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109975

Sigma-Aldrich

1,2-Epoxybutane

99%

Synonyma:

α-Butylene oxide, 1,2-Butylene oxide, 1-Butene oxide, Ethyloxirane

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen


About This Item

Empirický vzorec (Hillův zápis):
C4H8O
Číslo CAS:
Molekulová hmotnost:
72.11
Beilstein/REAXYS Number:
102411
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23

vapor density

2.2 (vs air)

vapor pressure

140 mmHg ( 20 °C)

assay

99%

autoignition temp.

698 °F

expl. lim.

19 %

refractive index

n20/D 1.384 (lit.)

bp

63 °C (lit.)

density

0.829 g/mL at 25 °C (lit.)

SMILES string

CCC1CO1

InChI

1S/C4H8O/c1-2-4-3-5-4/h4H,2-3H2,1H3

InChI key

RBACIKXCRWGCBB-UHFFFAOYSA-N

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Application

1,2-Epoxybutane can be used:
  • As a monomer to synthesize novel initiators via ring-opening polymerization. These initiators can be used to prepare complex macromolecules such as grafted polyamides.
  • To functionalize polyethyleneimine which is used in the synthesis of oxidation-stable adsorbents for CO2 capture.

Features and Benefits

  • High polymerizability
  • Low susceptibility to transfer reaction
  • Ease of handling

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

5.0 °F - closed cup

flash_point_c

-15 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves


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Osvědčení o analýze (COA)

Lot/Batch Number

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Zákazníci si také prohlíželi

T Nakamura et al.
Biochemical and biophysical research communications, 180(1), 124-130 (1991-10-15)
Halohydrin hydrogen-halide-lyase, which catalyzes the interconversion of halohydrins to epoxides, purified from a recombinant E. coli was found to catalyze the transformation of 1,2-epoxybutane into beta-hydroxyvaleronitrile in the presence of cyanide. Chloride inhibited competitively the formation of beta-hydroxyvaleronitrile. The enzyme
M Katz et al.
Journal of environmental pathology and toxicology, 3(5-6), 171-187 (1980-06-01)
Nitrosopiperidine, sodium nitrite and 1,2 epoxybutane were tested in the Ames agar incorporation assay in an attempt to establish exact criteria for detecting the activity of these weak mutagens. As regards minimum concentrations it was determined that at 500 microgram
A M Rossi et al.
Teratogenesis, carcinogenesis, and mutagenesis, 3(1), 75-87 (1983-01-01)
In vivo and in vitro methodologies that have employed the yeast Schizosaccharomyces pombe as genetic indicator have been utilized to investigate the mutagenicity of two trichloroethylene (TCE) samples of pure and technical grade. Mutagenicity assays were also performed on two
Hong Yuan Sun et al.
Carbohydrate research, 344(15), 1999-2004 (2009-08-26)
A new soluble cyclodextrin derivative 6-O-(2-hydroxybutyl)-beta-cyclodextrin (6-HB-beta-CD) was prepared. Its molecular binding and recognition ability were investigated with the comparison of beta-cyclodextrin (beta-CD), 2-O-(2-hydroxypropyl)-beta-cyclodextrin (2-HP-beta-CD), 6-O-(2-hydroxypropyl)-beta-cyclodextrin (6-HP-beta-CD), and 2-O-(2-hydroxybutyl)-beta-cyclodextrin (2-HB-beta-CD). The relationship between the complex stability constants and the possible
D B McGregor et al.
Environmental and molecular mutagenesis, 13(3), 197-202 (1989-01-01)
Trichloroethylene (TCE) is a high production volume chemical frequently stabilized with oxiranes. These oxiranes may be responsible for the mutagenic activity of TCE in Salmonella, which has been occasionally, but not consistently, reported. High purity and oxirane-stabilized TCE samples were

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