1,2-Ethanedithiol supplier

Name
1,2-Ethanedithiol
EINECS 208-752-3
CAS No. 540-63-6
Article Data75
CAS DataBase
Density 1.05 g/cm³
Solubility insoluble in water
Melting Point ?41 °C(lit.)
Formula C₂H₆S₂
Boiling Point 144.3 °C at 760 mmHg
Molecular Weight 94.2016
Flash Point 44.4 °C
Transport Information UN 3071 6.1/PG 2
Appearance Clear colorless solid
Safety 36/37/39-45-26-16-36/37-36-7/9
Risk Codes 10-23/24/25-23/25-21-36-23-21/22-36/37/38-20/21/22
Molecular Structure
Hazard Symbols T; Xn; F
Synonyms s-Ethylene dimercaptan;Ethylenedithiol;Dithioglycol;Ethylene mercaptan;Dithioethyleneglycol;FEMA No. 3484;Ethylene dithioglycol;Ethylene dimercaptan;1,2-Dithiol ethane;ethane-1,2-dithiol;Ethylene glycol, dithio-;Ethylenedimercaptan;1,2-Dimercaptoethane;Ethyl hydropersulfide;1,2-dithioglycol;
PSA 77.60000
LogP 0.84600

Synthetic route

: 645-96-5
Benzeneselenol

poly(ethylene disulfide): poly(ethylene disulfide)

A: 1666-13-3
diphenyl diselenide

B: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
at 50 - 55℃; for 0.5h; Reduction; oxidation;	A 94% B 96.4%

...Expand

: 5769-02-8
2-methyl-2-phenyl[1,3]dithiolane

A: 540-63-6
ethane-1,2-dithiol

B: 98-86-2
acetophenone

Conditions

Conditions	Yield
With magnesium(II) perchlorate; water; methylene green In acetonitrile Irradiation;	A n/a B 91%

: 66278-17-9
(2-Methyl-1,3-dithiolan-2-yl)essigsaeure-ethylester

A: 141-97-9
ethyl acetoacetate

B: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With magnesium(II) perchlorate; water; methylene green In acetonitrile Irradiation;	A 90% B n/a

: 822-38-8
1,3-dithiolane-2-thione

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With lithium aluminium tetrahydride In tetrahydrofuran	86%

polymer, product of thiylation with 0.19 g/mol of sulfur, where content of sulfur moieties 2.0 in repeating units; monomer(s): 1,2-dichloroethane, charged content 0.095 g/mol: polymer, product of thiylation with 0.19 g/mol of sulfur, where content of sulfur moieties 2.0 in repeating units; monomer(s): 1,2-dichloroethane, charged content 0.095 g/mol

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With potassium hydroxide; hydrazine hydrate at 80℃; for 2.5h;	56.8%

polymer: monomers(s): 1,2-dichloroethane; sulfur: polymer: monomers(s): 1,2-dichloroethane; sulfur

A: 3570-55-6
3-thiapentan-1,5-dithiol

B: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With sodium hydroxide; hydrazine hydrate Heating;	A 37% B 37%

polymer: monomers(s): 1,2-dibromoethane; sulfur: polymer: monomers(s): 1,2-dibromoethane; sulfur

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With sodium hydroxide; hydrazine hydrate Heating;	33%

: 420-12-2
thirane

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With methanol; hydrogen sulfide at 60℃; unter Druck;
With 2,2'-thiobis-ethanol; hydrogen sulfide at 45℃;

: 1,2-bis-sulfosulfanyl-ethane

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With hydrogenchloride

: 74-85-1
ethene

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With sulfur; benzene at 175℃; under 77228.3 - 88260.9 Torr; und Hydrieren des Reaktionsprodukts unter Druck an Co2S3 bei 150grad oder an Nickel-Kieselgur bei 160grad;

: 505-60-2
bis (2-chloroethyl) sulphide

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With ethanol; zinc

: 10017-60-4
S,S'-ethane-1,2-diyl diethanethioate

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With methanol; barium methoxide at -10℃;
With sodium hydroxide In acetone Ambient temperature;

: 201943-51-3
1,2-diphenylisothiocarbamidoethane

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
beim Schmelzen;

: 107-21-1
ethylene glycol

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With diphosphorus pentasulfide at 110 - 140℃; und Folgenden Destillieren mit Wasser;

: 107-06-2
1,2-dichloro-ethane

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With sodium hydrogensulfide; water at 80 - 100℃;
With sodium hydrogensulfide; ethanol at 80 - 100℃;
With magnesium hydroxide; sodium disulfide; water und Behandeln des entstandenen Polysulfid mit Natriumamalgam;
With ethanol; potassium hydrosulfide

: 107-06-2
1,2-dichloro-ethane

A: 25423-55-6
3,6-dithiaoctan-1,8-dithiol

B: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With sodium hydrogensulfide; water unter Druck;

: 106-93-4
ethylene dibromide

: 17356-08-0
thiourea

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With ethanol und Hydrolyse des entstandenen S.S'-Aethylen-diisothioharnstoff-dihydrobromids mit Kalilauge;

: 106-93-4
ethylene dibromide

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With potassium hydrosulfide Darstellung;
With sodium hydrogensulfide; ethanol
With ethanol; potassium hydrosulfide

: 1940-01-8
[1,2,5,6]tetrathiocane

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With 2-hydroxyethanethiol In d(4)-methanol; water-d2 at 25℃; Equilibrium constant; phosphate buffer(0.5 mM, pH7.0);

: 6317-10-8
2,2-diphenyl-1,3-dithiolane

A: 119-61-9
benzophenone

B: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With oxonium In 1,4-dioxane; water at 25℃; Rate constant; Mechanism; ionic strength: 0.053-0.95M; thallium ion concentration: 0-0.004M; hydrogen ion concentration: 0.05-0.95M; 25percent (v/v) dioxane-water.;

: 83318-96-1
1-(2-Mercapto-ethyl)-2-methylsulfanyl-4,6-diphenyl-pyridinium; iodide

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With sodium hydroxide; thiourea 1.) 130 deg C, 0.5 h; 2.) reflux, 3 h; Yield given. Multistep reaction;

: C6H14O2S6(75)Se2

: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
With hydrogenchloride; 75Se-sodium selenite; sodium acetate at 5℃; for 0.833333h; Equilibrium constant; pH= 1.8; apparent equilibrium constant;
With hydrogenchloride; 75Se-sodium selenite; sodium acetate at 5℃; for 0.833333h; Equilibrium constant; pH= 2.5; apparent equilibrium constant;
With hydrogenchloride; 75Se-sodium selenite; sodium acetate at 5℃; for 0.833333h; Equilibrium constant; pH= 3.7; apparent equilibrium constant;

: 822-38-8
1,3-dithiolane-2-thione

alcoholic potash: alcoholic potash

: 540-63-6
ethane-1,2-dithiol

: 930-35-8
1,3-dithiol-2-thione

: 60-29-7
diethyl ether

lithium alanate: lithium alanate

: 540-63-6
ethane-1,2-dithiol

...Expand

: 930-35-8
1,3-dithiol-2-thione

: 64-17-5
ethanol

sodium: sodium

A: 74-93-1
methylthiol

B: 540-63-6
ethane-1,2-dithiol

...Expand

: 822-38-8
1,3-dithiolane-2-thione

: 7664-41-7
ammonia

A: 1147550-11-5
ammonium thiocyanate

B: 540-63-6
ethane-1,2-dithiol

Conditions

Conditions	Yield
at 150℃; im Rohr;

...Expand

: 4472-81-5
2-imino-1,3-dithiolane

: 7647-01-0
hydrogenchloride

A: 1940-01-8
[1,2,5,6]tetrathiocane

B: 540-63-6
ethane-1,2-dithiol

C: 15719-64-9, 15719-76-3, 97762-63-5
methylammonium carbonate

Conditions

Conditions	Yield
at 120℃;

...Expand

: 5653-29-2
2-(1,3-dithiolan-2-yl)-1-phenylethan-1-one

: furan-2,3,5(4H)-trione pyridine (1:1)

zinc dust: zinc dust

A: 540-63-6
ethane-1,2-dithiol

B: 93-55-0
1-phenyl-propan-1-one

Conditions

Conditions	Yield
unter Durchleiten von Wasserdampf;

...Expand

: 5653-30-5
2-[1,3]dithiolan-2-ylidene-1-phenyl-ethanone

: furan-2,3,5(4H)-trione pyridine (1:1)

zinc: zinc

A: 540-63-6
ethane-1,2-dithiol

B: 93-55-0
1-phenyl-propan-1-one

Conditions

Conditions	Yield
im Wasserdampf-Strom;

...Expand

: 2080-58-2
1,3-dithiolan-2-one

: 7664-41-7
ammonia

A: 540-63-6
ethane-1,2-dithiol

B: 57-13-6
urea

Conditions

Conditions	Yield
at 100℃;

...Expand

: 108-94-1
cyclohexanone

: 540-63-6
ethane-1,2-dithiol

: 177-16-2
1,4-dithiaspiro[4.5]decane

Conditions

Conditions	Yield
With thionyl chloride; silica gel In toluene for 24h; Heating;	100%
With bentonite In toluene for 3h; Heating;	99%
With silica gel; iron(III) chloride In dichloromethane Ambient temperature;	99%

: 104-87-0
4-methyl-benzaldehyde

: 540-63-6
ethane-1,2-dithiol

: 23229-29-0
2-(4-methylphenyl)-1,3-dithiolane

Conditions

Conditions	Yield
With silica gel; toluene-4-sulfonic acid In dichloromethane for 1.5h; Heating;	100%
With Cu(OTf)2-SiO2 for 0.5h; Ambient temperature;	99%
With PPA; silica gel In 1,2-dichloro-ethane at 20℃; for 0.5h;	99%

: 100-52-7
benzaldehyde

: 540-63-6
ethane-1,2-dithiol

: 5616-55-7
2-phenyl-1,3-dithiane

Conditions

Conditions	Yield
With thionyl chloride; silica gel In benzene at 20℃; for 5h;	100%
With silica gel; toluene-4-sulfonic acid In dichloromethane for 3h; Heating;	100%
With acetophenone In dichloromethane at 20℃; for 0.5h; chemoselective reaction;	100%

: 119-61-9
benzophenone

: 540-63-6
ethane-1,2-dithiol

: 6317-10-8
2,2-diphenyl-1,3-dithiolane

Conditions

Conditions	Yield
Nafion-H In benzene Heating;	100%
With cobalt(II) bromide In dichloromethane for 4h; Ambient temperature;	99%
With amberlyst-15 In acetonitrile for 1h;	99.91%

: 566-88-1
dihydrocholesterone

: 540-63-6
ethane-1,2-dithiol

: 2791-43-7
5α-cholestan-3-one ethanediyl S,S-acetal

Conditions

Conditions	Yield
With zeolite HSZ-360 In dichloromethane for 15h; Ambient temperature;	100%
tellurium tetrachloride In 1,2-dichloro-ethane for 3h; Ambient temperature;	94%
With cadmium(II) iodide for 0.0222222h; Irradiation;	78%

: 540-63-6
ethane-1,2-dithiol

: 98-86-2
acetophenone

: 5769-02-8
2-methyl-2-phenyl[1,3]dithiolane

Conditions

Conditions	Yield
With perchloric acid; silica gel at 25 - 30℃; for 5h;	100%
With toluene-4-sulfonic acid In benzene Heating;	99%
With cobalt(II) bromide In dichloromethane for 1.25h; Ambient temperature;	99%

: 540-63-6
ethane-1,2-dithiol

: 24127-98-8
1,2-bis(chlorosulfanyl)ethane

Conditions

Conditions	Yield
With chlorine In tetrachloromethane at -20℃;	100%
With sulfuryl dichloride
With chlorine at -15 - -5℃; for 2h;

: 540-63-6
ethane-1,2-dithiol

: 4669-51-6
2-Chloro-1,3,2-dithiaphospholane

Conditions

Conditions	Yield
With phosphorus trichloride at 20℃; for 3h;	100%
With phosphorus trichloride at 20℃; for 3h;	95%
With phosphorus trichloride at 20℃; for 3h; Inert atmosphere;	95%

: 89-98-5
2-chloro-benzaldehyde

: 540-63-6
ethane-1,2-dithiol

: 83521-68-0
2-(2-chlorophenyl)-1,3-dithiolane

Conditions

Conditions	Yield
With Iron(III) nitrate nonahydrate; sodium iodide In dichloromethane at 20℃; for 16h;	100%
With phosphoric acid functionalized ethanolamine grafted polyacrylonitrile fiber In methanol at 65℃; for 4h; Solvent; Temperature; Green chemistry;	98%
tungsten(VI) chloride In dichloromethane at 0 - 5℃; for 0.0833333h;	96%

: 555-16-8
4-nitrobenzaldehdye

: 540-63-6
ethane-1,2-dithiol

: 41159-02-8
2-(4-nitrophenyl)-1,3-dithiolane

Conditions

Conditions	Yield
With PPA; silica gel In 1,2-dichloro-ethane at 20℃; for 0.5h;	100%
With boron trifluoride diethyl etherate In dichloromethane for 6h; Ambient temperature;	99%
With iron(III) In dichloromethane for 10h; Ambient temperature;	98%

: 120-14-9
3,4-dimethoxy-benzaldehyde

: 540-63-6
ethane-1,2-dithiol

: 69922-36-7
2-(3,4-dimethoxyphenyl)-1,3-dithiolane

Conditions

Conditions	Yield
amberlyst-15 In chloroform for 48h; Ambient temperature;	100%
With N-Bromosuccinimide for 0.05h;	98%
With silica-supported sulfuric acid at 20℃; for 0.133333h; Neat (no solvent); chemoselective reaction;	98%

: 112-45-8
10-Undecenal

: 540-63-6
ethane-1,2-dithiol

: 101033-01-6
2-(9-decenyl)-1,3-dithiolane

Conditions

Conditions	Yield
With thionyl chloride; silica gel In benzene at 20℃; for 5h;	100%
With PPA; silica gel In 1,2-dichloro-ethane at 20℃; for 0.5h;	100%

: 13984-50-4
methyl levulinate

: 540-63-6
ethane-1,2-dithiol

: 146405-06-3
methyl 5,5-ethylenedithiohexanoate

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In chloroform	100%

: 34713-70-7
2-Phenylpropanal

: 540-63-6
ethane-1,2-dithiol

: 83521-78-2
2-(1-Phenyl-ethyl)-[1,3]dithiolane

Conditions

Conditions	Yield
With thionyl chloride; silica gel In benzene at 20℃; for 5h;	100%
With trichloroisocyanuric acid In chloroform at 20℃; for 1.5h;	92%
	76%

: 434-22-0
19-nortestosterone

: 540-63-6
ethane-1,2-dithiol

: 74531-93-4
3,3-Ethandiyldimercapto-oestro-4-en-17β-ol

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In methanol; dichloromethane	100%

: 7554-95-2
kryptogenin diacetate

: 540-63-6
ethane-1,2-dithiol

: 96455-87-7
(25R)-22-oxocholest-5-ene-3β,26-diol 16,16-(cycloethylene dithioketal) 3,26-diacetate

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In acetic acid for 1.5h; Ambient temperature;	100%

: 120342-79-2
1,5-Bis<(9'-oxofluoren-2'-yl)oxy>-3-oxapentane

: 540-63-6
ethane-1,2-dithiol

: 120342-82-7
1,5-Bis<<9',9'-(ethylenedithio)fluoren-2'-yl>oxy>-3-oxapentane

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In acetic acid for 6h; Heating;	100%
With boron trifluoride diethyl etherate In acetic acid for 6h; Heating; Yield given;

: 120342-80-5
1,11-Bis<(9'-oxofluoren-2'-yl)oxy>-3,6,9-trioxaundecane

: 540-63-6
ethane-1,2-dithiol

: 120342-84-9
1,11-Bis<<9',9'-(ethylenedithio)fluoren-2'-yl>oxy>-3,6,9-trioxaundecane

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In acetic acid for 6h; Heating;	100%
With boron trifluoride diethyl etherate In acetic acid for 6h; Heating; Yield given;

: 149310-98-5
C17H23NO4

: 540-63-6
ethane-1,2-dithiol

: 130760-83-7
C19H27NO3S2

Conditions

Conditions	Yield
With thionyl chloride; silica gel In dichloromethane for 12h; Ambient temperature;	100%
With thionyl chloride; silica gel

: 104486-84-2
(-)-(1R,2R,6R,7R)-6,7-dimethyl-3-oxo-2,8-dioxabicyclo[3.3.0]octane

: 540-63-6
ethane-1,2-dithiol

: 104431-97-2
(-)-(3R,4R,5R)-4,5-dimethyl-3-(1,3-dithiolan-2-yl)pentanolide

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In dichloromethane at 0℃; for 0.5h; Cyclization;	100%
With boron trifluoride diethyl etherate In dichloromethane Ambient temperature;	81%

: 540-63-6
ethane-1,2-dithiol

: 151646-90-1
1-benzyl-3-formyl-9-methoxy-1H-benzindole

: 151646-91-2
1-benzyl-3-<2-(1,3-dithiolanyl)>-9-methoxy-1H-benzindole

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In acetic acid for 0.75h; Ambient temperature;	100%

: 540-63-6
ethane-1,2-dithiol

: <4R-<3(4R*,5S*),4α,5α>>-3,3'-(1,4,7-Trioxo-1,7-heptanediyl)bis<4-methyl-5-phenyl-2-oxazolidinone>

: <4R-<3(4R*,5S*),4α,5α>>-3,3'-<1,3-Dithiolan-2-ylidenebis(1-oxo-3,1-propanediyl)>bis<4-methyl-5-phenyl-2-oxazolidinone>

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate at 0℃; for 0.5h;	100%

: 540-63-6
ethane-1,2-dithiol

: 12-chloro-5-hydroxy-9-oxo-6a,7,8,9,10,10a-hexahydronaphthacene-6,11-dione

: 89564-59-0
12-chloro-9,9-ethylenedithio-5-hydroxy-6a,7,8,9,10,10a-hexahydronaphthacene-6,11-dione

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In dichloromethane for 2h; Ambient temperature;	100%

: 540-63-6
ethane-1,2-dithiol

: 2043-61-0
cyclohexanecarbaldehyde

: 70777-60-5
Cyclohexancarboxaldehyde dithioethyleneacetal

Conditions

Conditions	Yield
With zeolite HSZ-360 In dichloromethane for 15h; Ambient temperature;	100%
With cobalt(II) bromide In dichloromethane for 0.05h; Ambient temperature;	99%
With PPA; silica gel In 1,2-dichloro-ethane at 20℃; for 0.5h;	96%

: 540-63-6
ethane-1,2-dithiol

: 123-73-9
crotonaldehyde

: 61685-38-9
2-prop-1-enyl-1,3-dithiolane

Conditions

Conditions	Yield
With thionyl chloride; silica gel In benzene at 20℃; for 5h;	100%
With N-Bromosuccinimide In chloroform at 20℃; for 0.0833333h;	94%
With H-Rho zeolite In hexane for 2.5h; Heating;	89%
With iron(III) In dichloromethane for 4h; Ambient temperature;	75%
With natural kaolinitic clay In benzene for 2h; Heating;	70%

: 540-63-6
ethane-1,2-dithiol

: 502-42-1
cycloheptanone

: 184-32-7
1,4-dithia-spiro[4.6]undecane

Conditions

Conditions	Yield
Nafion-H In benzene Heating;	100%
With perchloric acid; silica gel at 25 - 30℃; for 0.05h;	97%
With P-benzyltriphenylphosphonium tribromide at 20℃; for 1.5h;	96%

: 540-63-6
ethane-1,2-dithiol

: 102-04-5
1,3-Diphenylpropanone

: 76312-47-5
2,2-bis(benzyl)-1,3-dithiolane

Conditions

Conditions	Yield
Nafion-H In benzene Heating;	100%
With silica gel; zirconium(IV) chloride In dichloromethane for 0.5h; Ambient temperature;	99%
With silica gel; iron(III) chloride In dichloromethane Ambient temperature;	98%

: 540-63-6
ethane-1,2-dithiol

: cis-bicyclo<5.3.1>undecan-3-one

: spiro(cis-bicyclo<5.3.1>undecane-3,2':1'3'-dithiolane)

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate for 0.0833333h;	100%

: 540-63-6
ethane-1,2-dithiol

: 163397-73-7
13α-acetyl-8β(H)-podocarpane

: 13α-acetyl-8β(H)-podocarpane ethylenedithioketal

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In dichloromethane Ambient temperature;	100%

: 61571-90-2
5,7-dimethoxy-4-oxo-1,2,3,4-tetrahydro-2-naphthoic acid methyl ester

: 540-63-6
ethane-1,2-dithiol

: 61571-94-6
methyl 3',4'-dihydro-6',8'-dimethoxyspiro[1,3-dithiolane-2,1'(2H)-naphthalene-3-carboxylate]

Conditions

Conditions	Yield
With boron trifluoride diethyl etherate In dichloromethane at 25℃; for 18h; Cyclization;	100%

1,2-Ethanedithiol Consensus Reports

Reported in EPA TSCA Inventory.

1,2-Ethanedithiol Specification

The 1,2-Ethanedithiol, with the CAS registry number 540-63-6, has the IUPAC name of ethane-1,2-dithiol. As to its usage, it is usually used as building block in organic synthesis and an excellent ligand for metal ions. And its product categories are including Phenoles and thiophenoles; Other Reagents; thiol Flavor; Chemistry.

The physical properties of this chemical are as below: (1)ACD/LogP: 1.31; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.31; (4)ACD/LogD (pH 7.4): 1.3; (5)ACD/BCF (pH 5.5): 5.82; (6)ACD/BCF (pH 7.4): 5.76; (7)ACD/KOC (pH 5.5): 122.84; (8)ACD/KOC (pH 7.4): 121.56; (9)#H bond acceptors: 0; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 3; (12)Polar Surface Area: 77.6; (13)Index of Refraction: 1.516; (14)Molar Refractivity: 27.1 cm³; (15)Molar Volume: 89.6 cm³; (16)Polarizability: 10.74×10^-24 cm³; (17)Surface Tension: 33.3 dyne/cm; (18)Density: 1.05 g/cm³; (19)Flash Point: 44.4 °C; (20)Enthalpy of Vaporization: 37.93 kJ/mol; (21)Boiling Point: 144.3 °C at 760 mmHg; (22)Vapour Pressure: 6.45 mmHg at 25°C; (23)Exact Mass: 93.991092; (24)MonoIsotopic Mass: 93.991092; (25)Topological Polar Surface Area: 2; (26)Heavy Atom Count: 4; (27)Complexity: 6.

Use of this chemical: 1,2-Ethanedithiol could react with diketene to produce 1,2-bis-(4-oxo-oxetan-2-ylmethylsulfanyl)-ethane, with the following condition: reagent: cyclohexane azoisobutyronitrile; other condition: unter Bestrahlung mit UV-Licht.

Production method of this chemical: [1,3]dithiolane-2-thione could react to produce 1,2-Ethanedithiol, with the following condition: reagent: LAH; solvent: tetrahydrofuran; yield: 86 %.

When you are dealing with this chemical, you should be much more cautious. For one thing, it is harmful which may cause damage to health. For another thing, it is toxic which at low levels cause damage to health. If by inhalation, in contact with skin and if swallowed, it will be very toxic. In addition, it is highly flammable which may catch fire in contact with air, only needing brief contact with an ignition source, and it has a very low flash point or evolve highly flammable gases in contact with water.

Therefore, you should take different measures to deal with different cases. Wear suitable protective clothing, gloves and eye/face protection. And if in case of contact with eyes, rinse immediately with plenty of water and seek medical advice and if in case of accident or if you feel unwell, seek medical advice immediately (show label where possible). Then while store it, keep the container tightly closed and in a well-ventilated place, away from sources of ignition - No smoking.

In addition, you could convert the following datas into the molecular structure:
(1)Canonical SMILES: C(CS)S
(2)InChI: InChI=1S/C2H6S2/c3-1-2-4/h3-4H,1-2H2
(3)InChIKey: VYMPLPIFKRHAAC-UHFFFAOYSA-N

Below are the toxicity information of this chemical:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Source
mouse	LD50	intraperitoneal	50mg/kg (50mg/kg)	European Journal of Medicinal Chemistry--Chimie Therapeutique. Vol. 17, Pg. 235, 1982.
mouse	LD50	intravenous	56200ug/kg (56.2mg/kg)	U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#02101,
mouse	LD50	oral	342mg/kg (342mg/kg)	Drug and Chemical Toxicology. Vol. 3, Pg. 249, 1980.

Product Name

1,2-Ethanedithiol

Synthetic route

1,2-Ethanedithiol Consensus Reports

1,2-Ethanedithiol Specification

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