| Weight | 178.143 g/mol |
|---|---|
| Formula | C9H6O4 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
NINHYDRIN (485-47-2)
Indantrione Monohydrate
Score:
#1397 in Biochemistry
,
#3347 in Biology
,
#4171 in Chemistry
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- A MODIFIED NINHYDRIN REAGENT FOR THE PHOTOMETRIC DETERMINATION OF AMINO ACIDS AND RELATED COMPOUNDS (Journal of Biological Chemistry, 1954)
- PHOTOMETRIC NINHYDRIN METHOD FOR USE IN THE CHROMATOGRAPHY OF AMINO ACIDS (Journal of Biological Chemistry, 1948)
- A modified ninhydrin colorimetric analysis for amino acids (Archives of Biochemistry and Biophysics, 1957)
- The determination of amino-acids with ninhydrin (Analyst, 1955)
- Quantitative monitoring of solid-phase peptide synthesis by the ninhydrin reaction (Analytical Biochemistry, 1981)
- Amino Acid Analysis: Aqueous Dimethyl Sulfoxide As Solvent for the Ninhydrin Reaction (Journal of Biological Chemistry, 1968)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Indantrione Monohydrate
-
SMILESC1=CC=C2C(=C1)C(=O)C(C2=O)(O)O
-
InChIKeyFEMOMIGRRWSMCU-UHFFFAOYSA-N
- Pubchem - NINHYDRIN
- Wikipedia - ninhydrin
Ninhydrin (2,2-dihydroxyindane-1,3-dione) is a chemical used to detect ammonia or primary and secondary amines. When reacting with these free amines, a deep blue or purple color known as Ruhemann's purple is produced. Ninhydrin is most commonly used to detect fingerprints, as the terminal amines of lysine residues in peptides and proteins sloughed off in fingerprints react with ninhydrin.
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NINHYDRIN
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