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3,4,5-Trimethoxybenzyl alcohol

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3,4,5-Trimethoxybenzyl alcohol Basic information

Product Name:
3,4,5-Trimethoxybenzyl alcohol
Synonyms:
  • Benzyl alcohol, 3,4,5-trimethoxy-
  • 3,4,5-TRIMETHOXYBENZYL ALCOHOL
  • (3,4,5-TRIMETHOXYPHENYL)METHANOL
  • RARECHEM AL BD 0063
  • 3,4,5-Trimethoxybenzyl alcohol, 97+%
  • 3,4,5-Trimethyxybencylalcohol
  • 3,4,5-Trimethoxybenzyl alcohol 97%
  • 3,4,5-TRIMETHOXYBENZENEMETHANOL
CAS:
3840-31-1
MF:
C10H14O4
MW:
198.22
EINECS:
223-331-4
Product Categories:
  • Building Blocks
  • C9 to C10
  • fine chemicals, specialty chemicals, intermediates, electronic chemical, organic synthesis
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C9 to C30
  • Oxygen Compounds
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
3840-31-1.mol
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3,4,5-Trimethoxybenzyl alcohol Chemical Properties

Melting point:
3°C
Boiling point:
228 °C25 mm Hg(lit.)
Density 
1.233 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.543(lit.)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform, Dichloromethane, Ethanol, Ethyl Acetate
form 
Oil
pka
13.99±0.10(Predicted)
color 
Yellow
Specific Gravity
1.20
BRN 
2104523
InChI
1S/C10H14O4/c1-12-8-4-7(6-11)5-9(13-2)10(8)14-3/h4-5,11H,6H2,1-3H3
InChIKey
QPHLRCUCFDXGLY-UHFFFAOYSA-N
SMILES
COc1cc(CO)cc(OC)c1OC
CAS DataBase Reference
3840-31-1(CAS DataBase Reference)
NIST Chemistry Reference
Benzenemethanol, 3,4,5-trimethoxy-(3840-31-1)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
23-24/25
WGK Germany 
3
HS Code 
2909.30.6000
HazardClass 
IRRITANT
Storage Class
10 - Combustible liquids

MSDS

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3,4,5-Trimethoxybenzyl alcohol Usage And Synthesis

Chemical Properties

clear colorless to light brown viscous liquid

Uses

Present in the leaves of Acer truncatum.

Synthesis Reference(s)

Tetrahedron Letters, 33, p. 5417, 1992 DOI: 10.1016/S0040-4039(00)79109-X

Synthesis

3,4,5-Trimethoxybenzaldehyde 2.729 g and sodium borohydride 0.459 g were dissolved in methanol 20 ml, the reaction was stirred at room temperature for 30 min, adjusted to pH with dilute hydrochloric acid, and extracted with chloroform (10 ml ?? 2). 8~9, extracted with chloroform (10 ml??2), the organic phases were combined and washed with water (10 ml??2), dried with anhydrous magnesium sulfate and filtered, the filtrate was evaporated to remove the solvent, to obtain oily 3,4,5-trimethoxybenzylalcohol 2.61 g, the yield was 95%.

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