Basic information Safety Supplier Related

TRASEOLIDE

Basic information Safety Supplier Related

TRASEOLIDE Basic information

Product Name:
TRASEOLIDE
Synonyms:
  • ATII
  • 5-ACETYL-3-ISOPROPYL-1,1,2,6-TETRAMETHYLINDANE
  • TRASEOLIDE
  • 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1h-inden-5-yl]-ethanon
  • 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]-Ethanone
  • Ethanone,1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]-
  • Ketone,3-isopropyl-1,1,2,6-tetramethyl-5-indanylmethyl
  • 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]ethan-1-one
CAS:
68140-48-7
MF:
C18H26O
MW:
258.4
EINECS:
268-799-0
Product Categories:
  • Aromatics
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
68140-48-7.mol
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TRASEOLIDE Chemical Properties

Boiling point:
350.0±31.0 °C(Predicted)
Density 
0.933±0.06 g/cm3(Predicted)
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
form 
Oil to Thick Oil
color 
Colourless
Odor
at 100.00 %. dry sweet amber musk herbal creamy
Odor Type
musk
LogP
5.018 (est)
NIST Chemistry Reference
Ethanone, 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1h-inden-5-yl]-(68140-48-7)
EPA Substance Registry System
Ethanone, 1-[2,3-dihydro-1,1,2,6-tetramethyl-3-(1-methylethyl)-1H-inden-5-yl]- (68140-48-7)
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Safety Information

Hazardous Substances Data
68140-48-7(Hazardous Substances Data)
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TRASEOLIDE Usage And Synthesis

Chemical Properties

Colourless Oil

Chemical Properties

TRASEOLIDE is a musk fragrance that is prepared from toluene and isobutanoyl chloride by a Friedel–Crafts reaction that yields p-tolyl isopropyl ketone; the ketone is reduced to the corresponding alcohol. Chlorination and treatment with 2-methyl-2-butene yield 1 (cipher)- isopropyl-2,3,3,5-tetramethylindane, which gives the title compound through a Friedel–Crafts reaction with acetyl chloride:
It is used in perfume compositions for soaps and detergents.

Uses

A component of Musk fragrances.

Definition

ChEBI: An indane derivative in which the indane skeleton is substituted by geminal methyl groups at C-1, by single methyl groups at C-2 and C-6, by an isopropyl group at C-3 and by an acetyl group at C-6. It is a constituent of musk odorant.

Flammability and Explosibility

Not classified

TRASEOLIDESupplier

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