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321273

Sigma-Aldrich

Ethane

10 ppm in nitrogen

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About This Item

Linear Formula:
CH3CH3
CAS Number:
Molecular Weight:
30.07
Beilstein:
1730716
MDL number:

vapor density

1.05 (vs air)

vapor pressure

37.95 atm ( 21.1 °C)

autoignition temp.

881 °F

expl. lim.

13 %

concentration

10 ppm in nitrogen

bp

−88 °C (lit.)

mp

−172 °C (lit.)

density

0.362 g/mL at 20 °C (lit.)

SMILES string

CC

InChI

1S/C2H6/c1-2/h1-2H3

InChI key

OTMSDBZUPAUEDD-UHFFFAOYSA-N

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Application

For calibrating analytical instruments.

Packaging

Packaged in lightweight no-return cylinder

Recommended products

Control valve Z166995 or regulator Z167002 is recommended.

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Reika Kanya et al.
The Journal of chemical physics, 136(20), 204309-204309 (2012-06-07)
Two-body Coulomb explosion processes of ethane (CH(3)CH(3)) and its isotopomers (CD(3)CD(3) and CH(3)CD(3)) induced by an intense laser field (800 nm, 1.0 × 10(14) W/cm(2)) with three different pulse durations (40 fs, 80 fs, and 120 fs) are investigated by
Ramiro F Quijano-Quiñones et al.
Molecules (Basel, Switzerland), 17(4), 4661-4671 (2012-04-24)
The energy change on each Occupied Molecular Orbital as a function of rotation about the C-C bond in ethane was studied using the B3LYP, mPWB95 functional and MP2 methods with different basis sets. Also, the effect of the ZPE on
Paul O Wennberg et al.
Environmental science & technology, 46(17), 9282-9289 (2012-08-03)
We use historical and new atmospheric trace gas observations to refine the estimated source of methane (CH(4)) emitted into California's South Coast Air Basin (the larger Los Angeles metropolitan region). Referenced to the California Air Resources Board (CARB) CO emissions
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
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•-)

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