| Identification | More | [Name]
2,5-Dichlorobenzene-1,4-diamine | [CAS]
20103-09-7 | [Synonyms]
1,4-DIAMINO-2,5-DICHLOROBENZENE
2.5-DICHLORO-1.4-BENZENEDIAMINE
2,5-DICHLORO-1,4-PHENYLENEDIAMINE
2,5-DICHLORO-4-PHENYLENEDIAMINE
2,5-dichlorobenzene-1,4-diamine
2,5 DICHLORO PPD
2,5-DICHLORO-P-PHENYLENEDIAMINE
2-CHLORO PPD
AURORA KA-7368
BUTTPARK 100\01-20
1,4-benzenediamine,2,5-dichloro-
1,4-diamino-3,6-dichlorobenzene
2,5-dichlor-1,4-fenylendiamin
2,5-dichlor-1,4-fenylendiamin(czech)
2,5-dichloro-4-benzenediamine
2,5-dichloro-p-phenylenediamin
benzene,2,5-dichloro,1,4-diamino
DICHLORO-PARA-PHENYLENEDIAMINE
DICHLOROPHENYLENEDIAMINE | [EINECS(EC#)]
243-512-1 | [Molecular Formula]
C6H6Cl2N2 | [MDL Number]
MFCD00007902 | [Molecular Weight]
177.03 | [MOL File]
20103-09-7.mol |
| Chemical Properties | Back Directory | [Appearance]
light brown to pinkish-grey powder | [Melting point ]
164-166 °C (dec.)(lit.)
| [Boiling point ]
291.88°C (rough estimate) | [density ]
1.4668 (rough estimate) | [refractive index ]
1.6400 (estimate) | [storage temp. ]
2-8°C
| [form ]
powder to crystal | [pka]
3.16±0.10(Predicted) | [color ]
White to Brown | [BRN ]
2803055 | [InChI]
InChI=1S/C6H6Cl2N2/c7-3-1-5(9)4(8)2-6(3)10/h1-2H,9-10H2 | [InChIKey]
QAYVHDDEMLNVMO-UHFFFAOYSA-N | [SMILES]
C1(N)=CC(Cl)=C(N)C=C1Cl | [CAS DataBase Reference]
20103-09-7(CAS DataBase Reference) | [EPA Substance Registry System]
20103-09-7(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [WGK Germany ]
3
| [RTECS ]
SS9150000
| [F ]
9 | [TSCA ]
Yes | [HS Code ]
29215900 | [Hazardous Substances Data]
20103-09-7(Hazardous Substances Data) |
| Hazard Information | Back Directory | [Chemical Properties]
light brown to pinkish-grey powder | [Synthesis]
Example 2: Add 200 mL of deionized water, 41.4 g of pulverized 2,5-dichloro-4-nitroaniline, 6 g of sodium hydroxide, 0.3 g of 1,4-naphthoquinone, and 25 g of 80% hydrazine hydrate solution to the reaction vessel. The reaction system was kept in an aqueous phase environment. The reaction mixture was stirred continuously for 9 hours at a temperature range of 85°C to 95°C to ensure complete reaction. Upon completion of the reaction, the product was separated by filtration, followed by washing the filter cake with deionized water and drying under appropriate conditions to yield 34.0 g of 2,5-dichloro-1,4-benzenediamine. The purity of the product was determined to be 96% by gas chromatography (G.C.) and the chemical purity analysis resulted in 99.6%. | [References]
[1] Patent: US5041672, 1991, A
[2] Patent: US5041672, 1991, A |
| Spectrum Detail | Back Directory | [Spectrum Detail]
2,5-Dichlorobenzene-1,4-diamine(20103-09-7)MS
2,5-Dichlorobenzene-1,4-diamine(20103-09-7)1HNMR
2,5-Dichlorobenzene-1,4-diamine(20103-09-7)13CNMR
2,5-Dichlorobenzene-1,4-diamine(20103-09-7)IR1
2,5-Dichlorobenzene-1,4-diamine(20103-09-7)IR2
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