478059
2-Methylpyrrolidine
96%
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About This Item
Empirical Formula (Hill Notation):
C5H11N
CAS Number:
Molecular Weight:
85.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
212-144-3
MDL number:
Assay:
96%
Product Name
2-Methylpyrrolidine, 96%
InChI key
RGHPCLZJAFCTIK-UHFFFAOYSA-N
InChI
1S/C5H11N/c1-5-3-2-4-6-5/h5-6H,2-4H2,1H3
SMILES string
CC1CCCN1
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.)
Quality Level
Application
2-Methylpyrrolidine may be used as a guest molecule for the synthesis of nonasil-[4158], a clatharate compound.
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.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
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
Regulatory Information
危险化学品
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On the Formation of Pentylpiperidine in the Hydrodenitrogenation of Pyridine.
Wang H and Prins R.
Catalysis Letters, 126(1-2), 1-9 (2008)
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)
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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