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280372

Sigma-Aldrich

1-Butylpyrrolidine

98%

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About This Item

Empirical Formula (Hill Notation):
C8H17N
CAS Number:
767-10-2
Molecular Weight:
127.23
EC Number:
212-179-4
MDL number:
MFCD00003184
UNSPSC Code:
12352100
PubChem Substance ID:
24856943
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.44 (lit.)

bp

155-157 °C/754 mmHg (lit.)

density

0.814 g/mL at 25 °C (lit.)

SMILES string

CCCCN1CCCC1

InChI

1S/C8H17N/c1-2-3-6-9-7-4-5-8-9/h2-8H2,1H3

InChI key

JSHASCFKOSDFHY-UHFFFAOYSA-N

Related Categories

Application

1-Butylpyrrolidine has been used in:
  • microwave-assisted synthesis of ionic liquid precursor, 1-butyl-1-methylpyrrolidinium methylcarbonate
  • [N,N-methylbutylpyrrolidinium] thiosalicylate, ionic liquid

Pictograms

FlameSkull and crossbones
GHS02,GHS06

Signal Word

Danger

Hazard Statements

H226,H301 + H311

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

96.8 °F - closed cup

Flash Point(C)

36 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP6159
MKCK1145
MKCC2662
MKBV8061V
MKBV8062V

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Giridhar Pulletikurthi et al.
Dalton transactions (Cambridge, England : 2003), 46(2), 455-464 (2016-12-14)
The mixtures of 1-butylpyrrolidine and ZnCl
Synthesis, characterization and thermal properties of thiosalicylate ionic liquids.
Wilfred CD and Mustafa FB.
Journal of Chemical Sciences (Bangalore), 125(6), 1511-1515 (2013)
Giridhar Pulletikurthi et al.
Chemistry, an Asian journal, 12(20), 2684-2693 (2017-08-05)
Electrostatic interactions are characteristic of ionic liquids (ILs) and play a pivotal role in determining the formation of species when solutes are dissolved in them. The formation of new species/complexes has been investigated for certain ILs. However, such investigations have
Optimised microwave-assisted synthesis of methylcarbonate salts: a convenient methodology to prepare intermediates for ionic liquid libraries.
Holbrey JD, et al.
Green Chemistry, 12(3), 407-413 (2010)

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