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3,5-Dimethoxybenzoic acid

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3,5-Dimethoxybenzoic acid Basic information

Product Name:
3,5-Dimethoxybenzoic acid
Synonyms:
  • 3,5-DIMETHOXYBENZOIC ACID
  • AKOS 227-39
  • AKOS BBS-00007826
  • AURORA 8636
  • OTAVA-BB BB7013191651
  • RARECHEM AL BO 0044
  • TIMTEC-BB SBB007798
  • 3,5-dimethoxy-benzoicaci
CAS:
1132-21-4
MF:
C9H10O4
MW:
182.17
EINECS:
214-473-8
Product Categories:
  • FINE Chemical & INTERMEDIATES
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
  • Organic acids
  • Building Blocks for Dendrimers
  • Functional Materials
  • C9
  • Carbonyl Compounds
  • Carboxylic Acids
  • bc0001
Mol File:
1132-21-4.mol
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3,5-Dimethoxybenzoic acid Chemical Properties

Melting point:
178-180 °C (lit.)
Boiling point:
275.56°C (rough estimate)
Density 
1.2481 (rough estimate)
refractive index 
1.4500 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
almost transparency in hot Methanol
pka
3.96±0.10(Predicted)
form 
Crystalline Powder
color 
Almost white to light beige-pink
BRN 
511834
InChIKey
IWPZKOJSYQZABD-UHFFFAOYSA-N
LogP
2.190
CAS DataBase Reference
1132-21-4(CAS DataBase Reference)
NIST Chemistry Reference
3,5-Dimethoxybenzoic acid(1132-21-4)
EPA Substance Registry System
Benzoic acid, 3,5-dimethoxy- (1132-21-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29189090

MSDS

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3,5-Dimethoxybenzoic acid Usage And Synthesis

Chemical Properties

almost white to light beige-pink cryst. powder

Uses

3,5-Dimethoxybenzoic acid (3,5-DmeoxBA) can be used as a reactant for the synthesis of:

  • 5,7-Dimethoxy-3,4-diphenylisocoumarin by coupling with diphenylacetylene.
  • Biotin dimedone, a reagent used in the study of protein sulfenation.

It can also be used as a ligand to synthesize lanthanide complexes [Ln(3,5-DmeoxBA)3(phen)]2; where phen is 1,10-phenanthroline.

Definition

ChEBI: 3,5-dimethoxybenzoic acid is a methoxybenzoic acid that is benzoic acid which is substituted by methoxy groups at positions 3 and 5. It has a role as a plant metabolite. It is a conjugate acid of a 3,5-dimethoxybenzoate.

Purification Methods

Crystallise the acid from water, EtOH or aqueous acetic acid and dry it in a vacuum. [Beilstein 10 H 405, 10 I 195, 10 III 1446, 10 IV 1501.]

3,5-Dimethoxybenzoic acid Preparation Products And Raw materials

Preparation Products

Raw materials

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