P46105
Piperidine hydrochloride
99%
Synonym(s):
Piperidinium chloride
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Recommended Products
vapor density
2.94 (vs air)
Quality Level
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:
Reactant for synthesis of phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors
Reactant for:
- 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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
Flash Point(F)
235.4 °F - closed cup
Flash Point(C)
113 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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
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
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
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