Synonym: (3R,4S,5R)-(−)-3,4,5-Trihydroxy-1-cyclohexenecarboxylic acid
CAS Number: 138-59-0
Empirical Formula (Hill Notation): C7H10O5
Molecular Weight: 174.15
EC Number: 205-334-2
MDL Number: MFCD00066278
Linear Formula: C7H10O5
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: S5375-1G
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: S5375-5G
| assay |
≥99% |
| color |
white to off-white |
| form |
powder |
| InChI |
1S/C7H10O5/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1,4-6,8-10H,2H2,(H,11,12)/t4-,5-,6-/m1/s1 |
| InChI key |
JXOHGGNKMLTUBP-HSUXUTPPSA-N |
| mp |
185-187 °C (lit.) |
| Quality Level |
200  |
| SMILES string |
O[C@@H]1CC(=C[C@@H](O)[C@H]1O)C(O)=O |
| technique(s) |
ligand binding assay: suitable |
| Application: |
Shikimic acid has been used as a standard for the quantification of shikimate in apical parts of roots. It has also been used as a substrate in shikimate kinase assay. |
| Biochem/physiol Actions: |
Shikimic acid is observed to be carcinogenic in rat models, when administered. It serves as a precursor for the biosynthesis of aromatic amino acids, alkaloids and other aromatic metabolites in microorganisms. Shikimic acid is known to inhibit adenosine diphosphate (ADP) induced platelet aggregation and blood coagulation in rabbits. |
| Packaging: |
1, 5 g in poly bottle |
| Packaging: |
10 mg in glass bottle |
| Purity |
≥99% |
| mp |
185-187 °C (lit.) |
| UNSPSC |
12352106 |