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133-38-0

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133-38-0 Usage

Description

DIHYDROXYFUMARIC ACID is a 2-hydroxydicarboxylic acid derived from fumaric acid, featuring two hydroxy groups at the 2and 3-positions. This organic compound exhibits unique chemical properties and potential applications across various industries.

Uses

Used in Pharmaceutical Industry:
DIHYDROXYFUMARIC ACID is used as a pharmaceutical intermediate for its potential role in the synthesis of various drug compounds. Its unique structure allows it to be a key component in the development of new medications.
Used in Chemical Synthesis:
In the chemical industry, DIHYDROXYFUMARIC ACID is used as a building block for synthesizing a range of chemical products. Its functional groups enable it to participate in various chemical reactions, contributing to the creation of novel compounds with specific applications.
Used in Research and Development:
DIHYDROXYFUMARIC ACID serves as a valuable research compound in scientific studies. It is utilized to investigate the properties of 2-hydroxydicarboxylic acids and their potential applications in different fields, including material science and biology.
Used in Cosmetics Industry:
DIHYDROXYFUMARIC ACID is used as an ingredient in cosmetic formulations for its potential benefits to skin health. Its chemical properties may contribute to the development of skincare products with improved efficacy and safety.
Used in Food and Beverage Industry:
In the food and beverage sector, DIHYDROXYFUMARIC ACID may be used as a flavoring agent or preservative. Its unique taste profile and ability to extend shelf life could make it a valuable addition to various food products.

Purification Methods

Crystallise the acid from water. [Beilstein 3 IV 1975.]

Check Digit Verification of cas no

The CAS Registry Mumber 133-38-0 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 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 133-38:
(5*1)+(4*3)+(3*3)+(2*3)+(1*8)=40
40 % 10 = 0
So 133-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C4H4O6/c5-1(3(7)8)2(6)4(9)10/h5-6H,(H,7,8)(H,9,10)/b2-1+

133-38-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name dihydroxyfumaric acid

1.2 Other means of identification

Product number -
Other names Dihydroxy-fumarsaeure

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:133-38-0 SDS

133-38-0Related news

The production of yellow pigments from (+)-catechin and DIHYDROXYFUMARIC ACID (cas 133-38-0) in a model wine system09/29/2019

The oxidation of tartaric acid by hydroxyl radicals, produced by gamma-irradiation of aqueous solutions of tartaric acid, was shown to generate dihydroxyfumaric acid. To confirm the importance of this oxidative degradation pathway in wine oxidation, dihydroxyfumaric acid was itself reacted with ...detailed

Diastereoselective Self‐Condensation of DIHYDROXYFUMARIC ACID (cas 133-38-0) in Water: Potential Route to Sugars10/01/2019

Vielseitige Salze: Bei der Kondensation wasserlöslicher DHF‐Salze unter Bildung des threo‐Diastereomers von Pentulosonsäure hängt der Reaktionsweg vom verwendeten Metallsalz ab. In dieser Umwandlung zeigen sich die unterschiedlichen Rollen von DHF als Nucleophil (Synthon für das α‐Hydroxyac...detailed

133-38-0Relevant articles and documents

Mechanism of the Catalytic Oxidation of Tartaric Acid in the Presence of Iron Ions

Sychev, A. Ya.,Duka, G. G.

, p. 43 - 46 (2007/10/02)

The oxidation of tartaric acid by hydrogen peroxide in the presence of iron ions has been studied polarimetrically.A mechanism qualitatively consistent with the kinetics of the oxidation of tartaric acid in both the peroxide (anaerobic) system and the mix

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