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2,3-dihydroxy-2-methylbutanoic acid is an organic compound that falls under the category of hydroxy acids. These are carboxylic acids with at least one hydroxyl (-OH) group. In this particular molecule, the presence of two hydroxyl groups and a methyl (-CH3) group attached to the butanoic acid backbone gives it its distinctive name. 2,3-dihydroxy-2-methylbutanoic acid is known for its versatile applications, particularly in the medical and cosmetics industries, owing to its hydroxy acid properties. While there is limited information on its toxicity or environmental impact, it is understood that as an organic compound, it participates in various metabolic processes. Additionally, it is predicted to predominantly exist in a protonated form within biological systems, which may lead to skin and eye irritation similar to other acids. Some individuals may also experience allergic reactions to 2,3-dihydroxy-2-methylbutanoic acid.

14868-24-7

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14868-24-7 Usage

Uses

Used in Medical Applications:
2,3-dihydroxy-2-methylbutanoic acid is used as a therapeutic agent for its potential benefits in the medical field. Its hydroxy acid properties may contribute to its effectiveness in treating certain conditions, although more research is needed to fully understand its impact and safety profile.
Used in Cosmetics Industry:
In the cosmetics industry, 2,3-dihydroxy-2-methylbutanoic acid is utilized as an ingredient in various skincare and beauty products. Its hydroxy acid nature allows it to potentially offer exfoliating and skin-brightening effects, making it a valuable component in formulations aimed at improving skin texture and appearance.
Used in Metabolic Research:
2,3-dihydroxy-2-methylbutanoic acid is employed as a subject of study in metabolic research. Given its classification as an organic compound, it is involved in numerous metabolic processes, making it an interesting candidate for investigations into how it interacts with biological systems and potentially contributes to overall health and wellness.

Check Digit Verification of cas no

The CAS Registry Mumber 14868-24-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,8,6 and 8 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14868-24:
(7*1)+(6*4)+(5*8)+(4*6)+(3*8)+(2*2)+(1*4)=127
127 % 10 = 7
So 14868-24-7 is a valid CAS Registry Number.

14868-24-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dihydroxy-2-methylbutanoic acid

1.2 Other means of identification

Product number -
Other names 2-methyl-4-deoxy-erythronic 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:14868-24-7 SDS

14868-24-7Downstream Products

14868-24-7Relevant academic research and scientific papers

PHENYLPROPANOIDS AND OTHER DERIVATIVES FROM THAPSIA VILLOSA

Teresa, J. De Pascual,Moran, Joaquin R.,Hernandez, Jose M.,Grande, M.

, p. 2071 - 2074 (1985)

Key Word Index - Thapsia villosa; Umbelliferae; roots; phenylpropanoids; hemanticine; guaianolides; thapsivillosin K. - Five phenylpropanoids related to hemanticine have been obtained from Thapsia villosa roots.We propose for these substances the trivial names isohelmanticine, neohelmanticine, isoneohelmanticine, epoxyhelmanticine and epoxyhelmanticine angelate.All these substances are based on (1S,2R)1-(3-methoxy-4,5-methylenedioxyphenyl)-1,2-propanediol, which is esterified variously by acetic, angelic, epoxyangelic and/or (2R,3S)2,3-dihydroxy-2-methylbutyric acids.We also report three C6-guaianolides and their hydrolysis products.The name thapsivillosin K is proposed for a new guaianolide.

ENZYMATIC ENANTIOSELECTIVE HYDROLYSIS OF 2,2-DIMETHYL-1,3-DIOXOLANE-4-CARBOXYLIC ESTERS

Pottie, M.,Eycken, J. Van der,Vandewalle, M.,Dewanckele, J. M.,Roeper, H.

, p. 5319 - 5322 (2007/10/02)

2,2-dimethyl-1,3-dioxolane-4-carboxylic acid derived chiral building blocks were prepared from substituted α,β-unsaturated acids with high enantiomeric purities by enzymatic hydrolysis of their n.butyl esters.

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