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ChemicalBook >> CAS DataBase List >>3-Hydroxypiperidine

3-Hydroxypiperidine

CAS No.
6859-99-0
Chemical Name:
3-Hydroxypiperidine
Synonyms
PIPERIDIN-3-OL;3-PIPERIDINOL;Benidipine Impurity 17;3-hydroxyperidine;3-HYDROXYPIPERIDINE;3-Hydroxypiperadine;OEM 3-Hydroxypiperidin;3-Hydroxypiperidine>3-HYDROXYPIPERIDINE 98%;(3R)-3-piperidin-1-iumol
CBNumber:
CB7687884
Molecular Formula:
C5H11NO
Molecular Weight:
101.15
MDL Number:
MFCD00014591
MOL File:
6859-99-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-17 18:53:45
Product description Number Pack Size Price
3-Hydroxypiperidine 99% 56210 10g $70.6
3-Hydroxypiperidine ≥98.0% (NT) 56210 50g $212
3-Hydroxypiperidine >98.0%(GC) H0412 5g $30
3-Hydroxypiperidine >98.0%(GC) H0412 25g $93
3-Hydroxypiperidine 426073 10g $340
More product size

3-Hydroxypiperidine Properties

Melting point 57-61 °C
Boiling point 67-69 °C (2 mmHg)
Density 1.016±0.06 g/cm3(Predicted)
Flash point >100°C
storage temp. 2-8°C
solubility ethanol: 0.1 g/mL, clear
pka 14.91±0.20(Predicted)
form Crystalline Powder and Lumps
color White to light yellow
PH 11.5-11.7 (H2O)Aqueous solution
Water Solubility soluble
Sensitive Air Sensitive & Hygroscopic
BRN 102696
InChI 1S/C5H11NO/c7-5-2-1-3-6-4-5/h5-7H,1-4H2
InChIKey BIWOSRSKDCZIFM-UHFFFAOYSA-N
SMILES OC1CCCNC1
LogP -0.35
CAS DataBase Reference 6859-99-0(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Corrosion (GHS05)
GHS05
Signal word  Danger
Hazard statements  H315-H318
Precautionary statements  P264-P280-P302+P352-P305+P351+P338-P332+P313-P362+P364
PPE Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Hazard Codes  C,Xi
Risk Statements  34-20/21/22-36/37/38
Safety Statements  26-36/37/39-45-27
RIDADR  UN 3263 8/PG 2
WGK Germany  3
HazardClass  8
PackingGroup  III
HS Code  29333990
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Dam. 1
Skin Irrit. 2
REACH Registrations Active
NFPA 704
1
3 0

3-Hydroxypiperidine price More Price(60)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 56210 3-Hydroxypiperidine 99% 6859-99-0 10g $70.6 2026-04-30 Buy
Sigma-Aldrich 56210 3-Hydroxypiperidine ≥98.0% (NT) 6859-99-0 50g $212 2026-04-30 Buy
TCI Chemical H0412 3-Hydroxypiperidine >98.0%(GC) 6859-99-0 5g $30 2026-04-30 Buy
TCI Chemical H0412 3-Hydroxypiperidine >98.0%(GC) 6859-99-0 25g $93 2026-04-30 Buy
Usbiological 426073 3-Hydroxypiperidine 6859-99-0 10g $340 2026-06-03 Buy
Product number Packaging Price Buy
56210 10g $70.6 Buy
56210 50g $212 Buy
H0412 5g $30 Buy
H0412 25g $93 Buy
426073 10g $340 Buy

3-Hydroxypiperidine Chemical Properties,Uses,Production

Background

Many piperidine derivatives have multiple pharmacological activities such as antibacterial, antitumor, treatment of Alzheimer's disease and anesthesia. They are also important drugs for the treatment of viral infections (including AIDS) and diabetes. 3-Hydroxypiperidine or its derivatives are one of the important intermediates, which are widely used in the synthesis of drug intermediates such as chiral 3-aminopiperidine. It is of great significance to develop a synthesis method suitable for industrial production.

Chemical Properties

White to light yellow crystalline powder and lumps

Application

3-Hydroxypiperidine may be used to synthesize the following:
2-pyrrolidinone via oxidation with iodosylbenzene
1-[2,8-bis(trifluoromethyl)quinolin-4-yl]piperidin-3-ol via reaction with 4-bromoquinoline
Reactant for:
Synthesis of unsymmetrical ureas
Synthesis of piperidine nucleoside analogs
Fluorination reactions
Synthesis of substituted pyridines

Uses

3-Hydroxypiperidine is usually used for Synthesis of unsymmetrical ureas,Synthesis of piperidine nucleoside analogs,Fluorination reactions,Synthesis of substituted pyridines.

General Description

3-Hydroxypiperidine can be obtained from the reduction of 3-hydroxypyridine.

Synthesis

Dissolve 86.0g of 5-bromo-2-hydroxypentylamine hydrobromide in 150mL of water, and add a solution of 60mL of water containing 15.0g of sodium carbonate at 10-15°C, and drip it for about 1 hour. After dripping, react at about 15°C for 2 hours. Then heat to 30-40°C and react for 2 hours. Stop the reaction, cool it to room temperature, and concentrate the reaction solution under reduced pressure to remove most of the water. Filter it to remove salt, wash it with cold water, and continue to concentrate the mother liquor. The crude product is distilled under reduced pressure to obtain 26.5g of colourless oily 3-hydroxypiperidine, yielding 80%.

References

[1] Patent: CN108017572, 2018, A. Location in patent: Paragraph 0018-0020; 0023
[2] Synlett, 2006, # 9, p. 1440 - 1442
[3] Chemistry - A European Journal, 2009, vol. 15, # 28, p. 6953 - 6963
[4] Patent: CN105367484, 2016, A. Location in patent: Paragraph 0018
[5] Patent: CN105439939, 2016, A. Location in patent: Paragraph 0041; 0042

85275-45-2
6859-99-0
Synthesis of 3-Hydroxypiperidine from 1-Boc-3-hydroxypiperidine
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