Identifiers | |
---|---|
CAS Number | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.006.965 |
Chemical and physical data | |
Formula | C9H9NO4 |
Molar mass | 195.174 g·mol−1 |
3D model ( JSmol) | |
Melting point | 164–165 °C (327–329 °F) |
| |
|
Salicyluric acid is the glycine conjugate of salicylic acid and is the primary form in which salicylates are excreted from the body, [1] via the kidneys. The pathway is very similar to the pathway of benzoic acid excretion as hippuric acid.
{{
cite book}}
: CS1 maint: location missing publisher (
link)
Identifiers | |
---|---|
CAS Number | |
ChemSpider | |
UNII | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.006.965 |
Chemical and physical data | |
Formula | C9H9NO4 |
Molar mass | 195.174 g·mol−1 |
3D model ( JSmol) | |
Melting point | 164–165 °C (327–329 °F) |
| |
|
Salicyluric acid is the glycine conjugate of salicylic acid and is the primary form in which salicylates are excreted from the body, [1] via the kidneys. The pathway is very similar to the pathway of benzoic acid excretion as hippuric acid.
{{
cite book}}
: CS1 maint: location missing publisher (
link)