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W322504

Sigma-Aldrich

Phenyl disulfide

≥98%

Sinonimo/i:

Diphenyl disulfide, NSC 2689

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About This Item

Formula condensata:
C6H5SSC6H5
Numero CAS:
882-33-7
Peso molecolare:
218.34
Numero FEMA:
3225
Beilstein:
639794
Numero CE:
212-926-4
N° CoE:
11757
Numero MDL:
MFCD00003065
Codice UNSPSC:
12164502
ID PubChem:
24901566
Numero Flavis:
12.043

Origine biologica

synthetic

Grado

Halal
Kosher

Saggio

≥98%

Punto di fusione

58-60 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Organolettico

earthy; sulfurous

Stringa SMILE

S(Sc1ccccc1)c2ccccc2

InChI

1S/C12H10S2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10H
GUUVPOWQJOLRAS-UHFFFAOYSA-N

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Altre note

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Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H410

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
MKBW1993V
MKBT7955V
MKBD6836
08219HH
08326LE

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S C Mitchell et al.
Drug metabolism and drug interactions, 16(3), 191-206 (2000-12-16)
Radiolabelled [UL-14C]-diphenyl sulphide, [UL-14C]-diphenyl sulphoxide and [UL-14C]-diphenyl sulphone were administered by gavage (1.0 mmol/kg body weight) to adult male Wistar rats following an overnight fast. For all compounds, faeces were the major route of excretion of radioactivity (50%). Urinary elimination
Ana Mijovilovich et al.
The journal of physical chemistry. A, 114(35), 9523-9528 (2010-08-19)
Sulfur K-edge XANES was measured for two divalent sulfurs (dibenzyl and benzyl phenyl) and two disulfides (dibenzyl and diphenyl). The absorption spectra could be assigned using density functional theory with the "half core hole" approximation for the core hole including
C W Nogueira et al.
Toxicology, 191(2-3), 169-178 (2003-09-11)
Organochalcogens are important intermediates and useful reagents in organic synthesis, which can increase human exposure risk to these chemicals in the workplace. As well, there are a number of reported cases of acute toxicity following organochalcogen ingestion of vitamins and
J I Rossato et al.
Neurochemical research, 27(4), 297-303 (2002-04-18)
Ebselen (2-phenyl- 1,2-benzisoselenazole-3 (2H)-one) is a seleno-organic compound with antioxidant properties, and anti-inflammatory actions. Recently, ebselen improved the outcome of acute ischemic stroke in humans. In the present study, the potential antioxidant capacity of organochalcogenide compounds diphenyl diselenide (PhSe)2, diphenyl
Y Ito et al.
Mutation research, 393(3), 307-316 (1997-12-11)
The suppressive effect of S-methyl methanethiosulfonate (MMTS) on aflatoxin B1 (AFB1)- or methyl methanesulfonate (MMS)-induced chromosome aberrations (CA) in rat bone marrow cells was studied. MMTS significantly suppressed CA induced by both AFB1 (an indirect-acting carcinogen) and MMS (a direct-acting
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