Salicylaldehyde

Salicylaldehyde

Salicylaldehyde

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10 Gram

Negotiable

  • Min.Order :10 Gram
  • Purity: 99%
  • Payment Terms : T/T,,MoneyGram,Other

Keywords

Salicylaldehyde 90-02-8,chemical research,C7H6O2

Quick Details

  • Appearance:Solid
  • Application:Orally active estrogenic steroid. It was the estrogen used in many of the first oral contraceptives
  • PackAge:in foil bag or customized
  • ProductionCapacity:10|Kilogram|Week
  • Storage:Refrigerator
  • Transportation:shipping by courier or by sea

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Details:

alicylaldehyde Chemical Properties
mp  1-2 °C(lit.)
bp  197 °C(lit.)
density  1.146 g/mL at 25 °C(lit.)
vapor density  4.2 (vs air)
vapor pressure  1 mm Hg ( 33 °C)
FEMA  3004
refractive index  n20/D 1.573(lit.)
Fp  170 °F
Water Solubility  slightly soluble
Sensitive  Air & Light Sensitive
Merck  14,8326
BRN  471388
Stability: Stable. Combustible. Incompatible with strong bases, strong reducing agents, strong acids, strong oxidizing agents.
CAS DataBase Reference 90-02-8(CAS DataBase Reference)
NIST Chemistry Reference Benzaldehyde, 2-hydroxy-(90-02-8)
EPA Substance Registry System Benzaldehyde, 2-hydroxy-(90-02-8)
 
Safety Information
Hazard Codes  Xn,N
Risk Statements  21/22-36/38-68-36/37/38-20/21/22-51-36-51/53-22
Safety Statements  26-36/37-36/37/39-36-61-64-29/35
RIDADR  3082
WGK Germany  2
RTECS  VN5250000
8-10-23
HazardClass  6.1(b)
PackingGroup  II
Hazardous Substances Data 90-02-8(Hazardous Substances Data)
 
 
Salicylaldehyde Usage And Synthesis
Chemical Properties colourless to yellow oily liquid with a bitter almond odour
General Description Liquid; colorless or pale yellow; bitter almond odor. Sinks and mixes slowly in water.
Reactivity Profile Salicylaldehyde is an aldehyde. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation.
Health Hazard LIQUID: Irritating to skin and eyes. Harmful if swallowed.
Fire Hazard Combustible. Can react with oxidizing materials.

 

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