| Weight | 604.483 g/mol |
|---|---|
| Formula | C20H11N2Na3O10S3 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 5 |
AMARANTH (915-67-3)
Red Dye No. 2 · Amaranth Dye · FD and C Red No. 2
Score:
#1448 in Biology
,
#1696 in Chemistry
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- Photo-catalytic degradation of toxic dye amaranth on TiO2/UV in aqueous suspensions (Materials Science and Engineering: C, 2012)
- Glyphosate-resistant Palmer amaranth ( Amaranthus palmeri ) confirmed in Georgia (Weed Science, 2006)
- Polyphenol composition and in vitro antioxidant activity of amaranth, quinoa buckwheat and wheat as affected by sprouting and baking. (Food Chemistry, 2010)
- Use of waste materialsBottom Ash and De-Oiled Soya, as potential adsorbents for the removal of Amaranth from aqueous solutions (Journal of Hazardous Materials, 2005)
- A Compositional Study of Amaranth Grain (Journal of Food Science, 1981)
- Photocatalytic degradation of the alimentary azo dye amaranth: Mineralization of the azo group to nitrogen (Applied Catalysis B-environmental, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Red Dye No. 2
- Amaranth Dye
- FD and C Red No. 2
-
SMILESC1=CC=C2C(=C1)C(=CC=C2S(=O)(=O)[O-])NN=C3C4=C(C=C(C=C4)S(=O)(=O)[O-])C=C(C3=O)S(=O)(=O)[O-].[Na+].[Na+].[Na+]
-
InChIKeyVOBHRQFELWTZFS-UHFFFAOYSA-K
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