Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3
SKU: S1848

1,3-Propene sultone | 21806-61-1 |Sarcham Labs

SKU: S1848

Description

10898703

Synonyms: 5H-1,2-Oxathiole 2,2-Dioxide

Melting Point 85°C
Boiling Point 118°C
Color White
Formula Weight 120.12
Physical Form Crystal-Powder at 20°C
Chemical Name or Material 1-Propene 1,3-Sultone

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SPECIFICATION

AppearanceN/A
Content of ZincN/A
Boiling PointN / A
Melting PointN/A
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A

Safety Information

Classification of the substance or mixture

GHS Label elements, including precautionary statements

Hazards not otherwise classified (HNOC) or not covered by GHS

 

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1,3-Propene sultone | 21806-61-1 FAQs

Propene is a molecular formula that includes three carbon atoms and six hydrogens. Its unsaturated hydrocarbon structure and the fact that it has a double bond between two carbon atoms give it the chemical formula C3H6.

Propene is chemically represented as C3H6. This straightforward alkene is a member of the hydrocarbon class characterized by its reactivity in addition and polymerization processes; it has a single carbon-carbon double bond.

Propene is an alkene, as shown by its chemical formula: C3H6. Its molecular composition may be inferred from its formula, which directs its function in synthesis processes, such as those that produce polypropylene and other organic molecules.

Because of its double-bond structure, propene is very reactive. This makes it essential in many chemical processes, including hydrogenation, halogenation, and hydrohalogenation.

Propane has three carbon and six hydrogen atoms, as in its formula C3H6. Its unsaturated character is reflected in the ratio, allowing it to behave chemically differently than alkanes and has distinct commercial and laboratory uses.