on the specific application and formulation.

Check Digit Verification of cas no

The CAS Registry Mumber 39925-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 39925-38:
(7*3)+(6*9)+(5*9)+(4*2)+(3*5)+(2*3)+(1*8)=157
157 % 10 = 7
So 39925-38-7 is a valid CAS Registry Number.

39925-38-7SDS

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 2-phenyl-2-sulfoacetic acid

1.2 Other means of identification

Product number -
Other names D-SULFOPHENYLACETIC 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:39925-38-7 SDS

39925-38-7Relevant academic research and scientific papers

Asymmetric synthesis of allylic sulfonic acids: Enantio-And regioselective iridium-catalyzed allylations of Na2SO3

Liu, Wei,Zhao, Xiao-Ming,Zhang, Hong-Bo,Zhang, Liang,Zhao, Ming-Zhu

, p. 16873 - 16876 (2014)

An enantioselective allylation reaction of allylic carbonates with sodium sulfite (Na2SO3) catalyzed by Ir complex was accomplished, providing allylic sulfonic acids in good to excellent yields with a high level of enantioand regioselectivities. (R)-2-Phenyl-2-sulfoacetic acid, a key intermediate for the synthesis of Cefsulodin and Sulbenicillin, was synthesized as well.

Preparation method of sulbenicillin sodium

-

Paragraph 0058; 0060, (2018/09/08)

The invention discloses a preparation method of sulbenicillin sodium. According to the invention, L-amino acid is firstly adopted to perform splitting on D, L-sulfonylphenylacetic acid to obtain D(-)-sulfonylphenylacetic acid, then D(-)-sulfonylphenylacetic acid is compounded with D, L-sulfonylphenylacetic acid to prepare a sulfonylphenylacetic acid mixture with D(-)-sulfonylphenylacetic acid to L(+)-sulfonylphenylacetic acid ratio being about 78%:22%, the sulfonylphenylacetic acid mixture is chlorinated and then reacts with 6-APA, and then reacts with sodium iso-octoate, to directly obtain asulbenicillin sodium mixture with the ratio of D(-)-sulbenicillin sodium to L(+)-sulbenicillin sodium being about 78%:22%. According to the invention, post-treatment process is simplified, no water isused in the step of producing sulbenicillin sodium, hydrolysis impurity level is reduced, product purity is more than 99.0%, and product mole rate is more than 90%.

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