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High purity ! 7400-08-0 C9H8O3 p-Hydroxy-cinnamic acid

CAS NO.7400-08-0

  • Min.Order: 1 Metric Ton
  • Payment Terms: L/C,T/T,Other
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  • 7400-08-0
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Quick Details

  • ProName: High purity ! 7400-08-0 C9H8O3 p-Hydr...
  • CasNo: 7400-08-0
  • Molecular Formula: C9H8O3
  • Appearance: white crystalline powder
  • Application: 7400-08-0
  • DeliveryTime: Within 7 working days since received y...
  • PackAge: 25kg/drum or 180kg/drum
  • Port: Any Chinese main ports
  • ProductionCapacity: 100 Metric Ton/Month
  • Purity: 98% purity
  • Storage: 2-8, cold storage, to avoid light stor...
  • Transportation: BY SEA /BY AIR /BY COURIER
  • LimitNum: 1 Metric Ton
  • Valid Period: 2years
  • function: Enhances The Effects of Injecta

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7400-08-0

Details

p-Hydroxy-cinnamic acid Basic information
Product Name: p-Hydroxy-cinnamic acid
Synonyms: LABOTEST-BB LT00452637;COUMARIC ACID, TRANS-P-;3-(4-HYDROXYPHENYL)ACRYLIC ACID;AKOS 221-47;AKOS BAR-2479;(2E)-3-(4-Hydroxyphenyl)-2-propenoic acid;3-(4-Hydroxyphenyl)-2-propenoic acid;3-(4-hydroxyphenyl)-2-propenoicaci
CAS: 7400-08-0
MF: C9H8O3
MW: 164.16
EINECS: 231-000-0
Product Categories: Cinnamic acid
Mol File: 7400-08-0.mol
p-Hydroxy-cinnamic acid Structure
 
p-Hydroxy-cinnamic acid Chemical Properties
mp  214 °C (dec.)(lit.)
storage temp.  -20°C
CAS DataBase Reference 7400-08-0(CAS DataBase Reference)
NIST Chemistry Reference 2-Propenoic acid, 3-(4-hydroxyphenyl)-(7400-08-0)
EPA Substance Registry System 2-Propenoic acid, 3-(4-hydroxyphenyl)-(7400-08-0)
 
Safety Information
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-36/37/39-22
WGK Germany  2
RTECS  GD9095000
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
 
p-Hydroxy-cinnamic acid Usage And Synthesis
Chemical Properties Light yellow to beige crystalline powder
Usage p-Coumaric Acid is the hydroxy derivative of Cinnamic Acid with antioxidant properties. p-Coumaric acid is a is a major component of lignocellulose. Studies suggest that p-Coumaric Acid may reduce the risk of cancer by reducing the formation of carcinogenic nitrosamines.

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