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Sigma-Aldrich

2-Methylpyrrolidine

96%

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About This Item

Empirical Formula (Hill Notation):
C5H11N
CAS Number:
765-38-8
Molecular Weight:
85.15
EC Number:
212-144-3
MDL number:
MFCD00014491
UNSPSC Code:
12352100
PubChem Substance ID:
24871446
NACRES:
NA.22

assay

96%

refractive index

n20/D 1.437 (lit.)

bp

97-99 °C/744 mmHg (lit.)

density

0.834 g/mL at 25 °C (lit.)

SMILES string

CC1CCCN1

InChI

1S/C5H11N/c1-5-3-2-4-6-5/h5-6H,2-4H2,1H3

InChI key

RGHPCLZJAFCTIK-UHFFFAOYSA-N

General description

2-Methylpyrrolidine is a substituted pyrrolidine. It is one of the major bioactive compounds found in Teucrium manghuaense. The hydrodenitrogenation of 2-methylpyrrolidine in the presence of sulfided NiMo/γ-Al2O3 catalyst has been studied.

Application

2-Methylpyrrolidine may be used as a guest molecule for the synthesis of nonasil-[4158], a clatharate compound.

signalword

Danger

Hazard Classifications

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

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

37.4 °F - closed cup

flash_point_c

3 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Jennifer Zablocki et al.
Chirality, 32(5), 619-631 (2020-03-11)
An enantiomerically pure (R)-2-methylpyrrolidine-based anilino squaraine crystallizes in two chiral polymorphs adopting a monoclinic C2 and an orthorhombic P21 21 21 structure, respectively. By various thin-film preparation techniques, a control of the polymorph formation is targeted. The local texture of
Extraction of Teucrium manghuaense and evaluation of the bioactivity of its extract.
Yin G, et al.
International Journal of Molecular Sciences, 10(10), 4330-4341 (2009)
On the Formation of Pentylpiperidine in the Hydrodenitrogenation of Pyridine.
Wang H and Prins R.
Catalysis Letters, 126(1-2), 1-9 (2008)
Nagaraju Rajana et al.
Journal of chromatographic science, 57(9), 769-777 (2019-09-11)
Acetamide is a potential genotoxic impurity; it should control in drug substance based on daily dosage level. It forms from base-contaminated acetonitrile and by-product of some drug substances. The available methods for acetamide in drug substance and water samples were

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