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3,4-Dimethoxybenzoic acid - 99%, high purity , CAS No.93-07-2

1 Citations COA COA
    Grade & Purity:
  • ≥99%
In stock
Item Number
D102883
Grouped product items
SKU Size
Availability
 Price Qty
D102883-5g
5g
4
$9.90
D102883-25g
25g
3
$17.90
D102883-100g
100g
4
$61.90
D102883-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$122.90
Wish List
Bulk Order  SDS  DATASHEET  Specification Sheet


View related series
carboxylic acid (2098) COX (258) Glucose Metabolism (1943) Immunology/Inflammation (1929) Non heterocyclic block (8163)

Basic Description

Synonyms MLS002207141 | KBioGR_002164 | SMR000112092 | DTXSID6059077 | NSC7721 | NSC-7721 | STK397279 | Q425928 | MFCD00002500 | BRD-K14520048-001-04-2 | SDCCGMLS-0066972.P001 | Veratrylic acid | 3,4dimethoxy benzoic acid | 3,4-Dimethoxy benzoic acid | CCG-39276 |
Specifications & Purity ≥99%
Shipped In Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Benzenoids
Class Benzene and substituted derivatives
Subclass Benzoic acids and derivatives
Intermediate Tree Nodes Methoxybenzoic acids and derivatives
Direct Parent P-methoxybenzoic acids and derivatives
Alternative Parents M-methoxybenzoic acids and derivatives  Dimethoxybenzenes  Benzoic acids  Phenoxy compounds  Benzoyl derivatives  Anisoles  Alkyl aryl ethers  Monocarboxylic acids and derivatives  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic homomonocyclic compounds
Substituents P-methoxybenzoic acid or derivatives - M-methoxybenzoic acid or derivatives - O-dimethoxybenzene - Dimethoxybenzene - Benzoic acid - Phenoxy compound - Anisole - Methoxybenzene - Phenol ether - Benzoyl - Alkyl aryl ether - Carboxylic acid derivative - Carboxylic acid - Ether - Monocarboxylic acid or derivatives - Organooxygen compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aromatic homomonocyclic compound
Description This compound belongs to the class of organic compounds known as p-methoxybenzoic acids and derivatives. These are benzoic acids in which the hydrogen atom at position 4 of the benzene ring is replaced by a methoxy group.
External Descriptors benzoic acids

Associated Targets(Human)

CA14 Tclin Carbonic anhydrase 14 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TYR Tclin Tyrosinase (717 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA6 Tclin Carbonic anhydrase VI (993 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA1 Tclin Carbonic anhydrase I (13240 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA14 Tclin Carbonic anhydrase XIV (1305 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA12 Tclin Carbonic anhydrase XII (6231 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TPMT Tchem Thiopurine S-methyltransferase (45 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA9 Tclin Carbonic anhydrase IX (8255 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
HepG2 (196354 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Ca7 Carbonic anhydrase VII (3 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CA4 Carbonic anhydrase IV (1713 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Escherichia coli (133304 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Aspergillus niger (16508 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Candida albicans (78123 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PPO Polyphenol oxidase (10 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Heterodera zeae (651 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Hylobius abietis (106 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 488180303
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488180303
IUPAC Name 3,4-dimethoxybenzoic acid
INCHI InChI=1S/C9H10O4/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3,(H,10,11)
InChIKey DAUAQNGYDSHRET-UHFFFAOYSA-N
Smiles COC1=C(C=C(C=C1)C(=O)O)OC
Isomeric SMILES COC1=C(C=C(C=C1)C(=O)O)OC
WGK Germany 3
RTECS DG8598750
Molecular Weight 182.17
Beilstein 518285
Reaxy-Rn 518285
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=518285&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

8 results found

Lot Number Certificate Type Date Item
F2101116 Certificate of Analysis Mar 04, 2025 D102883
F2101117 Certificate of Analysis Mar 04, 2025 D102883
E2509220 Certificate of Analysis Jul 15, 2024 D102883
E2509221 Certificate of Analysis Jul 15, 2024 D102883
B2317146 Certificate of Analysis Dec 08, 2021 D102883
B2317151 Certificate of Analysis Dec 08, 2021 D102883
B2317129 Certificate of Analysis Dec 08, 2021 D102883
H2315303 Certificate of Analysis Dec 08, 2021 D102883

Chemical and Physical Properties

Solubility Soluble in water (0.5 mg/ml at 15°C), chloroform, methanol, and 95% ethanol (50 mg/ml).
Sensitivity Moisture sensitive.
Melt Point(°C) 180-181°C
Molecular Weight 182.170 g/mol
XLogP3 1.600
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 3
Exact Mass 182.058 Da
Monoisotopic Mass 182.058 Da
Topological Polar Surface Area 55.800 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 180.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Haichuan Zhang, Yang Liu, Shiyu Fu, Yulin Deng.  (2021)  Selective hydrodeoxygenation of lignin model compound (3,4-dimethoxybenzyl alcohol) by Pd/CNX catalyst.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,  169  (274). 

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