Basic information Safety Supplier Related

1,1-Dibutoxytrimethylamine

Basic information Safety Supplier Related

1,1-Dibutoxytrimethylamine Basic information

Product Name:
1,1-Dibutoxytrimethylamine
Synonyms:
  • N,N-Dimethylformamide di-n-butyl acetal, 98+%
  • 1,1-Dibutoxy-N,N-dimethylmethylamine, 1,1-Dibutoxytrimethylamine
  • dibutoxymethyl(dimethyl)amine
  • 1,1-Dibutoxy-N,N-dimethylmethanamine
  • α,α-Dibutoxy-N,N-dimethylmethanamine
  • N,N-Dimethylformamide Dibutyl Acetal 
  • N,N-Dimethylformamide Dibutyl Acetal [for Esterification]
  • 1,1-DIBUTOXY-N,N-DIMETHYLMETHYLAMINE
CAS:
18503-90-7
MF:
C11H25NO2
MW:
203.32
EINECS:
242-387-0
Product Categories:
  • GC Derivatizing Reagents
  • N,N-Dimethylformamide Dialkylacetals (GC Derivatizing Reagents)
  • Acetals/Ketals/Ortho Esters
  • Building Blocks
  • Chemical Synthesis
  • Organic Building Blocks
  • Analytical Chemistry
  • Esterification & Alkylation (GC Derivatizing Reagents)
  • Oxygen Compounds
Mol File:
18503-90-7.mol
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1,1-Dibutoxytrimethylamine Chemical Properties

Boiling point:
93 °C12 mm Hg(lit.)
Density 
0.853 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.417
Flash point:
53°C
pka
5.22±0.50(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
Specific Gravity
0.852
BRN 
1098693
CAS DataBase Reference
18503-90-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
10-36/37/38
Safety Statements 
26-36
RIDADR 
UN 1993 3/PG 3
WGK Germany 
3
HS Code 
2924.19.8000
HazardClass 
3.2
PackingGroup 
III

MSDS

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1,1-Dibutoxytrimethylamine Usage And Synthesis

Uses

N,N-Dimethylformamide dibutyl acetal is the suitable reagent used for the simultaneous quantification of cocaine and its primary metabolite, benzoyl ecgonine, from a urine matrix by gas-chromatography. It may be used as reagent for the esterification of fatty acids.

General Description

N,N-Dimethylformamide dibutyl acetal (1,1-Dibutoxytrimethylamine, 1,1-Dibutoxy-N,N-dimethylmethylamine) is a dimethylformamide dialkyl acetal. Its synthesis has been reported by Meerwin and coworkers by reaction of N,N-Dimethylformamide diethyl acetal with butanol.

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