推荐产品
等级
JIS special grade
表单
solid
存货情况
available only in Japan
dilution
(for analytical testing)
mp
111 °C (dec.) (lit.)
SMILES字符串
CN(C)c1ccc(cc1)N=Nc2ccccc2
InChI
1S/C14H15N3/c1-17(2)14-10-8-13(9-11-14)16-15-12-6-4-3-5-7-12/h3-11H,1-2H3
InChI key
JCYPECIVGRXBMO-UHFFFAOYSA-N
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警示用语：
Danger
危险声明
预防措施声明
危险分类
Acute Tox. 3 Oral - Carc. 2
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Joshua Balsam et al.
Lab on a chip, 11(5), 941-949 (2011-01-19)
In this paper, we describe a simple charge-coupled device (CCD) based lensless fluorometer with sensitivity in the range of current ELISA plate readers. In our lensfree fluorometer, a multi-wavelength LED light source was used for fluorophore excitation. To collimate the
Debadutta Mishra et al.
Toxicology letters, 203(1), 40-47 (2011-03-08)
The azo-dye p-dimethylaminoazobenzene (p-DAB) is a potential tumor initiator in rodents, but the underlying mechanism is not clear. Following chronic feeding of the carcinogen for 3, 5 and 7 weeks, trace elemental status, free radical generation, oxidative damage, antioxidant profile
Michalina Oplatowska et al.
The Analyst, 136(11), 2403-2410 (2011-04-22)
Sensitive and specific enzyme-linked immunosorbent assays (ELISAs) were developed for the detection of two illegal synthetic dyes: Methyl Yellow (MY) and Rhodamine B (RB) in food. Polyclonal antibodies were raised against synthesised immunogens and employed in unique direct disequilibrium ELISAs.
Akira Abe et al.
Analytical biochemistry, 434(1), 78-83 (2012-11-14)
Lysosomal phospholipase A2 (group XV PLA2, LPLA2) is a lysosomal enzyme linked to drug-induced phospholipidosis. We developed phospholipid "smart probes" based on the conversion of a quenched fluorogenic substrate to a fluorescent product. Due to the preference of LPLA2 for
Derek Ho et al.
Biochemistry, 50(22), 4830-4842 (2011-05-03)
The membrane topology of the colicin E1 channel domain was studied by fluorescence resonance energy transfer (FRET). The FRET involved a genetically encoded fluorescent amino acid (coumarin) as the donor and a selectively labeled cysteine residue tethered with DABMI (4-(dimethylamino)phenylazophenyl-4'-maleimide)
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