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8.08159

Sigma-Aldrich

Thiophenol

Synonym(s):

Phenyl mercaptan, Mercaptobenzene

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About This Item

UNSPSC Code:
12352107
NACRES:
NA.22

vapor pressure

2.7 hPa ( 25 °C)

Quality Level

Assay

≥99.0% (GC)

form

liquid

autoignition temp.

450 °C

potency

46.2 mg/kg LD50, oral (rat)
134 mg/kg LD50, skin (rabbit)

reaction suitability

reagent type: reductant

pH

5 (20 °C in H2O, saturated aqueous solution)

bp

168.3 °C/1013 hPa

mp

-15 °C

transition temp

flash point 50 °C

solubility

0.94 g/L

density

1.08 g/cm3 at 20 °C

General description

for synthesis

Application

Thiophenol for synthesis. CAS 108-98-5, pH 5 (H₂O, 20 °C) (saturated aqueous solution).

Storage and Stability

Store below +30°C.

Analysis Note

Assay (GC, area%):≥ 99.0 % (a/a)
Density (d 20 °C/ 4 °C):1.077 - 1.079
Identity (IR):passes test

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Flam. Liq. 3 - Repr. 2 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

122.0 °F - closed cup

Flash Point(C)

50 °C - closed cup


Certificates of Analysis (COA)

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Protocols

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

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