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等级
purum
方案
≥98.0% (CHN)
表单
solid
mp
173-176 °C
175-177 °C (lit.)
溶解性
dioxane: soluble 0.1 g/10 mL, clear, colorless
储存温度
2-8°C
SMILES字符串
NC1=C(N)C=CC(C2=CC(N)=C(N)C=C2)=C1
InChI
1S/C12H14N4/c13-9-3-1-7(5-11(9)15)8-2-4-10(14)12(16)6-8/h1-6H,13-16H2
InChI key
HSTOKWSFWGCZMH-UHFFFAOYSA-N
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一般描述
The photooxidation of 3,3′-diaminobenzidine by Chlamydomonas reinhardii and blue-green algae has been investigated. Electropolymerization of 3,3′-diaminobenzidine on solid substrate electrode (Platinum, Gold and Glassy Electrode) affords stable and water insoluble films.
应用
过氧化物酶底物；分光光度法测定硒的试剂。
3,3′-Diaminobenzidine, a dark brown dye, was used as an antibody-specific stain to identify the paired antibodies in breast tissue. 3,3′-Diaminobenzidine may be used for the determination of selenium and for the synthesis of a useful, linear, Schiff-base coordination polymer.
警示用语：
Danger
危险分类
Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Muta. 2
储存分类代码
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Synthesis and characterization of the thermally stable copolymer of tetrakis (salicylaldehydato-O, O') zirconium (IV) and 3, 3'-diaminobenzidine.
Archer RD and Wang B.
Inorganic Chemistry, 29(1), 39-39 (1990)
Photooxidation of 3,3'-diaminobenzidine by blue-green algae and Chlamydomonas reinhardii.
N H Chua
Biochimica et biophysica acta, 267(1), 179-189 (1972-04-20)
Poly (3, 3'-diaminobenzidine) film on a gold electrode for selective preconcentration and stripping analysis of selenium (IV).
Cai Q and Khoo SB.
Analytical Chemistry, 66(24), 4543-4550 (1994)
Determination of traces of selenium 3, 3-diaminobenzidine as selenium (lV) organic reagent.
Cheng K L.
Analytical Chemistry, 28(11), 1738-1742 (1956)
Jimmy C Azar et al.
Computational and mathematical methods in medicine, 2014, 647273-647273 (2014-07-26)
Comparing staining patterns of paired antibodies designed towards a specific protein but toward different epitopes of the protein provides quality control over the binding and the antibodies' ability to identify the target protein correctly and exclusively. We present a method
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