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Sigma-Aldrich

Ethylene

≥99.5%

Synonym(s):

Ethene

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About This Item

Linear Formula:
CH2=CH2
CAS Number:
Molecular Weight:
28.05
Beilstein:
1730731
EC Number:
MDL number:
UNSPSC Code:
12142100
PubChem Substance ID:
NACRES:
NA.22

vapor density

0.97 (vs air)

Quality Level

vapor pressure

35.04 atm ( 20 °C)

Assay

≥99.5%

autoignition temp.

842 °F

expl. lim.

36 %

bp

−104 °C (lit.)

mp

−169 °C (lit.)

SMILES string

C=C

InChI

1S/C2H4/c1-2/h1-2H2

InChI key

VGGSQFUCUMXWEO-UHFFFAOYSA-N

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General description

Ethylene is an alkene used in Friedel-Crafts alkylation, cycloaddition, electrophilic addition, and vinylation reactions.

Application

Ethylene is mainly used as a precursor to synthesize polyethylene, ethylbenzene and ethylene dichloride. It is also used in the preparation of single- layer graphene by thermal chemical vapor deposition.

Packaging

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

Other Notes

Legal Information

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

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purge valve

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Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Gas 1 - Press. Gas Liquefied gas - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

2A - Gases

WGK

nwg

Flash Point(F)

-148.0 °F - closed cup

Flash Point(C)

-100 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Addition of arenes to ethylene and propene catalyzed by ruthenium.
Lail, Marty and Arrowood, Benjamin N and Gunnoe, T Brent
Journal of the American Chemical Society, 125(25), 7506-7507 (2003)
Ethylene
Crimmins MT and Kim-Meade AS
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
Catalytic hydroarylation of ethylene using TpRu (L)(NCMe) Ph (L= 2, 6, 7-Trioxa-1-phosphabicyclo [2, 2, 1] heptane): Comparison to TpRu (L?)(NCMe) Ph systems (L?= CO, PMe3, P (pyr) 3, or P (OCH2) 3CEt).
Joslin, Evan E et al.
Organometallics, 31(19), 6851-6860 (2012)
Pyridinic N doped graphene: synthesis, electronic structure, and electrocatalytic property.
Luo, Zhiqiang et al.
Journal of Materials Chemistry, 21(22), 8038-8044 (2011)
Ethylene.
Kirk-Othmer Encyclopedia of Chemical Technology, 1-39 (2000)

Protocols

Separation of Methane; Acetylene; Carbon monoxide; Water; Nitrogen; Carbon dioxide; Ethane; Ethylene

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