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539775

Sigma-Aldrich

Ethane

99.99%

Sinonimo/i:

Ethane gas

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About This Item

Formula condensata:
CH3CH3
Numero CAS:
74-84-0
Peso molecolare:
30.07
Beilstein:
1730716
Numero CE:
200-814-8
Numero MDL:
MFCD00009023
Codice UNSPSC:
12142100
ID PubChem:
24878421
NACRES:
NA.22

Densità del vapore

1.05 (vs air)

Tensione di vapore

37.95 atm ( 21.1 °C)

Saggio

99.99%

Forma fisica

gas

Temp. autoaccensione

881 °F

Limite di esplosione

13 %

P. eboll.

−88 °C (lit.)

Punto di fusione

−172 °C (lit.)

Densità

0.362 g/mL at 20 °C (lit.)

Stringa SMILE

CC

InChI

1S/C2H6/c1-2/h1-2H3
OTMSDBZUPAUEDD-UHFFFAOYSA-N

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Applicazioni

  • High-pressure oxidation of ethane: The paper discusses the oxidation properties of ethane under high pressure, providing insights crucial for developing combustion models and understanding ethane′s behavior in various industrial processes (H Hashemi, JG Jacobsen, CT Rasmussen, 2017).
  • Progress and prospects in catalytic ethane aromatization: This review highlights the advancements in converting ethane to more valuable aromatic hydrocarbons, showcasing the potential of ethane as a petrochemical feedstock (Y Xiang, H Wang, J Cheng, J Matsubu, 2018).

Confezionamento

Supplied in a carbon steel lecture bottle with a CGA180M/CGA110F needle valve installed.

Compatible with the following:
  • Aldrich® lecture-bottle station systems
  • Aldrich® lecture-bottle gas regulators

Altre note

See Technical Information Bulletin AL-151 Gas Regulators: Selection, Installation, and Operation

Note legali

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC

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Pittogrammi

FlameGas cylinder
GHS02,GHS04

Avvertenze

Danger

Indicazioni di pericolo

H220,H280

Classi di pericolo

Flam. Gas 1A - Press. Gas Liquefied gas

Codice della classe di stoccaggio

2A - Gases

Classe di pericolosità dell'acqua (WGK)

nwg

Punto d’infiammabilità (°F)

-211.0 °F - closed cup

Punto d’infiammabilità (°C)

-135 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificati d'analisi (COA)

Lot/Batch Number
MKCM0398
MKCL1723
MKCJ9241
MKCH7597
MKCF7483

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Dario Frascari et al.
Bioresource technology, 128, 479-486 (2012-12-04)
A novel aerobic/anaerobic/aerobic treatment was implemented in batch reactors containing aquifer materials from a site contaminated by tetrachloroethylene (PCE), trichloroethylene (TCE), vinyl chloride (VC), 1,1,2-trichloroethane (1,1,2-TCA) and chloroform (CF). Consortia grown aerobically on methane, propane, n-pentane and n-hexane completely biodegraded
Margaret A Greene et al.
Organic letters, 14(16), 4293-4296 (2012-05-10)
Stereospecific nickel-catalyzed cross-coupling reactions of benzylic 2-methoxyethyl ethers are reported for the preparation of enantioenriched 1,1-diarylethanes. The 2-methoxyethyl ether serves as a traceless directing group that accelerates cross-coupling. Chelation of magnesium ions is proposed to activate the benzylic C-O bond
Isobel J Simpson et al.
Nature, 488(7412), 490-494 (2012-08-24)
After methane, ethane is the most abundant hydrocarbon in the remote atmosphere. It is a precursor to tropospheric ozone and it influences the atmosphere's oxidative capacity through its reaction with the hydroxyl radical, ethane's primary atmospheric sink. Here we present
Sachiko Tojo et al.
The Journal of organic chemistry, 78(5), 1887-1893 (2012-11-29)
A central carbon–carbon (C–C) σ bond dissociation of polyphenylethane radical anions (Ph(n)E•-, n = 3–6), mesolysis, was investigated by the transient absorption measurement during pulse radiolysis of Ph(n)E in 2-methyltetrahydrofuran. The charge resonance (CR) band of 1,1,2,2-tetraphenylethane radical anion (1,1,2,2-Ph4E•-)
Prantik Maity et al.
Journal of the American Chemical Society, 135(1), 280-285 (2012-12-28)
We have developed a nickel-catalyzed cross coupling of benzylic ammonium triflates with aryl boronic acids to afford diarylmethanes and diarylethanes. This reaction proceeds under mild reaction conditions and with exceptional functional group tolerance. Further, it transforms branched benzylic ammonium salts
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