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394238

Sigma-Aldrich

Pyrrolidine

≥99.5%, purified by redistillation

Synonym(s):

Tetrahydropyrrole, Tetramethyleneimine

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About This Item

Empirical Formula (Hill Notation):
C4H9N
CAS Number:
123-75-1
Molecular Weight:
71.12
Beilstein/REAXYS Number:
102395
EC Number:
204-648-7
MDL number:
MFCD00005249
UNSPSC Code:
12352100
PubChem Substance ID:
24864581
NACRES:
NA.22

vapor density

2.45 (vs air)

vapor pressure

128 mmHg ( 39 °C)
49 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

653 °F

purified by

redistillation

expl. lim.

10.6 %

refractive index

n20/D 1.443 (lit.)

solubility

water: miscible

density

0.852 g/mL at 25 °C (lit.)

SMILES string

C1CCNC1

InChI

1S/C4H9N/c1-2-4-5-3-1/h5H,1-4H2

InChI key

RWRDLPDLKQPQOW-UHFFFAOYSA-N

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General description

Pyrrolidine is a five membered cyclic amine. It is a nitrogen heterocycle that forms the nucleus of various bioactive molecules. It can be synthesized by reacting 1,4-diaminobutanes with acids. It behaves as a strong base in employed in certain homogeneous nonaqueous reactions. Its crystalline structure has been investigated. Its reaction on the Ge(100)-2×1 surface and Si(100)-2×1 surface has been investigated. Pyrrolidine has been found to be one of the component of volatile amine fraction in the brewing process. A study on the kinetics of pyrrolidinolysis of phthalimide (PTH) shows second- and third-order terms in the rate law. Biodegradation of pyrrolidine by Mycobacterium strains has been studied.

Application

Pyrrolidine may be used in the following studies:
  • Synthesis of pyrrolidine derivatives of pyrimidine.
  • As a catalyst in the selective monoallylation of allylic alcohols.
  • To capture carbondioxide in a bubble column reactor using pyrrolidine aqueous solutions by gas–liquid absorption.

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Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

37.4 °F - closed cup

flash_point_c

3 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN2189
SHBJ3184
SHBF5731V
SHBC1836V
SHBB3338V

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P Poupin et al.
Canadian journal of microbiology, 45(3), 209-216 (1999-07-17)
Nine bacterial strains that grew on morpholine and pyrrolidine as sole carbon, nitrogen, and energy sources were isolated from three different environments with no known morpholine contamination. One of these strains could also degrade piperidine. These bacteria were identified as
CO2 capture by pyrrolidine: Reaction mechanism and mass transfer.
Garcia-Abuin, A, et al.
AIChE Journal, 60(3), 1098-1106 (2014)
Azetidine, pyrrolidine and hexamethyleneimine at 170 K.
Bond AD, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 64(10), o543-o546 (2008)
Reactions of cyclic aliphatic and aromatic amines on Ge (100)-2? 1 and Si (100)-2? 1.
Wang GT, et al.
The Journal of Physical Chemistry B, 107(21), 4982-4996 (2003)
Ryozo Shibuya et al.
Angewandte Chemie (International ed. in English), 53(17), 4377-4381 (2014-03-08)
A dual platinum- and pyrrolidine-catalyzed direct allylic alkylation of allylic alcohols with various active methylene compounds to produce products with high monoallylation selectivity was developed. The use of pyrrolidine and acetic acid was essential, not only for preventing undesirable side
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