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2,3,4-Trihydroxybenzaldehyde - 98%, high purity , CAS No.2144-08-3

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2,3,4-Trihydroxybenzaldehyde - 98%, high purity , CAS No.2144-08-3

8 Citations

COA

Grade & Purity:

≥98%

Cas Number: 2144-08-3
Molecular Weight: 154.12
Beilstein Registry Number: 2328658
EC Number: 218-404-2
MDL number: MFCD00003325
PubChem CID: 75064
PubChem SID: 488185024

In stock

Item Number

T107278

Grouped product items
SKU	Size	Availability	Price
T107278-1g	1g	5	$9.90
T107278-5g	5g	6	$25.90
T107278-25g	25g	6	$76.90
T107278-100g	100g	7	$277.90
T107278-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$1,246.90

View related series

aldehyde (388) Non heterocyclic block (8163)

Basic Description

Synonyms	DTXCID0031473 \| 2,3,4-trihydroxy benzaldehyde \| 2,4-Trihydroxybenzaldehyde \| Benzaldehyde,3,4-trihydroxy- \| Tox21_113928 \| EN300-21495 \| Pyrogallol-4-carboxaldehyde \| SY037740 \| 4-(2-Hydroxyethyl)piperazine-1-ethanesulfonic acid \| Isothiocyanic acid, (4-p
Specifications & Purity	≥98%
Storage Temp	Argon charged
Shipped In	Normal
Product Description	Antimicrobial activity of carbohydrazone derived from 2,3,4-trihydroxybenzaldehyde against bacteria and fungi has been investigated. 2,3,4-trihydroxybenzaldehyde forms Schiff bases via [1+1] condensation with anthranilic acid Application 2,3,4-Trihydroxybenzaldehyde has been used in the preparation of 1,5-dimethyl-2-phenyl-4-[(1E)-(2,3,4-trihydroxybenzylidene)amino]-1H-pyrazol-3(2H)-one

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenols
    - Subclass Benzenetriols and derivatives
      - Level5 Pyrogallols and derivatives
        Level6 5-unsubstituted pyrrogallols

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenols
Subclass	Benzenetriols and derivatives
Intermediate Tree Nodes	Pyrogallols and derivatives
Direct Parent	5-unsubstituted pyrrogallols
Alternative Parents	Hydroxybenzaldehydes Benzoyl derivatives 1-hydroxy-4-unsubstituted benzenoids 1-hydroxy-2-unsubstituted benzenoids Vinylogous acids Polyols Organic oxides Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	5-unsubstituted pyrrogallol - Hydroxybenzaldehyde - Benzaldehyde - Benzoyl - 1-hydroxy-4-unsubstituted benzenoid - 1-hydroxy-2-unsubstituted benzenoid - Aryl-aldehyde - Monocyclic benzene moiety - Vinylogous acid - Polyol - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Aldehyde - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as 5-unsubstituted pyrrogallols. These are pyrrogallols that are unsubstituted at th5-position of the benzene ring.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(non-human)

Vibrio harveyi (399 Activities)

Explore this target

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	488185024
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488185024
IUPAC Name	2,3,4-trihydroxybenzaldehyde
INCHI	InChI=1S/C7H6O4/c8-3-4-1-2-5(9)7(11)6(4)10/h1-3,9-11H
InChIKey	CRPNQSVBEWWHIJ-UHFFFAOYSA-N
Smiles	C1=CC(=C(C(=C1C=O)O)O)O
Isomeric SMILES	C1=CC(=C(C(=C1C=O)O)O)O
WGK Germany	2
RTECS	CU8439800
PubChem CID	75064
Molecular Weight	154.12
Beilstein	2328658
Reaxy-Rn	2328658

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.

22 results found

Lot Number	Certificate Type	Date	Item
A2330502	Certificate of Analysis	Apr 18, 2025	T107278
L2216486	Certificate of Analysis	Apr 17, 2025	T107278
L2216480	Certificate of Analysis	Mar 10, 2025	T107278
L2216517	Certificate of Analysis	Feb 17, 2025	T107278
B2317194	Certificate of Analysis	Nov 04, 2024	T107278
L2216483	Certificate of Analysis	Sep 19, 2024	T107278
L2216579	Certificate of Analysis	Sep 19, 2024	T107278
L2216388	Certificate of Analysis	Sep 19, 2024	T107278
L2216487	Certificate of Analysis	Sep 19, 2024	T107278
L2216478	Certificate of Analysis	Sep 19, 2024	T107278
H2415367	Certificate of Analysis	Jun 17, 2024	T107278
H2415368	Certificate of Analysis	Jun 17, 2024	T107278
H2415369	Certificate of Analysis	Jun 17, 2024	T107278
F2222159	Certificate of Analysis	Mar 21, 2024	T107278
F2222158	Certificate of Analysis	Mar 21, 2024	T107278
F2222160	Certificate of Analysis	Mar 21, 2024	T107278
B1807134	Certificate of Analysis	Jun 05, 2023	T107278
B1807123	Certificate of Analysis	Jun 05, 2023	T107278
B2317195	Certificate of Analysis	Feb 27, 2023	T107278
L2216485	Certificate of Analysis	Nov 18, 2022	T107278
H2422115	Certificate of Analysis	Nov 18, 2022	T107278
C1911187	Certificate of Analysis	Oct 19, 2022	T107278

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Chemical and Physical Properties

Solubility	Soluble in Methanol
Sensitivity	Air Sensitive
Melt Point(°C)	159-161°C
Molecular Weight	154.120 g/mol
XLogP3	0.900
Hydrogen Bond Donor Count	3
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	1
Exact Mass	154.027 Da
Monoisotopic Mass	154.027 Da
Topological Polar Surface Area	77.800 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	147.000
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

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