the library

Makrut lime

Citrus· citrus

Makrut lime

What it is

Makrut lime is Citrus hystrix, grown mainly for its double leaves and knobbled peel rather than its juice.

What it tastes like

On the nose: lemon-citronella-rose, pine, floral, citrus. Among its measured molecules: Pseudolimonene, Linalyl oxide, Citronellal, citronellol, sabinene.

What goes with it

255 more go with it. See them all in the full library →

Salt and acid

Salt

Salt not measured yet.

Acid

0 %Apple2 %Cranberry4 %Apple cider vinegar6 %Balsamic vinegar8 %Makrut lime

Acid 7.474 % (g/100 g) — the library's own composition sheet.

Unusual pairings

Pairs the library can cite that almost nobody makes.

15 of 133 compounds on file carry a paper the library can cite.

On file, no cited source yet ✳

These molecules are on record for it from the library's earlier sources. We are buying and requesting the papers; each one that lands moves its molecule up into the cited list.

  • β-bisaboleneterpenoid
  • 1.Xi.,6.xi.,7.xi.-cadina-4,9-dieneterpenoid
  • Narirutin 4'-O-glucosideflavonoid
  • delta-cadineneterpenoid
  • 1,6-dimethyl-4-isopropyltetralinterpenoid
  • citronellic acidterpenoid
  • beta-farneseneterpenoid
  • hesperidinflavonoid
  • 2-methylfuranfuran
  • (+)-sabineneterpenoid
  • β-phellandreneterpenoidreads as burning taste (PubChem)
  • neoeriocitrinflavonoid
  • terpinoleneterpenoidreads as terpene taste (PubChem)
  • Obacunoneterpenoid
  • 5-Geranoxypsoralen;Bergamottin; Bergaptincoumarin
  • dihydroxybergamottincoumarin
  • δ-elemeneterpenoid
  • pentadecaneacid
  • (+)-alpha-thujeneterpenoid
  • 2,6-Dimethyl-2,4,6-octatrieneacid
  • (2S)-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-2,3-dihydrochromen-4-oneflavonoid
  • 7-[4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-2,3-dihydrochromen-4-oneflavonoid
  • (1R,2R,4S,7S,8S,11R,12R,13S,18R)-7-(furan-3-yl)-13-hydroxy-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosane-5,15,20-trioneterpenoid
  • neryl acetateterpenoid
  • geranyl acetateterpenoidreads as lavender (PubChem)
  • 1-O-[(3R)-2-hydroxy-2,6-dimethyl-8-(7-oxofuro[3,2-g]chromen-4-yl)oxyoct-6-en-3-yl] 5-O-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-propan-2-yloxyoxan-2-yl]methyl] 3-hydroxy-3-methylpentanedioatecoumarin
  • 4-[(6R)-6,7-dihydroxy-3,7-dimethyloct-2-enoxy]furo[3,2-g]chromen-7-onecoumarin
  • perillaldehydealdehyde
  • Didyminsugar
  • isopulegolterpenoid
  • (R)-oxypeucedanin hydratecoumarin
  • limoninterpenoid
  • acetoneketonereads as fruity (PubChem)
  • beta-ocimeneterpenoid
  • α-copaeneterpenoid
  • 1-O-isopropyl-beta-D-glucopyranosidesugar
  • beta-sitosterolalcohol
  • benzenehydrocarbonreads as aromatic (PubChem)
  • Limonin 17-beta-D-glucopyranosidesugar
  • camphorterpenoidreads as pungent aromatic taste (PubChem)
  • 3-careneterpenoid
  • rose oxideterpenoid
  • nonanalaldehydereads as orange-rose (PubChem)
  • isopropyl alcoholalcoholreads as burning taste (PubChem)
  • D-limoneneterpenoidreads as citrus (PubChem)
  • (-)-beta-pineneterpenoid
  • (-)-alpha-pineneterpenoid
  • Nomilinic acid 17-beta-D-glucopyranosideterpenoid
  • Nomilin 17-beta-D-glucopyranosideterpenoid
  • (-)-alpha-curcumeneterpenoid
  • narirutinflavonoid
  • (+)-3-careneterpenoid
  • (S)-(-)-citronellalterpenoid
  • (-)-linaloolalcohol
  • octanalaldehydereads as fruity (PubChem)
  • citrusoside Aterpenoid
  • citrusoside Bcoumarin
  • (1R,2S,6S,7S,8R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-eneterpenoid
  • safrolereads as sassafras (PubChem)
  • α-myrceneterpenoid
  • 4-isopropyl-1-methylcyclohex-2-en-1-olterpenoid
  • phytolalcohol
  • rutinflavonoid
  • β-farneseneterpenoid
  • humuleneterpenoid
  • beta-ocimeneterpenoid
  • diosminflavonoid
  • nerolidolalcohol
  • germacrene Dterpenoid
  • (R)-(+)-6'-hydroxy-7'-methoxybergamottincoumarin
  • 3,4,5,8-tetrahydro-2H-cuban-1-olterpenoid
  • cosmeneterpenoid
  • allo-ocimeneacid
  • (4E,6Z)-alloocimeneterpenoid
  • (3E)-3,7-dimethylocta-1,3-dieneacid
  • vitamin Cacidreads as sharp, acidic taste (PubChem)
  • bergamottincoumarin
  • 2-(4-Ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl)propan-2-olterpenoid
  • 1,3,5,7-Octatetraene, 2,6-dimethyl-terpenoid
  • sitoglusideterpenoid
  • phenylethyl alcoholalcoholreads as sharp burning taste (PubChem)
  • hexanalaldehydereads as sharp, aldehyde (PubChem)
  • trans-Sabinene hydrateterpenoid
  • geraniolalcoholreads as sweet rose (PubChem)
  • geranialterpenoidreads as lemon (PubChem)
  • Cadinolterpenoid
  • cis-Calameneneterpenoid
  • (5S)-1-isopropyl-4-methylidenebicyclo[3.1.0]hexaneterpenoid
  • (-)-endo-alpha-bergamoteneterpenoid
  • neralterpenoid
  • nerolalcoholreads as sweet rose (PubChem)
  • methyl acetateester
  • campheneterpenoidreads as camphor (PubChem)
  • isoimperatorincoumarin
  • beta-elemeneterpenoid
  • p-menthan-3-oneterpenoid
  • ethanolalcoholreads as burning (PubChem)
  • neo-isopulegol, rel-terpenoid
  • (+)-4-epi-cryptomeridiolterpenoid
  • Nomilinterpenoid
  • α-phellandreneterpenoid
  • α-terpineneterpenoid
  • ethylbenzenehydrocarbonreads as pungent (PubChem)
  • 1-O-[3-hydroxy-3-methyl-1-(7-oxofuro[3,2-g]chromen-4-yl)oxybutan-2-yl] 5-O-[(3,4,5-trihydroxy-6-propan-2-yloxyoxan-2-yl)methyl] 3-hydroxy-3-methylpentanedioatecoumarin
  • citrusoside Dcoumarin
  • 1H-indolenitrogen compoundreads as light jasmine (PubChem)
  • 1-hexanolalcoholreads as fatty, fruity (PubChem)
  • (1S,5S)-carvyl acetateterpenoid
  • decanalaldehydereads as citrus (PubChem)
  • eriocitrinflavonoid
  • methyl anthranilateesterreads as grape (PubChem)
  • Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-terpenoid
  • citronellyl acetateterpenoid
  • 3,7-Dimethyl-1,3-octadieneacid
  • (3R,5Z)-2,6-dimethylocta-1,5,7-trien-3-olterpenoid
  • α-eudesmolalcohol
  • (+)-oxypeucedanincoumarin
  • 6-methyl-5-hepten-2-oneketonereads as fruity taste (PubChem)

Sources

  • Katerina et al. 2023, Molecules
  • Efendi et al. 2021, Metabolites