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CAS NO.138-59-0
| Shikimic acid Basic information |
| Product Name: | Shikimic acid |
| Synonyms: | L-SHIKIMIC ACID;(3R,4S,5R)-3,4,5-TRIHYDROXY-1-CYCLOHEXENECARBOXYLIC ACID;(3R,4S,5R)-3,4,5-TRIHYDROXY-CYCLOHEX-1-ENECARBOXYLIC ACID;(3R,4S,5R)-3,4,5-TRIHYDROXYL-1-CYCLOHEXENE-1-CARBOXYLIC ACID;(3R,4S,5R)-TRIHYDROXY-1-CYCLOHEXENE-1-CARBOXYLIC ACID;(-)3ALPHA,4ALPHA,5BETA-TRIHYDROXY-1-CYCLOHEXENE-1-CARBOXYLIC ACID;1-CYCLOHEXENE-1-CARBOXYLIC ACID, 3,4,5-TRIHYDROXY-, (3R,4S,5R);3,4,5-TRIHYDROXY-1-CYCLOHEXENE-1-CARBOXYLIC ACID |
| CAS: | 138-59-0 |
| MF: | C7H10O5 |
| MW: | 174.15 |
| EINECS: | 205-334-2 |
| Product Categories: | API intermediates;Chiral Reagents;Chiral Building Blocks;Simple Alcohols (Chiral);Synthetic Organic Chemistry;Natural Plant Extract;API;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;Antibiotic;Plant Extract;Inhibitors |
| Mol File: | 138-59-0.mol |
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| Shikimic acid Chemical Properties |
| mp | 185-187 °C(lit.) |
| alpha | -180 º (c=4, H2O 25 ºC) |
| refractive index | -180 ° (C=1, H2O) |
| storage temp. | -20°C Freezer |
| Water Solubility | 18 g/100 mL (20 ºC) |
| Sensitive | Hygroscopic |
| Merck | 14,8480 |
| BRN | 4782717 |
| CAS DataBase Reference | 138-59-0(CAS DataBase Reference) |
| NIST Chemistry Reference | Shikimic acid(138-59-0) |
| Safety Information |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 22-24/25-36-26 |
| WGK Germany | 3 |
| RTECS | GW4600000 |
| F | 3-10 |
| HS Code | 29181980 |
| Hazardous Substances Data | 138-59-0(Hazardous Substances Data) |
| MSDS Information |
| Provider | Language |
|---|---|
| Shikimic acid | English |
| SigmaAldrich | English |
| ACROS | English |
| ALFA | English |
| Shikimic acid Usage And Synthesis |
| Chemical Properties | White Solid |
| Usage | Naturally occurring (-)-form is a major biosynthetic precursor of phenylalanine, tyrosine, and tryptophan and hence of the majority of plant alkaloids. It is also involved in the biosynthesis of lignin, flavonpids and other important aromatic compounds. |
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