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07-5640

Diphenyl ether

Name: Diphenyl ether
Brand: SAJ

SAJ first grade, ≥98.0%

Synonyme(s) :

Diphenyl oxide, Phenyl ether

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About This Item

Formule linéaire :

(C₆H₅)₂O

Numéro CAS:

101-84-8

Poids moléculaire :

170.21

Beilstein:

1364620

Numéro CE :

202-981-2

Numéro MDL:

MFCD00003034

Code UNSPSC :

12352112

ID de substance PubChem :

329748483

Qualité

SAJ first grade

Densité de vapeur

>5.86 (25 °C, vs air)

Pression de vapeur

<1 mmHg ( 20 °C)

Essai

≥98.0%

Forme

crystalline

Température d'inflammation spontanée

1144 °F

Limite d'explosivité

1.5 %

Disponibilité

available only in Japan

Indice de réfraction

n20/D 1.579 (lit.)

pb

259 °C (lit.)

Pf

25-27 °C (lit.)

Densité

1.073 g/mL at 25 °C (lit.)

Chaîne SMILES

O(c1ccccc1)c2ccccc2

InChI

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

Clé InChI

USIUVYZYUHIAEV-UHFFFAOYSA-N

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Pictogrammes

GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H319,H410

Conseils de prudence

P264 - P273 - P280 - P305 + P351 + P338 - P337 + P313 - P391

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

239.0 °F - closed cup

Point d'éclair (°C)

115 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number

A3149

A8647

A1230

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Determinants of prenatal exposure to polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) in an urban population.

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

Solvent effects on the hydrogenolysis of diphenyl ether with Raney nickel and their implications for the conversion of lignin.

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

Synthesis and herbicidal activity of diphenyl ether derivatives containing unsaturated carboxylates.

Haibo Yu et al.

Journal of agricultural and food chemistry, 59(21), 11718-11726 (2011-10-01)

A series of novel diphenyl ether derivatives containing unsaturated carboxylates were designed and synthesized. Their structures were identified by (1)H nuclear magnetic resonance and elemental analyses. The bioassays indicated that the compounds 5b and 5c exhibited good herbicidal activities against

Mechanism and inhibition of saFabI, the enoyl reductase from Staphylococcus aureus.

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

Formation of toxic species and precursors of PCDD/F in thermal decomposition of alpha-cypermethrin.

Sindra L Summoogum et al.

Chemosphere, 85(2), 143-150 (2011-07-09)

This article examines the thermal decomposition of alpha-cypermethrin, one of the most common pyrethroid pesticides. The objective was to identify its decomposition pathways and to gain an understanding into the formation of toxic species in the environment, including those that

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