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方案
≥97.0% (N)
mp
134-137 °C
SMILES字符串
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
警示用语：
Warning
危险声明
危险分类
Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2
储存分类代码
11 - Combustible Solids
WGK
WGK 2
闪点(°F)
>334.4 °F - closed cup
闪点(°C)
> 168 °C - closed cup
个人防护装备
Eyeshields, Gloves, type N95 (US)
Jessica L Reiner et al.
Environmental science & technology, 41(11), 3815-3820 (2007-07-07)
Synthetic musk compounds are used as additives in many consumer products, including perfumes, deodorants, and detergents. Earlier studies have reported the occurrence of synthetic musks in environmental and wildlife samples collected in the United States. In this study, human breast
Haruhiko Nakata
Environmental science & technology, 39(10), 3430-3434 (2005-06-15)
In this study, the occurrence of the polycyclic musk fragrances HHCB (1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta[g]-2-benzopyran) and AHTN (7-acetyl-1,1,3,4,4,6-hexamethyltetrahydeonaphthalene) in marine mammals and sharks collected from Japanese coastal waters is reported. HHCB was present in the blubbers of all finless porpoises (Neophocaena phocaenoides) analyzed
Laurence Roosens et al.
Chemosphere, 69(10), 1540-1547 (2007-07-17)
Synthetic musks, such as 7-acetyl-1,1,3,4,4,6-hexamethyl-1,2,3,4-tetrahydronaphthalene (AHTN) and 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethylcyclopenta-gamma-2-benzopyran (HHCB), musk ketone (MK) and musk xylene (MX), are used as an alternative for natural musk. Due to their widespread use, these synthetic compounds turned up in different environmental compartments, such as
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
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
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