Skip to Content
Merck
All Photos(1)

Documents

Safety Information

180173

Sigma-Aldrich

Carbon disulfide

ACS reagent, ≥99.9%

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
CS2
CAS Number:
Molecular Weight:
76.14
Beilstein:
1098293
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

vapor density

2.67 (vs air)

vapor pressure

5.83 psi

Assay

≥99.9%

form

liquid

autoignition temp.

212 °F

expl. lim.

50 %

impurities

H2S, passes test (lim. ~1.5 ppm)
SO2, passes test (lim ~2.5 ppm)
≤0.05% water

evapn. residue

≤0.002%

color

APHA: ≤10

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

Looking for similar products? Visit Product Comparison Guide

General description

Carbon disulfide (CS2) is a colorless liquid. It is present in atmosphere and natural waters in the form of sulfur gas. It is responsible for the production of sulfur dioxide (SO2) in the atmosphere (stratosphere and/or troposphere). Its lifetime in the atmosphere has been proposed to be around 12 days. It is a non-polar solvent.
Carbon disulfide is a highly volatile, flammable liquid with low ignition temperature. It can be synthesized by reacting hydrocarbon gas with sulfur. It is an important raw material for preparing viscose rayon and cellophane film.

Application

Carbon disulfide has been used for the desorption of air samples during analysis of trihalomethanes (THMs) in those samples.
It may be used in the preparation of dibenzyl trithiocarbonate, a RAFT (Reversible Addition-Fragmentation Transfer) chain-transfer agent (CTA). It may be employed as a solvent in the preparation of benzyl chlorodithioformate.
Carbon disulfide may be used in the xanthogenation of cellulose and in the synthesis of poly(ethylene trithiocarbonate) and dithiocarbamates. C2S may undergo hydrolysis catalyzed by nanosized titania and zirconia to form CO2 and H2S. It can also generate 1,3-dithiolium carbenes via cycloaddition with acetylenes.

related product

Product No.
Description
Pricing

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


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PRTR

Class I Designated Chemical Substances

FSL

Group 4: Flammable liquids
Special flammables
Hazardous rank I

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

180173-18L-KL:
180173-VAR:
180173-BULK:
180173-500ML:4548173110752
180173-2L:4548173110745
180173-1L:4548173110738
180173-2L-PW:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Copolymerization of ethylene sulfide and carbon disulfide.
Soga K, et al.
Journal of Polymer Science, 14(3), 677-684 (1976)
Carbon Disulfide.
Smith DE and Timmerman RW.
Kirk-Othmer Encyclopedia of Chemical Technology (2003)
Cyril Catto et al.
International journal of environmental research and public health, 9(8), 2562-2586 (2012-10-16)
In order to improve disinfection by-product (DBP) exposure assessment, this study was designed to document both water and air levels of these chemical contaminants in two indoor swimming pools and to analyze their within-day and day-to-day variations in both of
Xanthogenation of lignocarbohydrates by carbon disulfide.
Efanov MV and Pershina LA.
Chemistry of Natural Compounds, 38(1), 90-94 (2002)
1, 3-Dithiolium carbenes from acetylenes and carbon disulfide.
Hartzler HD.
Journal of the American Chemical Society, 95(13), 4379-4387 (1973)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service