D176605
4,5-Dimethyl-1,2-phenylenediamine
98%
Sinónimos:
4,5-Diamino-o-xylene
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About This Item
Fórmula lineal:
(CH3)2C6H2(NH2)2
Número de CAS:
Peso molecular:
136.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
assay
98%
form
powder
mp
127-129 °C (lit.)
storage temp.
2-8°C
SMILES string
Cc1cc(N)c(N)cc1C
InChI
1S/C8H12N2/c1-5-3-7(9)8(10)4-6(5)2/h3-4H,9-10H2,1-2H3
Inchi Key
XSZYBMMYQCYIPC-UHFFFAOYSA-N
Application
Employed in the preparation of transition metal complexes and quinoxalinones.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Los clientes también vieron
K Mori et al.
Chemical & pharmaceutical bulletin, 46(9), 1474-1476 (1998-10-17)
A simple and accurate method for determination of vitamin C (ascorbic acid (AsA) and dehydroascorbic acid (DHA)) using 4,5-dimethyl-o-phenylenediamine (DMPD) was investigated. It was found that DMPD is a useful fluorescent reagent. The reaction product of DMPD with DHA showed
M Katayama et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 110(10), 776-782 (1990-10-01)
Twelve purines oxidized with 4,5-dimethyl-o-phenylenediamine (DMPD) was found to react with N-bromosuccinimide (NBS) to give fluorescent derivatives. In this paper, the identification of oxidation and fluorescent products have been described. In compliance with the substituent on purine skelton, three alloxans
Bull. Korean Chem. Soc., 15, 1122-1122 (1994)
Tijana Bugarcic et al.
Inorganic chemistry, 48(19), 9444-9453 (2009-09-29)
The synthesis and characterization of ruthenium(II) arene complexes of the general formula [(eta(6)-arene)Ru(XY)Z](+), where arene = p-cymene (p-cym), hexamethylbenzene (hmb), or biphenyl (bip), XY = o-phenylenediamine (o-pda), o-benzoquinonediimine (o-bqdi), or 4,5-dimethyl-o-phenylenediamine (dmpda), and Z = Cl, Br, or I, are
M L Karnovsky et al.
Environmental health perspectives, 102 Suppl 10, 43-44 (1994-12-01)
Although great progress has been made in understanding the respiratory burst of leukocytes that produce superoxide (O2-), it is possible that a component or components, might have been overlooked. Furthermore, O2- production and its sequels, though cardinal in bactericidal action
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