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295183

Sigma-Aldrich

Cyclopropane

≥99%

Synonym(s):

Trimethylene (6CI)

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About This Item

Empirical Formula (Hill Notation):
C3H6
CAS Number:
75-19-4
Molecular Weight:
42.08
EC Number:
200-847-8
MDL number:
MFCD00001268
UNSPSC Code:
12142100
PubChem Substance ID:
24857764
NACRES:
NA.22

vapor density

1.45 (vs air)

Quality Level

100

Assay

≥99%

autoignition temp.

928 °F

expl. lim.

10.4 %

bp

−33 °C (lit.)

mp

−128 °C (lit.)

SMILES string

C1CC1

InChI

1S/C3H6/c1-2-3-1/h1-3H2

InChI key

LVZWSLJZHVFIQJ-UHFFFAOYSA-N

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Application

Cyclopropane has been used as the pseudo-π unsaturated hydrocarbon prototype to study the rotational spectrum of its complex formed with chlorine monofluoride and the similarity of this complex with isotopomers.

Packaging

Supplied in a Sure/Pac™ cylinder and has a brass needle valve with a male 1/4" NPTF outlet thread installed. Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.

Compatible with the following:

Legal Information

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

also commonly purchased with this product

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hose barb

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Z146811

Hose adapter, brass

recommended

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regulator

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Pictograms

FlameGas cylinder
GHS02,GHS04

Signal Word

Danger

Hazard Statements

H220,H280

Precautionary Statements

P410 + P403

Hazard Classifications

Flam. Gas 1 - Press. Gas Liquefied gas

Storage Class Code

2A - Gases

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBP7402
SHBH9047
STBC3584V
SHBB6363V
STBC3318V

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Timothy R Newhouse et al.
Organic letters, 15(7), 1591-1593 (2013-03-09)
A highly effective acid-catalyzed cyclopropyl ester to γ-lactone skeletal rearrangement has been demonstrated and applied to the synthesis of a variety of bi- and tricyclic functionalized lactones, rigid and highly compact structures for use as biological probes.
Enzymatic chemistry of cyclopropane, epoxide, and aziridine biosynthesis.
Christopher J Thibodeaux et al.
Chemical reviews, 112(3), 1681-1709 (2011-10-25)
Pedro S Coelho et al.
Science (New York, N.Y.), 339(6117), 307-310 (2012-12-22)
Transition metal-catalyzed transfers of carbenes, nitrenes, and oxenes are powerful methods for functionalizing C=C and C-H bonds. Nature has evolved a diverse toolbox for oxene transfers, as exemplified by the myriad monooxygenation reactions catalyzed by cytochrome P450 enzymes. The isoelectronic
Shuhei Kawamura et al.
Journal of medicinal chemistry, 56(9), 3689-3700 (2013-04-04)
The natural product belactosin A (1) with a trans-cyclopropane structure is a useful prototype compound for developing potent proteasome (core particle, CP) inhibitors. To date, 1 and its analogues are the only CP ligands that bind to both the nonprimed
Thomas Schalck et al.
Microorganisms, 9(2) (2021-02-04)
Fuels and polymer precursors are widely used in daily life and in many industrial processes. Although these compounds are mainly derived from petrol, bacteria and yeast can produce them in an environment-friendly way. However, these molecules exhibit toxic solvent properties
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