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145-39-1

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145-39-1 Structure

145-39-1 Structure
IdentificationBack Directory
[Name]

MUSK TIBETEN
[CAS]

145-39-1
[Synonyms]

TIBETEN
MUSK TIBETEN
musktibetine
Tibetene musk
Musk Tibetine
MUSK TIBETENE
MUSK TIBETEN USP/EP/BP
Tibetene musk Solution, 100ppm
4,6-DINITRO-5-TERT-BUTYLHEMIMELLITENE
5-t-Butyl-4,6-dinitro-1,2,3-trimethylbenzene
2,6-DINITRO-3,4,5-TRIMETHYL-TERT-BUTYLBENZENE
1-tert-Butyl-3,4,5-trimethyl-2,6-dinitrobenzol
5-tert-Butyl-1,2,3-trimethyl-4,6-dinitrobenzene
5-tert-Butyl-4,6-dinitro-1,2,3-trimethylbenzene
1-tert-butyl-2,6-dinitro-3,4,5-trimethyl-benzen
1-tert-Butyl-2,6-dinitro-3,4,5-trimethylbenzene
1-(1,1-DIMETHYLETHYL)-2,6-DINITRO-3,4,4-TRIMETHYL
1-(TERT-BUTYL)-3,4,5-TRIMETHYL-2,6-DINITROBENZENE
Benzene, 1-tert-butyl-2,6-dinitro-3,4,5-trimethyl-
Benzene, 1-tert-butyl-3,4,5-trimethyl-2,6-dinitro-
1-(1,1-Dimethylethyl)-2,6-dinitro-3,4,5-trimethylbenzene
1-(1,1-dimethylethyl)-2,6-dinitro-3,4,5-trimethyl-benzen
1-(1,1-dimethylethyl)-3,4,5-trimethyl-2,6-dinitro-benzen
1-(1,1-dimethylethyl)-3,4,5-trimethyl-2,6-dinitro-Benzene
Benzene, 1-(1,1-dimethylethyl)-2,6-dinitro-3,4,5-trimethyl-
Benzene, 1-(1,1-dimethylethyl)-3,4,5-trimethyl-2,6-dinitro-
[EINECS(EC#)]

205-651-6
[Molecular Formula]

C13H18N2O4
[MDL Number]

MFCD00024266
[MOL File]

145-39-1.mol
[Molecular Weight]

266.29
Chemical PropertiesBack Directory
[Boiling point ]

409.5°C (rough estimate)
[density ]

1.1738 (rough estimate)
[refractive index ]

1.6450 (estimate)
[Odor]

at 10.00 % in benzyl benzoate. musk ketone sweet powdery fatty
[Odor Type]

musk
[LogP]

4.931 (est)
[EPA Substance Registry System]

Benzene, 1-(1,1-dimethylethyl)-3,4,5-trimethyl-2,6-dinitro- (145-39-1)
Safety DataBack Directory
[TSCA ]

TSCA listed
[HS Code ]

2904200090
[Toxicity]

The acute oral LD50 in rats was reported as > 6 g/kg and the acute dermal LD50 in rabbits as > 5 g/kg (Weir, 1971)
Hazard InformationBack Directory
[Occurrence]

Has apparently not been reported to occur in nature.
[Uses]

Musk tibetine is used as fragrance and fixative in after-shave lotions, perfumes, ete.
[Preparation]

By nitration of the corresponding benzene derivative (Bedoukian, 1967).
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