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Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3
SKU: S2697

1,2-Dibromobutane | 533-98-2 | Sarchem Labs

SKU: S2697

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Description

10792

Synonym : butane, 1,2-dibromo, .alpha.-butylene dibromide, alpha-butylene dibromide, 1,2-dibomobutane, 1,2 dibromobutane, butane,2-dibromo, 1,2-dibromo-butane, alpha-butylene bromide, 1,2-butylene bromide, .alpha.-butylene bromide

Color Yellow
Boiling Point 166°C
Formula Weight 215.92
Physical Form Clear Liquid at 20°C
Chemical Name or Material 1,2-Dibromobutane

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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1,2-Dibromobutane | 533-98-2 FAQs

1,2-Dibromobutane has the formula C4H8Br2. It has four carbon atoms, eight hydrogen atoms, and two bromine atoms. The bromine atoms are connected to nearby carbon atoms, which makes them reactive in different chemical uses.

The 1,2-dibromobutane structure has a four-carbon backbone with bromine atoms on adjacent carbons. This arrangement improves its utility in synthesis, enabling halogen substitution and elimination reactions essential for producing complex organic compounds in industrial applications.

1,2-dibromobutane melting point is -65°C. The presence of bromine atoms affects its physical effects, changing how it moves between different states and how easily it dissolves in different chemicals.

1,2-Dibromobutane is used in organic synthesis, acting as an intermediate for pharmaceuticals, agrochemicals, and specialized polymers. Its bromine structure helps it add distinct groups during chemical changes.

1,2-Dibromobutane is made by adding bromine to butene or its related compounds using specific ways to control the reaction. Adding bromine carefully creates a product with a clear reaction, making it useful for both industry and lab work.

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