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Merck
CN

13807

Carbon disulfide

puriss., ≥99.5% (GC)

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About This Item

Empirical Formula (Hill Notation):
CS2
CAS Number:
75-15-0
Molecular Weight:
76.14
EC Number:
200-843-6
UNSPSC Code:
12352200
PubChem Substance ID:
329750353
Beilstein/REAXYS Number:
1098293
MDL number:
MFCD00011321

Key Documents

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InChI key

QGJOPFRUJISHPQ-UHFFFAOYSA-N

InChI

1S/CS2/c2-1-3

SMILES string

S=C=S

vapor density

2.67 (vs air)

grade

puriss.

assay

≥99.5% (GC)

autoignition temp.

212 °F

expl. lim.

50 %

impurities

≤0.0005% H2S + foreign org. S-comp., ≤0.002% non-volatile matter, ≤0.02% water (Karl Fischer)

bp

46 °C (lit.)

mp

−112-−111 °C (lit.)

density

1.266 g/mL at 25 °C (lit.)

anion traces

sulfate (SO42-): ≤5 mg/kg, sulfite (SO32-): ≤20 mg/kg

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

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

-22.0 °F - closed cup

flash_point_c

-30 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
20380
92450

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M Schuster et al.
Fungal genetics and biology : FG & B, 79, 132-140 (2015-06-21)
The use of fluorescent proteins (FPs) in plant pathogenic fungi provides valuable insight into their intracellular dynamics, cell organization and invasion mechanisms. Compared with green-fluorescent proteins, their red-fluorescent "cousins" show generally lower fluorescent signal intensity and increased photo-bleaching. However, the
S Kilaru et al.
Fungal genetics and biology : FG & B, 79, 125-131 (2015-06-21)
Fluorescent proteins (FPs) are powerful tools to investigate intracellular dynamics and protein localization. Cytoplasmic expression of FPs in fungal pathogens allows greater insight into invasion strategies and the host-pathogen interaction. Detection of their fluorescent signal depends on the right combination
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
[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
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