Basic information Application Safety Supplier Related

3,4-DIETHOXYBENZALDEHYDE

Basic information Application Safety Supplier Related

3,4-DIETHOXYBENZALDEHYDE Basic information

Product Name:
3,4-DIETHOXYBENZALDEHYDE
Synonyms:
  • AKOS B000267
  • (diaminophosphorylthio)methane
  • 3,4-DIETHOXYBENZALDEHYDE
  • ASISCHEM R43189
  • OTAVA-BB BB7020401740
  • 3,4-diethoxy-benzaldehyd
  • Benzaldehyde, 3,4-diethoxy-
  • 3,4-DIETHOXYBENZALDE
CAS:
2029-94-9
MF:
C11H14O3
MW:
194.23
EINECS:
217-979-7
Product Categories:
  • Aldehydes
  • C10 to C21
  • Aromatic Aldehydes & Derivatives (substituted)
  • BenzaldehydeDerivative
  • Carbonyl Compounds
Mol File:
2029-94-9.mol
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3,4-DIETHOXYBENZALDEHYDE Chemical Properties

Melting point:
22°C
Boiling point:
293-294 °C (lit.)
Density 
1.097 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5570(lit.)
Flash point:
225 °F
storage temp. 
2-8°C, stored under nitrogen
form 
powder to lump to clear liquid
color 
White or Colorless to Light yellow
Cosmetics Ingredients Functions
PERFUMING
InChI
1S/C11H14O3/c1-3-13-10-6-5-9(8-12)7-11(10)14-4-2/h5-8H,3-4H2,1-2H3
InChIKey
SSTRYEXQYQGGAS-UHFFFAOYSA-N
SMILES
[H]C(=O)c1ccc(OCC)c(OCC)c1
LogP
2.385 (est)
CAS DataBase Reference
2029-94-9(CAS DataBase Reference)
EPA Substance Registry System
Benzaldehyde, 3,4-diethoxy- (2029-94-9)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
23-24/25
WGK Germany 
2
TSCA 
TSCA listed
HazardClass 
IRRITANT
HS Code 
29124990
Storage Class
10 - Combustible liquids

MSDS

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3,4-DIETHOXYBENZALDEHYDE Usage And Synthesis

Application

3,4-Diethoxybenzaldehyde is an important organic synthesis intermediate, mainly used in the production of fragrances, dyes, pharmaceuticals, and fluorescent whitening agents.

Synthesis

3,4-dihydroxybenzaldehyde aniline synthesis of 3,4-diethoxybenzaldehyde as an example: in a 50mL three-port round bottom flask, add 15.0mL toluene, 3g aldehyde aniline Schiff base (0.015mol), 5mL (7.3g, 0.067mol) of bromoethane and tert-butanol potassium 1.68g (0.015mol), add magnetic stirrer. Argon protection, reflux and stirring oil bath heating to 80 C, the reaction 12 h. After the reaction, cooling reaction solution, filtration to remove potassium tert-butanol, the solution was added 10 mL of distilled water, 10 mL of ethyl acetate, and fully shaken. The organic phase was separated, and the aqueous phase was extracted with 5mL of ethyl acetate for 3 times, the organic phase was combined and dried with anhydrous sodium sulfate. The organic solvent was removed by rotary evaporation, and the mixed solvent of ethyl acetate and petroleum ether was used as the eluent, by changing the polarity gradient of the solvent, thin-layer plate detection, and column chromatography yielded 1.63g of colorless liquid 3,4-diethoxybenzaldehyde in 72% yield.

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