62875-07-4

Basic information

• Product Name: 2-methylbutane-1,2,4-triol
• Synonyms: 2-methylbutane-1,2,4-triol;2-Methyl-1,2,4-butanetriol
• CAS NO: 62875-07-4
• Molecular Formula: C₅H₁₂O₃
• Molecular Weight: 120.14698
• EINECS: 263-746-8
• Mol File: 62875-07-4.mol

Chemical Properties

• Boiling Point: 286.7 °C at 760 mmHg
• Flash Point: 145.5 °C
• Appearance: /
• Density: 1.159 g/cm³
• Vapor Pressure: 0.000292mmHg at 25°C
• Refractive Index: 1.486
• CAS DataBase Reference: 2-methylbutane-1,2,4-triol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylbutane-1,2,4-triol(62875-07-4)
• EPA Substance Registry System: 2-methylbutane-1,2,4-triol(62875-07-4)

Safety Data

• Hazardous Substances Data: 62875-07-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-methylbutane-1,2,4-triol is used as an active ingredient in the production of various pharmaceuticals due to its potential antioxidant and anti-inflammatory properties. It contributes to the development of medications that can help in treating various health conditions.
Used in Cosmetics and Personal Care Products:
In the cosmetics and personal care industry, 2-methylbutane-1,2,4-triol is used as a key component in the formulation of products such as creams, lotions, and shampoos. Its sweet taste and solubility in water and ethanol make it an ideal ingredient for enhancing the sensory experience and improving the efficacy of these products.
Used in Organic Synthesis:
2-methylbutane-1,2,4-triol is utilized in the synthesis of various organic compounds, serving as a versatile building block for the creation of new molecules with potential applications in different fields.
Used as a Biofuel Additive:
Due to its high octane rating, 2-methylbutane-1,2,4-triol has been studied for its potential use as a biofuel additive. It can improve the performance and efficiency of biofuels, making them more environmentally friendly and sustainable energy sources.
Used in Medicine and Health Research:
The potential antioxidant and anti-inflammatory properties of 2-methylbutane-1,2,4-triol have attracted the attention of researchers in the field of medicine and health. It is being investigated for its potential to contribute to the development of new treatments and therapies for various diseases and conditions.

InChI:InChI=1/C5H12O3/c1-5(8,4-7)2-3-6/h6-8H,2-4H2,1H3

Upstream product

• 597-44-4 2-hydroxy-2-methylbutane-1,4-dioic acid 
• 59954-67-5 3,4-epoxy-3-methylbutanol 
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• 6236-09-5 (S)-citramalic acid 
• 107127-75-3 (+/-)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane 
• 78947-95-2 3-(iodomethyl)-3-methyl-2,6-dioxacyclohexanone 
• 763-32-6 2-methyl-1-buten-4-ol 
• 58558-53-5 (((3-methylbut-3-en-1-yl)oxy)methyl)benzene 

Relevant articles and documents

Molybdenum-Catalyzed Hydroxyl-Directed Anti-Dihydroxylation of Allylic and Homoallylic Alcohols

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The regio- and stereoselective synthesis of cyclic iodo carbonates 1-10, resulting from allylic and homoallylic alcohols was investigated.These useful intermediates were easily hydrolyzed to epoxy alcohols 11-20 or triols 21-30, depending on the polymeric reagent employed (Amberlyst A 26 in the OH- or CO32- form, respectively).Stereochemical assignments were carried out by 13C NMR or 1H NMR correlations and by conversion of the compounds to products of known stereostructures.

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