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Key Documents

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46528

Supelco

Diphenyl sulfide

PESTANAL®, analytical standard

Sinonimo/i:

Phenyl sulfide

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About This Item

Formula condensata:
(C6H5)2S
Numero CAS:
139-66-2
Peso molecolare:
186.27
Beilstein:
1907932
Numero CE:
205-371-4
Numero MDL:
MFCD00003064
Codice UNSPSC:
41116107
ID PubChem:
329757207
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.6327 (lit.)

P. eboll.

296 °C (lit.)

Punto di fusione

−40 °C (lit.)

Densità

1.113 g/mL at 20 °C (lit.)

Formato

neat

Stringa SMILE

S(c1ccccc1)c2ccccc2

InChI

1S/C12H10S/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H
LTYMSROWYAPPGB-UHFFFAOYSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Note legali

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H410

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
BCBV2099
SZBG033XV
SZB9168XV
SZE9168X
SZE7262X

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Xuesheng Zhang et al.
Environmental toxicology and chemistry, 31(7), 1485-1493 (2012-05-03)
Polychlorinated diphenyl sulfides (PCDPSs), a series of dioxin-like compounds, have been detected in various environmental samples. However, information on the toxicity of these compounds is limited. In the present study, the toxic effects of PCDPSs were assessed after acute and
X Yang et al.
Guang pu xue yu guang pu fen xi = Guang pu, 21(4), 475-477 (2003-08-30)
Substitution of diphenyl sulfurine to dodecarbonyl-triruthenium and dodecarbonyl-triiron were studied respectively. Infrared spectra were used in characterization of the reactions and to follow the reaction processes from starting to finishing. Spectra data showed that the new compounds appeared and starting
Jiaqi Shi et al.
Chemosphere, 88(7), 844-854 (2012-05-02)
Twenty-nine congeners of polychlorinated diphenyl sulfide (PCDPS) theoretically possible were synthesized and purified, and their octanol-water partition coefficients (logK(ow)) and high performance liquid chromatography capacity factors (HPLC-logk') were determined. Then the constitutional and structural descriptors were obtained respectively to establish
Julia Wellsow et al.
Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques, 5(3), 245-257 (2003-01-30)
Imaging the serotonin transporter (SERT) with Positron Emission Tomography (PET) provides a useful tool for understanding alterations of the serotonergic system. However, no optimal PET radiotracer for the SERT yet exists. The main purpose of this study was to design
Ruijuan Qu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 261-269 (2011-07-15)
Tetrachlorinated diphenyl sulfides (TCDPSs) are environmentally interesting compounds. In this paper, both experimental and theoretical studies on IR and (1)H NMR as well as (13)C NMR chemical shifts of 4 synthesized TCDPSs have been carried out. The optimized geometries were
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