| Identification | More | [Name]
1,5-DIAMINOANTHRAQUINONE | [CAS]
129-44-2 | [Synonyms]
1,5-ANTHRAQUINONYLDIAMINE
1,5-DIAMINOANTHRAQUINONE
TIMTEC-BB SBB000769
1,5-diamino-10-anthracenedione
1,5-diamino-9,10-anthraquinone
1,5-diaminoanthrachinon
1,5-diamino-anthraquinon
10-Anthracenedione,1,5-diamino-9
9,10-Anthracenedione,1,5-diamino-
smokeredf
1,5-diaminoanthracene-9,10-dione
1,5-DIAMINOANTHRAQUINONE, TECH., 85%
1,5-DIAMINOATHRAQUINONE
1,5-diamino-9，10-Anthracenedione
1,5-Diaminoanthra-9,10-quinone | [EINECS(EC#)]
204-947-2 | [Molecular Formula]
C14H10N2O2 | [MDL Number]
MFCD00001226 | [Molecular Weight]
238.24 | [MOL File]
129-44-2.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
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 .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [RTECS ]
CB6400000
| [TSCA ]
Yes | [HS Code ]
29147000 |
| Hazard Information | Back Directory | [Uses]
1,5-Diaminoanthraquinone (DAAQ) may be used in the preparation of vertical nanowire arrays. It may be used in the synthesis of poly(1,5-diaminoanthraquinone) (PDAA) particles, via chemically oxidative polymerization of DAAQ. | [Uses]
1,5-Diaminoanthraquinone (DAAQ) may be used in the preparation of vertical nanowire arrays. It may be used in the synthesis of poly(1,5-diaminoanthraquinone) (PDAA) particles, via chemically oxidative polymerization of DAAQ. | [General Description]
1,5-Diaminoanthraquinone (DAAQ) is an organic dye compound. Rapid preparation of 1,5-diaminoanthraquinone nanofibers (DAAQNFs) decorated with small platinum nanoparticles (PtNPs) has been reported. The absorption and fluorescence spectra of DAAQ has been investigated in various organic solvents. Preparation of vertical organic nanowire arrays of DAAQ on solid substrates by a facile physical vapor transport method has been reported. | [Synthesis]
1,5-Diaminoanthraquinone is prepared by SO3H exchange
from anthraquinone-1,5-disulfonic acid, by replacing
NO2 in 1,5-dinitroanthraquinone,
, or by reducing 1,5-dinitroanthraquinone
with sodium sulfide or by catalytic hydrogenation
. | [Purification Methods]
Recrystallise it from aniline (m 313-314o) EtOH or acetic acid [Flom & Barbara J Phys Chem 89 4481 1985]. [Beilstein 14 H 303, 14 I 467, 14 II 116, 14 III 466, 14 IV 479.] |
|
|