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1728-46-7

1728-46-7 Structure

1728-46-7 Structure
IdentificationMore
[Name]

2-TERT-BUTYLCYCLOHEXANONE
[CAS]

1728-46-7
[Synonyms]

2-TERT-BUTYLCYCLOHEXANONE
ORTHO TERTIARY BUTYL CYCLOHEXANONE
O-TERT-BUTYLCYCLOHEXANONE
VERDONE
2-(1,1-dimethylethyl)-cyclohexanon
2-(1,1-dimethylethyl)-Cyclohexanone
2-t-Butylcyclohexanone
Cyclohexanone, 2-(1,1-dimethylethyl)-
2-ter-Butyl-cyclohexanone
2-tert-Butylcyclohexanone 97%
2-tert-Butylcyclohexane-1-one
[EINECS(EC#)]

217-043-8
[Molecular Formula]

C10H18O
[MDL Number]

MFCD00009696
[Molecular Weight]

154.25
[MOL File]

1728-46-7.mol
Chemical PropertiesBack Directory
[Appearance]

clear colorless to light yellow-greenish liquid
[Melting point ]

38.55°C
[Boiling point ]

62.5 °C4 mm Hg(lit.)
[density ]

0.896 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.457(lit.)
[Fp ]

162 °F
[storage temp. ]

Sealed in dry,2-8°C
[form ]

liquid
[color ]

Colourless
[Odor]

at 10.00 % in dipropylene glycol. powerful woody camphor orris minty
[Odor Type]

woody
[BRN ]

2041417
[Cosmetics Ingredients Functions]

PERFUMING
[LogP]

2.630 (est)
[CAS DataBase Reference]

1728-46-7(CAS DataBase Reference)
[EPA Substance Registry System]

Cyclohexanone, 2-(1,1-dimethylethyl)- (1728-46-7)
Questions And AnswerBack Directory
[Uses]

2-tert-butylhexane, also known as o-tert-butylcyclohexanone, is a synthetic fragrance with a woody and camphor-like aroma. It is widely used in the food and cosmetics industries and is also an important intermediate, for example, it can be used to synthesize fragrances such as 2-hydroxy-2-acetyl-6-tert-butylcyclohexanone.
Safety DataBack Directory
[Hazard Codes ]

Xi
[Safety Statements ]

S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

1
[Hazard Note ]

Irritant
[TSCA ]

TSCA listed
[HS Code ]

2914290090
Hazard InformationBack Directory
[Description]

2-Tert-butylcyclohexanone, although of very limited application in perfumery, can be used with some advantage in soap and detergent fragrances to increase the power and introduce more “lift” to the perfume. This is particularly noticeable in functional products in hot water (detergents, etc.). The effect of Verdone is apparently enhanced by heat and steam since the material is quite volatile with steam, and it also sublimes when heated. It was produced by hydrogenation of ortho-terriary-Butylphenol.
[Chemical Properties]

clear colorless to light yellow-greenish liquid
[Synthesis Reference(s)]

Journal of the American Chemical Society, 107, p. 4679, 1985 DOI: 10.1021/ja00302a014
Synthesis, p. 456, 1976 DOI: 10.1055/s-1976-24079
Spectrum DetailBack Directory
[Spectrum Detail]

2-TERT-BUTYLCYCLOHEXANONE(1728-46-7)MS
2-TERT-BUTYLCYCLOHEXANONE(1728-46-7)1HNMR
2-TERT-BUTYLCYCLOHEXANONE(1728-46-7)13CNMR
2-TERT-BUTYLCYCLOHEXANONE(1728-46-7)IR1
2-TERT-BUTYLCYCLOHEXANONE(1728-46-7)Raman
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

2-tert-Butylcyclohexanone, 99%(1728-46-7)
[Sigma Aldrich]

1728-46-7(sigmaaldrich)
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