| Weight | 134.134 g/mol |
|---|---|
| Formula | C8H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
o-Phthalaldehyde (643-79-8)
o Phthaldialdehyde · ortho Phthalic Aldehyde · ortho-Phthalaldehyde
Score:
#1607 in Biochemistry
,
#3668 in Biology
,
#4605 in Chemistry
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- High performance liquid chromatographic determination of subpicomole amounts of amino acids by precolumn fluorescence derivatization with o-phthaldialdehyde (Analytical Chemistry, 1979)
- Spectrophotometric Assay Using o-Phthaldialdehyde for Determination of Proteolysis in Milk and Isolated Milk Proteins (Journal of Dairy Science, 1983)
- Determination of cholesterol using o-phthalaldehyde (Journal of Lipid Research, 1973)
- Amino Acid Analysis and Enzymatic Sequence Determination of Peptides by an Improved o-Phthaldialdehyde Precolumn Labeling Procedure (Journal of Liquid Chromatography & Related Technologies, 1981)
- o-Phthaldialdehyde precolumn derivatization and reversed-phase high-performance liquid chromatography of polypeptide hydrolysates and physiological fluids. (Journal of Chromatography A, 1983)
- O-phthalaldehyde: fluorogenic detection of primary amines in the picomole range. Comparison with fluorescamine and ninhydrin. (Proceedings of the National Academy of Sciences of the United States of America, 1975)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o Phthaldialdehyde
- ortho Phthalic Aldehyde
- ortho-Phthalaldehyde
- ortho-Phthalic Aldehyde
- o Phthalaldehyde
- Orthophthaldialdehyde
- ortho Phthalaldehyde
- o-Phthaldialdehyde
-
SMILESC1=CC=C(C(=C1)C=O)C=O
-
InChIKeyZWLUXSQADUDCSB-UHFFFAOYSA-N
- Pubchem - o-Phthalaldehyde
- Wikipedia - O-phthalaldehyde
o-Phthalaldehyde or ortho-phthalaldehyde (OPA) is the chemical compound with the formula C6H4(CHO)2. Often abbreviated OPA, the molecule is a dialdehyde, consisting of two formyl (CHO) groups attached to adjacent carbon centres on a benzene ring. This pale yellow solid is a building block in the synthesis of heterocyclic compounds and a reagent in the analysis of amino acids.
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o-Phthalaldehyde
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