88-29-9 Usage
Uses
Used in Perfumery Industry:
7-acetyl-6-ethyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene is used as a musk ingredient in perfumes for its distinctive scent and ability to provide a long-lasting fragrance.
Used in Cosmetics Industry:
In the cosmetics industry, 7-acetyl-6-ethyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene is used as a musk component in various cosmetic products to impart a pleasant and lasting aroma.
Used in Soap Industry:
7-acetyl-6-ethyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene is used as a musk additive in soaps to enhance their scent and provide a unique olfactory experience for the users.
Safety Profile
Poison by ingestion. Moderately toxic by skin contact. A sktn and eye irritant. Exposure causes blue coloration of internal organs and central nervous system effects, e.g., hyperexcitabdity, tremors, lack of coordination, hunched back, and loss of weight. It is slowly metabolized and excreted via feces. Symptoms persist for 90 days after exposure. Severity of symptoms seems proportional to length of exposure. It is freely absorbed via human skin. When heated to decomposition it emits acrid smoke and fumes.
Check Digit Verification of cas no
The CAS Registry Mumber 88-29-9 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88-29:
(4*8)+(3*8)+(2*2)+(1*9)=69
69 % 10 = 9
So 88-29-9 is a valid CAS Registry Number.
InChI:InChI=1/C18H26O/c1-7-13-10-15-16(11-14(13)12(2)19)18(5,6)9-8-17(15,3)4/h10-11H,7-9H2,1-6H3
88-29-9Relevant academic research and scientific papers
Ketone precursors for organoleptic compounds
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, (2008/06/13)
The invention discloses ketones of formula I: wherein, Y is an optionally substituted alkyl, cycloalkyl, or cycloalkylalkyl, wherein each alkyl group is straight or branched and each alkyl and cycloalkyl group is saturated or unsaturated; R1is hydrogen or a C1-6alkyl group that is substituted, saturated or unsaturated, straight or branched; A is a chromophoric substituted aromatic ring or ring system; n is an integer; and with the proviso that formula I is not 2-ethoxy-1-phenyl-ethanone. These compositions are useful for the delivery of organoleptic compounds, especially of flavors, fragrances, masking agents and antimicrobial compounds.
Process for the production of compounds useful in perfumery
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, (2008/06/13)
Process for producing compounds useful in perfumery including isochromans and acylated indane hydrocarbons with an alkylene oxide or with a lower acyl halide in the presence of a hydrocarbon or hydrocarbon mixture containing C5 to C10 alkanes at a temperature of from -20° C. up to -5° C. In the case of forming isochromans, the resulting alcohol is reacted, in situ, with a lower alkanol and a formaldehyde precursor at temperatures of from 20° C. up to 80° C.
