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Cyclic compounds (13)
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ISOPHORONE (78-59-1)  
diisophorone
Isophorone is an α,β-unsaturated cyclic ketone. It is a colorless liquid with a characteristic peppermint-like odor, although commercial samples can appear yellowish. Used as a solvent and as a precursor to polymers, it is produced on a large scale industrially.
(+)-Pulegone (89-82-7)  
pulegone  ·  isopulegone  ·  pulegone, (R)-isomer
Pulegone is a naturally occurring organic compound obtained from the essential oils of a variety of plants such as Nepeta cataria (catnip), Mentha piperita, and pennyroyal. It is classified as a monoterpene. Pulegone is a clear colorless oily liquid and has a pleasant odor similar to pennyroyal, peppermint and camphor.
Pulegone (89-82-7, 15932-80-6)  
isopulegone  ·  pulegone, (R)-isomer  ·  pulegone, (S)-isomer
Pulegone is a naturally occurring organic compound obtained from the essential oils of a variety of plants such as Nepeta cataria (catnip), Mentha piperita, and pennyroyal. It is classified as a monoterpene. Pulegone is a clear colorless oily liquid and has a pleasant odor similar to pennyroyal, peppermint and camphor.
CARVONE (99-49-0, 8008-79-5)  
2-methyl-5-(1-methylethenyl)-2-cyclohexene-1-one  ·  limonen-6-one  ·  carvone, (S)-isomer
Carvone is a member of a family of chemicals called terpenoids. Carvone is found naturally in many essential oils, but is most abundant in the oils from seeds of caraway (Carum carvi), spearmint (Mentha spicata), and dill.
androstenedione (63-05-8)  
4 Androstene 3,17 dione  ·  delta-4-Androstenedione  ·  4-Androstene-3,17-dione
Androstenedione, or 4-androstenedione (abbreviated as A4 or Δ4-dione), also known as androst-4-ene-3,17-dione, is an endogenous weak androgen steroid hormone and intermediate in the biosynthesis of testosterone from dehydroepiandrosterone (DHEA) and of estrone. It is closely related to androstenediol (androst-5-ene-3β,17β-diol).
NOOTKATONE (4674-50-4, 28834-25-5)  
nootkatone, (4R-(4alpha,4aalpha,6beta))-isomer
Nootkatone is a natural organic compound and is the most important and expensive aromatic of grapefruit. It is a sesquiterpene and a ketone. Nootkatone was previously thought to be one of the main chemical components of the smell and flavour of grapefruits.
PERILLALDEHYDE (2111-75-3)  
perilla aldehyde  ·  4-mentha-1,8-dien-7-al  ·  perillaldehyde, (+)-isomer
Perillaldehyde, or perilla aldehyde, is a natural organic compound found most abundantly in the annual herb perilla, but also in a wide variety of other plants and essential oils. It is a monoterpenoid containing an aldehyde functional group. Perillaldehyde, or volatile oils from perilla that are rich in perillaldehyde, are used as food additives for flavoring and in perfumery to add spiciness.
4-Cholesten-3-one (601-57-0)  
cholest-4-en-3-one
beta-Damascone (639-99-6, 23726-91-2, 35044-68-9, 23726-91-2)  
damascone  ·  alpha-damascone
Damascones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascones belong to a family of chemicals known as rose ketones, which also includes damascenones and ionones. beta-Damascone is a contributor to the aroma of roses, despite its relatively low concentration, and is an important fragrance chemical used in perfumery.
1125-21-9 (1125-21-9)  
ketoisophorone
alpha-Damascone (43052-87-5, 24720-09-0)  
1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2-butenone  ·  TMCHB
16-Dehydroprogesterone (1096-38-4)  
delta(16)-progesterone
19-Norandrostenedione (734-32-7)  
19-nor-A-dione  ·  19-norandrost-4-ene-3,17-dione  ·  19-nor-4-androstene-3,17-dione
19-Norandrostenedione may refer to: Bolandione (19-nor-4-androstenedione) 19-Nor-5-androstenedione
ADRENOSTERONE (911474-75-4, 382-45-6)  
11-ketoandrostenedione  ·  adrenosterone, 3H-labeled  ·  4-androstene-3,11,17-trione
Adrenosterone, also known as Reichstein's substance G , as well as 11-ketoandrostenedione (11-KA4), 11-oxoandrostenedione (11-OXO), and androst-4-ene-3,11,17-trione, is a steroid hormone with a weak androgenic effect, and an intermediate/prohormone of 11-ketotestosterone. It was first isolated in 1936 from the adrenal cortex by Tadeus Reichstein at the Pharmaceutical Institute in the University of Basel. Originally, adrenosterone was called Reichstein's substance G.
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