Basic information Safety Supplier Related

N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL

Basic information Safety Supplier Related

N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Basic information

Product Name:
N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL
Synonyms:
  • 1,1-DINEOPENTYLOXYTRIMETHYLAMINE
  • 1,1-bis(2,2-dimethylpropoxy)-N,N,N-trimethylamine
  • Methanamine, 1,1-bis(2,2-dimethylpropoxy)-N,N-dimethyl-
  • 1,1-dineopentyloxy-n,n-dimethylmethylamine
  • N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL
  • N,N-Dimethyl[bis(neopentyloxy)]methanamine
  • Dimethylformamide dineopentyl acetal.
  • N,N-Dimethylformamide Dineopentyl Acetal [for Esterification]
CAS:
4909-78-8
MF:
C13H29NO2
MW:
231.37
EINECS:
225-536-4
Product Categories:
  • Analytical Chemistry
  • Esterification & Alkylation (GC Derivatizing Reagents)
  • GC Derivatizing Reagents
  • N,N-Dimethylformamide Dialkylacetals (GC Derivatizing Reagents)
Mol File:
4909-78-8.mol
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N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Chemical Properties

Melting point:
253.5℃
Boiling point:
85-87 °C/10 mmHg (lit.)
Density 
0.829 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.412(lit.)
Flash point:
125 °F
storage temp. 
Store at 0-5°C
pka
5.24±0.50(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
Water Solubility 
Hydrolyzes with water.
Sensitive 
Moisture Sensitive
BRN 
741992
CAS DataBase Reference
4909-78-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
1993
WGK Germany 
3
9-21
HazardClass 
3
PackingGroup 
III
HS Code 
29110000

MSDS

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N,N-DIMETHYLFORMAMIDE DINEOPENTYL ACETAL Usage And Synthesis

Chemical Properties

Colorless to slight yellow liquid

Uses

N,N-Dimethylformamide dineopentyl acetal helps in the lactonization of ω-hydroxyacids, giving lactones of up to 16-membered rings. It can be used to convert primary alcohols to alkylating agents for use in the alkylation of thiols. It is used in the esterification of Nα-9-fluorenylmethyloxycarbonylamino acids. It was used in the synthesis of 1,3-dialkyl, benzyl and cyclohexyl barbiturate derivatives. It was used as reagent during the synthesis of L-serine and L-cystine stereospecifically labeled with deuterium at the β-position.

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