Skip to Content
MilliporeSigma
All Photos(1)

Documents

P46105

Sigma-Aldrich

Piperidine hydrochloride

99%

Synonym(s):

Piperidinium chloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C5H11N · HCl
CAS Number:
6091-44-7
Molecular Weight:
121.61
Beilstein/REAXYS Number:
3611699
EC Number:
228-033-8
MDL number:
MFCD00012770
UNSPSC Code:
12352100
PubChem Substance ID:
24898558
NACRES:
NA.22

vapor density

2.94 (vs air)

Quality Level

200

vapor pressure

63.6 mmHg ( 37.8 °C)

assay

99%

form

powder

mp

245-248 °C (lit.)

SMILES string

Cl[H].C1CCNCC1

InChI

1S/C5H11N.ClH/c1-2-4-6-5-3-1;/h6H,1-5H2;1H

InChI key

VEIWYFRREFUNRC-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Reagent for synthesis of:
  • Quinoline selenium compounds
  • Peripheral seratonin 5-HT3 receptor ligands

Reactant for synthesis of phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors

Reactant for:
  • Mannich reactions
  • Asymmetric hydrogenation of quinolines
  • Chemoselective reductive amination of carbonyl compounds

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 4

1 of 4

1-(2-Chloroethyl)piperidine hydrochloride 98%

Sigma-Aldrich

C42602

1-(2-Chloroethyl)piperidine hydrochloride

4-Acetylbenzoic acid 98%

Sigma-Aldrich

177458

4-Acetylbenzoic acid

Piperidine for synthesis

Sigma-Aldrich

8.22299

Piperidine

Syringaldehyde 98%

Sigma-Aldrich

S7602

Syringaldehyde

Qingtong Wang et al.
Scientific reports, 7, 45364-45364 (2017-03-30)
T cell infiltration to synovial tissue is an early pathogenic mechanism of rheumatoid arthritis (RA). In the present work, we reveal that G protein coupled receptor kinase 2 (GRK2) is abundantly expressed in T cells of collagen-induced arthritis (CIA). A
Željko Pavković et al.
Progress in neuro-psychopharmacology & biological psychiatry, 96, 109733-109733 (2019-08-17)
Adolescent neurodevelopment confer vulnerability to the actions of treatments that produce adaptations in neurocircuitry underlying motivation, impulsivity and reward. Considering wide usage of a sedative-hypnotic agent propofol in clinical practice, we examined whether propofol is a challenging treatment for peripubertal
Reza Shamsimeymandi et al.
Archiv der Pharmazie, 352(7), e1800352-e1800352 (2019-05-29)
A series of novel chroman-4-one derivatives were designed and synthesized successfully with good to excellent yield (3a-l). In addition, the obtained products were evaluated for their cholinesterase (ChE) inhibitory activities. The results show that among the various synthesized compounds, analogs
Xiao-Xi Huang et al.
Nucleic acids research, 42(13), 8719-8731 (2014-06-19)
Ligands that can interact specifically with telomeric multimeric G-quadruplexes could be developed as promising anticancer drugs with few side effects related to other G-quadruplex-forming regions. In this paper, a new cationic porphyrin derivative, m-TMPipEOPP, was synthesized and characterized. Its multimeric

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service