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2,4-Pentanedione, 1,3-dihydroxy-, (S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 147523-70-4 Structure
  • Basic information

    1. Product Name: 2,4-Pentanedione, 1,3-dihydroxy-, (S)- (9CI)
    2. Synonyms: 2,4-Pentanedione, 1,3-dihydroxy-, (S)- (9CI)
    3. CAS NO:147523-70-4
    4. Molecular Formula: C5H8O4
    5. Molecular Weight: 132.11462
    6. EINECS: N/A
    7. Product Categories: ACETYLGROUP
    8. Mol File: 147523-70-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2,4-Pentanedione, 1,3-dihydroxy-, (S)- (9CI)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-Pentanedione, 1,3-dihydroxy-, (S)- (9CI)(147523-70-4)
    11. EPA Substance Registry System: 2,4-Pentanedione, 1,3-dihydroxy-, (S)- (9CI)(147523-70-4)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 147523-70-4(Hazardous Substances Data)

147523-70-4 Usage

Physical Properties

Colorless, odorless liquid

Function

Used in self-tanning products to react with amino acids in the skin to produce a brown pigment, giving the appearance of a tan

Safety

Considered safe for topical use, but may cause skin irritation in some individuals

Instructions

It is important to follow product instructions and seek medical advice if irritation occurs

Precautions

Inhalation or ingestion should be avoided as it may cause irritation to the respiratory and gastrointestinal systems

Industry Use

Widely used in the cosmetic industry for achieving a sun-kissed glow without exposure to harmful UV rays

Check Digit Verification of cas no

The CAS Registry Mumber 147523-70-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,5,2 and 3 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 147523-70:
(8*1)+(7*4)+(6*7)+(5*5)+(4*2)+(3*3)+(2*7)+(1*0)=134
134 % 10 = 4
So 147523-70-4 is a valid CAS Registry Number.

147523-70-4SDS

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 (3S)-1,3-dihydroxypentan-2,4-dione

1.2 Other means of identification

Product number -
Other names (S)-1,3-Dihydroxy-pentane-2,4-dione

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:147523-70-4 SDS

147523-70-4Downstream Products

147523-70-4Relevant articles and documents

Enzyme-catalysed Carbon-Carbon Bond Formation: Use of Transketolase from Escherichia coli

Hobbs, Gordon R.,Lilly, Malcolm D.,Turner, Nicholas J.,Ward, John M.,Willets, Andrew J.,Woodley, John M.

, p. 165 - 166 (2007/10/02)

Transketolase has been obtained in greater quantities from an over-expressed E. coli transformant carrying the transketolase gene.Crude extracts of this organism are suitable for use in small scale biotransformations to provide mmol quantities of product.Initial results indicate that the transketolase from E. coli is relatively non-specific for the aldehyde component of the reaction.

ENZYME-CATALYZED SYNTHESIS OF CARBOHYDRATES: SYNTHETIC POTENTIAL OF TRANSKETOLASE

Demuynck, Colette,Bolte, Jean,Hecquet, Laurence,Dalmas, Valerie

, p. 5085 - 5088 (2007/10/02)

The synthetic potential of yeast or spinach transketolases was studied, using hydroxypyruvate as a donor substrate and 31 aldehydes as acceptors.All of them react, including aromatic, heteroaromatic and α,β unsaturated aldehydes.

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