odorant

Molecules can have smell {odorant} to humans. Odorants must be volatile. Airborne-molecule chemical-bond configurations (shapes) and vibration and rotation frequencies and intensities cause smell. Odorant molecules have molecular weight greater than 35 and less than 350, not too small nor too large for olfactory receptors. Odorants are typically hydrophobic.

Pungent odorants are compact non-polar aryl compounds. Sweet odorants are non-polar chain esters. Sweaty odorants are polar chain organic acids. Right-handed and left-handed chiral molecules, like spearmint and caraway, smell different.

primary

People can distinguish 30 primary odorants:

alliaceous and garlicy: cysteine sulfur compounds

aromatic: benzene alkyls

asparagusy, bitter: carboxylic-acid thiols

biting, hanging, alcoholy: small alcohols

burnt, smoky: monophenols and polycyclic aromatic hydrocarbons

buttery: small aldehydes

camphorous, resinous: polycyclic aryls

cool and minty: cyclic alcohols

earthy, moldy, potatoey: cyclic ethers

fishy: alkyl and aryl monoamines

flowery, fresh: monoterpenoid alcohols

foul, rotten, sulfurous: small thiol sulfur compounds

fragrant, floral, flowery, ethereal: linear ethers

fruity, sweet: medium-chain alcohols and non-polar chain esters

goaty, hircine: medium-length polar chain carboxylic acids

grassy, herby: alkene aldehydes

malty: short-chain aldehydes

minty, spearminty, pepperminty: cyclic alkene ketones

musky, ambrosial: macrocyclic ketones

nutty, earthy, green peppery: heterocyclic aromatic amines

pharmaceutical, medicinal, pungent, unpleasant: halogens

pungent, acrid, vinegary: small carboxylic acids

putrid, sweaty, rancid: medium-short polar chain carboxylic acids

roasted, fermented, popcorny: heterocyclic aromatic amines

rubber: monoterpenes (isoprenes)

cabbage-like, rotten: methyl sulfides

savory, spicy: heterocyclic ketones

spermous: alkyl multi-amines and heterocyclic amines

tarry, oily: polyphenols

tobacco: alkenes-with-one-ring ketones

urinous: steroid ketones

woody: triterpenes (sesquiterpenes)

Odorants mix to make odor, and people can distinguish 10,000 different odors.

categories

Smells can range through sweet/flowery/fruity, mild/vegetably, mild/animaly, mild/mineraly, strong/vegetably, strong/animaly, putrid/animaly, and sharp/mineraly.

The smell-category sequence correlates with molecule reactivity:

Ether -C-O-C-

Alcohol -CH2OH

Ester -COO-

Aryl =CHC=

Terpene =CC2

Ketone -COC-

Aldehyde -CHO

Acid -COOH

Amine -CH2NH2

Sulfhydryl -CH2SH

Halogens Br2

similarities based on chemical group

Similar chemical types make similar smells. Similar chemical origins make similar smells.

Alcohols are similar: biting, fruity, sweet.

Aldehydes are similar: malty, grassy (herby).

Amines are similar: spermous, fishy, nutty, roasted.

Aryls are similar: aromatic, burnt (smoky), camphorous (resinous), tarry (oily).

Carboxylic acids are similar: pungent (acrid, vinegary), putrid (sweaty, rancid), goaty (hircine).

Ethers are similar: fragrant, floral, fruity and sweet.

Ketones are similar: minty, spicy, savory, tobacco, musky (ambrosial), urinous.

Sulfur compounds are similar: asparagusy, cabbage-like, alliaceous (garlicy), foul, rotten.

Terpenes are similar: minty, flowery (fresh), rubbery, woody.

similarities based on similar chemical groups

Alcohols and aryl ketones are similar: biting, fruity, minty, musky.

Alcohols and esters are similar: fruity, sweet.

Aldehydes and alkene ketones are similar: malty, grassy, tobacco.

Aldehydes and ethers are similar: malty, grassy, earthy.

Aldehydes and terpenes are similar: malty, grassy, rubbery, woody.

Amines and steroid ketones are similar: spermous, fishy, nutty, roasted, urinous.

Amines and carboxylic acids are similar: spermous, fishy, nutty, roasted, pungent, putrid, goaty.

Polycyclic aryls and halogens are similar: camphorous, pharmaceutical.

Carboxylic acids and steroid ketones are similar: pungent, putrid, goaty, urinous.

Alkene ketones and terpenes are similar: tobacco, rubbery, woody.

Polycyclic aryl ketones and ethers are similar: minty, camphorous, musky, fragrant, flowery, fruity.

similarities based on organism type

Vegetable smells are similar: alcohols, aldehydes, ethers, aryl and alkene ketones, sulfur compounds, terpenes.

Animal smells are similar: carboxylic acids, amines, polycyclic aryl ketones, steroid ketones.

opposites

Carboxylic acids (sour, putrid, animal) and esters (sweet, fruity, vegetable) are opposites.

Carboxylic acids (sour, putrid, animal) and alcohols (sweet, fruity, vegetable) are opposites.

Amines (animal) and aldehydes (vegetable) are opposites.

Amines (animal) and terpenes (vegetable) are opposites.

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Date Modified: 2022.0224