578576
1,2-环氧-3-苯氧基丙烷
technical grade
别名:
2,3-环氧丙基苯醚, 缩水甘油基苯基醚, 苯基缩水甘油醚
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经验公式（希尔记法）:
C9H10O2
化学文摘社编号:
分子量:
150.17
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
204-557-2
Beilstein/REAXYS Number:
2744
MDL number:
InChI key
FQYUMYWMJTYZTK-UHFFFAOYSA-N
InChI
1S/C9H10O2/c1-2-4-8(5-3-1)10-6-9-7-11-9/h1-5,9H,6-7H2
SMILES string
C1OC1COc2ccccc2
grade
technical grade
vapor density
5.2 (vs air)
vapor pressure
0.03 mmHg ( 20 °C)
refractive index
n20/D 1.53 (lit.), n20/D 1.530 (lit.)
bp
245 °C (lit.)
mp
3.5 °C (lit.)
density
1.109 g/mL at 25 °C (lit.)
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Carc. 1B - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
237.2 °F - closed cup
flash_point_c
114 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Shijin Wu et al.
Applied microbiology and biotechnology, 76(6), 1281-1287 (2007-08-22)
Bacillus sp. Z018, a novel strain producing epoxide hydrolase, was isolated from soil. The epoxide hydrolase catalyzed the stereospecific hydrolysis of (R)-phenyl glycidyl ether to generate (R)-3-phenoxy-1,2-propanediol. Epoxide hydrolase from Bacillus sp. Z018 was inducible, and (R)-phenyl glycidyl ether was
M Garrido et al.
Analytica chimica acta, 585(2), 277-285 (2007-03-28)
This paper reports the validation of the results obtained by combining near infrared spectroscopy and multivariate curve resolution-alternating least squares (MCR-ALS) and using high performance liquid chromatography as a reference method, for the model reaction of phenylglycidylether (PGE) and aniline.
Manfred T Reetz et al.
Organic letters, 6(2), 177-180 (2004-01-16)
[reaction: see text] The epoxide hydrolase (EH) from Aspergillus niger, which shows a selectivity factor of only E = 4.6 in the hydrolytic kinetic resolution of glycidyl phenyl ether, has been subjected to directed evolution for the purpose of enhancing
Ida B Niklasson et al.
Chemical research in toxicology, 22(11), 1787-1794 (2009-09-04)
Epoxy resins can be prepared from numerous chemical compositions. Until recently, alternatives to epoxy resins based on diglycidyl ethers of bisphenol A (DGEBA) or bisphenol F (DGEBF) monomers have not received commercial interest, but are presently doing so, as epoxy
Dermatitis from phenyl glycidyl ether.
E Rudzki et al.
Contact dermatitis, 9(1), 90-91 (1983-01-01)
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