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P46105

Sigma-Aldrich

Piperidin -hydrochlorid

99%

Synonym(e):

Piperidinium chloride

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About This Item

Empirische Formel (Hill-System):
C5H11N · HCl
CAS-Nummer:
6091-44-7
Molekulargewicht:
121.61
Beilstein:
3611699
EG-Nummer:
228-033-8
MDL-Nummer:
MFCD00012770
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24898558
NACRES:
NA.22

Dampfdichte

2.94 (vs air)

Qualitätsniveau

200

Dampfdruck

63.6 mmHg ( 37.8 °C)

Assay

99%

Form

powder

mp (Schmelzpunkt)

245-248 °C (lit.)

SMILES String

Cl[H].C1CCNCC1

InChI

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

InChIKey

VEIWYFRREFUNRC-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

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

Piktogramme

Skull and crossbones
GHS06

Signalwort

Danger

H-Sätze

H301

P-Sätze

P301 + P310

Gefahreneinstufungen

Acute Tox. 3 Oral

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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Qingtong Wang et al.
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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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