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Merck

676918

Disulfuro de carbono

ACS reagent, ≥99.9%

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Fórmula empírica (notación de Hill):
CS2
Número CAS:
Peso molecular:
76.14
UNSPSC Code:
12352100
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-843-6
Beilstein/REAXYS Number:
1098293
MDL number:
Assay:
≥99.9%
Grade:
ACS reagent
Bp:
46 °C (lit.)
Vapor pressure:
5.83 psi
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grade

ACS reagent

Quality Level

vapor density

2.67 (vs air)

vapor pressure

5.83 psi

assay

≥99.9%

form

liquid

autoignition temp.

212 °F

expl. lim.

50 %

dilution

(for analytical testing)

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

General description

Carbon disulfide is a widely used solvent in the production of rayon fibers, carbon tetrachloride, pesticides, vulcanizers, cellophane, adhesives, and other chemicals. It is also used as a starting material in the synthesis of various sulfur-containing derivatives.
Our premium ACS solvents are ideal for routine chemical synthesis, drying, purification, and critical labware cleaning. They meet or exceed the rigorous standards of the American Chemical Society (ACS), ensuring high-quality results for your research needs.

Premium ACS Solvents: Our solvents meet or exceed the stringent standards set by the American Chemical Society, ensuring high quality and reliability for your laboratory applications.

Replicable and Publishable Results: Designed for consistency, our solvents deliver results that can be reliably reproduced, making them ideal for research that requires publication.

Versatile Applications: Suitable for routine chemical synthesis, drying, purification, and critical labware cleaning, our solvents cater to a wide range of research needs in the laboratory.

Application

Carbon disulfide can be used as a solvent:
  • To synthesize hydroxynaphthyl ketones via Friedel-Crafts acylation and demethylation.
  • In the regioselective bromination of binaphthols.


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signalword

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

Clase de almacenamiento

3 - Flammable liquids

wgk

WGK 2

flash_point_f

-22.0 °F - closed cup

flash_point_c

-30 °C - closed cup



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[11C]carbon disulfide: a versatile reagent for PET radiolabelling.
Philip W Miller et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(2), 433-436 (2011-12-14)
Marjan J Smeulders et al.
Nature, 478(7369), 412-416 (2011-10-21)
Extremophilic organisms require specialized enzymes for their exotic metabolisms. Acid-loving thermophilic Archaea that live in the mudpots of volcanic solfataras obtain their energy from reduced sulphur compounds such as hydrogen sulphide (H(2)S) and carbon disulphide (CS(2)). The oxidation of these
Margherita Maiuri et al.
Physical chemistry chemical physics : PCCP, 14(18), 6312-6319 (2012-02-15)
In carotenoids internal conversion between the allowed (S(2)) and forbidden (S(1)) excited states occurs on a sub-picosecond timescale; the involvement of an intermediate excited state(s) (S(x)) mediating the process is controversial. Here we use high time resolution (sub-20 fs) broadband