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1-Bromotetradecane

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1-Bromotetradecane Basic information

Product Name:
1-Bromotetradecane
Synonyms:
  • 1-Bromtetradecan
  • 1-Tetradecyl bromide
  • 1-tetradecylbromide
  • 1-BROMOTETRADECANE
  • BROMOTETRADECANE
  • TETRADECYL BROMIDE
  • MYRISTYL BROMIDE
  • N-TETRADECYL BROMIDE
CAS:
112-71-0
MF:
C14H29Br
MW:
277.28
EINECS:
203-999-3
Product Categories:
  • Alkyl Bromides
  • Monofunctional & alpha,omega-Bifunctional Alkanes
  • Monofunctional Alkanes
Mol File:
112-71-0.mol
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1-Bromotetradecane Chemical Properties

Melting point:
5-6 °C(lit.)
Boiling point:
175-178 °C20 mm Hg(lit.)
Density 
0.932 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.460(lit.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
Chloroform
form 
Liquid
color 
Clear yellow
Water Solubility 
insoluble
BRN 
1742640
Dielectric constant
3.8399999999999999
Stability:
Stable. Incompatible with strong bases, strong oxidizing agents.
CAS DataBase Reference
112-71-0(CAS DataBase Reference)
NIST Chemistry Reference
Tetradecane, 1-bromo-(112-71-0)
EPA Substance Registry System
Tetradecane, 1-bromo- (112-71-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-22
Safety Statements 
26-36-24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29033036

MSDS

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1-Bromotetradecane Usage And Synthesis

Chemical Properties

colorless or pale yellow liquid. soluble in acetone, benzene and chloroform. intermediates for organic synthesis.

Uses

1-Bromotetradecane was used in the synthesis of tetradecylferrocene, cationic and zwitterionic gemini surfactants, and 9-tetradecylcarbazole. Also used for synthesis of metallomesogenic polymers based on bis[η1(N)-3,4-dialkyloxybenzylidene-4?-dodecyloxyaniline]dichloropalladium(II) with octyl, decyl, dodecyl, tetradecyl and hexadecyl alkyl groups.

Preparation

1-Bromotetradecane is synthesized from 1-tetradecanol by bromination. The 1-tetradecanol was added to the reaction pot, and the sulfuric acid was added dropwise with stirring, and the stirring was continued for half an hour after the addition. Then add hydrobromic acid, heat to 99-101°C, and react for 8h. Cool to 30°C, stop stirring, stand for 12 hours, and separate the upper layer of oil, and adjust the pH to 8 with 10% sodium carbonate solution. The water layer was separated, the oily substance was washed twice with an equal volume of 50% ethanol, the washed oily substance was added with sodium carbonate, stirred intermittently, and dried for 24h. Filtration to obtain 1-bromotetradecane.

1-Bromotetradecane Preparation Products And Raw materials

Preparation Products

Raw materials

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