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Polycyclic organic compounds, Organic compound, Cosmetics chemicals, Neurotoxins, Perfume ingredients, Cyclopentanes

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5-HT3 antagonists (4)
Antiemetics (4)
Bicyclic compounds (4)
Convulsants (4)
Cyclic compounds (4)
Cycloalkanes (4)
Drugs acting on the gastrointestinal system and metabolism (4)
Five-membered rings (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 It was withdrawn from FDA review by the manufacturer after phase III clinical trials showed elevated transaminases (a sign of possible liver toxicity) in a significant number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.
2,4-DIMETHYLPHENOL (105-67-9)  
2,4-dimethylphenol titanium (+4)  ·  2,4-dimethylphenol potassium  ·  2,4-DMP
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.
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.
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.
1,1,1,2-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.
Anisole, p-propenyl- (104-46-1, 50770-19-9)  
Anethole (anise camphor) is an organic compound that is widely used as a flavoring substance. It is a derivative of phenylpropene, a type of aromatic compound that occurs widely in nature, in essential oils. It contributes a large component of the odor and flavor of anise and fennel (both in the botanical family Apiaceae), anise myrtle (Myrtaceae), liquorice (Fabaceae), camphor, magnolia blossoms, and star anise (Illiciaceae).
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.
Benz[a]anthracene (56-55-3)  
benzanthracene  ·  benzo(b)phenanthrene  ·  1,2-benzanthracene
Benz[a]anthracene or benzo[a]anthracene is a polycyclic aromatic hydrocarbon with the chemical formula C18H12. In February 2014, NASA announced a greatly upgraded database for tracking polycyclic aromatic hydrocarbons (PAHs), including benz[a]anthracene, in the universe. According to scientists, more than 20% of the carbon in the universe may be associated with PAHs, possible starting materials for the formation of life.
1,1,2-TRICHLOROETHANE (79-00-5)  
1,1,2-trichloroethane, 14C-2-labeled  ·  1,1,2-trichloroethane, 36Cl-labeled
1,1,2-Trichloroethane, or 1,1,2-TCA, is an organochloride solvent with the molecular formula C2H3Cl3. It is a colourless, sweet-smelling liquid that does not dissolve in water, but is soluble in most organic solvents. It is an isomer of 1,1,1-trichloroethane.
FLUORANTHENE (206-44-0, 76774-50-0)  
Fluoranthene is a polycyclic aromatic hydrocarbon (PAH). The molecule can be viewed as the fusion of naphthalene and benzene unit connected by a five-membered ring. Although samples are often pale yellow, the compound is colorless.
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.
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Polycyclic organic compounds
Organic compound
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Neurotoxins
Perfume ingredients
Cyclopentanes
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