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经验公式(希尔记法):
C18H26O
化学文摘社编号:
分子量:
258.40
NACRES:
NA.24
PubChem Substance ID:
UNSPSC Code:
85151701
EC Number:
244-240-6
MDL number:
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
InChI key
DNRJTBAOUJJKDY-UHFFFAOYSA-N
SMILES string
CC1CC(C)(C)c2cc(C(C)=O)c(C)cc2C1(C)C
grade
analytical standard
assay
≥97.0% (GC)
shelf life
limited shelf life, expiry date on the label
impurities
≤1.0% water
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
Quality Level
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General description
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.
Application
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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)
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)
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