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Polycyclic organic compounds, Cosmetics chemicals, Drugs acting on the gastrointestinal system and metabolism

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5-HT3 antagonists (4)
Antiemetics (4)
Bicyclic compounds (4)
Convulsants (4)
Cyclic compounds (4)
Cycloalkanes (4)
Cyclopentanes (4)
Five-membered rings (4)
Neurotoxins (4)
Perfume ingredients (4)

(+)-Isothujone (471-15-8)  
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
Isothujone (471-15-8)  
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
3-Thujanone (546-80-5, 1125-12-8)  
thujone  ·  beta-thujone, 1S-(1alpha,4beta,5alpha)-isomer  ·  alpha-thujone
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.
alpha-Thujone (546-80-5, 59573-80-7)  
thujone  ·  beta-thujone, 1S-(1alpha,4beta,5alpha)-isomer  ·  3-isothujone
Thujone ( ( listen)) is a ketone and a monoterpene that occurs naturally in two diastereomeric forms: (−)-α-thujone and (+)-β-thujone. It has a menthol odor. Though it is best known as a chemical compound in the spirit absinthe, which contains only small quantities of thujone, it is unlikely to be responsible for absinthe's alleged psychedelic effects.

Related Results:
TASOSARTAN (145733-36-4)  
Tasosartan is an angiotensin II receptor antagonist. It was withdrawn from FDA review by the manufacturer after phase III clinical trials showed elevated transaminases (a sign of possible liver toxicity) in a significant number of participants given the drug.
2-CHLORONAPHTHALENE (1321-65-9, 1335-88-2, 91-58-7)  
2-Chloronaphthalene is an organochlorine chemical compound, a chlorinated derivative of naphthalene. Its chemical formula is C 10H 7Cl. The compound is an isomer for 1-chloronaphthalene.
Biphenyl (92-52-4, 68409-73-4)  
diphenyl  ·  diphenyl, 14C-labeled
Biphenyl (or diphenyl or phenylbenzene or 1,1′-biphenyl or lemonene) is an organic compound that forms colorless crystals. Particularly in older literature, compounds containing the functional group consisting of biphenyl less one hydrogen (the site at which it is attached) may use the prefixes xenyl or diphenylyl. It has a distinctively pleasant smell.
naphthalene (91-20-3, 68412-25-9)  
Naphthalene is an organic compound with formula C 10H 8. It is the simplest polycyclic aromatic hydrocarbon, and is a white crystalline solid with a characteristic odor that is detectable at concentrations as low as 0.08 ppm by mass. As an aromatic hydrocarbon, naphthalene's structure consists of a fused pair of benzene rings.
1,1,1,2-TETRACHLOROETHANE (23425-39-0, 630-20-6)  
1,1,1,2-Tetrachloroethane is a chlorinated hydrocarbon. It is a colorless liquid with a sweet chloroform-like odor. It is used as a solvent and in the production of wood stains and varnishes.
2,4-DIMETHYLPHENOL (105-67-9)  
2,4-dimethylphenol titanium (+4)  ·  2,4-dimethylphenol potassium  ·  2,4-DMP
P-XYLENE (68650-36-2, 68411-39-2, 106-42-3)  
paraxylene  ·  4-xylene  ·  para-xylene
p-Xylene (para-xylene) is an aromatic hydrocarbon. It is one of the three isomers of dimethylbenzene known collectively as xylenes. The p- stands for para-, indicating that the two methyl groups in p-xylene occupy the diametrically opposite substituent positions 1 and 4.
2-METHYLNAPHTHALENE (7419-61-6, 91-57-6)  
2-methylnaphthalene, methyl-13C-labeled  ·  2-methylnaphthalene, lithium salt, ion(1-)  ·  2-methylnaphthalene, naphthalene-1-(13)C-labeled
2-Methylnaphthalene is a polycyclic aromatic hydrocarbon (PAH). On February 22, 2014, NASA announced a greatly upgraded database for detecting and monitoring PAHs, including 2-methylnaphthalene, in the universe. According to NASA scientists, over 20% of the carbon in the universe may be associated with PAHs, possible starting materials for the formation of life.
CHRYSENE (65996-93-2, 50-32-8, 218-01-9)  
Chrysene is a polycyclic aromatic hydrocarbon (PAH) with the molecular formula C 18H 12 that consists of four fused benzene rings. It is a natural constituent of coal tar, from which it was first isolated and characterized. It is also found in creosote at levels of 0.5-6 mg/kg.
1-METHYLNAPHTHALENE (90-12-0, 1321-94-4)  
1-Methylnaphthalene is a polycyclic aromatic hydrocarbon (PAH). It has a cetane number of zero, and was previously used as the lower reference for cetane number. However, due to the expense and handling difficulty of 1-methylnaphthalene, it was replaced in this capacity by isocetane, with a CN of 15.
PENTACHLOROETHANE (76-01-7)  
Pentachloroethane is a non-flammable but toxic chemical compound of chlorine, hydrogen, and carbon. It is used as a solvent for oil and grease, in metal cleaning, and in the separation of coal from impurities.
2-CHLOROPHENOL (25167-80-0, 95-57-8)  
o-chlorophenol  ·  2-monochlorophenol  ·  o-monochlorophenol
2-Chlorophenol or ortho-chlorophenol is an organic compound, a derivative of phenol. Related compounds are used as a disinfectant agents and various pesticides. This particular compound has few other applications, but is an intermediate in the polychlorination of phenol.
Dioxin (1746-01-6)  
TCDD  ·  PCDD  ·  Tetrachlorodibenzodioxin
2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is a polychlorinated dibenzo-p-dioxin (sometimes shortened, though inaccurately, to simply "dioxin") with the chemical formula C 12H 4Cl 4O 2. TCDD is a colorless solid with no distinguishable odor at room temperature. It is usually formed as a side product in organic synthesis and burning of organic materials.
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Polycyclic organic compounds
Cosmetics chemicals
Drugs acting on the gastrointestinal system and metabolism
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