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cis-3-hexenol

floral alcohol Key food odorant

Found in 8 ingredients across the CompKitchen flavor graph.

Look up another compound — search by name, CAS number, PubChem CID, or FEMA #.

Key food odorant (individualist)

Dunkel et al. 2014

Identified in the meta-analysis of 227 food samples as one of 151 individualist odorants — appears in <5% of foods, carries the diagnostic signature of specific ingredients.

Source: Angew. Chem. Int. Ed. 2014, 53, 7124–7143

Properties

Odor description
green, grassy, leafy, fresh
Odor threshold — orthonasal, in clean water
70.0 ppb 1 published value · see all 3 with sources
CAS number
928-96-1
Not in FEMA GRAS publications 1-33. Of 3,367 listed flavoring substances, none match this compound name. May still be food-safe under other regulatory routes (FDA 21 CFR 172, EFSA, JECFA) — check femaflavor.org for the authoritative current list.

How this molecule is described

Sources disagree about odour more often than they disagree about chemistry. Rather than show one answer, here is every description on file with how many ingredient records carry it.

Also filed as
z-3-hexenol

Same molecule, unified here — previously counted and displayed as separate compounds.

Descriptions on file

Ordered by how many independent descriptor streams give each wording, then by how often it appears. The bar is still replication — one source copied onto many ingredients scores high there — so the two can disagree.

fruity, sweet, fatty, camphor FlavorDB 2.0, Flavordb Odor Column 2 sources agree
1
green, honey, burnt, rose, oily, vanilla, apple FlavorDB 2.0
5
apple, chemical, citrus, fatty FlavorDB 2.0
1
green, grassy, leafy, fresh shown above Llm Adjudicated
—
chemical Flavordb Odor Column
—
green, honey, burnt, rose, oily Flavordb Odor Column
—

Bars are the share of ingredient records carrying each description. High agreement means the sources replicate each other — not necessarily that they are right.

Published thresholds

3 measured values from the literature. Grouped by what was actually measured — a threshold smelled in clean water, tasted in the mouth, or measured in a real food are three different quantities and are not pooled.

Orthonasal, in clean water

70.0 ppb

The reference measurement — smelled in water. OAV is computed against this.

Threshold Matrix Source Paper
70.0 ppb water_odor Leffingwell —

In a food matrix

3.9 ppb – 13.0 ppb

Measured in a real food, where the matrix shifts detection — not a clean-water value.

Threshold Matrix Source Paper
3.9 ppb water (food: green tea infusion (jingshan cha)) Literature corpus —
13.0 ppb water (food: reference standard (water)) Literature corpus —

Only values we can attribute are listed. Where a compendium's licence does not permit public attribution its figures are omitted here, so every number on this page traces to a citable source.

Where you'd actually smell it

Odor Activity Value = measured concentration ÷ odor threshold (13.0 ppb, the engine's canonical value — see the 3 published values). OAV ≥ 1 = perceptible.

Food Concentration (ppb) OAV Source
vinegar 20000.0 1538 ⚡ Corpus paper
olive 20000.0 1538 ⚡ DOI

Concentrations from PubMed Central Open Access papers (free literature corpus, MIT-style licensed). Copper = OAV ≥ 10 (strongly perceptible). Green = OAV ≥ 1 (perceptible).

Thresholds in published tables

Numbers printed in open-access papers, grouped by the medium the table states. Median and full range of the values; “agree” means two or more papers whose middle 80% of values sit within 100×. Not reviewed.

MediumMedianRangeValuesPapersPapers agree?
air 8.45 µg/L air 0.013–200 66 no (3.0 decades)
ethanol solution 1000 ppb 40–1.26e+03 54 yes
food matrix 400 ppb 3.9–1e+04 3433 yes
model wine or beer 400 ppb 400–1e+03 54 yes
not applicable 400 ppb 400–400 11 one paper
unstated 400 ppb 0.2–1.5e+05 6860 no (2.6 decades)
water 13 ppb 0.004–1.9e+03 3833 yes

Found in

Measured impact first, then profile share

Every ingredient known to contain cis-3-hexenol. Ingredients with a measured concentration come first, ranked by odour activity; the rest follow by how large a share of that ingredient's profile this molecule is. The figure beside each is how many different compounds that ingredient has in total — not the concentration of cis-3-hexenol in it. Full concentrations are in the OAV table above.

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