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1-Bromodecane

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1-Bromodecane Basic information

Product Name:
1-Bromodecane
Synonyms:
  • 1-Bromodecane ,98%
  • 10-Bromodecane
  • 1-BroModecane, 98% 500GR
  • BroMine decane
  • 1-BROMODECANE FOR SYNTHESIS 250 ML
  • n-Decyl bromide Decyl bromide
  • DECYL BROMIDE
  • BROMO DECANE
CAS:
112-29-8
MF:
C10H21Br
MW:
221.18
EINECS:
203-955-3
Product Categories:
  • Alkyl
  • Building Blocks
  • Bromine Compounds
  • Chemical Synthesis
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • ALKYL BROMIDE
  • Alkyl Bromides
  • Monofunctional & alpha,omega-Bifunctional Alkanes
  • Monofunctional Alkanes
Mol File:
112-29-8.mol
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1-Bromodecane Chemical Properties

Melting point:
-29.6 °C
Boiling point:
238 °C(lit.)
Density 
1.066 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.456(lit.)
Flash point:
202 °F
storage temp. 
Store below +30°C.
solubility 
Chloroform, Ethyl Acetate (Slightly)
form 
Liquid
color 
Clear colorless to slightly yellow
Water Solubility 
SLIGHTLY SOLUBLE
BRN 
1735227
Dielectric constant
4.4(24℃)
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
InChIKey
MYMSJFSOOQERIO-UHFFFAOYSA-N
CAS DataBase Reference
112-29-8(CAS DataBase Reference)
NIST Chemistry Reference
Decane, 1-bromo-(112-29-8)
EPA Substance Registry System
Decane, 1-bromo- (112-29-8)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
23-24/25
RIDADR 
2810
WGK Germany 
3
RTECS 
HD6850000
8
TSCA 
Yes
HazardClass 
6.1
HS Code 
29033036
Toxicity
LD50 orally in Rabbit: > 2000 mg/kg

MSDS

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1-Bromodecane Usage And Synthesis

Chemical Properties

Colorless to light yellow liqui

Uses

1-Bromodecane is used to produce decanal. It is also used in organic synthesis.

Uses

1-Bromodecane was used in the synthesis of ferrocene containing hexacatenar metallomesogen.

General Description

1-Bromodecane participates in alkylation of pentaerythritol and introduces two lipophilic groups in pentaerythritol. It reacts with 1,2-dimethylimidazole to yield 1-decyl-2,3-dimethylimidazolium bromide.

Purification Methods

Shake the it with H2SO4, wash with H2O, dry with K2CO3, and fractionally distil it. [Beilstein 1 IV 470.]

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