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Safety Information

W424401

Sigma-Aldrich

2-Methylpiperidine

98%

Synonym(s):

α-Pipecoline, 2-Pipecoline, NSC 31047, NSC 462

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About This Item

Empirical Formula (Hill Notation):
C6H13N
CAS Number:
109-05-7
Molecular Weight:
99.17
FEMA Number:
4244
Beilstein:
79804
EC Number:
203-642-1
MDL number:
MFCD00005982
UNSPSC Code:
12164502
PubChem Substance ID:
24901992
Flavis number:
14.133

biological source

synthetic

Assay

98%

refractive index

n20/D 1.445 (lit.)

bp

118-119 °C/753 mmHg (lit.)

density

0.844 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

Organoleptic

fishy

SMILES string

CC1CCCCN1

InChI

1S/C6H13N/c1-6-4-2-3-5-7-6/h6-7H,2-5H2,1H3

InChI key

NNWUEBIEOFQMSS-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

50.0 °F - closed cup

Flash Point(C)

10 °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.

FSL

Group 4: Flammable liquids
Type 1 petroleums
Hazardous rank II
Water soluble liquid

JAN Code

W424401-BULK:
W424401-1KG:
W424401-SAMPLE:
W424401-4KG:
W424401-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBK8570V
STBC7273V
MKBF3712
03324AE

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Ahmed M Ali et al.
Angewandte Chemie (International ed. in English), 48(11), 2024-2026 (2009-02-05)
Double protection: Efficient Fmoc-based solid-phase synthesis (SPPS) of sulfotyrosine (sY) peptides is achieved by incorporating the sY residue(s) as a dichlorovinyl-protected (DCV) sulfodiester(s) and using 2-methylpiperidine for Fmoc removal. After removal of the other protecting groups, the DCV group could
Yusuf Erdogdu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(1), 162-167 (2009-07-04)
The experimental and theoretical vibrational spectra of 2 and 3-methylpiperidine (abbreviated as 2-MP and 3-MP) were studied. The FT-Infrared spectra of 2-MP and 3-MP molecules were recorded in the liquid phase. The structural and spectroscopic analysis of the title molecules
J W Sloan et al.
Journal of medicinal chemistry, 28(9), 1245-1251 (1985-09-01)
Previous studies have shown that (+/-)-[3H]nicotine binds to multiple sites in the rat brain P2 preparation. Using a series of pyridine, piperidine and pyrrolidine analogues, the present studies identified drugs with specificity for a separate up-regulatory site that increases the
W R Martin et al.
Pharmacology, biochemistry, and behavior, 29(4), 725-731 (1988-04-01)
The effects of ethylketazocine (EKC) administered intraperitoneally and the nicotinic ligands (-)- and (+)-nicotine, (-)-cytisine, (-)-lobeline, and (+)-2-methylpiperidine administered into the 4th ventricle on the latency of the thermally evoked withdrawal reflex of the decerebrate rat were investigated. EKC administered
J W Sloan et al.
Life sciences, 37(15), 1367-1372 (1985-10-14)
(+/-)-2-Methylpiperidine has a high degree of specificity in enhancing the binding of (-)-[3H]nicotine in the rat brain P2 preparation. (-)- and (+)-2-Methylpiperidine have been resolved. The (+) but not the (-) isomer increased the binding of (-)-[3H]nicotine. The two isomers
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