Shikimic acid

Shikimic acid Basic information
Product Name:Shikimic acid
Synonyms:Shikimic acid,(3R,4S,5R)-()-3,4,5-Trihydroxy-1-cyclohexenecarboxylic acid;Illicium Verum P.E.;Shikimic acid methyl esther;ShikiMic acid, 98% 1GR;3,4,5-Trihydroxycyclohex-1-enecarboxylic acid;Shikimic acid,98%;ShikiMic acid API;ShikiMic acid (ShikiMate)
CAS:138-59-0
MF:C7H10O5
MW:174.15
EINECS:205-334-2
Product Categories:Inhibitors;Plant Extract;chemical reagent;pharmaceutical intermediate;phytochemical;reference standards from Chinese medicinal herbs (TCM).;standardized herbal extract;API;Antibiotic;Chiral Building Blocks;Simple Alcohols (Chiral);Synthetic Organic Chemistry;Natural Plant Extract;Chiral Reagents;API intermediates;138-59-0
Mol File:138-59-0.mol
Shikimic acid Structure
Shikimic acid Chemical Properties
Melting point 185-187 °C (lit.)
Boiling point 225.11°C (rough estimate)
alpha -180 º (c=4, H2O 25 ºC)
density 1.52 g/cm3 (27.2℃)
vapor pressure 0Pa at 25℃
refractive index -180 ° (C=1, H2O)
storage temp. 2-8°C
solubility 180g/l
form Powder
pkapK (14.1°) 5.19
color White to light beige or light gray
optical activity[α]/D -180.0±5.0°, c = 4 in H2O
Water Solubility 18 g/100 mL (20 ºC)
Sensitive Hygroscopic
Merck 14,8480
BRN 4782717
InChIKeyJXOHGGNKMLTUBP-HSUXUTPPSA-N
LogP-1.5 at 21℃ and pH1
Surface tension49.86mN/m at 1g/L and 20℃
CAS DataBase Reference138-59-0(CAS DataBase Reference)
NIST Chemistry ReferenceShikimic acid(138-59-0)
IARC3 (Vol. 40, Sup 7) 1987
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
RTECS GW4600000
3-10
HS Code 29181980
Hazardous Substances Data138-59-0(Hazardous Substances Data)
ToxicityLD5 i.p. in mice: 1000 mg/kg (Evans, Osman)
MSDS Information
ProviderLanguage
Shikimic acidEnglish
SigmaAldrichEnglish
ACROSEnglish
ALFAEnglish
Shikimic acid Usage And Synthesis
Chemical PropertiesWhite Solid
UsesShikimic 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.
UsesNaturally 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.
DefinitionChEBI: A cyclohexenecarboxylic acid that is cyclohex-1-ene-1-carboxylic acid substituted by hydroxy groups at positions 3, 4 and 5 (the 3R,4S,5R stereoisomer). It is an intermediate metabolite in plants and micro rganisms.
Biochem/physiol ActionsShikimic 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.
Shikimic acid Preparation Products And Raw materials
Preparation ProductsEthyl 3,4-O-isopropylideneshikiMate–>ShikiMic Acid Ethyl Ester–>CHORISMIC ACID–>1-cyclohexene-1-carboxylic acid-5-hydroxy-3,4-isopropylidine-dioxy

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