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103404-58-6

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103404-58-6 Usage

Description

(+/-)-2-HYDROXYBUTANOIC ACID BARIUM SALT is a chemical compound consisting of a barium ion and the 2-hydroxybutanoic acid molecule. It is known for its ability to form complex compounds with other substances and is often used as a reagent in chemical reactions.
Used in Research and Development:
(+/-)-2-HYDROXYBUTANOIC ACID BARIUM SALT is used as a reagent in chemical reactions for its ability to form complex compounds with other substances.
Used in Laboratory Settings:
(+/-)-2-HYDROXYBUTANOIC ACID BARIUM SALT is used as a catalyst and a source of barium for other chemical reactions.
Used in Pharmaceutical Applications:
(+/-)-2-HYDROXYBUTANOIC ACID BARIUM SALT may have pharmaceutical applications, although its main use is in research and development.
Used in Industrial Applications:
(+/-)-2-HYDROXYBUTANOIC ACID BARIUM SALT may also have industrial applications, but its primary use remains in the scientific and research fields.

Check Digit Verification of cas no

The CAS Registry Mumber 103404-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,4,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 103404-58:
(8*1)+(7*0)+(6*3)+(5*4)+(4*0)+(3*4)+(2*5)+(1*8)=76
76 % 10 = 6
So 103404-58-6 is a valid CAS Registry Number.

103404-58-6SDS

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 2-Hydroxybutanoic acid

1.2 Other means of identification

Product number -
Other names (2R)-2-hydroxy-4-phenylbutanoic 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:103404-58-6 SDS

103404-58-6Upstream product

103404-58-6Downstream Products

103404-58-6Relevant articles and documents

Enzymatic Synthesis of Optically Pure (R)-(-)-Mandelic Acid and Other 2-Hydroxycarboxylic Acids: Screening for the Enzyme, and Its Purification, Characterization and Use

Yamazaki, Yoshimitsu,Maeda, Hidekatsu

, p. 2621 - 2632 (2007/10/02)

An enzyme that reduces benzoylformate with NADH to form (R)-mandelate was extracted from cells of Streptococcus faecalis IFO 12964 and purified to more than 95percent purity as evidenced by gel electrophoresis.Physicochemical and enzymic properties were studied.From the substrate specificity, we concluded that the enzyme was a kind of (R)-2-hydroxyisocaproate dehydrogenase.Optically pure (R)-(-)-mandelic acid was prepared with the enzyme, NADH, and alcohol, formate or glucose dehydrogenase in 84 ca. 93percent yield.Five (R)-2-hydroxyalkanoic acids (C4 - C6) or their Ba salts, (R)-(+)-3-phenyllactic acid and (S)-(-)-3-chlorolactic acid were also prepared with the enzyme.

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