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Merck

07770

Millipore

N,N-Dimethyl-p-phenylenediamine dihydrochloride

suitable for microbiology, ≥99.0%

Sinónimos:

4-Amino-N,N-dimethylaniline dihydrochloride, DMPD · 2HCl, DMPPDA · 2HCl

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About This Item

Fórmula lineal:
(CH3)2NC6H4NH2 · 2HCl
Número de CAS:
Peso molecular:
209.12
Beilstein/REAXYS Number:
3913463
EC Number:
MDL number:
UNSPSC Code:
41171621
PubChem Substance ID:
NACRES:
NA.85

Quality Level

assay

≥99.0% (AT)
≥99.0%

form

powder

loss

≤0.05% loss on ignition

mp

210-215 °C (dec.)
222 °C (dec.) (lit.)

cation traces

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤500 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

application(s)

food and beverages
microbiology

SMILES string

Cl[H].Cl[H].CN(C)c1ccc(N)cc1

InChI

1S/C8H12N2.2ClH/c1-10(2)8-5-3-7(9)4-6-8;;/h3-6H,9H2,1-2H3;2*1H

InChI key

IAEDWDXMFDKWFU-UHFFFAOYSA-N

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General description

N,N-Dimethyl-p-phenylenediamine dihydrochloride is an azoreduction product of acid orange 52 (AO52). It is useful in the oxidase test which differentiates bacteria based on their ability to utilise the dye.

Application

N,N-Dimethyl-p-phenylenediamine dihydrochloride has been used to determine the plasma oxidant capacity in terms of plasma ferric equivalent oxidative potential (PFEOP).

Caution

May discolor to red on storage.

pictograms

Skull and crossbones

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

Storage Class

6.1A - Combustible, acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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An HPLC micro-method with fluorescence detection has been developed to determine total vitamin C (vit C) and dehydroascorbic acid (DHA) concentrations in human plasma samples. This method is based on the rapid, specific reaction of DHA with dimethyl-o-phenylenediamine (DMPD) to
Joseph B Issa et al.
The journal of physical chemistry. B, 111(24), 6878-6886 (2007-06-02)
Photoinduced intramolecular charge separation across proline-bridged donor-acceptor complexes of the type Pyr-(Pro)n-DMPD (where Pyr=pyrene-1-sulfonyl and DMPD=N,N-dimethyl-1,4-phenylenediamine) was studied. The steady-state emission spectrum for n=0, 1, 2, 3 showed an increase in emission intensity with the number of proline residues. Time-dependent
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The interactions of reductants with dopamine beta-monooxygenase (DbetaM) were examined using two novel classes of reductants. The steady-state kinetics of the previously characterized DbetaM reductant, N,N-dimethyl-1,4-p-phenylenediamine (DMPD), were parallel to the ascorbic acid-supported reaction with respect to pH dependence and

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