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Fast Delivery Cinnamaldehyde factory sells 104-55-2 Cinnamaldehyde
Fast Delivery Cinnamaldehyde factory sells 104-55-2 Cinnamaldehyde

Fast Delivery Cinnamaldehyde factory sells 104-55-2 Cinnamaldehyde

Min.Order / FOB Price:Get Latest Price

1 Kilogram

FOB Price:USD 11.0000 -12.0000

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

Keywords

Fast Delivery Cinnamaldehyde factory sells 104-55-2 Cinnamaldehyde factory Cinnamaldehyde

Quick Details

  • Appearance:slightly yellow liquid
  • Application:Cinnamaldehyde is one of the important pharmaceutical materials.
  • PackAge:210kg/drum,or according to the requirements of the customers
  • ProductionCapacity:2000|Metric Ton|Year
  • Storage:Keep undercool, dry and well ventilated warehouses, guard against fire
  • Transportation:by sea or by air

Superiority:

Fast Delivery Cinnamaldehyde factory sells 104-55-2 Cinnamaldehyde

Application field
 
Use1] It is used as a flavoring agent for making soap flavors and cakes and other foods
 
[Use 2] China's regulations can be used for fruit preservation, according to the production needs of appropriate use. It can also be used as an edible spice.
 
[Use3] It can be used as a preservative. According to the regulations of China, it can be used for the preservation of fruits. It should be used appropriately according to the production needs. It can also be used as an edible spice.
 
[Use 4] Spices; Antistaling agent. GB 2760 1:96 provides for the permitted use of edible spices. Mainly used in the preparation of cinnamon, cinnamon, Cola flavor, also used in alcohol and tobacco. Regulations can also be used for fruit preservation, dosage GMP; Residual amount ≤0.3 mg/kg.
 
[Use5] Solvent, flavoring, pharmaceutical raw material intermediate, essence and fragrance.
 
 
[English Name]
 
3-PHENYL-2-PROPENAL
 
3-PHENYLPROPENAL
 
AKOS B004060
 
AKOS BBS-00003207
 
CINNAMALDEHYDE
 
CINNAMALDEHYDE, TRANS-
 
CINNAMIC ALDEHYDE
 
FEMA 2286
 
LABOTEST-BB LT00939010
 
STYRONE
 
TRANS-3-PHENYL-2-PROPEN-1-AL
 
TRANS-3-PHENYL-2-PROPENAL
 
TRANS-ALPHA CINNAMALDEHYDE
 
TRANS-CINNAMAL
 
TRANS-CINNAMALDEHYDE
 
TRANS-CINNAMIC ALDEHYDE
 
TRANS-PHENYLACROLEIN
 
TRANS-PHENYLACRYLALDEHYDE
 
2-Propenal, 3-phenyl-
 
2-propenal,3-phenyl-

Details:

The preparation methods
 
[Method 1]
(1) Hydroxyl shrinkage. Benzaldehyde and acetaldehyde as raw materials. The cinnamaldehyde is formed by condensation under alkaline conditions. 133kg benzaldehyde, 400kg water, 10kg 40%-50% sodium hydroxide, 66.6kg acetaldehyde and 40-50kg benzene were added to the reaction pot successively, and stirred at 20℃ for 5h. At the end of the reaction, the benzene layer was stratified, then dilute acid and water until neutral. After recovery of benzene by vacuum distillation, the distillate at 130℃ (2.67Kpa) was collected to obtain 55-60kg cinnamaldehyde.
(2) Separation method of essential oil. Cinnamic oil and Ceylon oil contain about 55%-85% cinnamic aldehyde, which can be separated by sodium bisulfite addition method. The addition was separated by centrifugation, decomposed by dilute acid or alkali, distilled by steam and reduced pressure.
 
[Method 2]
Hydroxyaldehyde method
Cinnamaldehyde was synthesized from benzaldehyde and acetaldehyde under alkaline conditions. 133kg benzaldehyde, 400kg water, 10kg 40%-50% sodium hydroxide, 66.6kg acetaldehyde and 40-50kg benzene were added to the reaction pot successively, and stirred at 20℃ for 5h. At the end of the reaction, the benzene layer was stratified, then dilute acid and water until neutral. After recovery of benzene by vacuum distillation, the fraction of 130℃(2.67kPa) was collected to obtain 55~60kg cinnamaldehyde.
Single separation of essential oils
Cinnamic oil and Ceylon oil contain 55% ~ 85% cinnamic aldehyde which can be separated by sodium bisulfite addition method. The addition was separated by centrifugation, decomposed by dilute acid or alkali, distilled by steam and reduced pressure.
 
[Method 3]
By adding cinnamon oil or cinnamon oil with sodium bisulfite method, so that the adduct of cinnamaldehyde and sodium bisulfite with centrifugation method, washed with ether, and then with dilute alkali or acid solution decomposition, by water, and so on distillation and by vacuum distillation.
In the presence of sodium hydroxide, benzaldehyde and acetaldehyde were condensed together: benzaldehyde, acetaldehyde, water and sodium hydroxide solution were mixed and oscillated at room temperature for a week, and the oil was extracted by ether, dried by benzyl alcohol and distilled by vacuum.

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