398020
1,2-Ethanedithiol
technical grade, ≥90%
Synonym(s):
1,2-Dimercaptoethane, Dithioglycol, Ethylene mercaptan
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About This Item
Linear Formula:
HSCH2CH2SH
CAS Number:
Molecular Weight:
94.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-752-3
Beilstein/REAXYS Number:
505946
MDL number:
Assay:
≥90%
Form:
liquid
grade
technical grade
Quality Level
vapor density
>1 (vs air)
vapor pressure
4.8 mmHg ( 20 °C)
assay
≥90%
form
liquid
refractive index
n20/D 1.558 (lit.)
bp
144-146 °C (lit.)
mp
−41 °C (lit.)
density
1.123 g/mL at 25 °C (lit.)
functional group
thiol
SMILES string
SCCS
InChI
1S/C2H6S2/c3-1-2-4/h3-4H,1-2H2
InChI key
VYMPLPIFKRHAAC-UHFFFAOYSA-N
General description
1,2-Ethanedithiol (1,2-Dimercaptoethane, Dithioglycol, Ethylene mercaptan) is an organo sulfur compound. It affords monomeric, dimeric and polymeric complexes on reaction with Pt(PPh3)4, Pd(PPh3)4 and Ni(PPh3)4. It has been synthesized by refluxing 1,2-dichloroethane with thiourea in ethanol.
Application
1,2-Ethanedithiol may be used in the following studies:
- Synthesis of membrane-permeant, fluorogenic biarsenicals.
- Development of microarrays of protein interaction and quantifying the domain-peptide interactions in high throughput using fluorescently labeled synthetic peptides.
- As insolubilizing agent in a study to evaluate the structural, optical, and electrical properties of high-quality films of PbSe nanocrystals fabricated by a layer-by-layer (LbL) dip-coating method.
- Quantitation of the extent of protein phosphorylation using a phosphoprotein isotope-coded affinity tag (PhIAT).
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
111.2 °F - closed cup
flash_point_c
44 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Synthesis and reactions of new complexes of nickel, palladium, and platinum with 1, 2-ethanedithiol, 2-(methylthio) ethanethiol, and 2-(methylthio) ethane disulfide.
Rauchfuss TB and Roundhill DM.
Journal of the American Chemical Society, 97(12), 3386-3392 (1975)
M B Goshe et al.
Analytical chemistry, 73(11), 2578-2586 (2001-06-14)
A method has been developed that utilizes phosphoprotein isotope-coded affinity tags (PhIAT) that combines stable isotope and biotin labeling to enrich and quantitatively measure differences in the O-phosphorylation states of proteins. The PhIAT labeling approach involves hydroxide ion-mediated beta-elimination of
The vibrational assignment, rotational isomerism and force constants of 1, 2-ethanedithiol.
Hayashi M, et al.
Bulletin of the Chemical Society of Japan, 38(10), 1734-1740 (1965)