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Safety Information

83275

Sigma-Aldrich

4-Pyrrolidinopyridine

purum, ≥98.0% (NT)

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About This Item

Empirical Formula (Hill Notation):
C9H12N2
CAS Number:
2456-81-7
Molecular Weight:
148.20
Beilstein:
472443
EC Number:
219-534-2
MDL number:
MFCD00006415
UNSPSC Code:
12352100
PubChem Substance ID:
329769286
NACRES:
NA.22

grade

purum

Quality Level

200

Assay

≥98.0% (NT)

form

crystals

mp

54-58 °C (lit.)
55-61 °C

solubility

methanol: 0.1 g/mL, clear

SMILES string

C1CCN(C1)c2ccncc2

InChI

1S/C9H12N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h3-6H,1-2,7-8H2

InChI key

RGUKYNXWOWSRET-UHFFFAOYSA-N

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Related Categories

Other Notes

Hypernucleophilic acylation catalyst. Reviews

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H314

Hazard Classifications

Acute Tox. 3 Oral - Skin Corr. 1B

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

83275-VAR:
83275-BULK:
83275-5G:
83275-25G:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG9248
BCCF4186
BCCB4143
BCBM9852V
1430931V

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A. Hassner
Tetrahedron, 34, 2069-2069 (1978)
Brian L Hodous et al.
Journal of the American Chemical Society, 124(34), 10006-10007 (2002-08-22)
The first method for the catalytic enantioselective addition of amines (specifically, pyrroles) to ketenes has been developed, and it has been demonstrated that the resulting acylpyrroles can be transformed into a broad spectrum of useful derivatives. On the basis of
A method for the synthesis of isomerically pure saturated mixed-chain phosphatidylcholines.
J T Mason et al.
Analytical biochemistry, 113(1), 96-101 (1981-05-01)
E.F. Scriven
Chemical Society Reviews, 12, 129-129 (1983)
H Kai et al.
The Journal of pharmacy and pharmacology, 48(1), 53-56 (1996-01-01)
We have examined the effects of pyridine derivatives on phosphatidylcholine secretion in primary cultures of rat type II pneumocytes. Of 12 pyridine derivatives, 4-aminopyridine, 4-dimethylaminopyridine and 4-pyrolidinopyridine had a stimulatory effect on phosphatidylcholine secretion, whereas other derivatives had little effect.
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