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Merck
CN

532355

(R)-(+)-1,2-Epoxybutane

98%

Synonym(s):

(2R)-Ethyloxirane

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About This Item

Empirical Formula (Hill Notation):
C4H8O
CAS Number:
Molecular Weight:
72.11
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
98%
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Quality Level

assay

98%

optical activity

[α]20/D 10°, neat

refractive index

n20/D 1.386 (lit.)

bp

63 °C (lit.)

density

0.837 g/mL at 25 °C (lit.)

functional group

ether

SMILES string

CC[C@@H]1CO1

InChI

1S/C4H8O/c1-2-4-3-5-4/h4H,2-3H2,1H3/t4-/m1/s1

InChI key

RBACIKXCRWGCBB-SCSAIBSYSA-N



signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

10.0 °F - closed cup

flash_point_c

-12.2 °C - closed cup

ppe

Faceshields, Gloves, Goggles

Regulatory Information

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Zhengyuan Zhou et al.
International journal of pharmaceutics, 354(1-2), 82-87 (2007-12-08)
Ethylene oxide and 1,2-butylene oxide were sequentially polymerised to form the diblock copolymer E13B10 (E=oxyethylene, B=oxybutylene, subscripts denote number-average block lengths in repeat units). Dynamic and static light scattering over the temperature range 10-30 degrees C demonstrated a transition from
D Weinstein et al.
Environmental mutagenesis, 3(1), 1-9 (1981-01-01)
Based on the findings of Nagao et al [1978] that phenacetin is negative in the standard Ames test with Aroclor induced rat S-9 and positive with hamster S-9, the test was performed with a mixture of rat/hamster S-9. Phenacetin was
A Ohnishi et al.
Environmental research, 60(2), 242-247 (1993-02-01)
Axonal neuropathy occurs due to occupational ethylene oxide (EtO) exposure. The experimental model of human EtO neuropathy was established. In addition, the neurotoxic effects of propylene oxide (PpO) and butylene oxide (BtO) were demonstrated in rats. Although no human neuropathy



Global Trade Item Number

SKUGTIN
532355-1G04061832558943
532355-5G04061837395291