Carbon disulphide supplier

Name
Carbon disulfide
EINECS 200-843-6
CAS No. 75-15-0
Article Data609
CAS DataBase
Density 1.259 g/cm³
Solubility 2.9 g/L (20 °C) in water
Melting Point -111 °C
Formula CS₂
Boiling Point 46.22 °C at 760 mmHg
Molecular Weight 76.143
Flash Point -30 °C
Transport Information UN 1131 3/PG 1
Appearance colourless to light yellow liquid with an unpleasant odour
Safety 16-33-36/37-45-7
Risk Codes 11-36/38-48/23-62-63-39/23/24/25-23/24/25
Molecular Structure
Hazard Symbols F, T
Synonyms Carbonbisulfide;Carbon bisulphide;Carbon sulfide (CS2);Dithiocarbonic anhydride;
PSA 64.18000
LogP 1.01810

Synthetic route

: 56-23-5
tetrachloromethane

: 10544-50-0
sulfur

A: 10025-67-9
disulfur dichloride

B: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
byproducts: S(x)Cl2; (N2), bomb reed, heated at 250°C for 24 h; cooled in liquid air in vac., distd.;	A 95% B n/a
byproducts: S(x)Cl2; (N2), bomb reed, heated at 250°C for 15 h; cooled in liquid air in vac., distd.;	A 86% B n/a
byproducts: S(x)Cl2; (N2), bomb reed, heated at 210°C for 8 d; cooled in liquid air in vac., distd.;	A 70% B n/a

...Expand

: 67-56-1
methanol

: 74-93-1
methylthiol

A: 75-15-0
carbon disulfide

B: 624-92-0
Dimethyldisulphide

C: 3658-80-8
dimethyltrisulfane

Conditions

Conditions	Yield
Stage #1: methanol; methylthiol With hydrogen sulfide; aluminum oxide with 14percent by weight of potassium tungstate at 400℃; Stage #2: With sulfur; N-cyclohexyl-cyclohexanamine	A n/a B 94.9% C n/a

...Expand

: C33H39CuN2S2

A: 75-15-0
carbon disulfide

B: C32H39CuN2

Conditions

Conditions	Yield
In melt at 180℃; for 0.166667h; Inert atmosphere;	A n/a B 88%

: graphite

: 7446-09-5
sulfur dioxide

A: 75-15-0
carbon disulfide

B: 23550-45-0
disulfur

C: 463-58-1
carbon oxide sulfide

Conditions

Conditions	Yield
byproducts: CO, CO2; at 1400 K, with excess of carbon;	A 81.16% B 10.82% C 8.02%
byproducts: CO, CO2; at 1000 K, with excess of carbon;	A 37.08% B 3.22% C 59.7%

...Expand

: 10544-50-0
sulfur

: 67-66-3
chloroform

A: 7647-01-0
hydrogenchloride

B: 10025-67-9
disulfur dichloride

C: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
(N2), bomb reed, heated at 205°C for 60 h; cooled in liquid air in vac. for a week, distd.; Raman spectr.;	A n/a B 80% C n/a

...Expand

: 56-23-5
tetrachloromethane

A: 7647-01-0
hydrogenchloride

B: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With hydrogen sulfide In neat (no solvent) reaction of H2S with gaseous CCl4 on heating to 870°C; catalyst: asbestos powder;;	A n/a B 71.5%
With hydrogen sulfide In neat (no solvent) reaction of H2S with gaseous CCl4 on heating to 870°C;;	A n/a B 58%
With hydrogen sulfide In neat (no solvent) reaction of H2S with gaseous CCl4 on heating to 870°C;;	A n/a B 22.1%

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

: 74-86-2
acetylene

A: 188290-36-0
thiophene

B: 75-15-0
carbon disulfide

C: 95-15-8
Benzo[b]thiophene

D: 71-43-2
benzene

Conditions

Conditions	Yield
With disulfide oil at 650℃; for 1.75h; Further byproducts given;	A 68% B 0.09 g C 0.12 g D 0.25 g

...Expand

: 17356-08-0
thiourea

A: 75-15-0
carbon disulfide

B: Triguanidinium-trithiophosphat

C: Triguanidinium-tetrathiophosphat

Conditions

Conditions	Yield
With tetraphosphorus decasulfide at 140℃; for 40h;	A n/a B 5% C 58%
With ammonium hydroxide; tetraphosphorus decasulfide 1.) 40 h, 140 deg C; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 101855-29-2
C13H11NO4S2

A: 75-15-0
carbon disulfide

B: 6974-10-3
phthalimidoacetic acid ethyl ester

Conditions

Conditions	Yield
at 150 - 200℃; for 0.5h; further O-alkyl-S-phthalylglycyl xanthates;	A n/a B 53%

: 143601-38-1
2,2-Dimethyl-1,3-diphenyl-7-thia-2-sila-bicyclo[3.2.0]hept-3-ene-6-thione

A: 75-15-0
carbon disulfide

B: 7688-03-1
1,1-dimethyl-2,5-diphenylsilole

Conditions

Conditions	Yield
In tetrahydrofuran for 67h; Irradiation; or 180 deg C, 15 h;	A n/a B 40%

: {(η2-CS4)(S)Mo(μ2-S)2Mo(S)(η2-CS4)}(2-)

: 762-42-5
dimethyl acetylenedicarboxylate

A: 75-15-0
carbon disulfide

: {(-eta-1-S-η1-SC2(CO2Me)2)2Mo(μ2-S)}2(2-)

Conditions

Conditions	Yield
	A n/a B 25%

...Expand

: calcium carbide

A: 75-15-0
carbon disulfide

B: calcium(II) sulfide

Conditions

Conditions	Yield
With sulfur at 270-360°C;;	A 19.8% B n/a
With sulfur glowing at 500°C;
With S glowing at 500°C;

: 352-93-2
diethyl sulphide

A: 188290-36-0
thiophene

B: 75-15-0
carbon disulfide

C hydrogen sulfide, hydrogen, thienothiophene: hydrogen sulfide, hydrogen, thienothiophene

Conditions

Conditions	Yield
at 580 - 610℃; for 0.0236111h; Mechanism; Product distribution; pyrolysis of dimethyl sulfide and "disulfide oil", var. reaction conditions;	A 6% B 9.5% C n/a

...Expand

: 23550-45-0
disulfur

A: 75-15-0
carbon disulfide

B: 463-58-1
carbon oxide sulfide

Conditions

Conditions	Yield
With carbon monoxide; platinum	A 1% B n/a

: 5069-23-8
2,5-diethyl-thiophene

: 75-36-5
acetyl chloride

A: 75-15-0
carbon disulfide

B: 500891-67-8
1-(2,5-diethyl-[3]thienyl)-ethanone

Conditions

Conditions	Yield
With aluminium trichloride

...Expand

: 56-23-5
tetrachloromethane

: 97-77-8
disulfiram

A: 75-15-0
carbon disulfide

B: 117122-68-6
diethylamino-thioxo-methanesulfenyl chloride

Conditions

Conditions	Yield
at 145℃;

...Expand

: 56-23-5
tetrachloromethane

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With aluminium trichloride; sulfur at 120℃;
With copper; sulfur
With sulfur; aluminium

: 3698-28-0
2-allylanisole

A: 75-15-0
carbon disulfide

B: 19997-53-6
(2,3-dihydro-2-benzofuranyl)-methyl bromide

Conditions

Conditions	Yield
With bromine at 0℃;

: 33776-96-4
4,6-dithioxo-[1,3,5]triazinan-2-one

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
at 360℃;

: 463-71-8
thiophosgene

: 60-29-7
diethyl ether

: 128-04-1
sodium dimethyldithiocarbamate

A: 75-15-0
carbon disulfide

B: 97-74-5
bis(dimethylthiocarbamoyl)sulfide

...Expand

: 463-71-8
thiophosgene

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With iron at 100℃;

: 463-71-8
thiophosgene

A: 75-15-0
carbon disulfide

B: 56-23-5
tetrachloromethane

Conditions

Conditions	Yield
With ammonium chloride at 200℃;
With aluminium trichloride at 100℃;
With iron at 37℃;
at 200℃;

: 60-29-7
diethyl ether

: 27193-12-0
(dimethyl-thiocarbamic acid )-phthalic acid-thioanhydride

A: 75-15-0
carbon disulfide

B: 6329-16-4
N,N,N',N'-tetramethyl-phthalamide

...Expand

: 60-29-7
diethyl ether

: 58758-29-5
tributylphosphine-carbon disulfide adduct

A: 75-15-0
carbon disulfide

B: 998-40-3
tributylphosphine

...Expand

: 463-58-1
carbon oxide sulfide

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With silica gel

: 34557-54-5
methane

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With aluminum oxide; silica gel; sulfur at 600℃;
With iron sulfide; sulfur at 800 - 1000℃;
With silver sulfide; sulfur at 800 - 1000℃;

: 64-17-5
ethanol

: 27193-12-0
(dimethyl-thiocarbamic acid )-phthalic acid-thioanhydride

A: 75-15-0
carbon disulfide

B: 6329-16-4
N,N,N',N'-tetramethyl-phthalamide

...Expand

: 64-17-5
ethanol

: 58758-29-5
tributylphosphine-carbon disulfide adduct

A: 75-15-0
carbon disulfide

B: 998-40-3
tributylphosphine

...Expand

: 74-98-6
propane

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With aluminum oxide; sulfur at 600℃;

: 558-13-4
carbon tetrabromide

: 75-15-0
carbon disulfide

Conditions

Conditions	Yield
With sulfur

: 75-15-0
carbon disulfide

: 108-91-8
cyclohexylamine

: 1212-29-9
1,3-dicyclohexylthiourea

Conditions

Conditions	Yield
at 100℃; for 12h; Ionic liquid; Green chemistry;	100%
In water at 20℃; for 1h; Green chemistry;	95%
In water at 20℃; for 0.833333h; Green chemistry;	95%

: 75-15-0
carbon disulfide

: 104-94-9
4-methoxy-aniline

: 2284-20-0
4-Methoxyphenyl isothiocyanate

Conditions

Conditions	Yield
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.;	100%
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In ethanol at 20℃; for 1h; Stage #2: With dmap; di-tert-butyl dicarbonate at 0 - 20℃; for 4h;	96%
Stage #1: carbon disulfide; 4-methoxy-aniline With triethylamine In methanol at 0 - 5℃; Stage #2: With bis(trichloromethyl) carbonate In chloroform at 0℃; for 4h; Further stages.;	95%

: 75-15-0
carbon disulfide

: 62-53-3
aniline

: 103-72-0
phenyl isothiocyanate

Conditions

Conditions	Yield
Stage #1: carbon disulfide; aniline With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.;	100%
Stage #1: carbon disulfide; aniline With potassium carbonate In water at 20℃; for 3h; Inert atmosphere; Stage #2: With 1,3,5-trichloro-2,4,6-triazine In dichloromethane; water at 0℃; for 0.5h; Inert atmosphere; Stage #3: With sodium hydroxide In dichloromethane; water pH=11; Inert atmosphere;	98%
Stage #1: carbon disulfide; aniline With potassium carbonate In water at 20℃; Stage #2: With 1,3,5-trichloro-2,4,6-triazine In dichloromethane; water at 0℃; for 0.5h;	98%

: 75-15-0
carbon disulfide

: 100-46-9
benzylamine

: 1424-14-2
dibenzyl thiourea

Conditions

Conditions	Yield
at 100℃; for 12h; Ionic liquid; Green chemistry;	100%
aluminum oxide; zinc(II) oxide at 100℃; for 2h; Condensation;	98%
In water at 20℃; for 1.33333h; Solvent; Time; Green chemistry;	97%

: 75-15-0
carbon disulfide

: 75-56-9, 16033-71-9
methyloxirane

: 3489-45-0
4-methyl-1,3-dithiolane-2-thione

Conditions

Conditions	Yield
(2-propanolato)-[(2,2',2''-nitrilotris[ethanolato])-(3)-N,O,O',O'']titanium at 120℃; for 48h;	100%
With [aluminum((1R,2R)-N,N′-bis(3,5-di-tert-butyl-salicylidene)cyclohexane-1,2-diamine)2O]; tetrabutylammomium bromide at 90℃; for 16h; Neat (no solvent); chemoselective reaction;	94%
With potassium hydroxide; ethanol

: 75-15-0
carbon disulfide

: 2627-86-3
(S)-1-phenyl-ethylamine

: 31172-77-7
N,N'-bis<(S)-(1-phenylethyl)>thiourea

Conditions

Conditions	Yield
In ethanol Inert atmosphere; Reflux;	100%
at 47℃;	97%
In ethanol for 20h; Heating;	79%

: 75-15-0
carbon disulfide

: 109-77-3
malononitrile

: 74-88-4
methyl iodide

: 5147-80-8
[Bis(methylthio)methylene]malononitrile

Conditions

Conditions	Yield
With potassium carbonate; tetrabutylammomium bromide In benzene at 60℃; for 3h;	100%
Stage #1: malononitrile With potassium carbonate In dimethyl sulfoxide at 20℃; for 0.166667h; Large scale reaction; Stage #2: carbon disulfide In dimethyl sulfoxide at 0 - 22℃; for 0.5h; Large scale reaction; Stage #3: methyl iodide In dimethyl sulfoxide at 5 - 20℃; Large scale reaction;	99%
Stage #1: carbon disulfide; malononitrile With potassium carbonate In dimethyl sulfoxide at 0 - 20℃; for 2h; Stage #2: methyl iodide In dimethyl sulfoxide at 0 - 20℃; for 12h;	93.9%

...Expand

: 75-15-0
carbon disulfide

: 108-93-0
cyclohexanol

: 74-88-4
methyl iodide

: 41320-40-5
<<(methylthio)thiocarbonyl>oxy>cyclohexane

Conditions

Conditions	Yield
Stage #1: carbon disulfide; cyclohexanol With 1H-imidazole; sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Addition; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 0.5h; Methylation; Further stages.;	100%
Stage #1: carbon disulfide; cyclohexanol In dimethyl sulfoxide at 20℃; for 0.333333h; Stage #2: With N-benzyl-trimethylammonium hydroxide In dimethyl sulfoxide at 20℃; for 1h; Stage #3: methyl iodide In dimethyl sulfoxide at 20℃; for 3h;	82%
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In water for 1h; Ambient temperature;	80%

...Expand

: 75-15-0
carbon disulfide

: 1724-39-6
cyclododecanol

: 74-88-4
methyl iodide

: 4373-12-0
O-cyclododecyl-S-methyl dithiocarbonate

Conditions

Conditions	Yield
Stage #1: carbon disulfide; cyclododecanol With 1H-imidazole; sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Addition; Stage #2: methyl iodide In tetrahydrofuran at 20℃; for 0.5h; Methylation; Further stages.;	100%
With sodium hydride	87%
Stage #1: carbon disulfide; cyclododecanol With n-butyllithium In tetrahydrofuran; hexane at 0 - 20℃; for 3h; Stage #2: methyl iodide at 20℃;	80%

...Expand

: 110-89-4
piperidine

: 75-15-0
carbon disulfide

: 121-44-8
triethylamine

: 59983-55-0
triethylammonium piperidinodithiocarbamate

Conditions

Conditions	Yield
In diethyl ether at 20℃; for 0.2h;	100%
In acetonitrile
In diethyl ether

...Expand

: 110-91-8
morpholine

: 75-15-0
carbon disulfide

: 873-58-5
sodium N-morpholinocarbamodithioate

Conditions

Conditions	Yield
Stage #1: morpholine With sodium hydroxide In methanol; water at 0℃; for 0.333333h; Stage #2: carbon disulfide In methanol; water at 0 - 20℃;	100%
With sodium hydroxide In acetonitrile for 5h;	92%
With sodium hydroxide In ethanol at 20 - 40℃;	71%

: 75-15-0
carbon disulfide

: 949-68-8
N-cycloheptatrienylidene-4-methyl-aniline

: 136472-58-7
3-p-Tolyl-3,8a-dihydro-cycloheptathiazole-2-thione

Conditions

Conditions	Yield
at 60℃; for 24h;	100%

: 75-15-0
carbon disulfide

: 768-94-5
1-Adamantanamine

: 4411-26-1
1-adamantylisothiocyanate

Conditions

Conditions	Yield
With dmap; di-tert-butyl dicarbonate; triethylamine	100%
With S,S'-bis(1-phenyl-1H-tetrazol-5-yl) dithiocarbonate; triethylamine In acetonitrile for 0.333333h;	95%
Stage #1: carbon disulfide; 1-Adamantanamine With triethylamine In ethanol at 0℃; for 1.5h; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 1h;	90%
Stage #1: carbon disulfide; 1-Adamantanamine With triethylamine In ethanol at 20℃; Stage #2: With dmap; di-tert-butyl dicarbonate In ethanol at 20℃; for 0.25h; Further stages.;	82%
With potassium hydroxide

: 75-15-0
carbon disulfide

: 2350-99-4
2-[(4-methylphenyl)amino]acetohydrazide

: 142787-64-2
C10H12N3OS2(1-)*K(1+)

Conditions

Conditions	Yield
With potassium hydroxide In ethanol for 16h;	100%

: 75-15-0
carbon disulfide

: 29111-46-4
N-phenylaminoacetyl hydrazide

: 142787-65-3
C9H10N3OS2(1-)*K(1+)

Conditions

Conditions	Yield
With potassium hydroxide In ethanol for 16h;	100%

: 75-15-0
carbon disulfide

: 2371-31-5
2-((4-chlorophenyl)amino)acetohydrazide

: 142787-63-1
C9H9ClN3OS2(1-)*K(1+)

Conditions

Conditions	Yield
With potassium hydroxide In ethanol for 16h;	100%

: 75-15-0
carbon disulfide

: 24344-23-8
Phenyl-bis-(dimethylamino)-arsin

: 24344-29-4
dimethylthiocarbamic acid phenylarsonous acid-thioanhydride

Conditions

Conditions	Yield
	100%

: 75-15-0
carbon disulfide

: 62965-98-4
N-p-bromophenyl-2,4,6-cycloheptatriene-1-imine

: 136472-60-1
3-(4-Bromo-phenyl)-3,8a-dihydro-cycloheptathiazole-2-thione

Conditions

Conditions	Yield
at 60℃; for 24h;	100%

: 75-15-0
carbon disulfide

: 62515-92-8
N-p-methoxyphenyl-2,4,6-cycloheptatriene-1-imine

: 136472-57-6
3-(4-Methoxy-phenyl)-3,8a-dihydro-cycloheptathiazole-2-thione

Conditions

Conditions	Yield
at 60℃; for 24h; Mechanism; other p-substituted phenyliminotropones;	100%
at 60℃; for 24h;	100%

: 75-15-0
carbon disulfide

: 127026-63-5
bis(N,N-diethylamido)-o-chlorophenylarsonite

: 127026-35-1
C16H24AsClN2S4

Conditions

Conditions	Yield
	100%

: 75-15-0
carbon disulfide

: 112392-70-8
C12H26ClP

A: 112392-74-2
2-(Di-tert-butyl-phosphinothioyl)-3-methyl-but-1-ene-1-thione

B: 112392-71-9
C12H27ClP(1+)*Cl(1-)

Conditions

Conditions	Yield
In pentane at 15 - 20℃; for 8h;	A 85% B 100%

...Expand

: 75-15-0
carbon disulfide

: 85997-29-1
2-butylbenzimidazo<1,2-d><1,2,4>thiadiazol-3(2H)-one

: 72885-90-6
3H-benzimidazo<2,1-c><1,2,4>dithiazol-3-thione

Conditions

Conditions	Yield
In dichloromethane for 24h; Ambient temperature;	100%

: 75-15-0
carbon disulfide

: 147168-89-6
(1S,2R,4R)-1-amino-2-exo-hydroxy-7,7-dimethyl-bicyclo[2.2.1]heptane

: 147168-90-9
(1S,5R,7R)-10,10-dimethyl-3-thioxo-2-aza-4-oxatricyclo<5.2.1.01,5>decane

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran for 15h; Heating;	100%
With triethylamine In tetrahydrofuran Heating;

: 75-15-0
carbon disulfide

: C24H43N2P

: C26H43N2PS4

Conditions

Conditions	Yield
In diethyl ether for 84h;	100%

: 75-15-0
carbon disulfide

: 553-53-7
Nicotinic acid hydrazide

: 88317-41-3
potassium N-(pyridine-4-carbonyl)-hydrazine carbodithiolate

Conditions

Conditions	Yield
With potassium hydroxide In ethanol at 0 - 20℃;	100%
With potassium hydroxide In ethanol for 1h;	94%
With potassium hydroxide In ethanol

: 75-15-0
carbon disulfide

: 54-85-3
isoniazid

: 61019-32-7
potassium 4-pyridinyldithiocarbazate

Conditions

Conditions	Yield
With potassium hydroxide In ethanol	100%
With potassium hydroxide In ethanol at 20℃;	100%
With potassium hydroxide In ethanol at 20℃; for 16h;	99%

: 75-15-0
carbon disulfide

: 54-85-3
isoniazid

: potassium 2-isonicotinoyl hydrazine carbothionate

Conditions

Conditions	Yield
With potassium hydroxide In ethanol for 16h; Cooling with ice;	100%
With potassium hydroxide In ethanol at 25℃; for 3h;

: 75-15-0
carbon disulfide

: 21909-51-3
2-(2-methyl-1H-indol-3-yl)acetohydrazide

: 88351-79-5
α-(2-Methylindol-3-yl)acetyldithiocarbazinic acid potassium salt

Conditions

Conditions	Yield
With potassium hydroxide In ethanol for 10h; Ambient temperature;	100%
With potassium hydroxide In ethanol at 20℃; for 24h;	100%

: 75-15-0
carbon disulfide

: 141-97-9
ethyl acetoacetate

: C7H8O3S2(2-)*2K(1+)

Conditions

Conditions	Yield
With potassium hydroxide In 1,4-dioxane	100%
With potassium hydroxide In N,N-dimethyl-formamide at 25℃; for 24h;
Stage #1: ethyl acetoacetate With potassium carbonate In N,N-dimethyl-formamide for 1h; Stage #2: carbon disulfide In N,N-dimethyl-formamide for 2h;

: 75-15-0
carbon disulfide

: 3290-99-1
4-methoxybenzoic acid hydrazide

: 85103-41-9
potassium N-(4-methoxybenzoyl)hydrazinecarbodithioate

Conditions

Conditions	Yield
With potassium hydroxide In ethanol at 20℃;	100%
With potassium hydroxide
With potassium hydroxide In ethanol

Carbon disulphide Chemical Properties

Molecular Formula: CS₂
Molecular Weight: 76.139 g/mol
EINECS: 200-843-6
Flashing point: -30 °C
Index of Refraction: 1.627
Density: 1.262 g/mL
Vapour Pressure: 352 mmHg at 25 °C
Boiling Point: 46 °C
Melting point: -111 °C
Storage tempreture: 2-8 °C
Water solubility: 2.9 g/L at 20 °C
Solubility: Soluble in water
Sensitive: Hygroscopic
Appearance: Colourless to light yellow liquid with an unpleasant odour
Structure of Carbon disulphide (CAS NO.75-15-0):

IUPAC Name: Methanedithione
Product Category of Carbon disulphide (CAS NO.75-15-0): Inorganics;Pesticides;Stable Isotopes;Aluminum Bottles;Alphabetical Listings

Carbon disulphide Uses

Carbon disulphide (CAS NO.75-15-0) is used frequently as a building block in organic chemistry as well as an industrial and chemical non-polar solvent.

Carbon disulphide Production

Carbon disulphide (CAS NO.75-15-0) once was manufactured by combining carbon and sulfur at high temperatures. A lower temperature reaction, requiring only 600 °C utilizes natural gas as the carbon source in the presence of silica gel or alumina catalysts.

Carbon disulphide Toxicity Data With Reference

1.	mmo-sat 100 µL/plate	NIOSH* National Institute for Occupational Safety and Health, U.S. Dept. of Health, Education, and Welfare, Reports and Memoranda 5AUG77 .
2.	sce-hmn:lym 10,200 µg/L	BCTKAG Bromatologia i Chemia Toksykologiczna. 14 (1981),115.
3.	ihl-hmn LCLo:4000 ppm/30M	29ZWAE Practical Toxicology of Plastics Lefaux, R.,Cleveland, OH.: Chemical Rubber Company,1968,118.
4.	ihl-hmn LCLo:2000 ppm/5M	TABIA2 Tabulae Biologicae. 3 (1933),231.
5.	unr-man LDLo:186 mg/kg	85DCAI Poisoning; Toxicology, Symptoms, Treatments. 2 (1970),73.
6.	orl-rat LD50:3188 mg/kg	GISAAA Gigiena i Sanitariya. 31 (1)(1966),13.
7.	ihl-rat LC50:25 g/m3/2H	85GMAT Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure Izmerov, N.F., et al.,Moscow, USSR.: Centre of International Projects, GKNT,1982,32.
8.	orl-mus LD50:2780 mg/kg	GISAAA Gigiena i Sanitariya. 31 (1)(1966),13.
9.	ihl-mus LC50:10 g/m3/2H	85GMAT Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure Izmerov, N.F., et al.,Moscow, USSR.: Centre of International Projects, GKNT,1982,32. GISAAA Gigiena i Sanitar

Carbon disulphide Consensus Reports

Reported in EPA TSCA Inventory. EPA Genetic Toxicology Program. Community Right-To-Know List. EPA Extremely Hazardous Substances List.

Carbon disulphide Safety Profile

Hazard Codes: F, Toxic T
Risk Statements: 11-36/38-48/23-62-63-39/23/24/25-23/24/25
R11:Highly flammable.
R23/24/25:Toxic by inhalation, in contact with skin and if swallowed.
R36/38:Irritating to eyes and skin.
R48:Danger of serious damage to health by prolonged exposure.
R62:Risk of impaired fertility.
R63:Possible risk of harm to the unborn child.
Safety Statements: 16-33-36/37-45-7
S7:Keep container tightly closed.
S16:Keep away from sources of ignition.
S33:Take precautionary measures against static discharges.
S36/37:Wear suitable protective clothing and gloves.
S45:In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)

Carbon disulphide Standards and Recommendations

OSHA PEL: TWA 4 ppm; STEL 12 ppm (skin)
ACGIH TLV: TWA 10 ppm (skin); BEI: 5 mg (2-thiothiazolidine-4-carboxylic acid (TTCA))/g creatinine in urine
DFG MAK: 5 ppm (16 mg/m³); BAT: 8 mg/L of 4-thio-4-thiazolidine carboxylic acid (TTCA) at end of shift
NIOSH REL: (Carbon Disulfide) TWA 1 ppm; CL 10 ppm/15M
DOT Classification: 3; Label: Flammable Liquid, Poison

Carbon disulphide Analytical Methods

For occupational chemical analysis use NIOSH: Carbon Disulfide, 1600.

Carbon disulphide Specification

Carbon disulphide , its cas register number is 75-15-0. At very high levels, carbon disulfide may be life-threatening because it affects the nervous system. Significant safety data come from the viscose rayon industry, where both carbon disulfide as well as small amounts of H₂S may be present. A human poison by unspecified route. Human reproductive effects on spermatogenesis by inhalation. Experimental teratogenic and reproductive effects. The main toxic effect is on the central nervous system, acting as a narcotic and anesthetic in acute poisoning with death following from respiratory failure. Flammable liquid. A dangerous fire hazard when exposed to heat, flame, sparks, friction, or oxidizing materials. Severe explosion hazard when exposed to heat or flame. Ignition and potentially explosive reaction when heated in contact with rust or iron. Mixtures with sodium or potassium-sodium alloys are powerful, shock-sensitive explosives. Explodes on contact with permanganic acid. Potentially explosive reaction with nitrogen oxide, chlorine (catalyzed by iron). Reacts with metal azides to produce shock- and heat-sensitive, explosive metal azidodithioformates.
Carbon disulphide (CAS NO.75-15-0) is hazardous, so the first aid measures and others should be known. Such as: When on the skin: first, should flush skin with plenty of water immediately for at least 15 minutes while removing contaminated clothing. Secondly, get medical aid. Or in the eyes: Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Then get medical aid soon. While, it's inhaled: Remove from exposure and move to fresh air immediately. Give artificial respiration while not breathing. When breathing is difficult, give oxygen. And as soon as to get medical aid. Then you have the ingesting of the product: Do not induce vomiting. If conscious and alert, rinse mouth and drink 2-4 cupfuls of milk or water, and get medical aid immediately. Notes to physician: Effects may be delayed. Observe patient.

Product Name

Carbon disulfide

Synthetic route

Carbon disulphide Chemical Properties

Carbon disulphide Uses

Carbon disulphide Production

Carbon disulphide Toxicity Data With Reference

Carbon disulphide Consensus Reports

Carbon disulphide Safety Profile

Carbon disulphide Standards and Recommendations

Carbon disulphide Analytical Methods

Carbon disulphide Specification

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