295183
Cyclopropane
≥99%
Synonym(s):
Trimethylene (6CI)
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About This Item
Empirical Formula (Hill Notation):
C3H6
CAS Number:
Molecular Weight:
42.08
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12142100
EC Number:
200-847-8
MDL number:
Assay:
≥99%
InChI key
LVZWSLJZHVFIQJ-UHFFFAOYSA-N
InChI
1S/C3H6/c1-2-3-1/h1-3H2
SMILES string
C1CC1
vapor density
1.45 (vs air)
assay
≥99%
autoignition temp.
928 °F
expl. lim.
10.4 %
bp
−33 °C (lit.)
mp
−128 °C (lit.)
Quality Level
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:
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
signalword
Danger
hcodes
pcodes
Hazard Classifications
Flam. Gas 1 - Press. Gas Liquefied gas
Storage Class
2A - Gases
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)
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Ya Zhang et al.
Frontiers in microbiology, 8, 2036-2036 (2017-11-04)
The occurrence of pathogenic bacteria in drinking water distribution systems (DWDSs) is a major health concern, and our current understanding is mostly related to pathogenic species such as
Lorenzo Cianni et al.
PLoS neglected tropical diseases, 14(3), e0007755-e0007755 (2020-03-13)
The cysteine protease cruzipain is considered to be a validated target for therapeutic intervention in the treatment of Chagas disease. A series of 26 new compounds were designed, synthesized, and tested against the recombinant cruzain (Cz) to map its S1/S1´
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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