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5-hydroxy-6-methyl-2,3-dihydro-4H-pyran-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

38877-21-3

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38877-21-3 Usage

Also known as

2-hydroxy-3-methyldihydrofuran-4-one or maltol

Natural occurrence

Found in roasted malt, barley, coffee, and bread

Aroma

Sweet

Uses in industries

Flavor enhancer and fragrance in food and cosmetic industries

Precursor

Used in synthesis of other compounds

Properties

Potential antioxidant, antimicrobial, and antitumor properties

Application

Added to food and beverage products as a natural sweetener and flavoring agent

Check Digit Verification of cas no

The CAS Registry Mumber 38877-21-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,8,7 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38877-21:
(7*3)+(6*8)+(5*8)+(4*7)+(3*7)+(2*2)+(1*1)=163
163 % 10 = 3
So 38877-21-3 is a valid CAS Registry Number.

38877-21-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hydroxy-6-methyl-2,3-dihydropyran-4-one

1.2 Other means of identification

Product number -
Other names dihydromaltol

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:38877-21-3 SDS

38877-21-3Downstream Products

38877-21-3Relevant academic research and scientific papers

A dihydro maltol and dihydro ethyl maltol synthetic method

-

Paragraph 0027; 0028; 0029; 0030, (2017/08/25)

The invention discloses a dihydro maltol and dihydro ethyl maltol synthesis method. The method includes A, according to a formula II, allowing 2-methyl-5, 6-dihydro-2H-pyran and hydrogen peroxide to perform dihydroxylation under the effect of strong acid ion exchange resin, and obtaining a 2-methyl-3 and 4-dihydro-tetrahydropyrane intermediates of a formula III; B, according to the formula III, oxidizing the 2-methyl-3 and 4-dihydro-tetrahydropyrane intermediates through oxidation agent, and obtaining a compound of a formula IV. When R = ethyl, the compound of the formula IV is dihydro ethyl maltol; when R = methyl, the compound of the formula IV is dihydro maltol. The method adopts conventional chemical raw materials, and the reaction condition is mild.

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