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Key Documents

D176605

Sigma-Aldrich

4,5-Dimethyl-1,2-phenylenediamine

98%

Synonym(s):

4,5-Diamino-o-xylene

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About This Item

Linear Formula:
(CH3)2C6H2(NH2)2
CAS Number:
Molecular Weight:
136.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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.
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

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