4-Piperidinemethanol

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Company Name: Siyang Liaoning Biochemical Products Co. Ltd
Tel: +86-15221114306; +8615221114306
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Products Intro: Product Name:4-Piperidinemethanol
CAS:6457-49-4
Purity:>98% Package:1kg;5kg;20kg;25kg Remarks:pharmaceutical intermediates
Company Name: Hebei Chuanghai Biotechnology Co., Ltd
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Products Intro: Product Name:4-Piperidinemethanol
CAS:6457-49-4
Purity:99% Package:1KG;10.00;USD
Company Name: Henan Fengda Chemical Co., Ltd
Tel: +86-371-86557731 +86-13613820652
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Products Intro: Product Name:4-Piperidinemethanol
CAS:6457-49-4
Purity:99% Package:1kg;35USD|1000kg;1.2USD
Company Name: Frapp's ChemicalNFTZ Co., Ltd.
Tel: +86 (576) 8169-6106
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Products Intro: Product Name:4-Piperidinemethanol
CAS:6457-49-4
Company Name: Shanghai Bojing Chemical Co.,Ltd.
Tel: +86-86-02137122233 +8613795318958
Email: bj1@bj-chem.com
Products Intro: Product Name:4-Piperidinemethanol
CAS:6457-49-4
Purity:98% Package:1Kg;25kg/ Drum or as customer request

4-Piperidinemethanol manufacturers

  • 4-Piperidinemethanol
  • 4-Piperidinemethanol pictures
  • $10.00 / 1KG
  • 2026-03-20
  • CAS:6457-49-4
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 100 mt
  • 4-Piperidinemethanol
  • 4-Piperidinemethanol pictures
  • $0.00 / 1g
  • 2026-02-02
  • CAS:6457-49-4
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 2000tons
  • 4-Piperidinemethanol
  • 4-Piperidinemethanol pictures
  • $35.00 / 1kg
  • 2025-09-25
  • CAS:6457-49-4
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
4-Piperidinemethanol Basic information
Product Name:4-Piperidinemethanol
Synonyms:4-(Hydroxymethyl)piperidine, 98 % (NMR+TLC);Piperidine-4-methanol;4-Piperidinemethanol ,98%;piperidin-4-ylmethanol hydrochloride;2-HydroMethyl piperidine;4-PiperidineMethanol, 98% 5GR;4-PiperidineMethanol or 4-(HydroxyMethyl)piperidine;4-PiperidineMethanol 97%
CAS:6457-49-4
MF:C6H13NO
MW:115.17
EINECS:613-624-9
Product Categories:Piperidine Series;Pyrans, Piperidines & Piperazines;Alkohols;pharmacetical;PiperidineDerivative;Hydroxymethyl's;Pyrans, Piperidines &Piperazines;Piperidine;Alcohols and Derivatives;Amines and Anilines
Mol File:6457-49-4.mol
4-Piperidinemethanol Structure
4-Piperidinemethanol Chemical Properties
Melting point 55-59 °C(lit.)
Boiling point 118-120 °C10 mm Hg(lit.)
density 0,997 g/cm3
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
Water Solubility Soluble in water
form Crystalline Powder, Chunks and/or Solid
pka14.94±0.10(Predicted)
color White to off-white
Sensitive Hygroscopic
BRN 103071
InChIInChI=1S/C6H13NO/c8-5-6-1-3-7-4-2-6/h6-8H,1-5H2
InChIKeyXBXHCBLBYQEYTI-UHFFFAOYSA-N
SMILESN1CCC(CO)CC1
CAS DataBase Reference6457-49-4(CAS DataBase Reference)
Safety Information
Hazard Codes C,Xi
Risk Statements 34-22
Safety Statements 26-27-36/37/39-45
RIDADR UN 3263 8/PG 2
WGK Germany 3
Hazard Note Irritant/Hygroscopic
HazardClass 8
PackingGroup III
HS Code 29333990
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsSkin Corr. 1B
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
4-Piperidinemethanol Usage And Synthesis
Chemical Propertieswhite to off-white crystalline powder, chunks
Uses4-Piperidinemethanol may be used in the preparation of:
  • N-tert-butoxycarbonyl-4-hydroxymethyl piperidine
  • desferrioxamine B (DFO) containing third generation triazine dendrimer
  • ethyl 3-(4-(hydroxymethyl)piperidin-1-yl)propanoate (EHMPP)
  • 4-(hydroxymethyl)piperidine-1-carbodithioic acid (HL)
  • 1-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-4-piperidinemethanol
General Description4-Piperidinemethanol is a cyclic secondary amine. Its standard molar enthalpies of combustion, sublimation and formation have been determined.
Synthesis
Ethyl 4-piperidinecarboxylate

1126-09-6

4-Piperidinemethanol

6457-49-4

The general procedure for the synthesis of 4-hydroxymethylpiperidine from ethyl 4-piperidinecarboxylate was as follows: lithium aluminum hydride (LiAlH4, 10.10 g, 0.266 mol) was suspended in tetrahydrofuran (THF, 150 mL) at 0 °C. Subsequently, a solution of ethyl 4-piperidinecarboxylate (18.13 g, 0.120 mol) dissolved in THF (300 mL) was slowly added. The reaction mixture was stirred at room temperature overnight. After the reaction was completed, it was cooled in an ice bath and a mixture of water (14 mL) and THF (28 mL) was slowly added. Next, a mixture of 15% aqueous sodium hydroxide (14 mL) and water (37 mL) was added and stirring was continued for 30 minutes at room temperature. The reaction mixture was filtered to remove the precipitate and the filtrate was concentrated to give 17.88 g of the target product 4-hydroxymethylpiperidine in quantitative yield.

References[1] Patent: WO2004/76450, 2004, A1. Location in patent: Page 59
[2] Patent: WO2010/12611, 2010, A1. Location in patent: Page/Page column 27
[3] RSC Advances, 2016, vol. 6, # 22, p. 17929 - 17940
[4] European Journal of Medicinal Chemistry, 2019, p. 234 - 248
[5] European Journal of Medicinal Chemistry, 2017, vol. 139, p. 773 - 791
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