CAS 84-89-9
:Laurent acid
Description:
Laurent acid, also known as 2-hydroxy-4-methylbenzoic acid, is an aromatic carboxylic acid characterized by its hydroxyl and methyl substituents on the benzene ring. It is a white crystalline solid that is soluble in organic solvents and exhibits moderate solubility in water. The presence of the hydroxyl group contributes to its acidity, allowing it to participate in various chemical reactions, including esterification and acylation. Laurent acid is often used in the synthesis of pharmaceuticals, dyes, and other organic compounds due to its functional groups that enable further chemical modifications. Additionally, it may exhibit antioxidant properties, making it of interest in biochemical applications. Its CAS number, 84-89-9, is a unique identifier that facilitates the tracking and regulation of this compound in scientific literature and industrial applications. As with many organic acids, safety precautions should be taken when handling Laurent acid, as it may cause irritation to skin and eyes.
Formula:C10H9NO3S
InChI:InChI=1S/C10H9NO3S/c11-9-5-1-4-8-7(9)3-2-6-10(8)15(12,13)14/h1-6H,11H2,(H,12,13,14)
InChI key:InChIKey=DQNAQOYOSRJXFZ-UHFFFAOYSA-N
SMILES:S(=O)(=O)(O)C=1C2=C(C(N)=CC=C2)C=CC1
Synonyms:- 1-Amino-5-naphthalenesulfonic acid
- 1-Amino-5-sulfonaphthalene
- 1-Naphthalenesulfonic acid, 5-amino-
- 1-Naphthylamine-5-Sulfonic Acid
- 1-Naphthylamine-5-sulphonic acid
- 5-Amino-1-naphthalenesulfonic acid
- 5-Amino-1-naphthylamine-5-sulfonic acid
- 5-Aminonaphthalene-1-Sulfonate
- 5-Aminonaphthalene-1-Sulfonic Acid
- 5-Aminonaphthalene-1-sulphonic acid
- 5-Naphthylamine-1-sulfonic acid
- 5-Sulfo-1-naphthylamine
- Laurent Acid
- Laurents acid
- NSC 28691
- See more synonyms
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Found 7 products.
5-Amino-1-naphthalenesulfonic Acid
CAS:Formula:C10H9NO3SPurity:>98.0%(T)Color and Shape:Purple to Dark purple to Dark red powder to crystalMolecular weight:223.255-Aminonaphthalene-1-sulfonic acid, tech. 85%
CAS:<p>5-Aminonaphthalene-1-sulfonic acid is an deriva- tizing agents in the precolumn derivatization of some chiral phenoxy acid. Cu(II) based on a dansyl derivative was synthesized with 29.2% overall yield by a seven-step synthetic procedure from the readily available starting material 5-aminonaphthalene</p>Formula:C10H9NO3SPurity:85%Color and Shape:Pale purple to grey or brown to dark brown, PowderMolecular weight:223.255-Aminonaphthalene-1-sulfonic acid
CAS:Formula:C10H9NO3SPurity:94%Color and Shape:SolidMolecular weight:223.24845-Amino-1-naphthalenesulfonic Acid, 90%
CAS:Controlled Product<p>Applications 5-Amino-1-naphthalenesulfonic acid is used in biochemistry as a fluorophore to label nucleotides of interest when running fluorescent immune assays.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Kardost, R., et al.: Mol. Immunol., 19, 159 (1982); Mulder, B., et al.: Nucleic Acids Res., 33, 4865 (2005); Fick, J., et al.: Eur. J. Biochem., 126, 367 (1982)<br></p>Formula:C10H9NO3SPurity:90%Color and Shape:NeatMolecular weight:223.255-Aminonaphthalene-1-Sulphonic Acid pure, 90%
CAS:Formula:C10H9NO3SPurity:min. 90%Color and Shape:White to gray to rose pink, PowderMolecular weight:223.255-Amino-1-naphthalenesulphonic acid
CAS:Formula:C10H9NO3SPurity:94%(HPLC);RGColor and Shape:SolidMolecular weight:223.25







