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138760-70-0

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138760-70-0 Usage

Chemical structure

A derivative of furanone with two hydroxyl groups (-OH) at the 3 and 4 positions, and a hydroxymethyl group (-CH2OH) at the 5 position.

Natural sources

Found in various natural sources.

Antioxidant properties

Has the potential to scavenge free radicals and protect against oxidative stress.

Anti-inflammatory properties

May have potential anti-inflammatory properties.

Therapeutic applications

Research has shown that this compound may have potential therapeutic applications in the treatment of various diseases and disorders.

Use in pharmaceutical and cosmetic products

Considered a promising candidate for use in pharmaceutical and cosmetic products.

Check Digit Verification of cas no

The CAS Registry Mumber 138760-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,7,6 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138760-70:
(8*1)+(7*3)+(6*8)+(5*7)+(4*6)+(3*0)+(2*7)+(1*0)=150
150 % 10 = 0
So 138760-70-0 is a valid CAS Registry Number.

138760-70-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name D-erythro-ascorbic acid

1.2 Other means of identification

Product number -
Other names D-Erythroascorbic 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:138760-70-0 SDS

138760-70-0Downstream Products

138760-70-0Relevant articles and documents

Production, stability, and antioxidative and antimicrobial activities of two l-ascorbate analogues from phycomyces blakesleeanus: D-erythroascorbate and d-erythroascorbate glucoside

Gutierrez-Larrainzar, Marta,De Castro, Cristina,Del Valle, Pilar,Rua, Javier,Garcia-Armesto, Maria Rosario,Busto, Felix,De Arriaga, Dolores

, p. 10631 - 10638 (2010)

D-Erythroascorbate (D-EAA), a five-carbon analogue of L-ascorbate (L-AA), and D-erythroascorbate monoglucoside (D-EAAG) are accumulated in Phycomyces blakesleeanus grown on glucose (99.5 and 1084 μg/g mycelial dry weight, respectively) and also excreted into the culture medium. Both compounds showed UV spectral properties and ionization constants similar to those of L-AA. D-EAAG was much more stable to aerobic oxidation than D-EAA and L-AA at acidic pH. D-EAAG is synthesized from D-erythroascorbate by a mycelial glucosyltransferase activity that uses UDP-glucose as glucose substrate donor with Km = 2.5 mM and 41.3 μM for D-EAA. This glucosyltransferase activity was maximal in the stationary growth phase in parallel with maximal production of D-EAAG. The presence of D-arabinose or D-arabinono-1,4-lactone in the culture medium produces the maximal accumulation of D-EAA and D-EAAG (about 30- and 4-fold with respect to that obtained in glucose culture). Both compounds showed greater antioxidant activity than L-AA and other standard antioxidants, with a capacity similar to that of L-AA to inhibit the growth of Escherichia coli.

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