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411027

Sigma-Aldrich

Piperidine

≥99.5%, purified by redistillation

Synonym(s):

Hexahydropyridine

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About This Item

Empirical Formula (Hill Notation):
C5H11N
CAS Number:
110-89-4
Molecular Weight:
85.15
Beilstein:
102438
EC Number:
203-813-0
MDL number:
MFCD00005979
UNSPSC Code:
12352005
PubChem Substance ID:
24865722
NACRES:
NA.22

vapor density

3 (vs air)

vapor pressure

23 mmHg ( 20 °C)

Assay

≥99.5%

form

liquid

purified by

redistillation

refractive index

n20/D 1.452 (lit.)

bp

106 °C (lit.)

mp

−13 °C (lit.)

density

0.862 g/mL at 20 °C (lit.)

SMILES string

C1CCNCC1

InChI

1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2

InChI key

NQRYJNQNLNOLGT-UHFFFAOYSA-N

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Application

Piperidine may be used as a base for the oxidative homocoupling of terminal alkynes to form symmetrical 1,4-disubstituted 1,3-diynes in the presence of copper nanoparticle on polyaniline support catalyst. It may also be used for cleaving the Fmoc-group in Nα-9-fluorenylmethyloxycarbonyl (Fmoc) amino acids.

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 1

Flash Point(F)

60.8 °F - closed cup

Flash Point(C)

16 °C - closed cup

Personal Protective Equipment

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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Solid?phase peptide synthesis using mild base cleavage of N?-fluorenylmethyloxycarbonylamino acids, exemplified by a synthesis of dihydrosomatostatin.
Chang CD
Chemical Biology & Drug Design, 11(3), 246-249 (1978)
Polymer-Supported Cu?Nanoparticle as an Efficient and Recyclable Catalyst for Oxidative Homocoupling of Terminal Alkynes.
Aziz ST
Catalysis Letters, 148(1), 205-213 (2018)
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A novel series of piperidine-linked amino-triazine derivatives were designed, synthesized and evaluated for in vitro anti-HIV activity as non-nucleoside reverse transcriptase inhibitors on the basis of our previous work. Screening results indicated that most compounds showed excellent activity against wild-type
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A de novo protein design strategy provides a powerful tool to elucidate how heavy metals interact with proteins.Cysteine derivatives of the TRI peptide family (Ac-G(LKALEEK)4G-NH2) have been shown to bind heavy metals in an unusual trigonal geometry. Our present objective
J Phillip Turner et al.
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