Shikimic acid

Shikimic acid

Shikimic acid

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1 Gram

FOB Price: USD 100.0000

  • Min.Order :1 Gram
  • Purity: 99
  • Payment Terms : L/C,T/T,

Keywords

Shikimic acid Shikimic acid ,C7H10O5 138-59-0,chemical

Quick Details

  • Appearance:powder
  • Application:Pharmaceutical Intermediates
  • PackAge:bag
  • ProductionCapacity:100|Metric Ton|Month
  • Storage:dry
  • Transportation: by air

Superiority:

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

 

Details:

 
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)
 
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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