1-Bromodecane
1-Bromodecane
  • CAS No.:112-29-8
Other grades of this product :
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
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.)
Fp 202 °F
storage temp. Store below +30°C.
form Liquid
color Clear colorless to slightly yellow
Water Solubility SLIGHTLY SOLUBLE
BRN 1735227
Stability:Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
InChIKeyMYMSJFSOOQERIO-UHFFFAOYSA-N
CAS DataBase Reference112-29-8(CAS DataBase Reference)
NIST Chemistry ReferenceDecane, 1-bromo-(112-29-8)
EPA Substance Registry SystemDecane, 1-bromo- (112-29-8)
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
ToxicityLD50 orally in Rabbit: > 2000 mg/kg
MSDS Information
ProviderLanguage
Decylbromide English
SigmaAldrich English
ACROS English
ALFA English
1-Bromodecane Usage And Synthesis
Chemical PropertiesColorless to light yellow liqui
Uses1-Bromodecane is used to produce decanal. It is also used in organic synthesis.
Uses1-Bromodecane was used in the synthesis of ferrocene containing hexacatenar metallomesogen.
General Description1-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 MethodsShake the it with H2SO4, wash with H2O, dry with K2CO3, and fractionally distil it. [Beilstein 1 IV 470.]

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