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经验公式(希尔记法):
C6H2ClN3O6
化学文摘社编号:
分子量:
247.55
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-864-3
Beilstein/REAXYS Number:
1588666
MDL number:
Assay:
≥98.0% (HPLC)
Form:
lumps
InChI key
HJRJRUMKQCMYDL-UHFFFAOYSA-N
InChI
1S/C6H2ClN3O6/c7-6-4(9(13)14)1-3(8(11)12)2-5(6)10(15)16/h1-2H
SMILES string
[O-][N+](=O)c1cc(c(Cl)c(c1)[N+]([O-])=O)[N+]([O-])=O
assay
≥98.0% (HPLC)
form
lumps
functional group
chloro, nitro
Quality Level
Other Notes
用 ~15% 的水润湿
signalword
Danger
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Sol. 1
supp_hazards
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
M Hagiyama et al.
The British journal of dermatology, 168(4), 771-778 (2012-10-31)
Neuroimmunological disorders are involved in the pathogenesis of atopic dermatitis (AD), partly through enhanced sensory nerve-skin mast cell interaction. Cell adhesion molecule 1 (CADM1) is a mast-cell adhesion molecule that mediates the adhesion to, and communication with, sympathetic nerves. To
Atsuto Ogata et al.
International immunopharmacology, 11(10), 1628-1632 (2011-06-07)
A chymase inhibitor SUN13834 has been shown to improve skin condition in animal models for atopic dermatitis. In the present study, effective dosages of SUN13834 for atopic dermatitis patients were predicted by pharmacokinetic/pharmacodynamic (PK/PD) analyses of SUN13834 in NC/Nga mice
Eujin Cho et al.
Journal of ethnopharmacology, 145(1), 294-302 (2012-11-15)
Korean red ginseng (KRG) has been shown to possess various biological activities including anti-inflammatory properties. We aimed to investigate the effects and mechanism of KRG on the prevention of atopic dermatitis (AD) using a mouse model. The effect of KRG
Andreas Natsch et al.
Chemical research in toxicology, 24(11), 2018-2027 (2011-10-26)
The skin sensitization potency of chemicals is partly related to their reactivity to proteins. This can be quantified as the rate constant of the reaction with a model peptide, and a kinetic profiling approach to determine rate constants was previously
T Fukuyama et al.
Toxicology letters, 213(3), 392-401 (2012-07-31)
Immunosuppressive environmental chemicals may exacerbate allergic diseases, including atopic dermatitis (AD). We examined the effects of the immunosuppressive environmental chemicals methoxychlor, parathion, piperonyl butoxide, dexamethasone, and cyclophosphamide on picryl-chloride-induced AD in NC/Nga mice. Mice were orally exposed (age, 5 weeks)
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