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251712

Sigma-Aldrich

tert-Butyl glycidyl ether

99%

Synonym(s):

(tert-Butoxymethyl)oxirane

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About This Item

Empirical Formula (Hill Notation):
C7H14O2
CAS Number:
7665-72-7
Molecular Weight:
130.18
Beilstein:
103483
EC Number:
231-640-0
MDL number:
MFCD00010050
UNSPSC Code:
12162002
PubChem Substance ID:
24855152
NACRES:
NA.23

Assay

99%

form

liquid

refractive index

n20/D 1.417 (lit.)

density

0.917 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)OCC1CO1

InChI

1S/C7H14O2/c1-7(2,3)9-5-6-4-8-6/h6H,4-5H2,1-3H3

InChI key

SFJRUJUEMVAZLM-UHFFFAOYSA-N

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Related Categories

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H302,H317,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Sens. 1

Supplementary Hazards

EUH019

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

105.8 °F - closed cup

Flash Point(C)

41 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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A F Frost et al.
Mutation research, 102(2), 193-200 (1982-09-01)
Unscheduled DNA synthesis (UDS) was examined in normal human peripheral blood lymphocytes (HPBL) exposed to n- and tert.-butyl glycidyl ethers (BGE). n-BGE, which is currently used as a major reactive diluent for industrial epoxy resin systems, has been implicated as
Michael Kotik et al.
Biochimica et biophysica acta, 1760(2), 245-252 (2005-12-14)
Purification of a novel enantioselective epoxide hydrolase from Aspergillus niger M200 has been achieved using ammonium sulphate precipitation, ionic exchange, hydrophobic interaction, and size-exclusion chromatography, in conjunction with two additional chromatographic steps employing hydroxylapatite, and Mimetic Green. The enzyme was

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