metanilic acid
benzenesulfonic acid, 3-amino-
Identification
| Name | metanilic acid |
| CAS Number | 121-47-1 |
| EINECS | 204-473-6 |
| FDA UNII | OT03NUM20P |
| Molecular Formula | C6 H7 N O3 S |
| Molecular Weight | 173.19139000 |
| MDL Number | MFCD00065345 |
| Nikkaji Number | J2.487B |
| Beilstein | 0473264 |
| XlogP3 | -0.20 (est) |
Regulatory
Physical Properties
| Appearance | white powder (est) |
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Flash Point | 32.00 °F. TCC ( 0.00 °C. ) (est) |
| logP (o/w) | -1.595 (est) |
| Soluble in | water, 3.562e+004 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Preferred SDS | View |
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | pharmaceuticals / chemical synthisis |
| Recommendation for metanilic acid usage levels up to | not for fragrance use. |
| Recommendation for metanilic acid flavor usage levels up to | not for flavor use. |
BOC Sciences
Best of Chemicals Supplier
Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...
Potential Uses
Natural Occurrence
Synonyms
3-
amino benzene sulfonic acid
m-
amino benzenesulfonic acid
3-
amino-benzenesulfonic acid
1-
aminobenzene-3-sulfonic acid
3-
aminobenzenesulfonic acid
m-
aminobenzenesulfonic acid
3-
aminobenzenesulphonic acid
meta-
aminophenylsulfonic acid
aniline-3-sulfonic acid
aniline-m-sulfonic acid
m-
anilinesulfonic acid
benzenesulfonic acid, 3-amino-
metanilicacid
m-
sulfanilic acid
PubMed:
Simultaneous dyeing and antibacterial finishing for cotton cellulose using a new reactive dye.
PubMed:
Synthesis and characterization of cytocompatible sulfonated polyanilines.
PubMed:
Aerobic biodegradation pathway for Remazol Orange by Pseudomonas aeruginosa.
PubMed:
Mechanism of Navitan Fast Blue S5R degradation by Pseudomonas aeruginosa.
PubMed:
A novel class of enkephalinase inhibitors containing a C-terminal sulfo group.
PubMed:
Metabolic disposition of 14C-metanil yellow in guinea pigs.
PubMed:
Metabolic disposition of [14C] metanil yellow in rats.
PubMed:
[Linkage of anthranilic and metanilic acid salts of diazonium to pyrazolones].
PubMed:
N-acetyl-(1-amino-2-naphthol-6-sulphonic acid), a common metabolite of sunset yellow FCF, orange GGN and 1-amino-2-naphthol-6-sulphonic acid in rat urine.
PubMed:
In vitro studies on the biotransformation of metanil yellow.
PubMed:
[Contrast media. V. Iodinated derivatives of metanilic acid].