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2,4,6-Trihydroxybenzaldehyde - >98.0%(HPLC), high purity , CAS No.487-70-7

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2,4,6-Trihydroxybenzaldehyde - >98.0%(HPLC), high purity , CAS No.487-70-7

1 Citations

COA

Grade & Purity:

≥98%(HPLC)

Cas Number: 487-70-7
Molecular Weight: 154.12
Beilstein Registry Number: 2254430
MDL number: MFCD00003329
PubChem CID: 68099
PubChem SID: 488184084

In stock

Item Number

T161492

Grouped product items
SKU	Size	Availability	Price
T161492-1g	1g	3	$30.90
T161492-5g	5g	3	$80.90
T161492-10g	10g	9	$144.90
T161492-25g	25g	2	$294.90
T161492-100g	100g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$1,060.90

View related series

aldehyde (388) NF-κB (747) Non heterocyclic block (8163)

Basic Description

Synonyms	SY047039 \| 2,4,6-Trihydroxybenzaldehyde \| 2,4,6-trihydroxy-benzaldehyde \| NSC38610 \| NSC-38610 \| AKOS015899852 \| Benzaldehyde,4,6-trihydroxy- \| EN300-177718 \| T1744 \| UNII-I70C45KRO9 \| EINECS 207-663-7 \| FT-0609876 \| Formylphloroglucinal \| Formylphloroglu
Specifications & Purity	≥98%(HPLC)
Storage Temp	Argon charged
Shipped In	Normal
Product Description	Reactant involved in the synthesis of biologically active molecules including: . 2,4,6-trichlorophenyl hydrazones with potential inhibition of protein glycation . Esculentoside A derivatives with haemolytic activity and LPS-induced nitric oxide production inhibition . α-Nucleophiles for hydrolysis of organophosphorus nerve agents . Xanthine oxidase inhibitors . Non-complexes Schiff base hydrazones . Methylated (±)-epigallocatechin gallate library for anticancer activity studies

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Phenols
    - Subclass Benzenetriols and derivatives
      - Level5 Phloroglucinols and derivatives
        Level6 Acylphloroglucinols and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Phenols
Subclass	Benzenetriols and derivatives
Intermediate Tree Nodes	Phloroglucinols and derivatives
Direct Parent	Acylphloroglucinols and derivatives
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	Acylphloroglucinol derivative - 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 oxygen compound - Organic oxide - Aldehyde - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as acylphloroglucinols and derivatives. These are phloroglucinol derivatives characterized by the presence of a COR group.
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(Human)

APP Tclin Amyloid-beta A4 protein (8510 Activities)

Discover Target: APP

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR1H3 Tchem LXR-alpha (2891 Activities)

Discover Target: NR1H3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NR1H2 Tchem LXR-beta (3841 Activities)

Discover Target: NR1H2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Rattus norvegicus (775804 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	488184084
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488184084
IUPAC Name	2,4,6-trihydroxybenzaldehyde
INCHI	InChI=1S/C7H6O4/c8-3-5-6(10)1-4(9)2-7(5)11/h1-3,9-11H
InChIKey	BTQAJGSMXCDDAJ-UHFFFAOYSA-N
Smiles	C1=C(C=C(C(=C1O)C=O)O)O
Isomeric SMILES	C1=C(C=C(C(=C1O)C=O)O)O
WGK Germany	2
RTECS	CU8440000
PubChem CID	68099
Molecular Weight	154.12
Beilstein	2254430
Reaxy-Rn	2254429

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.

7 results found

Lot Number	Certificate Type	Date	Item
K2416052	Certificate of Analysis	Jul 01, 2024	T161492
K2416053	Certificate of Analysis	Jul 01, 2024	T161492
E2014120	Certificate of Analysis	Mar 14, 2024	T161492
E2308089	Certificate of Analysis	May 19, 2023	T161492
C2324896	Certificate of Analysis	Apr 07, 2023	T161492
D1922076	Certificate of Analysis	Feb 02, 2023	T161492
L2209291	Certificate of Analysis	Dec 13, 2022	T161492

Chemical and Physical Properties

Sensitivity	Air sensitive
Melt Point(°C)	196 °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	135.000
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. Yanfei Zhang, Yong Sun, Hua Zhang, Qiying Mai, Bing Zhang, Hongyan Li, Zeyuan Deng. (2020) The degradation rules of anthocyanins from eggplant peel and antioxidant capacity in fortified model food system during the thermal treatments. Food Bioscience, 38 (100701).

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