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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)

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

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Z146811

Hose adapter, brass

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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

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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Lewis acid catalyzed formal intramolecular [3+2] cross-cycloaddition of cyclopropane 1,1-diesters with alkenes: general and efficient strategy for construction of bridged [n.2.1] carbocyclic skeletons.
Wenju Zhu et al.
Angewandte Chemie (International ed. in English), 52(7), 2032-2037 (2013-01-12)
Reymundo Villa et al.
Journal of medicinal chemistry, 56(17), 6576-6582 (2013-08-08)
Targeting the spliceosome with small molecule inhibitors provides a new avenue to target cancer by intercepting alternate splicing pathways. Although our understanding of alternate mRNA splicing remains poorly understood, it provides an escape pathway for many cancers resistant to current
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
Enzymatic chemistry of cyclopropane, epoxide, and aziridine biosynthesis.
Christopher J Thibodeaux et al.
Chemical reviews, 112(3), 1681-1709 (2011-10-25)
Han-Kun Zhang et al.
Journal of medicinal chemistry, 55(18), 8028-8037 (2012-08-30)
Structure-based drug design can potentially accelerate the development of new therapeutics. In this study, a cocrystal structure of the acetylcholine binding protein (AChBP) from Capitella teleta (Ct) in complex with a cyclopropane-containing selective α4β2-nicotinic acetylcholine receptor (nAChR) partial agonist (compound
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