Piperidin-4-olhydrochlorid

Suppliers

Names

[ Name ]:
Piperidin-4-olhydrochlorid

[Synonym ]:
Piperidin-4-ol hydrochloride
4-Hydroxypiperidinium chloride
4-Hydroxypiperidine Hydrochloride
4-Piperidinol hydrochloride (1:1)
Piperidin-4-olhydrochlorid
piperidin-4-ol,hydrochloride
MFCD00035298
Piperidin-4-ol hydrochloride (1:1)
EINECS 226-374-7
4-Piperidinol hydrochloride
4-Piperidinol, hydrochloride (1:1)

Chemical & Physical Properties

[ Boiling Point ]:
222ºC at 760 mmHg

[ Melting Point ]:
155-157 °C(lit.)

[ Molecular Formula ]:
C₅H₁₂ClNO

[ Molecular Weight ]:
137.608

[ Flash Point ]:
107.8ºC

[ Exact Mass ]:
137.060745

[ PSA ]:
32.26000

[ LogP ]:
0.86150

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933399090

Precursor & DownStream

Precursor

DownStream

1-(5-Nitro-2-pyridinyl)-4-piperidinol
N-BOC-4-Hydroxypiperidine
piperidin-4-yl acetate
tert-butyl 4-acetyloxypiperidine-1-carboxylate
4-Hydroxy Phencyclidine
4-hydroxypiperidine-1-carbonitrile

Customs

[ HS Code ]: 2933399090

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Microchip-based synthesis and analysis: control of multicomponent reaction products and intermediates.

Analyst 126(1) , 24-7, (2001)

A miniaturised-SYNthesis and Total Analysis System (mu SYNTAS) was used for the solution-phase synthesis and on-line analysis (TOF-MS) of Ugi multicomponent reaction (MCR) products. This approach prov...

1-[1-2-Benzo[b]thiopheneyl)cyclohexyl]piperidine hydrochloride (BTCP) yields two active primary metabolites in vitro: synthesis, identification from rat liver microsome extracts, and affinity for the neuronal dopamine transporter.

J. Med. Chem. 40(25) , 4019-25, (1997)

1-[1-(2-Benzo[b]thiopheneyl)cyclohexyl]piperidine hydrochloride (BTCP, 1) and cocaine bind to the neuronal dopamine transporter to inhibit dopamine (DA) reuptake. However, on chronic administration, c...

The Synthesis of Δ³-Tetrahydropyridine. Renshaw RR and Conn RC.

J. Am. Chem. Soc. 60(4) , 745-747, (1938)

piperidin-4-yl acetate
PIPERIDIN-4-YLIDENE-ACETIC ACID ETHYL ESTER
Piperidin-4-yl-pyridin-3-ylmethyl-amine
piperidin-4-one,2,2,2-trifluoroacetic acid
piperidin-4-yl(pyridin-2-yl)methanone
Piperidin-4-yl-carbamic acid allyl ester
4-bromo-1-(4-ethylcyclohexyl)-1H-pyrazol-3-amine
5-bromo-2-methoxy-N-(pyridin-3-ylmethyl)aniline
(5-methoxy-4-oxoquinazolin-3(4H)-yl)methyl pivalate
7-Isopropyl-1,3-dimethyl-1H-pyrazolo[4,3-b]pyridine
N-methyl-N-(piperidin-4-yl)benzo[d]thiazol-2-amine hydrochloride
2,3,4-Tris(dodecyloxy)phenol
6-(2,2-Dimethoxyethoxy)quinoline
3-Piperidinamine, 2-(2-fluorophenyl)-1-methyl-
N-butyl-6-chloro-N,2-dimethylpyrimidin-4-amine
(3-cyclopropyl-1,5-dimethyl-1H-pyrazolo[3,4-b]pyridin-6-yloxy)acetic acid

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