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About This Item
Linear Formula:
(NH2)2C6H3C6H3(NH2)2
CAS Number:
Molecular Weight:
214.27
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-110-6
Beilstein/REAXYS Number:
1212988
MDL number:
Assay:
97%
Form:
powder
Quality Level
assay
97%
form
powder
mp
175-177 °C (lit.)
SMILES string
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
Application
3,3′-Diaminobenzidine can be used as a starting material to prepare:
- Aromatic poly(imide) networks for hydrogen storage applications.
- Various derivatives of quinoxalines by condensation with diketones.
- Mesitylene-containing poly(benzimidazolium) analogs (Mes-PBI) for alkali anion-exchange membrane.
Peroxidase substrate; reagent for spectrophotometric determination of selenium.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 1B - Eye Irrit. 2 - Muta. 2
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A stable hydroxide-conducting polymer.
Thomas OD, et al.
Journal of the American Chemical Society, 134(26), 10753-10756 (2012)
Microporous networks of high-performance polymers: Elastic deformations and gas sorption properties.
Weber J, et al.
Macromolecules, 41(8), 2880-2885 (2008)
n-Type conjugated oligoquinoline and oligoquinoxaline with triphenylamine endgroups: efficient ambipolar light emitters for device applications.
Hancock JM, et al.
Chemistry of Materials, 18(20), 4924-4932 (2006)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D12384-5G | 04061835370245 |
| D12384-1G | 04061835370221 |
| D12384-25G | 04061835370238 |

