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Capsicum

Capsicum is a vegetable fruit with 404 known flavor compounds. The most distinctive molecule is 2-methoxy-3-(2-methylpropyl)-pyrazine. It pairs most strongly with onion, sharing 243 flavor compounds. Capsicum appears in 50,415 recipes, most commonly in creole cuisine.

Scientific name: Capsicum
genus of plants, vegetable
Capsicum — ingredient reference image
404
Flavor Compounds
8
Top Pairings of 856 scored

Flavor Science

Flavor Profile Breakdown

404 compounds

How Capsicum's 404 known compounds break down by aroma category. Percentages are of compounds with a known label.

sour 56 · 13.9%
fruity 55 · 13.6%
other 44 · 10.9%
floral 42 · 10.4%
roasted 35 · 8.7%
herbal 28 · 6.9%
green 27 · 6.7%
woody 19 · 4.7%
spicy 19 · 4.7%
caramel 13 · 3.2%

Most Used In

Flavor Compounds

137 of 404 are distinctive to capsicum — they appear in under 10% of foods. The remainder are the background most foods share.

Ordered by measured impact in capsicum — concentration against odour threshold where both are published, then by how distinctive the molecule is across the graph. Molecules measured here but not established as odorants sit below those that are.

Molecules volatile enough to reach the nose.
linalool nonanoic acid 2-methoxy-3-(2-methylpropyl)-pyrazine 3-isobutyl-2-methoxypyrazine p-menth-1-en-9-al 2-isobutyl-3-methoxypyrazine butane-2,3-diol 2-isopropyl-3-methoxypyrazine 3-methylbutyl butanoate ethylhexanol 3-hepten-2-one furan-2-pentyl 3-methyl-3-pentanol alpha-thujone (e,z)-2,6-nonadienal ethyl isobutyrate cis-3-hexenyl isovalerate 3-ethyl-2,5-dimethylpyrazine 1-methylpyrrole heneicosane citronellal butanol ethyl 2-methylbutyrate heptadecane biphenyl hexyl 2-methylbutanoate nonadecane p-xylene 2,4-decadienal methyl heptanoate +227 more citric acid catechin stearic acid capsaicin arachidic acid docosanoic acid resveratrol procyanidin b2 rutin procyanidin b1 (-)-epigallocatechin gallocatechin (-)-epicatechin dl-phenylalanine nervonic acid lutein isorhamnetin isoliquiritigenin thiamine hydrochloride taxifolin daidzein squalene genistein quercetin luteolin myricetin phloretin zeaxanthin aconitic acid stigmasterol 1h-indole 1-cyclohexene-1-carboxylic acid, 2,6,6-trimethyl-, ethyl ester 1-ethylindole 1-methyl-1,4-cyclohexadiene 2-furanmethanol, 5-methyl- 4-methylindole 4-methylpentyl 4-methylpentanoate pyrazine, 2-ethenyl-6-methyl alpha-cardinol dimethylheptane heptylisopentanoate isohexanol 1,3,5-cycloheptatriene 2-carene alpha-thujene caffeine α-tocopherol retinol dl-methionine 1-decanol, 2-octyl- docosanoic acid, docosyl ester hexanedial nonivamide 4-hepten-1-ol dl-valine l-ascorbic acid (z)-hex-3-en-1-ol amylamine cis-3-hexenyl pentanoate 3-methyl-2-cyclopenten-1-one

Most Abundant Molecules

2 of 404 quantified

Ranked by median concentration across published studies. Only 2 of Capsicum's 404 compounds have a measured concentration in the literature — the rest are confirmed present but not yet quantified. Bars are log-scaled.

1 linalool 50 µg/kg
2 nonanoic acid 50 µg/kg

Best Pairings for Capsicum

Ranked by how often cooks actually use them together, across 453,403 recipes — the familiar answer first. Each pairing still carries its molecular score and shared-compound count; only the ORDER differs. Counts cover every characterised molecule the two ingredients have in common, not only the aroma-active ones, so they can exceed an ingredient’s aroma-compound count. For the chemistry-first view — where the surprising pairings live — see the molecular network below, the side-by-side comparison, or the Pairing Tool.

Molecular Neighborhood

Capsicum and its 10 closest compound-sharing relatives. Spoke thickness = shared compounds; circle size = that ingredient's own compound count. Drag to rearrange, scroll to zoom, click to open.

Molecular neighborhood diagram of capsicum — top 10 ingredients ranked by shared volatile compounds

Recipes with Capsicum

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Research basis

Capsicum is supported by 1,849 peer-reviewed papers

Drawn from PubMed + Europe PMC + food-science journals. Click any title to read the full abstract on the original source.