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3-Hydroxy-3-methylpentane-2,4-dione, also known as dihydroxyacetone (DHA), is a natural organic compound that plays a significant role in various industrial and cosmetic applications. It is a colorless, water-soluble, and hygroscopic liquid with a molecular formula of C5H10O3. DHA is a three-carbon keto-diol, which means it contains two hydroxyl groups and a ketone group. It is an important intermediate in the metabolism of carbohydrates and is also used as a tanning agent in sunless tanning products due to its ability to react with the amino acids in the skin's surface proteins, creating a temporary bronzed appearance. Additionally, DHA has applications in the food industry as a sugar substitute and in the pharmaceutical industry as a precursor for the synthesis of various drugs.

7338-73-0

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7338-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7338-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,3 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7338-73:
(6*7)+(5*3)+(4*3)+(3*8)+(2*7)+(1*3)=110
110 % 10 = 0
So 7338-73-0 is a valid CAS Registry Number.

7338-73-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-hydroxy-3-methylpentane-2,4-dione

1.2 Other means of identification

Product number -
Other names Diacetylmethylcarbinol

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:7338-73-0 SDS

7338-73-0Relevant academic research and scientific papers

UV-LIGHT- AND RADIATION-INITIATED ADDITION OF ACETALDEHYDE TO ALLYL ALKANOATES

Liska, Frantisek,Valenta, Miroslav,Fikar, Jiri,Jandova, Martina,Pesek, Miroslav,Trska, Petr

, p. 1287 - 1296 (2007/10/02)

UV-light- and γ-60Co-initiated addition of acetaldehyde to allyl formate (I) and allyl acetate (II) yielded the 1:1 adducts - 4-oxopentyl formate (III) and 4-oxopentyl acetate (IV), respectively, together with the 1:2 telomers - 7-formyloxy-4-formyloxymethyl-2-heptanone (V) and 7-acetoxy-4-acetoxymethyl-2-heptanone (VI).The initial radiation yields are: G(III) = 200.8, G(IV) = 211.3, G(V) = 39.5, G(VI) = 37.9.Base-catalyzed transesterification of oxopentyl alkanoates III and IV afforded 5-hydroxy-2-pentanone (XIV), the same reaction of dialkylalkanoates VI and VII gave 5-hydroxy-4-hydroxymethyl-2-heptanone (XV).

Photolysis of Butane-2,3-dione in Fluorocarbon Solvents; a Chemically Induced Nuclear Polarization (CIDNP) Study

Broomhead, Eleanor J.,McLauchlan, Keith A.,Roe, Jonathan C.

, p. 796 - 804 (2007/10/02)

CIDNP observations of the polarized signals from products of radical reactions in solutions of neat butane-2,3-dione in perfluorocyclohexane and perfluorodecalin, and in solutions with added radical scavenger or hydrogen donor, are consistent with three primary processes.There are symmetric (probably) and unsymmetric fragmentation and hydrogen-abstraction by triplet butane-2,3-dione from the starting material, and each yields free radicals.In all solutions the mechanisms of ensuing reactions are suggested.In the presence of CCl4 and CCl3Br pair substitution effects dominate the CIDNP behaviour.When high concentrations of propan-2-ol are present evidence is given for reaction of the excited singlet state of the parent molecule.

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