1H-2-Benzoxacyclote...

1H-2-Benzoxacyclotetradecin-1,7(8H)-dione,3,4,5,6,9,10-hexahydro-14,16-dihydroxy-3-methyl-, (3S,11E)-

1H-2-Benzoxacyclotetradecin-1,7(8H)-dione,3,4,5,6,9,10-hexahydro-14,16-dihydroxy-3-methyl-, (3S,11E)-

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1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T,,MoneyGram,Other

Keywords

1H-2-Benzoxacyclotetradecin-1,7(8H)-dione,3,4,5,6,9,10-hexahydro-14,16-dihydroxy-3-methyl-, (3S,11E)- price 1H-2-Benzoxacyclotetradecin-1,7(8H)-dione,3,4,5,6,9,10-hexahydro-14,16-dihydroxy-3-methyl-, (3S,11E)- CAS 17924-92-4 1H-2-Benzoxacyclotetradecin-1,7(8H)-dione,3,4,5,6,9,10-hexahydro-14,16-dihydroxy-3-methyl-, (3S,11E)- supplier in China

Quick Details

  • Appearance: white powder
  • Application:Used as Pharmaceutical Intermediates
  • PackAge:5g/tin;250k/tin;1kg/tin
  • ProductionCapacity:150|Kilogram|Month
  • Storage: keep away from heat,sparks and flames
  • Transportation:by air or by courier

Superiority:

Superior quality, moderate price & quick delivery.

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Zearalenone Chemical Properties
mp  164-165°C
Fp  6 °C
storage temp.  −20°C
Merck  13,10169
CAS DataBase Reference 17924-92-4(CAS DataBase Reference)
EPA Substance Registry System 1H-2-Benzoxacyclotetradecin- 1,7(8H)-dione, 3,4,5,6,9,10-hexahydro-14, 16-dihydroxy-3-methyl-, (3S,11E)-(17924-92-4)
 
Safety Information
Hazard Codes  C,Xn,F
Risk Statements  34-62-63-36-20/21/22-11
Safety Statements  26-36/37/39-45-36-16-36/37
RIDADR  UN 3261 8/PG 2
WGK Germany  3
RTECS  DM2550000
10
Hazardous Substances Data 17924-92-4(Hazardous Substances Data)
 
Zearalenone Usage And Synthesis
Chemical Properties Crystalline Solid
Usage Estrogenic mycotoxin produced by Fusarium fungi commonly found in grains. One of a group of compounds known as resorcylic acid lactones
Usage Zearalenone is a resorcylic acid lactone produced by a number of Fusarium sp.. Zearalenone acts as a non-steroidal estrogen, binding to estrogen receptor and is uterotropic. Zearalenone induces reproductive problems in animals and, in some animal models, is thought to be a primary initiator of hepatic tumours. In vivo, zearalenone undergoes metabolic reduction to the more estrogenic zearalenol. Contamination of grains, notably maize, by Fusarium species gives rise to high levels of zearalenone and is regarded as an important food quality issue for both humans and animal health.
General Description White microcrystals or white powder.
Air & Water Reactions Zearalenone may be sensitive to prolonged exposure to air. Insoluble in water.
Reactivity Profile Zearalenone is an ester. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Zearalenone may be incompatible with alkalis.
Fire Hazard Flash point data for Zearalenone are not available. Zearalenone is probably combustible.

 

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