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Merck
모든 사진(1)

주요 문서

424641

Sigma-Aldrich

Carbon disulfide

ReagentPlus®, purified by redistillation, ≥99.9%

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About This Item

실험식(Hill 표기법):
CS2
CAS Number:
Molecular Weight:
76.14
Beilstein:
1098293
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.21
분석:
≥99.9%
bp:
46 °C (lit.)
vapor pressure:
5.83 psi

vapor density

2.67 (vs air)

Quality Level

vapor pressure

5.83 psi

제품 라인

ReagentPlus®

분석

≥99.9%

양식

liquid

autoignition temp.

212 °F

정제법

redistillation

expl. lim.

50 %

불순물

≤0.03% (water)
≤1.5 ppm hydrogen sulfide
≤2.5 ppm sulfur dioxide
<100 ppb benzene (No single impurity > 100 ppb, measured as benzene)
<500 ppb total hydrocarbon content

색상

APHA: ≤10

refractive index

n20/D 1.627 (lit.)

bp

46 °C (lit.)

mp

−112-−111 °C (lit.)

solubility

alcohol: miscible(lit.)
benzene: miscible(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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일반 설명

Carbon disulfide is a toxic, 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. It shows fat solvent property. CS2 in water assists the peptide bond formation in amino acids.

애플리케이션

Carbon disulfide may be used in the xanthogenation of cellulose and in the synthesis of poly(ethylene trithiocarbonate).
Suitable for industrial hygiene analysis

법적 정보

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

FlameHealth hazardExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

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

표적 기관

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


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문서 라이브러리 방문

Luke J Leman et al.
Astrobiology, 15(9), 709-716 (2015-08-27)
Demonstrating plausible nonenzymatic polymerization mechanisms for prebiotic monomers represents a fundamental goal in prebiotic chemistry. While a great deal is now known about the potentially prebiotic synthesis of amino acids, our understanding of abiogenic polymerization processes to form polypeptides is
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)
Xanthogenation of lignocarbohydrates by carbon disulfide.
Efanov MV and Pershina LA.
Chemistry of Natural Compounds, 38(1), 90-94 (2002)
Continuous direct spinning of fibers of single-walled carbon nanotubes with metallic chirality.
Rajyashree M Sundaram et al.
Advanced materials (Deerfield Beach, Fla.), 23(43), 5064-5068 (2011-10-11)

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