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335266

Sigma-Aldrich

Carbon disulfide

anhydrous, ≥99%

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About This Item

Empirical Formula (Hill Notation):
CS2
CAS Number:
Molecular Weight:
76.14
Beilstein:
1098293
EC Number:
MDL number:
UNSPSC Code:
12352107
PubChem Substance ID:
NACRES:
NA.21

grade

anhydrous

Quality Level

vapor density

2.67 (vs air)

vapor pressure

5.83 psi ( 20 °C)

Assay

≥99%

form

liquid

autoignition temp.

212 °F

expl. lim.

50 %

impurities

<0.005% water

refractive index

n20/D 1.627 (lit.)

bp

46 °C (lit.)

mp

−112-−111 °C (lit.)

density

1.266 g/mL at 25 °C (lit.)

SMILES string

S=C=S

InChI

1S/CS2/c2-1-3

InChI key

QGJOPFRUJISHPQ-UHFFFAOYSA-N

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General description

Carbon disulfide is a highly volatile, flammable liquid with low ignition temperature. It is an important raw material for preparing viscose rayon and cellophane film. C2S may undergo hydrolysis catalyzed by nanosized titania and zirconia to form CO2 and H2S.

Application

Carbon disulfide may be used in the xanthogenation of cellulose and in the synthesis of poly(ethylene trithiocarbonate) and dithiocarbamates. It can also generate 1,3-dithiolium carbenes via cycloaddition with acetylenes.

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Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1

Target Organs

Peripheral nervous system,Central nervous system,Cardio-vascular system,Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

-22.0 °F - closed cup

Flash Point(C)

-30 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Customers Also Viewed

1, 3-Dithiolium carbenes from acetylenes and carbon disulfide.
Hartzler HD.
Journal of the American Chemical Society, 95(13), 4379-4387 (1973)
Nanosized titania and zirconia as catalysts for hydrolysis of carbon disulfide.
Yue Y, et al.
Applied Catalysis. B, Environmental, 46(3), 561-572 (2003)
Carbon Disulfide.
Smith DE and Timmerman RW.
Kirk-Othmer Encyclopedia of Chemical Technology (2003)
Copolymerization of ethylene sulfide and carbon disulfide.
Soga K, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 14(3), 677-684 (1976)
An efficient, one-pot, synthesis of dithiocarbamates from the corresponding alcohols using Mitsunobu's reagent.
Chaturvedi D and Ray S.
Tetrahedron Letters, 47(8), 1307-1309 (2006)

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