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Shikimic acid

CAS No.
138-59-0
Chemical Name:
Shikimic acid
Synonyms
Shikimate;sikimic acid;(-)-SHIKIMIC ACID;Skikimic acid;L-SHIKIMIC ACID;Kava root extract;(3R,4S,5R)-3,4,5-TRIHYDROXY-1-CYCLOHEXENECARBOXYLIC ACID;(3R,4S,5R)-3,4,5-TRIHYDROXY-CYCLOHEX-1-ENECARBOXYLIC ACID;Shikimic;NSC 59257
CBNumber:
CB2293550
Molecular Formula:
C7H10O5
Molecular Weight:
174.15
MDL Number:
MFCD00066278
MOL File:
138-59-0.mol
MSDS File:
SDS
Last updated:2024-04-07 12:04:01

Shikimic acid 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
pka pK (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
InChIKey JXOHGGNKMLTUBP-HSUXUTPPSA-N
LogP -1.5 at 21℃ and pH1
Surface tension 49.86mN/m at 1g/L and 20℃
CAS DataBase Reference 138-59-0(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 29MS2WI2NU
NIST Chemistry Reference Shikimic acid(138-59-0)
IARC 3 (Vol. 40, Sup 7) 1987

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS05
Signal word  Danger
Hazard statements  H318
Precautionary statements  P280-P305+P351+P338
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
Toxicity LD5 i.p. in mice: 1000 mg/kg (Evans, Osman)
NFPA 704
1
0 1

Shikimic acid price More Price(54)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich S5375 Shikimic acid ≥99% 138-59-0 1g $158 2024-03-01 Buy
Sigma-Aldrich 8.24476 (-)-Shikimic acid for synthesis 138-59-0 250mg $29.76 2024-03-01 Buy
Sigma-Aldrich 8.24476 (-)-Shikimic acid for synthesis 138-59-0 1g $175 2024-03-01 Buy
Sigma-Aldrich 69686 Shikimic acid analytical standard 138-59-0 50mg $147 2024-03-01 Buy
TCI Chemical S0038 Shikimic Acid >97.0%(T) 138-59-0 100mg $23 2024-03-01 Buy
Product number Packaging Price Buy
S5375 1g $158 Buy
8.24476 250mg $29.76 Buy
8.24476 1g $175 Buy
69686 50mg $147 Buy
S0038 100mg $23 Buy

Shikimic acid Chemical Properties,Uses,Production

Description

Shikimic acid (3,4,5-trihydroxy-1-cyclohexene-1-carboxylic acid) is a natural organic compound. Plant and microbial sources are the only sources of this compound. The isolation of shikimic acid from the fruit of Illicium religiosum was primarily reported by Ekmann in 1885. The name shikimic acid was derived from the oriental plant shikimi-no-ki in Japanese. It is now available in more quantities through the extraction from the fruit Illicium verum (Chinese star anise). This compound is generally utilized as a starting material for the industrial synthesis of the antiviral oseltamivir, a drug against the H1N1 influenza virus. It is also an essential intermediate in the biosynthesis of lignin, aromatic amino acids (phenylalanine, tyrosine, and tryptophan), and most alkaloids of plants and microorganisms[1]. The neuraminidase inhibitors oseltamivir or Tamiflu derived from the shikimic acid pathway are potent influenza viral neuraminidase inhibitors against most influenza strains ( influenza A and B infections). The mode of application is by mouth, either in the form of a pill or liquid.

Chemical Properties

White Solid

Uses

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.

Uses

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.

Definition

ChEBI: 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 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.

References

[1] Priyanka Singh. “Shikimic acid as intermediary model for the production of drugs effective against influenza virus.” Phytochemicals as Lead Compounds for New Drug Discovery 14 1 (2020): 245–256.

88400-31-1
138-59-0
Synthesis of Shikimic acid from 1,3-Benzodioxole-5-carboxylic acid, 3a,6,7,7a-tetrahydro-7-hydroxy-2-methoxy-2-methyl-, methyl ester
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View Lastest Price from Shikimic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
shikimic acid pictures 2024-04-23 shikimic acid
138-59-0
US $0.00-0.00 / kg 1kg 98% 1000kg Changsha Staherb Natural Ingredients Co., Ltd.
Puer Natural Shikimic Acid pictures 2024-04-23 Puer Natural Shikimic Acid
138-59-0
US $10.00 / kg 1kg 98.0% Shikimic Acid Test by HPLC 10000 Changsha Staherb Natural Ingredients Co., Ltd.
shikimic acid pictures 2024-04-22 shikimic acid
138-59-0
US $160.00 / KG 1KG 99% 1000kg Hebei Yime New Material Technology Co., Ltd.
  • shikimic acid pictures
  • shikimic acid
    138-59-0
  • US $0.00-0.00 / kg
  • 98%
  • Changsha Staherb Natural Ingredients Co., Ltd.
  • shikimic acid pictures
  • shikimic acid
    138-59-0
  • US $160.00 / KG
  • 99%
  • Hebei Yime New Material Technology Co., Ltd.
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) ShikiMic acid SynonyMs: 3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid (3R,4S,5R)-3,4,5-trihydroxycyclohex-1-ene-1-carboxylic 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) SHIKIMIC ACID 1-Cyclohexene-1-carboxylic acid, 3,4,5-trihydroxy- 1-Cyclohexene-1-carboxylic acid, 3,4,5-trihydroxy-, [3R-(3alpha,4alpha,5beta)]- Bracken fern toxic component Kava Kava Extract 3,4,5-Trihydroxy-1-Cyclohexene-1-Carboxylic Acid (Shikimic acid) Shikimic (3R,4S,5R)-3,4,5-trihydroxycyclohexene-1-carboxylic acid SHIKIMIC ACID 98% SHIKIMIC ACID(RG) 3,4,5-TRIHYDROXY-1-CYCLOHEXENE-1-CARBOXYLIC ACID Shikimik Acid (3R,4S,5R)-3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic Acid NSC 59257 )-3,4,5-Trihydroxy-1-cyclohexenecarboxylic acid 3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic Acid (-)-Shikimic acid for synthesis Shikimic Scid Shikimic Acid > Oseltamivir Impurity 93 (-)-Shikimicacid Shikimic acid USP/EP/BP Shikimic Acid / Shikimicacid ShikiShikimic acidmic acid Puer Natural Shikimic Acid L-SHIKIMIC ACID (3R,4S,5R)-3,4,5-TRIHYDROXY-CYCLOHEX-1-ENECARBOXYLIC ACID (-)-SHIKIMIC ACID Shikimate Skikimic acid sikimic acid Kava root extract (3R,4S,5R)-3,4,5-TRIHYDROXY-1-CYCLOHEXENECARBOXYLIC ACID 138-59-0 C7H9O5 Biosynthetic precursor of aromatic amino acids, as well as many alkaloids and other aromatic metabolites. Organic Building Blocks Metabolomics Metabolic Libraries Simple Alcohols (Chiral) Chiral Building Blocks Amino Acid Library BioChemical Carboxylic Acids Asymmetric Synthesis