| Weight | 932.768 g/mol |
|---|---|
| Formula | C32H20N6Na4O14S4 |
| Hydrogen Acceptors | 20 |
| Hydrogen Donors | 4 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 9 |
DIRECT BLUE 6 (2602-46-2)
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- TCI - DIRECT BLUE 666.00 USD
- Biodegradation of benzidine based dye Direct Blue-6 by Pseudomonas desmolyticum NCIM 2112 (Bioresource Technology, 2007)
- Thirteen-week subchronic toxicity studies of Direct Blue 6, Direct Black 38, and Direct Brown 95 dyes (Toxicology and Applied Pharmacology, 1980)
- Total Synthesis of Flavocommelin, a Component of the Blue Supramolecular Pigment from Commelina communis, on the Basis of Direct 6-C-Glycosylation of Flavan (Journal of Organic Chemistry, 2004)
- Direct observation of adsorbed H{sub 2}-framework interactions in the Prussian Blue analogue Mn{sup II}{sub 3} [CO{sup III}(CN){sub 6}]{sub 2} : the relative importance of accessible coordination sites and Van Der Waals interactions. (Chemical Communications, 2006)
- Enhanced photo-catalytic activity of Sr and Ag co-doped TiO2 nanoparticles for the degradation of Direct Green-6 and Reactive Blue-160 under UV & visible light (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2015)
- Rapid decomposition of Direct Blue 6 in neutral solution by FeB amorphous alloys (RSC Advances, 2015)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H350: May cause cancer
Danger Carcinogenicity - Category 1A, 1B - H373: Causes damage to organs through prolonged or repeated exposure
Warning Specific target organ toxicity, repeated exposure - Category 2 -
SMILESC1=CC(=CC=C1C2=CC=C(C=C2)NN=C3C(=CC4=CC(=CC(=C4C3=O)N)S(=O)(=O)[O-])S(=O)(=O)[O-])NN=C5C(=CC6=CC(=CC(=C6C5=O)N)S(=O)(=O)[O-])S(=O)(=O)[O-].[Na+].[Na+].[Na+].[Na+]
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InChIKeyHOPRIFATEWRIEO-UHFFFAOYSA-J
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