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58957-60-1

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58957-60-1 Usage

General Description

(R*,S*)-()-dihydro-5-(1-hydroxyethyl)-3H-furan-2-one, also known as maltol, is a naturally occurring organic compound that is commonly found in various food products, especially those that have been subjected to heat treatment or fermentation processes. It is widely used as a flavor enhancer and fragrance ingredient in the food and beverage industry. Maltol has a sweet, caramel-like aroma and is often used to impart a pleasant, sweet taste to a range of products, including baked goods, confectionery, and beverages. It also has antioxidant properties and is being investigated for potential therapeutic applications in the treatment of various diseases. Maltol is generally recognized as safe for consumption by regulatory authorities, and its use in food and cosmetic products is widespread.

Check Digit Verification of cas no

The CAS Registry Mumber 58957-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,9,5 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 58957-60:
(7*5)+(6*8)+(5*9)+(4*5)+(3*7)+(2*6)+(1*0)=181
181 % 10 = 1
So 58957-60-1 is a valid CAS Registry Number.

58957-60-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-5-((R)-1-hydroxyethyl)dihydrofuran-2(3H)-one

1.2 Other means of identification

Product number -
Other names -

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:58957-60-1 SDS

58957-60-1Relevant articles and documents

(+/-)-erythro-γ,δ-Dihydroxycarboxylic Acid Lactones from a β-Lithiopropionate Equivalent and α-Chloroaldehydes

Plewe, Michael,Schmidt, Richard R.

, p. 534 - 536 (2007/10/02)

Reaction of β-ethylthio-β-lithioacrylate 1A with α-chloroaldehydes furnished predominantly the erythro products 3, which were isolated as γ-lactones 4.At room temperature intermediates 3 are transformed into the (+/-)-erythro-γ,δ-dihydroxycarboxylic acid γ-lactones 8.Raney nickel treatment provided interesting natural γ-lactone derivatives; thus, from erythro-8c the socalled L-factor erythro-9c was obtained.Similarly, from β-methoxy β-lithioacrylate 10A the (+/-)-erythro-γ,δ-dihydroxycarboxylic acid δ-lactone erythro-11 was gained.

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