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07-5640

Diphenyl ether

SAJ first grade, ≥98.0%

Synonym(s):

Diphenyl oxide, Phenyl ether

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About This Item

Linear Formula:
(C6H5)2O
CAS Number:
101-84-8
Molecular Weight:
170.21
EC Number:
202-981-2
UNSPSC Code:
12352112
PubChem Substance ID:
329748483
Beilstein/REAXYS Number:
1364620
MDL number:
MFCD00003034
Assay:
≥98.0%
Form:
crystalline
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grade

SAJ first grade

vapor density

>5.86 (25 °C, vs air)

vapor pressure

<1 mmHg ( 20 °C)

assay

≥98.0%

form

crystalline

autoignition temp.

1144 °F

expl. lim.

1.5 %

availability

available only in Japan

refractive index

n20/D 1.579 (lit.)

bp

259 °C (lit.)

mp

25-27 °C (lit.)

density

1.073 g/mL at 25 °C (lit.)

SMILES string

O(c1ccccc1)c2ccccc2

InChI

1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H

InChI key

USIUVYZYUHIAEV-UHFFFAOYSA-N

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wgk

WGK 2

flash_point_f

239.0 °F - closed cup

flash_point_c

115 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

signalword

Danger

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 1B

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
A3149
A8647
A1230

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Julie B Herbstman et al.
Environmental health perspectives, 115(12), 1794-1800 (2007-12-19)
Recent studies have reported blood levels of polybrominated diphenyl ethers (PBDEs) in the U.S. population. Information about neonatal levels and about the relationship to polychlorinated biphenyls (PCBs) exposures is limited. The objective was to characterize levels and determinants of fetal
Hua Xu et al.
Biochemistry, 47(14), 4228-4236 (2008-03-14)
Approximately one-third of the world's population carries Staphylococcus aureus. The recent emergence of extreme drug resistant strains that are resistant to the "antibiotic of last resort", vancomycin, has caused a further increase in the pressing need to discover new drugs
Xingyu Wang et al.
ChemSusChem, 5(8), 1455-1466 (2012-05-03)
The conversion of lignin, the most recalcitrant of the biopolymers, is necessary for a carbon-efficient utilization of lignocellulosic materials. In this context, hydrogenolysis of lignin is a process receiving increasing attention. In this report, the solvent effects on the hydrogenolysis
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