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P46105

Sigma-Aldrich

Piperidine hydrochloride

99%

Sinónimos:

Piperidinium chloride

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About This Item

Fórmula empírica (notación de Hill):
C5H11N · HCl
Número de CAS:
6091-44-7
Peso molecular:
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

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Categorías relacionadas

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
Elisabeth Kaltenegger et al.
FEBS open bio, 11(1), 10-25 (2020-11-29)
Deoxyhypusine synthase transfers an aminobutyl moiety from spermidine to the eukaryotic translation initiation factor 5A (eIF5A) in the first step of eIF5A activation. This exclusive post-translational modification is conserved in all eukaryotes. Activated eIF5A has been shown to be essential
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
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
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

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