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5-Hexen-1-ol

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Products Intro: Product Name:5-Hexen-1-ol
CAS:821-41-0
Purity:98% Min. Package:1KG;0.00;USD|20KG;0.00;USD|150KG;0.00;USD
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Products Intro: Product Name:5-Hexen-1-Ol
CAS:821-41-0
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Products Intro: Product Name:1-Hexen-6-ol
CAS:821-41-0
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Products Intro: Product Name:5-HEXEN-1-OL
CAS:821-41-0
Purity:NLT 98% Package:1G;1KG;100KG
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Products Intro: Product Name:5-HEXEN-1-OL
CAS:821-41-0
Purity:99% Package:25KG;5KG;1KG

5-Hexen-1-ol manufacturers

  • 5-HEXEN-1-OL
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  • CAS:821-41-0
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  • Purity: 99%
  • Supply Ability: 100kg
  • 5-Hexen-1-Ol
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  • $5.00 / 1KG
  • 2025-05-26
  • CAS:821-41-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 10000kg
5-Hexen-1-ol Basic information
Background
Product Name:5-Hexen-1-ol
Synonyms:5-HEXEN-1-OL;6-HYDROXY-1-HEXENE;1-Hexen-6-ol;5-Hexen-1-ol, 97+%;5-HEXEN-1-OL 99%;5-Hexen-1-ol,99%;5-hexeen-1-ol;5-Hexen-1-ol, 99% 5ML
CAS:821-41-0
MF:C6H12O
MW:100.16
EINECS:212-477-4
Product Categories:omega-Functional Alkanols, Carboxylic Acids, Amines & Halides;omega-Unsaturated Alkanols
Mol File:821-41-0.mol
5-Hexen-1-ol Structure
5-Hexen-1-ol Chemical Properties
Melting point <-20°C
Boiling point 78-80 °C/25 mmHg (lit.)
density 0.834 g/mL at 25 °C (lit.)
FEMA 4351 | 5-HEXENOL
refractive index n20/D 1.435(lit.)
Fp 117 °F
storage temp. Sealed in dry,2-8°C
solubility 18.6g/l
form Liquid
pka15.17±0.10(Predicted)
Specific Gravity0.846
color Clear colorless
PH7 (H2O)
Odorgreen
Odor Typegreen
biological sourcesynthetic
Water Solubility Miscible with water.
JECFA Number1623
BRN 1236458
Stability:Volatile
InChI1S/C6H12O/c1-2-3-4-5-6-7/h2,7H,1,3-6H2
InChIKeyUIZVMOZAXAMASY-UHFFFAOYSA-N
SMILESOCCCCC=C
LogP1.50
CAS DataBase Reference821-41-0(CAS DataBase Reference)
EPA Substance Registry System5-Hexen-1-ol (821-41-0)
Safety Information
Hazard Codes F
Risk Statements 10
Safety Statements 16-24/25
RIDADR UN 1987 3/PG 3
WGK Germany 1
9
Hazard Note Flammable
TSCA TSCA listed
HazardClass 3
PackingGroup III
HS Code 29052290
Storage Class3 - Flammable liquids
Hazard ClassificationsEye Dam. 1
Flam. Liq. 3
Skin Corr. 1B
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
5-Hexen-1-ol Usage And Synthesis
Background Enol is an important fine chemical, such as isophytol, folyl alcohol, etc. It can be further used as a critical intermediate for synthesizing medicines, pesticides, essences, spices and the like with high economic added values. It has a large market demand. 5-Hexen-1-ol is a common organic synthesis and medical intermediate and an essential raw material for chemical engineering and medicine.
Chemical PropertiesClear, colorless liquid with a green aroma.
Uses5-Hexen-1-ol is used in cyclization to a tetrahydropyran by phenylselenoetherification. It is also used as a building block in synthetic chemistry. Further, it is used to prepare 6-bromo-hex-1-ene by reaction with phosphorus tribromide.
Preparation5-hexen-1-ol may be prepared from 2-(chloromethyl)tetrahydropyran according to the literature procedure for the preparation of 4-penten-1-ol (Brooks, L. A.; Snyder, H. R. Org. Synth. Coll. Vol. III 1955, 698).
Application5-Hexen-1-ol is used as a food flavouring agent and as a raw material in organic synthesis for cyclisation to other compounds such as tetrahydropyran via phenylselenide etherification.
Aroma threshold valuesMedium strength odor; recommend smelling in a 10.00% solution or less
Synthesis 6-bromo-1-hexene is used as a raw material, and tetrabutylammonium bromide is used as a catalyst. In an acetonitrile solvent, it is heated to react with potassium acetate. The mixed solution is then cooled to room temperature (18-25°C), the reaction solution is concentrated under reduced pressure, and then water is added to dissolve; methyl tert-butyl ether is added and stirred to separate the layers, the water layer is extracted once with methyl tert-butyl ether, the organic phases are combined and filtered, and the filtrate is concentrated under reduced pressure. The concentrated solution begins to hydrolyze, and 15% alkaline aqueous solution and methanol are added to the concentrated solution. The mixture is stirred at room temperature to dissolve each other; after the hydrolysis is completed, the methanol is concentrated under reduced pressure. After concentration to dryness, the system begins to separate into layers, with an upper organic phase and a lower aqueous phase. The aqueous phase is extracted twice with dichloromethane, and the combined organic phases are concentrated under reduced pressure to obtain 5-Hexen-1-ol.
5-Hexen-1-ol
Tag:5-Hexen-1-ol(821-41-0) Related Product Information
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