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Key Documents

8.00795

Sigma-Aldrich

1,2-Ethanedithiol

for synthesis

Synonym(s):

1,2-Ethanedithiol

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About This Item

Empirical Formula (Hill Notation):
C2H6S2
CAS Number:
Molecular Weight:
94.20
MDL number:
UNSPSC Code:
12352105
EC Index Number:
208-752-3
NACRES:
NA.22

vapor pressure

6.4 hPa ( 20 °C)

Quality Level

Assay

≥99.0% (GC)

form

liquid

potency

120 mg/kg LD50, oral (Rat)
197 mg/kg LD50, skin (Rabbit)

mp

-41 °C

transition temp

flash point 50 °C

density

1.12 g/cm3 at 20 °C

storage temp.

2-30°C

InChI

1S/C2H6S2/c3-1-2-4/h3-4H,1-2H2

InChI key

VYMPLPIFKRHAAC-UHFFFAOYSA-N

Application

1,2-Ethanedithiol can be used as a reactant to synthesize:
  • Aryl thiols via copper-catalyzed single-step reaction with aryl halides.
  • 1,3-Dithiolanes via Lewis acid-catalyzed chemoselective condensation with carbonyl compounds.
  • Polyalkylene sulfides via polycondensation with dibromides in the presence of NaH.

Analysis Note

Assay (GC, area%): ≥ 99.0 % (a/a)
Density (d 20 °C/ 4 °C): 1.123 - 1.126
Identity (IR): passes test

Pictograms

FlameSkull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

111.2 °F - closed cup

Flash Point(C)

44 °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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