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2-Hydroxypropane-1-sulfonic acid, with the molecular formula C3H8O4S, is an organosulfur compound that features a hydroxyl group and a sulfonic acid group attached to a propane backbone. This versatile chemical is known for its ability to participate in various chemical reactions and processes due to its functional groups.

1561-96-2

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1561-96-2 Usage

Uses

Used in Organic Synthesis:
2-Hydroxypropane-1-sulfonic acid is utilized as a reagent in organic synthesis, where its hydroxyl and sulfonic acid groups contribute to the formation of a wide range of organic compounds. Its reactivity and stability make it a valuable component in the synthesis of various organic molecules.
Used in Metal Ion Coordination Chemistry:
As a chelating agent, 2-hydroxypropane-1-sulfonic acid is employed in metal ion coordination chemistry. Its ability to form complexes with metal ions is crucial for applications in areas such as catalysis, where metal complexes are often used to facilitate chemical reactions.
Used in Pharmaceutical Production:
2-hydroxypropane-1-sulfonic acid finds application in the production of specialty chemicals and pharmaceuticals, where its unique properties can be harnessed to create new drugs or improve the synthesis of existing ones.
Used in Detergent and Cleaning Product Formulation:
2-Hydroxypropane-1-sulfonic acid is used in the formulation of detergents and cleaning products due to its surfactant properties. Its ability to reduce the surface tension of water and form micelles makes it an effective ingredient for cleaning and washing applications across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1561-96-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,6 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1561-96:
(6*1)+(5*5)+(4*6)+(3*1)+(2*9)+(1*6)=82
82 % 10 = 2
So 1561-96-2 is a valid CAS Registry Number.

1561-96-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-hydroxypropane-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names 1,3-bis-docosanoyloxy-propan-2-ol

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:1561-96-2 SDS

1561-96-2Relevant academic research and scientific papers

Fatty acyl oxide isopropylacrylamides sodium sulfonate and synthetic method and application

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Paragraph 0024-0025, (2017/07/23)

A structural formula of sodium fatty acyl oxyisopropyl sulfonate is described in the specification, wherein R is C7-C17 saturated or unsaturated straight-chain hydrocarbyl. The sodium fatty acyl oxyisoproyl sulfonate has the advantages of greatly lowered Krafft point which is below 1 DEG C, good water solubility, good foaming performance, strong hard water resistance, high detersive power, wider application range, simple synthetic process and easy implementation of industrial production.

3-(N-morpholine)-2-hydroxyl propanesulfonic acid synthesizing technology

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Paragraph 0011; 0012; 0013; 0014, (2017/04/28)

The invention relates to a 3-(N-morpholine)-2-hydroxyl propanesulfonic acid synthesizing technology, and discloses a preparation method of a N-substituted morpholine organic compound. The preparation method comprises the following steps that cyclodehydration is conducted to obtain morpholine, neutralizing, filtering, rectifying and synthesizing are conducted to obtain 3-(N-morpholine)-2-hydroxyl propanesulfonic acid, and chromatography and purification are conducted to obtain the final product. According to the method, reaction conditions are mild, operation is easy and convenient, the safety is high, industrialization is easy to achieve, and the yield is stably 95% or above; in addition, reagents are low in cost and easy to obtain, and therefore obvious cost and technique advantages are achieved.

PROCESS COMPOSITIONS AND PRODUCTION OF ACYL ALKYLISETHIONATE COMPOSITIONS

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Page/Page column 30-31, (2008/06/13)

Methods and compositions are provided for forming ester based compositions. The ester based compositions may be used in consumer products. In one aspect, a method is provided for producing acyl alkylisethionate esters by the esterification of a sulfonate composition having two or more sulfonate isomers with fatty acid(s). In another aspect, a method is provided for forming an ester based composition including a blend of acyl alkylisethionate and acylisethionate esters.

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