127574
3,4-Epoxy-1-butene
98%
Synonym(s):
2-Vinyloxirane, 3,4-Epoxy-1-butene, Butadiene monoxide
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About This Item
Empirical Formula (Hill Notation):
C4H6O
CAS Number:
Molecular Weight:
70.09
Beilstein:
103170
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.417 (lit.)
bp
65-66 °C (lit.)
density
0.87 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C=CC1CO1
InChI
1S/C4H6O/c1-2-4-3-5-4/h2,4H,1,3H2
InChI key
GXBYFVGCMPJVJX-UHFFFAOYSA-N
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Related Categories
accessory
Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
-58.0 °F - closed cup
Flash Point(C)
-50 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Ewan D Booth et al.
Chemico-biological interactions, 147(2), 195-211 (2004-03-12)
Male Sprague-Dawley rats and B6C3F1 mice were exposed to either a single 6h or a multiple (5) daily (6h) nose-only dose of 1,3-[2,3-(14)C]-butadiene at exposure concentrations of nominally 1, 5 or 20 ppm. The aim was to compare the results
Quanxin Meng et al.
Chemico-biological interactions, 166(1-3), 207-218 (2006-07-21)
The carcinogenicity of 1,3-butadiene (BD) is related to its bioactivation to several DNA-reactive metabolites; accumulating evidence suggests that the stereochemistry of these BD intermediates may play a significant role in the mutagenic and carcinogenic actions of the parent compound. The
Barry M Trost et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 12(25), 6607-6620 (2006-06-30)
Palladium catalyzed asymmetric allylic alkylation reaction of an amine with two equivalents of butadiene monoxide allows for the expedient synthesis of trans- and cis-2,5-dihydropyrroles. The versatility of these chiral synthons towards the synthesis of a wide variety of iminosugar natural
Valeria Di Bussolo et al.
The Journal of organic chemistry, 69(21), 7383-7386 (2004-10-09)
The reaction of alpha vinyl oxirane 5, prepared through a new route to the d-gulal system, with O-nucleophiles (alcohols and di-O-isopropylidene-alpha-d-monosaccharides) and C-nucleophiles (lithium alkyls) affords, in a completely stereoselective way, the corresponding 2-unsaturated alpha O- and C-glycosides having the
Hitesh V Motwani et al.
Chemico-biological interactions, 288, 57-64 (2018-04-14)
DNA adducts can be formed from covalent binding of electrophilic reactive compounds to the nucleophilic N- and O-atoms of the biomolecule. The O-sites on DNA, with nucleophilic strength (n) of ca. 2, is recognized as a critical site for mutagenicity.
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