D176605
4,5-Dimethyl-1,2-phenylenediamine
98%
Synonyma:
4,5-Diamino-o-xylene
Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
About This Item
Lineární vzorec:
(CH3)2C6H2(NH2)2
Číslo CAS:
Molekulová hmotnost:
136.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Doporučené produkty
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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Zákazníci si také prohlíželi
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
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
E Mikiciuk-Olasik et al.
Acta poloniae pharmaceutica, 51(3), 231-233 (1994-01-01)
Some of new derivatives of 4-acylquinoxalin-2-one obtained in the reaction of N,N'-bis(chloroacetyl)-4,5-dimethyl-o-phenylenediamine with primary amines are described. Compounds were tested for their anti-HIV activity and as ligands for 99mTc.
A Bishop et al.
Free radical biology & medicine, 17(4), 311-320 (1994-10-01)
PQQ, also called methoxatin, has been isolated from guinea-pig neutrophils. The organic cations diphenyleneiodonium (DPI) and diphenyliodonium (BPI) and the aromatic o-diamine 4,5-dimethylphenylenediamine (DIMPDA) sequester synthetic PQQ and inhibit its redox-cycling activity in a model system. Standards were made of
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
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