![]() 2,6,6-Trimethyl-2-cyclohexene-1,4-dione structure
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Common Name | 2,6,6-Trimethyl-2-cyclohexene-1,4-dione | ||
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CAS Number | 1125-21-9 | Molecular Weight | 152.190 | |
Density | 1.0±0.1 g/cm3 | Boiling Point | 214.2±0.0 °C at 760 mmHg | |
Molecular Formula | C9H12O2 | Melting Point | 26-28 °C(lit.) | |
MSDS | Chinese USA | Flash Point | 96.1±0.0 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Use of 2,6,6-Trimethyl-2-cyclohexene-1,4-dioneKetoisophorone (4-Oxoisophorone) is a key intermediate in the synthesis of carotenoids and flavouring agents. Ketoisophorone is an industrially important cyclic endione[1]. |
Name | 2,6,6-Trimethyl-2-cyclohexene-1,4-dione |
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Synonym | More Synonyms |
Description | Ketoisophorone (4-Oxoisophorone) is a key intermediate in the synthesis of carotenoids and flavouring agents. Ketoisophorone is an industrially important cyclic endione[1]. |
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Related Catalog | |
References |
Density | 1.0±0.1 g/cm3 |
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Boiling Point | 214.2±0.0 °C at 760 mmHg |
Melting Point | 26-28 °C(lit.) |
Molecular Formula | C9H12O2 |
Molecular Weight | 152.190 |
Flash Point | 96.1±0.0 °C |
Exact Mass | 152.083725 |
PSA | 34.14000 |
LogP | 0.76 |
Vapour Pressure | 0.2±0.4 mmHg at 25°C |
Index of Refraction | 1.469 |
Symbol |
![]() GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H317 |
Precautionary Statements | P280 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Faceshields;Gloves |
Hazard Codes | Xi:Irritant |
Risk Phrases | R36/37/38 |
Safety Phrases | S26-S36/37-S37/39 |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
HS Code | 29142900 |
Precursor 6 | |
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DownStream 5 | |
HS Code | 2914299000 |
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Summary | 2914299000. other cyclanic, cyclenic or cyclotherpenic ketones without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0% |
Engineering towards nitroreductase functionality in ene-reductase scaffolds.
ChemBioChem. 16(5) , 811-8, (2015) Nitroreductases (NRs) and ene-reductases (ERs) both utilize flavin mononucleotide cofactors but catalyze distinct reactions. NRs reduce nitroaromatics, whereas ERs reduce unsaturated C=C double bonds,... |
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Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.
Bioresour. Technol. 102(5) , 3993-8, (2011) The bioreduction of α,β-unsaturated ketones (ketoisophorone, 2-methyl- and 3-methyl-cyclopentenone) and aldehydes [(S)-(-)-perillaldehyde and α-methyl-cinnamaldehyde] by 23 "non-conventional" yeasts (... |
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An engineered old yellow enzyme that enables efficient synthesis of (4R,6R)-Actinol in a one-pot reduction system.
ChemBioChem. 16(3) , 440-5, (2015) (4R,6R)-Actinol can be stereo-selectively synthesized from ketoisophorone by a two-step conversion using a mixture of two enzymes: Candida macedoniensis old yellow enzyme (CmOYE) and Corynebacterium a... |
2-Cyclohexene-1,4-dione, 2,6,6-trimethyl- |
2,6,6-Trimethyl-2-cyclohexen-1,4-dione |
4-Oxoisophorone,Ketoisophorone |
EINECS 214-406-2 |
2,6,6-trimethylcyclohex-2-ene-1,4-dione |
MFCD00043119 |
4-Oxoisophorone |
4-Ketoisophorone |
2,6,6-Trimethyl-2-cyclohexene-1,4-dione |