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54730

Supelco

6-Acetyl-1,1,2,4,4,7-hexamethyltetralin

analytical standard

Sinonimo/i:

1,2,3,4-Tetrahydro-1,1,3,4,4,6-hexamethyl-7-naphthyl methyl ketone, 1-(5,6,7,8-Tetrahydro-3,5,5,6,8,8-hexamethyl-2-naphthalenyl)ethanone, 5′,6′,7′,8′-Tetrahydro-3′,5′,5′,6′,8′,8′-hexamethyl-2′-acetonaphthone, 6-Acetyl-1,1,2,4,4,7-hexamethyl-1,2,3,4-tetrahydronaphthalene, AHMT, Fixolide, Musk tonalid, NSC 19550

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About This Item

Formula empirica (notazione di Hill):
C18H26O
Numero CAS:
Peso molecolare:
258.40
Numero CE:
Numero MDL:
Codice UNSPSC:
85151701
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Saggio

≥97.0% (GC)

Durata

limited shelf life, expiry date on the label

Impurezze

≤1.0% water

applicazioni

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Formato

neat

Stringa SMILE

CC1CC(C)(C)c2cc(C(C)=O)c(C)cc2C1(C)C

InChI

1S/C18H26O/c1-11-8-16-15(9-14(11)13(3)19)17(4,5)10-12(2)18(16,6)7/h8-9,12H,10H2,1-7H3
DNRJTBAOUJJKDY-UHFFFAOYSA-N

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Descrizione generale

6-Acetyl-1,1,2,4,4,7-hexamethyltetralin (musk tonalide) is a polycyclic musk which belongs to the class of tetralin compounds. It is widely used as a fragrance ingredient in consumer products, mainly soaps, detergents, cosmetics, and cleaning agents.

Applicazioni

6-Acetyl-1,1,2,4,4,7-hexamethyltetralin may be used as an analytical reference standard for the determination of the analyte in water samples, fish and perfumes by chromatography-based techniques.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Gas chromatography-mass spectrometry screening methods for select UV filters, synthetic musks, alkylphenols, an antimicrobial agent, and an insect repellent in fish
Mottaleb MA, et al.
Journal of Chromatography A, 1216(5), 815-823 (2009)
Examination of the in vitro (anti) estrogenic,(anti) androgenic and (anti) dioxin-like activities of tetralin, indane and isochroman derivatives using receptor-specific bioassays
Schreurs Richard HMM, et al.
Toxicology Letters, 156(2), 261-275 (2005)
Chromogenic derivatives of AHTN (6-acetyl-1, 1, 2, 4, 4, 7-hexamethyltetralin) react with amino acids and protein in vitro. Spectral characteristics of the colour products
Pipino S, et al.
Food And Chemical Toxicology, 42(5), 785-790 (2004)
Multicomponent analytical methodology to control phthalates, synthetic musks, fragrance allergens and preservatives in perfumes
Sanchez-Prado L, et al.
Talanta, 85(1), 370-379 (2011)
Semi-automated hollow-fibre membrane extraction, a novel enrichment technique for the determination of biologically active compounds in water samples
Muller S, et al.
Journal of Chromatography A, 985(1-2), 99-106 (2003)

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