86161-40-2

Basic information

• Product Name: 3-BUTENE-1,2-DIOL
• Synonyms: 3,4-DIHYDROXY-1-BUTENE;3-BUTENE-1,2-DIOL;EPB(TM) DIOL;BUT-3-ENE-1,2-DIOL;R,S-3-BUTENE-1,2-DIOL
• CAS NO: 86161-40-2
• Molecular Formula: C4H8O2
• Molecular Weight: 88.11
• EINECS: 207-835-1
• Mol File: 86161-40-2.mol
• Article Data: 68

Chemical Properties

• Melting Point: 15.1°C (estimate)
• Boiling Point: 196.5 °C(lit.)
• Flash Point: 222 °F
• Appearance: /
• Density: 1.047 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.462
• Storage Temp.: 0-6°C
• CAS DataBase Reference: 3-BUTENE-1,2-DIOL(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BUTENE-1,2-DIOL(86161-40-2)
• EPA Substance Registry System: 3-BUTENE-1,2-DIOL(86161-40-2)

Safety Data

• Hazard Codes: Xn
• Statements: 36/37/38
• Safety Statements: 36
• WGK Germany: 3
• F: 10
• Hazardous Substances Data: 86161-40-2(Hazardous Substances Data)

Usage

General Description

3-Butene-1,2-diol is a chemical compound with the molecular formula C4H8O2. It is a type of diol, which means it contains two hydroxyl (OH) functional groups. 3-Butene-1,2-diol is a colorless, viscous liquid at room temperature and is soluble in water. It is commonly used as a chemical intermediate in the production of various polymers and industrial chemicals. Additionally, it serves as a crosslinking agent in the production of resins and coatings. 3-Butene-1,2-diol also has potential applications in the pharmaceutical and cosmetic industries. Overall, this compound plays a significant role in the synthesis of a wide range of products and is important in various industrial processes.

Upstream product

• 930-22-3 epoxybutene 
• 110-57-6 trans-1,4-dichlorobut-2-ene 
• 6974-12-5 1,4-dibromo-2-butene 
• 821-06-7 (E)-1,4-dibromobutene 
• 909878-64-4 meso-erythritol 
• 590-19-2 2,3-dimethylbutene 
• 106-99-0 buta-1,3-diene 
• 671-56-7 1-chloro-2-hydroxy-3-butene 
• 18866-73-4 cis-1,4-dibromo-2-butene 
• 62214-38-4 (S)-1,2-O-isopropylidene-but-3-ene-1,2-diol 
• 497-06-3 3,4-butenediol 
• 87-69-4 L-Tartaric acid 
• 4427-96-7 (R)-(+)-4-vinyl-1,3-dioxolan-2-one 
• 821-11-4 1,4-butenediol 

Downstream Products

• 86106-09-4 (R)-(+)-3,4-dihydroxy-1-butene 
• 133095-74-6 (S)-2-hydroxy-3-buten-1-yl p-tosylate 
• 138249-07-7 2-hydroxy-(2R)-3-butenyl-4-methyl-1-benzenesulfonate 
• 17177-50-3 (+/-)-(1,2-Dihydroxyethyl)oxirane 
• 62214-39-5 (2S)-but-3-ene-1,2-diol 
• 4427-96-7 4-vinyl-1,3-dioxolan-2-one 
• 1411949-68-2 2-(2,2,3-trimethylcyclopent-3-enylmethyl)-4-vinyl-[1,3]dioxolane 
• 1411949-33-1 2-ethyl-2-(2-methylbutyl)-4-vinyl-[1,3]dioxolane 
• 151864-82-3 Ethyl 4-(4-hydroxy-3-oxobutyl)benzoate 
• 83968-02-9 2,2-dimethyl-4-vinyl-1,3-dioxolane 

Relevant articles and documents

Preparation method of vinylethylene sulfite

The invention belongs to the field of additives, and particularly relates to a preparation method of vinylethylene sulfite. The invention discloses a preparation method of vinylethylene sulfite, whichcomprises the following step: reacting 3-butylene-1,2-diol with thionyl chloride to obtain vinylethylene sulfite. The preparation method has the advantages of simple operation, easily available raw materials, greenness, environmental protection, and great implementation value and social and economic benefits.

An Amphiphilic (salen)Co Complex – Utilizing Hydrophobic Interactions to Enhance the Efficiency of a Cooperative Catalyst

An amphiphilic (salen)Co(III) complex is presented that accelerates the hydrolytic kinetic resolution (HKR) of epoxides almost 10 times faster than catalysts from commercially available sources. This was achieved by introducing hydrophobic chains that increase the rate of reaction in one of two ways – by enhancing cooperativity under homogeneous conditions, and increasing the interfacial area under biphasic reaction conditions. While numerous strategies have been employed to increase the efficiency of cooperative catalysts, the utilization of hydrophobic interactions is scarce. With the recent upsurge in green chemistry methods that conduct reactions ‘on water’ and at the oil-water interface, the introduction of hydrophobic interactions has potential to become a general strategy for enhancing the catalytic efficiency of cooperative catalytic systems. (Figure presented.).

Olefin reaction in the catalyst and the olefin production

PROBLEM TO BE SOLVED: To provide a catalyst for obtaining an olefin in high selectivity with a vicinal diol as a raw material.SOLUTION: A catalyst for olefination reaction for use in a reaction to produce an olefin by a reaction of a polyol, having two adjacent carbon atoms each having a hydroxy group, with hydrogen comprises: a carrier; at least one oxide selected from the group consisting of oxides of the group 6 elements and oxides of the group 7 elements supported on the carrier; and at least one metal selected from the group consisting of silver, iridium, and gold supported on the carrier.SELECTED DRAWING: None