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2,5-Dihydroxybenzoic acid

CAS No.
490-79-9
Chemical Name:
2,5-Dihydroxybenzoic acid
Synonyms
GENTISIC ACID;DHB;Gentisate;Gentisic;2,5-Dhba;Phloretate;Gensigen;2,5-dihydroxybenzoic;2,5-Dihydroxybenzoes?ure;Kyselina 2,5-dihydroxybenzoova
CBNumber:
CB5853669
Molecular Formula:
C7H6O4
Molecular Weight:
154.12
MDL Number:
MFCD00002460
MOL File:
490-79-9.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-06-03 18:11:14
Product description Number Pack Size Price
2,5-Dihydroxybenzoic acid matrix substance for MALDI-MS, >99.0% (HPLC) 85707 10mg $23.4
2,5-Dihydroxybenzoic acid matrix substance for MALDI-MS, >99.0% (HPLC) 85707 250mg $311
2,5-Dihydroxybenzoic acid certified reference material, pharmaceutical secondary standard PHR3329 50MG $882
2,5-Dihydroxybenzoic acid matrix substance for MALDI-MS, >99.0% (HPLC) 85707 1g $1000
2,5-Dihydroxybenzoic acid 98% 149357 10g $50.2
More product size

2,5-Dihydroxybenzoic acid Properties

Melting point 204-208 °C(lit.)
Boiling point 237.46°C (rough estimate)
Density 1.3725 (rough estimate)
refractive index 1.6400 (estimate)
storage temp. Store below +30°C.
solubility It is soluble in alcohol and ether.
pka 2.97(at 25℃)
form Crystalline Powder
color White to light beige
PH 3.21(1 mM solution);2.56(10 mM solution);2.01(100 mM solution)
Water Solubility soluble
ε(extinction coefficient) >2000 at 337nm
Merck 14,4398
BRN 2209119
Cosmetics Ingredients Functions SKIN CONDITIONING
InChI 1S/C7H6O4/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,8-9H,(H,10,11)
InChIKey WXTMDXOMEHJXQO-UHFFFAOYSA-N
SMILES OC(=O)c1cc(O)ccc1O
LogP 1.740
CAS DataBase Reference 490-79-9(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII VP36V95O3T
NIST Chemistry Reference 2,5-Dihydroxybenzoic acid(490-79-9)
EPA Substance Registry System Benzoic acid, 2,5-dihydroxy- (490-79-9)
UNSPSC Code 77101502
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
RTECS  LY3850000
Hazard Note  Harmful
TSCA  TSCA listed
HS Code  29182990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
NFPA 704
1
2 0

2,5-Dihydroxybenzoic acid price More Price(126)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 85707 2,5-Dihydroxybenzoic acid matrix substance for MALDI-MS, >99.0% (HPLC) 490-79-9 10mg $23.4 2026-04-30 Buy
Sigma-Aldrich 85707 2,5-Dihydroxybenzoic acid matrix substance for MALDI-MS, >99.0% (HPLC) 490-79-9 250mg $311 2026-04-30 Buy
Sigma-Aldrich PHR3329 2,5-Dihydroxybenzoic acid certified reference material, pharmaceutical secondary standard 490-79-9 50MG $882 2026-04-30 Buy
Sigma-Aldrich 85707 2,5-Dihydroxybenzoic acid matrix substance for MALDI-MS, >99.0% (HPLC) 490-79-9 1g $1000 2026-04-30 Buy
Sigma-Aldrich 149357 2,5-Dihydroxybenzoic acid 98% 490-79-9 10g $50.2 2026-04-30 Buy
Product number Packaging Price Buy
85707 10mg $23.4 Buy
85707 250mg $311 Buy
PHR3329 50MG $882 Buy
85707 1g $1000 Buy
149357 10g $50.2 Buy

2,5-Dihydroxybenzoic acid Chemical Properties,Uses,Production

Description

Gentisic acid is a dihydroxy benzoic acid. It is a derivative of benzoic acid and a minor (1 %) product of the metabolic break down of aspirin, excreted by the kidneys.
It is also found in the African tree Alchornea cordifolia and in wine.

Description

Gentisic acid is a benzoic acid that has been found in Gentiana and an active metabolite of aspirin with diverse biological activities. It decreases radiation-induced production of thiobarbituric acid reactive substances (TBARS), hydrogen peroxide, and protein carbonyls, increases superoxide dismutase activity, and prevents hemolysis in isolated human erythrocytes when used at concentrations ranging from 5 to 100 μM. Gentisic acid (1-10 μM) inhibits LDL oxidation and formation of cholesterol ester hydroperoxides in isolated human plasma. It induces relaxation of isolated guinea pig trachea (EC50 = 20 μM), an effect that is reduced by the large-conductance calcium-activated potassium channel blocker charybdotoxin . Gentisic acid (10 and 100 mg/kg) reduces cardiac hypertrophy and fibrosis and pulmonary remodeling, suppresses the renin-angiotensin-aldosterone system, and inhibits cardiac dysfunction in a mouse model of transverse aortic constriction-induced cardiac hypertrophy. It also prevents cardiovascular collapse and lactic acidemia in a canine model of P. aeruginosa-induced septic shock.

Chemical Properties

White to light beige crystalline powder. 2,5-Dihydroxybenzoic Acid [490-79-9] (gentisic acid, 2,5-DHBA), C7H6O4, Mr 154.1, mp 205 C, is soluble in water and alcohols but insoluble in benzene and chloroform. The acid is stable in boiling water and gives a deep blue color with iron(III) chloride. Here, the acid decomposes to form p-benzoquinone [106-51-4] and carbon dioxide. 2–5-Dihydroxybenzoic acid is used as an antirheumatic drug and, more recently, as a color developer for thermal paper.

Uses

Medicine, as sodium gentisate (analgesic).

Uses

2,5-dihydroxybenzoic acid areused as intermediates for pharmaceuticals (especially for antipyetic anlgesic, antirheumatism) and other organic synthesis. They are used as matrix for ionization of peptides, proteins and carbohydrates. In industrial field, they areused as intermediates for the production of other organic chemicals, resins, polyesters, plasticizers, dyestuffs, preservatives, and rubber chemicals.

Definition

ChEBI: 2,5-dihydroxybenzoic acid is a dihydroxybenzoic acid having the two hydroxy groups at the 2- and 5-positions. It has a role as a MALDI matrix material, an EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor, a human metabolite, a fungal metabolite and a mouse metabolite. It is functionally related to a benzoic acid. It is a conjugate acid of a 2,5-dihydroxybenzoate.

Production Methods

Gentisic acid is produced by carboxylation of hydroquinone.
C6H4(OH)2 + CO2 → C6H3(CO2H)(OH)2
This conversion is an example of a Kolbe–Schmitt reaction.

Application

As a hydroquinone , gentisic acid is readily oxidized and is used as an antioxidant excipient in some pharmaceutical preparations. In the laboratory, it is used as a sample matrix in matrix-assisted laser desorption/ionization (MALDI) mass spectrometry , and has been shown to conveniently detect peptides incorporating the boronic acid moiety by MALDI .

Synthesis Reference(s)

Journal of the American Chemical Society, 72, p. 3292, 1950 DOI: 10.1021/ja01163a521

General Description

Aspirin metabolite.

Safety Profile

Poison bp intravenous route. Moderately toxic by ingestion and intraperitoneal routes. Experimental teratogenic and reproductive effects. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes.

Purification Methods

Crystallise gentisic acid from hot water or *benzene/acetone. Dry it in a vacuum desiccator over silica gel. [Beilstein 10 H 384, 10 IV 1441.]

References

[1] RAVI JOSHI. Antioxidant activity and free radical scavenging reactions of gentisic acid: in-vitro and pulse radiolysis studies.[J]. Free Radical Research, 2012, 46 1: 11-20. DOI: 10.3109/10715762.2011.633518
[2] KEIKO ASHIDATE . Gentisic acid, an aspirin metabolite, inhibits oxidation of low-density lipoprotein and the formation of cholesterol ester hydroperoxides in human plasma[J]. European journal of pharmacology, 2005, 513 3: Pages 173-179. DOI: 10.1016/j.ejphar.2005.03.012
[3] J. F. CUNHA. The mechanism of gentisic acid-induced relaxation of the guinea pig isolated trachea: the role of potassium channels and vasoactive intestinal peptide receptors.[J]. Brazilian Journal of Medical and Biological Research, 2001, 4 1: 381-388. DOI: 10.1590/s0100-879x2001000300013
[4] SIMEI SUN. Gentisic acid prevents the transition from pressure overload-induced cardiac hypertrophy to heart failure.[J]. Scientific Reports, 2019: 3018. DOI: 10.1038/s41598-019-39423-8
[5] STEVEN MINK. Gentisic acid sodium salt, a phenolic compound, is superior to norepinephrine in reversing cardiovascular collapse, hepatic mitochondrial dysfunction and lactic acidemia in Pseudomonas aeruginosa septic shock in dogs.[J]. Intensive Care Medicine Experimental, 2016, 4 1: 24. DOI: 10.1186/s40635-016-0095-0

2,5-Dihydroxybenzoic acid Preparation Products And Raw materials

Global( 634)Suppliers
Supplier Tel Email Country ProdList Advantage
Shandong Vital Biotechnology Co., Ltd.
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Henan Tianfu Chemical Co.,Ltd.
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Related Qustion

Ask a question
Q:What is the connection between 2,5-dihydroxybenzoic acid and salicylic acid?STAR - Dec 3,2025
A:2,5-Dihydroxybenzoic acid (2,5-DHBA, also known as gentisic acid) is an oxidative metabolite of salicylic acid (SAL) at high doses. Salicylic acid is primarily utilised in the form of acetylsalicylic acid or aspirin; consequently, it may also be regarded as an aspirin metabolite. Furthermore, 2,5-DHBA is closely associated with the nephrotoxicity of SAL, with its effects intensifying as the SAL dosage increases[1].[1] TIMOTHY F. MCMAHON . Comparative acute nephrotoxicity of salicylic acid, 2,3-dihydroxybenzoic acid, and 2,5-dihydroxybenzoic acid in young and middle aged Fischer 344 rats[J]. Toxicology, 1991, 66 3: Pages 297-311. DOI:10.1016/0300-483X(91)90201-B.

View Lastest Price from 2,5-Dihydroxybenzoic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,5-Dihydroxybenzoic acid pictures 2026-07-17 2,5-Dihydroxybenzoic acid
490-79-9
1kg 99%min 2000KGS HANGZHOU HAILAN CHEMICAL CO.,LTD.
DHB pictures 2026-07-17 DHB
490-79-9
$10.00 1box 99.99% 9999 Ningbo Qingteng Plastic Cost.,Ltd.
2,5-Dihydroxybenzoic acid pictures 2026-06-30 2,5-Dihydroxybenzoic acid
490-79-9
1kg 99% 10000KGS Shaanxi Dideu New Materials Co. Ltd
  • DHB pictures
  • DHB
    490-79-9
  • $10.00
  • 99.99%
  • Ningbo Qingteng Plastic Cost.,Ltd.
Hydroguinonecarboxylicacid Kyselina 2,5-dihydroxybenzoova Kyselina gentisinova kyselina2,5-dihydroxybenzoova kyselinagentisinova Salicylic acid, 5-hydroxy- 2,5-Dihydroxybenzoic acid, 99% 5GR MesalaMine IMpurity G 2,5-Dihydroxybenzoic acid, tech Gentisic acid, 2-Carboxyhydroquinone, 2-Carboxybenzene-1,4-diol 2,5-Dihydroxybenzoic Acid, 97+% 2,5-Dihydroxyb Gentisic Acid 〔2,5-Dihydroxybenzoic Acid〕 2,5-Dhba Mesalazine (Mesalamine) EP Impurity G 2,5-DIHYDROXYBENZOIC ACID HYDROQUINONECARBOXYLIC ACID DIHYDROXYBENZOIC(2,5-) ACID Gentiana scabra P.E Hydrochinon acid GENTISIC ACID FREE ACID 2,5-dihdyroxybenzoic acid 2,5-Dihydroxybenzoic acid,DHB, Gentisic acid, Hydroquinonecarboxylic acid 5-Dihydroxybenzoic acid 2,5-Dihydroxybenzoic acid, 99% 50GR 2,5-dihydroxy-benzoicaci 2,5-Dioxybenzoic acid 5-Hydroxysalicylic acid 5-hydroxy-salicylicaci 5-hydroxysalicylicacid acido2,5-diidrossibenzoico Benzoic acid, 2,5-dihydroxy- Benzoicacid,2,5-dihydroxy- Gensigon 2,5-Dihydroxybenzoic acid(2,5-DHBA、DHB) 2,5-Dihydroxybenzoic Acid [Matrix for MALDI-TOF/MS] DHB, Gentisic acid, Hydroquinonecarboxylic acid 3,6-Dihydroxybenzoic acid Carboxyhydroquinone RARECHEM AL BE 0043 Mesalazine Impurity 7(Mesalazine EP Impurity G) DHB, 2,5-Dihydroxybenzoic acid Mesalazine Impurity G Mesalamine EP Impurity G 2,5-DihydroxybenzoicAcid[MatrixforMALDI-TOF/MS]> 2,5-Dihydroxybenzoic Acid > Dihydroxybenzoic MS Phloretate 2,5-DIHYDROXYBENZOIC ACID FOR SYNTHESIS GENTISIC ACID CAS 490-79-9 Mesalamine Impurity-G(2,5-dihydrobenzoic acid) 5-Dihydroxybenzoic Mesalazine EP Impurity GQ: What is Mesalazine EP Impurity G Q: What is the CAS Number of Mesalazine EP Impurity G Q: What is the storage condition of Mesalazine EP Impurity G Q: What are the applications of Mesalazine EP Impurity G 13C6]-2,5-Dihydroxybenzoic acid Mesalazine EP Impurity G 2,5-dihydroxybenzoic acid. 2,5-Dihydroxy Benzoic Acid (Mesalamine Impurity G) Mesalazine Impurity 7 2,5-Dihydroxybenzoic acid (Mesalazine Impurity)