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3-Hexenol chemical structure, C6H12O, CAS 928-96-1
2D chemical structure

Key facts

What buyers check first

Appearance
Colorless liquid
Boiling point
156 to 157
Density
0.846 at 22/15 °C
Flash point
54 °C
Solubility
Very soluble in ethanol and ether
HS code
290529
Category
Synthetic aroma chemicals
Illustrative photo, 200 litre blue HDPE drums of liquid in a warehouse
Typical packagingIllustrative packaging image, not the actual product

What is 3-Hexenol?

Plain description, key identifiers and synonyms

(Z)-hex-3-en-1-ol is a hex-3-en-1-ol in which the double bond adopts a Z-configuration. Also known as leaf alcohol, it is emitted by green plants upon mechanical damage. Used as a flavourant in tea. It has a role as an insect attractant, a fragrance and a plant metabolite.

Identifiers

Registry numbers, names and line notations, tap to copy

IUPAC name
(Z)-hex-3-en-1-ol
CAS number
928-96-1 CAS number cross-checked
EC number
213-192-8
Molecular formula
C6H12O
UNII
V14F8G75P4
MDL number
MFCD00063217
INCI name
3-HEXENOL
InChIKey
UFLHIIWVXFIJGU-ARJAWSKDSA-N
InChI
InChI=1S/C6H12O/c1-2-3-4-5-6-7/h3-4,7H,2,5-6H2,1H3/b4-3-
Canonical SMILES
CCC=CCCO
Isomeric SMILES
CC/C=C\CCO

Synonyms

  • cis-3-Hexen-1-ol
  • (Z)-Hex-3-en-1-ol
  • Leaf alcohol
  • cis-3-Hexenol
  • (Z)-3-Hexen-1-ol
  • Blatteralkohol
  • Z-3-Hexenol
  • (3Z)-hex-3-en-1-ol
  • 3-Hexen-1-ol, (Z)-
  • 3-Hexen-1-ol, cis-
  • 3-Hexen-1-ol, (3Z)-
  • beta-gamma-Hexenol
  • 3-Hexenol, cis-
  • (Z)-3-Hexenol
  • cis-3-Hexenol (natural)
  • (3Z)-3-Hexen-1-ol
  • cis-Hex-3-en-1-ol
  • Blaetteralkohol
  • Folic alcohol
  • (Z)-hex-3-en-ol
  • cis-1-hydroxy-3-hexene
  • Green leaf alcohol
  • (3e)-hexenol
  • 4-01-00-02141 (Beilstein Handbook Reference)
  • ENT 25091
Show all 36 synonyms
  • (E)-3-Hexenol
  • cis-3-Hexene-1-ol
  • 3Z-hexenol
  • 3-(Z)-Hexenol
  • beta,gamma-Hexenol
  • HEXEN-30L-1
  • (Z)-3-hexenyl alcohol
  • cis-hexenol
  • cis-3-Hexen-1-ol, 98%
  • cis-Hex-3-enol
  • cis-Hex-3-en-1ol

Physical and chemical properties

Measured values and descriptors computed from the structure

Physical and chemical properties

Measured values, check the supplier specification for your grade

Appearance
Colorless liquidexp.
Odour
Powerful grassy-green odorexp.
Taste
Fresh, green, raw fruity with a pungent depthexp.
Boiling point
156 to 157exp.
Density
0.846 at 22/15 °Cexp.
Flash point
54 °Cexp.
Solubility
Very soluble in ethanol and etherexp.

Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.

Computed descriptors

Calculated from the structure, useful for screening and formulation

Molecular weight
100.16 g/molcalc.
Exact mass
100.0888 Dacalc.
LogP (octanol/water)
1.33calc.
Topological polar surface area
20.23 Ųcalc.
Hydrogen bond donors
1calc.
Hydrogen bond acceptors
1calc.
Rotatable bonds
3calc.
Heavy atoms
7calc.
Rings
0calc.
Aromatic rings
0calc.
Fraction sp3 carbons
0.67calc.
Formal charge
0calc.
Stereocentres
0calc.
Lipinski rule of five
Passes (0 violations)calc.

Calculated for screening. Confirm critical figures with the supplier.

Safety and hazards

GHS classification summary, not a safety data sheet

GHS signal word
Warning
GHS02: Flammable
Flammable
GHS07: Harmful or irritant
Harmful or irritant
210NFPA 704 rating

Hazard statements

  • H226Flammable liquid and vapour.
  • H319Causes serious eye irritation.
Precautionary statements (14)
  • P210Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking.
  • P233Keep container tightly closed.
  • P240Ground and bond container and receiving equipment.
  • P241Use explosion-proof electrical, ventilating and lighting equipment.
  • P242Use non-sparking tools.
  • P243Take action to prevent static discharges.
  • P264 + P265Wash skin thoroughly after handling. Do not touch eyes.
  • P280Wear protective gloves, protective clothing, eye protection and face protection.
  • P303 + P361 + P353If on skin (or hair): Take off immediately all contaminated clothing. Rinse skin with water or shower.
  • P305 + P351 + P338If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
  • P337 + P317If eye irritation persists: Get medical help.
  • P370 + P378In case of fire: Use appropriate media to extinguish.
  • P403 + P235Store in a well-ventilated place. Keep cool.
  • P501Dispose of contents and container in accordance with local regulations.

GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.

Full safety data and first aid

3-Hexenol suppliers

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Where suppliers are based

55 suppliers in 10 countries

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3-Hexenol price

Indicative price range per kg from live supplier offers

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Uses and applications

What the substance is used for, by industry and function

In public use since the 1940's. In the United States, use in fragrances amounts to less than 20,000 lbs/ year.

Odorant in perfumery.

Used to obtain natural green top notes in perfumes and flavors. In addition, it is the starting material for the synthesis of 2-trans-6-cis-nonadien-1-ol and 2-trans-6-cis-nonadien-1-al.

Reported uses (ppm):

Table: Reported uses (ppm): (Flavor and Extract Manufacturers' Association, 1994) [Table#8255].

Industrial uses: Fragrance, Other.

Consumer uses: Other, Fragrance.

Use classes: Cosmetics.

Cosmetic ingredient, INCI name 3-HEXENOL(fragrance, skin conditioning, perfuming)

Roles

  • eukaryotic metabolite
  • fragrance
  • insect attractant
  • metabolite
  • plant metabolite

Functional uses

  • Deodorizer
  • Flavouring and nutrient
  • Fragrance
  • Humectant
  • Softener and conditioner
  • Solvent
  • Viscosity modifier

Cosmetic functions

  • Fragrance
  • Perfuming
  • Skin conditioning

How it is made

Preparation by the reaction of butyne-1 with ethylene oxide and subsequent selective reduction to the cis isomer.

Extracted from various essential oils and purified by reacting it to the corresponding phthalate or allophanate.

A stereospecific synthesis for cis-3-hexen-1-ol starts with the ethylation of sodium acetylide to 1-butyne, which is reacted with ethylene oxide to give 3-hexyn-1-ol. Selective hydrogenation of the triple bond in the presence of palladium catalysts yields cis-3-hexen-1-ol.

Regulatory status

Inventories, regulations and trade controls that list this substance

Health and food

  • EU cosmetic ingredient inventory

United States

  • TSCA inventory (USA)
    Status: Active in US commerce

HS code and trade data

Customs classification and reported world trade statistics

Global trade

World import and export statistics for the HS code 3-Hexenol is traded under.

HS 2905.29Indicative HS code

Unsaturated monohydric alcohols, other

World exports in 2024
$361M
−8.5% vs 2023, imports $367M
2019 to 2024
Top exporters
  1. China26.8%
  2. Japan20.6%
  3. India * partner reported11.6%
Top importers
  1. China15.7%
  2. United States14.7%
  3. Germany8.2%

* Partner reported figures, a lower bound.

Reported customs values in USD, not prices.Full trade data

The HS code shown for 3-Hexenol is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.

Frequently asked questions

Quick answers about 3-Hexenol, based on the data on this page

What is 3-Hexenol?

(Z)-hex-3-en-1-ol is a hex-3-en-1-ol in which the double bond adopts a Z-configuration. Also known as leaf alcohol, it is emitted by green plants upon mechanical damage. Used as a flavourant in tea. It has a role as an insect attractant, a fragrance and a plant metabolite.

What is the CAS number of 3-Hexenol?

The CAS registry number of 3-Hexenol is 928-96-1.

What is the molecular formula and weight of 3-Hexenol?

The molecular formula of 3-Hexenol is C6H12O and its molar mass is 100.16 g/mol.

What is 3-Hexenol used for?

In public use since the 1940's. In the United States, use in fragrances amounts to less than 20,000 lbs/ year. Odorant in perfumery. Used to obtain natural green top notes in perfumes and flavors. In addition, it is the starting material for the synthesis of 2-trans-6-cis-nonadien-1-ol and 2-trans-6-cis-nonadien-1-al.

Is 3-Hexenol hazardous?

3-Hexenol carries the GHS signal word "Warning". Main hazards: flammable liquid and vapour, causes serious eye irritation. This summary is not an SDS, always read the supplier safety data sheet.

What is the HS code of 3-Hexenol?

3-Hexenol is usually classified under HS code 290529 (Unsaturated monohydric alcohols, other). This is indicative, confirm it with your customs broker before shipping.

Where can I buy 3-Hexenol?

CompoundList lists 55 suppliers of 3-Hexenol in China, India, United States, Switzerland and 6 more. Send one free request to get and compare quotes. Your contact details stay private until you accept a quote.

Where can I buy 3-Hexenol in India?

16 suppliers in India list 3-Hexenol on CompoundList. Filter the suppliers list by country and send a request to compare prices, grades and delivery times.

What is the price of 3-Hexenol?

Suppliers quote 3-Hexenol on request because prices depend on grade, purity, quantity and destination. A free request on CompoundList gets you several quotes to compare.

Guides for buyers

Practical guides that help when you source, ship or handle 3-Hexenol

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Data last updated 7 Oct 2026. Details may have changed, please confirm them with the supplier. Report an error on this page
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