60720
Ketone Moschus
≥97.0% (N)
Synonym(s):
4-tert-Butyl-2,6-dimethyl-3,5-dinitroacetophenone, Musk ketone
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About This Item
Empirical Formula (Hill Notation):
C14H18N2O5
CAS Number:
Molecular Weight:
294.30
Beilstein/REAXYS Number:
2062638
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
≥97.0% (N)
mp
134-137 °C
SMILES string
CC(=O)c1c(C)c(c(c(c1C)[N+]([O-])=O)C(C)(C)C)[N+]([O-])=O
InChI
1S/C14H18N2O5/c1-7-10(9(3)17)8(2)13(16(20)21)11(14(4,5)6)12(7)15(18)19/h1-6H3
InChI key
WXCMHFPAUCOJIG-UHFFFAOYSA-N
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
>334.4 °F - closed cup
flash_point_c
> 168 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Leah Wollenberger et al.
The Science of the total environment, 305(1-3), 53-64 (2003-04-03)
A nitro musk (musk ketone) and three polycyclic musks (Tonalide, Galaxolide and Celestolide) were tested for acute and subchronic effects on a marine crustacean, the calanoid copepod Acartia tonsa. Sublethal effects on A. tonsa larvae were investigated with a rapid
Sabine Schnell et al.
Environmental science & technology, 43(24), 9458-9464 (2009-11-26)
Synthetic musks are widely used as perfuming agents in products, such as cosmetics, detergents, and soaps. The increased detection of these substances in the aquatic environment and their high bioconcentration potential raises concerns about potential effects on aquatic species. This
Yan Lv et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 25(9), 1125-1130 (2009-09-12)
This study intended to develop a robust and sensitive method for simultaneous determination of polycyclic musks (HHCB and AHTN) and nitro musks (musk xylene (MX) and musk ketone (MK)) in water samples using optimized solid-phase extraction (SPE) by gas chromatography
G G Rimkus et al.
Toxicology letters, 111(1-2), 5-15 (2000-01-12)
The monoamino metabolites of the nitro musk fragrances musk xylene (MX) and musk ketone (MK) were analysed simultaneously with their parent compounds by GC/ECD, GC/PND and GC/EI/MS in the various compartments of the aquatic environment. In this review the data
Ana Rita M Silva et al.
Analytical and bioanalytical chemistry, 396(5), 1853-1862 (2010-01-06)
Stir-bar-sorptive extraction with liquid desorption followed by large-volume injection and capillary gas chromatography coupled to mass spectrometry in selected ion monitoring acquisition mode (SBSE-LD/LVI-GC-MS(SIM)) has been developed to monitor ultra-traces of four musks (celestolide (ADBI), galaxolide (HHCB), tonalide (AHTN) and
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