Basic information Safety Supplier Related

1-Butylpyrrolidine

Basic information Safety Supplier Related

1-Butylpyrrolidine Basic information

Product Name:
1-Butylpyrrolidine
Synonyms:
  • N-BUTYL PYRROLIDINE
  • 1-BUTYLPYRROLIDINE
  • 1-BUTYLPYRROLIDINE FOR SYNTHESIS
  • 1-butyl-pyrrolidin
  • N-butyl-Tetrahydropyrrole
  • Pyrrolidine, 1-butyl-
CAS:
767-10-2
MF:
C8H17N
MW:
127.23
EINECS:
212-179-4
Product Categories:
  • API intermediates
  • Building Blocks
  • Heterocyclic Building Blocks
  • Pyrrolidines
  • Building Blocks
  • C4 to C10
  • Chemical Synthesis
  • Heterocyclic Building Blocks
Mol File:
767-10-2.mol
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1-Butylpyrrolidine Chemical Properties

Boiling point:
155-157 °C/754 mmHg (lit.)
Density 
0.814 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.44(lit.)
Flash point:
97 °F
storage temp. 
Refrigerator, Under inert atmosphere
solubility 
Chloroform (Sparingly), Ethyl Acetate (Slightly)
pka
10.62±0.20(Predicted)
form 
Oil
color 
Colourless
LogP
2.209 (est)
CAS DataBase Reference
767-10-2(CAS DataBase Reference)
NIST Chemistry Reference
1-Butylpyrrolidine(767-10-2)
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Safety Information

Hazard Codes 
T
Risk Statements 
10-24/25
Safety Statements 
16-36/37-45
RIDADR 
UN 2929 6.1/PG 2
WGK Germany 
2
RTECS 
UX9800000
HazardClass 
3.2
PackingGroup 
III

MSDS

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1-Butylpyrrolidine Usage And Synthesis

Uses

1-Butylpyrrolidine can be used in the composition for alcohol recovery solution.

Uses

1-Butylpyrrolidine has been used in:
microwave-assisted synthesis of ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate.
[N,N-methylbutylpyrrolidinium] thiosalicylate, ionic liquid.
The reaction of 1-butylpyrrolidine with dimethyl carbonate to yield the ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate, has been investigated under microwave heating conditions and the reaction parameters optimised to achieve 100% yield of the pyrrolidinium salt with no by-products in under 1h.

Preparation

The synthesis of 1-butylpyrrolidine and its derivatives (1-butylpyrrolidine with a little of 1-butenylpyrrolidines) was developed via a one-pot method from ammonia and 1,4-butandiol. Here, the product of 1-butylpyrrolidine was emphatically investigated, and the yield was 76% under the optimized conditions. Such a route was realized through successive N-alkylation using aqueous ammonia as the nitrogen source over the CuNiPd/ZSM-5 catalyst, which was prepared by a simple incipient wetness method. In this route, 1,4-butandiol not only participated in the formation of the N-heterocycle, but also acted as an alkylating reagent. This work offers a straightforward, economical route for 1-butylpyrrolidine and its derivatives.

One-pot synthesis of 1-butylpyrrolidine and its derivatives from aqueous ammonia and 1,4-butandiol over CuNiPd/ZSM-5 catalysts

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