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779202

Sigma-Aldrich

Ethylene oxide solution

2.5-3.3 M in THF

Synonym(s):

Dimethylene oxide, Epoxyethane, Ethyleneoxy, Oxacyclopropane, Oxidoethane

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About This Item

Empirical Formula (Hill Notation):
C2H4O
CAS Number:
Molecular Weight:
44.05
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

form

solution

Quality Level

reaction suitability

reaction type: C-C Bond Formation

concentration

2.5-3.3 M in THF

SMILES string

C1CO1

InChI

1S/C2H4O/c1-2-3-1/h1-2H2

InChI key

IAYPIBMASNFSPL-UHFFFAOYSA-N

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Application

Ethylene oxide solution can be used for the conversion of ortho-carborane to (2′-hydroxyethyl)-1,2-dicarba-closo-dodecaborane, a key step in the synthesis of ortho-carborane-modified N-alkyl-deoxynojirimycin (DNMs).

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Eye Dam. 1 - Flam. Liq. 2 - Muta. 1B - Repr. 1B - Skin Corr. 1 - STOT RE 1 - STOT SE 3

Target Organs

Central nervous system, Nervous system, Respiratory system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

1.4 °F

Flash Point(C)

-17 °C


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ortho?Carborane?Modified N?Substituted Deoxynojirimycin.
Hoogendoorn S
European Journal of Organic Chemistry, 2015(20), 4437-4446 (2015)
Faisal I Khan et al.
Journal of hazardous materials, 108(3), 147-159 (2004-05-04)
This paper discusses a methodology for the design of an optimum inspection and maintenance program. The methodology, called risk-based maintenance (RBM) is based on integrating a reliability approach and a risk assessment strategy to obtain an optimum maintenance schedule. First
V E Walker et al.
Mutation research, 233(1-2), 151-164 (1990-11-01)
The results of efforts to identify and quantify macromolecular adducts of ethylene oxide (ETO), to determine the source and significance of background levels of these adducts, and to generate molecular dosimetry data on these adducts are reviewed. A time-course study
Régis Coco et al.
International journal of pharmaceutics, 440(1), 3-12 (2012-07-24)
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Caught in the oxirane: Naphthalene diimides conjugated to a quinone methide and an oxirane have been synthesized and investigated as selective DNA G-quadruplex alkylating agents. The oxirane derivative generates a stable adduct with a G-quadruplex and shows selective alkylation of

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