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Supelco

2,5-Dihydroxybenzoic acid

analytical standard

Synonyme(s) :

2,5-DHBA, DHB, Gentisic acid, Hydroquinonecarboxylic acid

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About This Item

Formule linéaire :
(HO)2C6H3CO2H
Numéro CAS:
490-79-9
Poids moléculaire :
154.12
Numéro Beilstein :
2209119
Numéro CE :
207-718-5
Numéro MDL:
MFCD00002460
Code UNSPSC :
77101502
ID de substance PubChem :
329768120
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥99.0% (HPLC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

204-208 °C (lit.)

Application(s)

pharmaceutical

Format

neat

Chaîne SMILES 

OC(=O)c1cc(O)ccc1O

InChI

1S/C7H6O4/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,8-9H,(H,10,11)

Clé InChI

WXTMDXOMEHJXQO-UHFFFAOYSA-N

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Catégories apparentées

Application

2,5-Dihydroxybenzoic acid may be used as a reference standard in the determination of 2,5-dihydroxybenzoic acid in biopsy samples using high-performance liquid chromatography coupled with electrochemical detector.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302

Classification des risques

Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG6805
BCCF8915
BCCF3202
BCCF1325
BCCD1596

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Consulter la Bibliothèque de documents

G Palumbo et al.
Journal of pharmaceutical and biomedical analysis, 14(1-2), 175-180 (1995-12-01)
A high-performance liquid chromatographic method for the simultaneous determination of 5-aminosalicylic acid (5-ASA), acetyl-5-aminosalicylic acid (Ac-5-ASA) and 2,5-dihydroxybenzoic acid (5-HSA) in human endoscopic intestinal biopsy with electrochemical detection has been developed and validated. A liquid-liquid extraction procedure was used to
Laurent Salphati et al.
Drug metabolism and disposition: the biological fate of chemicals, 42(7), 1110-1116 (2014-04-24)
Glioblastoma multiforme (GBM) is the most common primary brain tumor in adults, and the limited available treatment options have not meaningfully impacted patient survival in the past decades. Such poor outcomes can be at least partly attributed to the inability
H Ma et al.
Oncogene, 34(6), 726-740 (2014-02-18)
Aberrant cell surface sialylation patterns have been shown to correlate with tumor progression and metastasis. However, the role of sialylation regulation of cancer multidrug resistance (MDR) remains poorly understood. This study investigated sialylation in modification on MDR in acute myeloid
Shadi Toghi Eshghi et al.
ACS chemical biology, 9(9), 2149-2156 (2014-07-17)
Aberrant glycosylation is associated with most of the diseases. Direct imaging and profiling of N-glycans on tissue sections can reveal tissue-specific and/or disease-associated N-glycans, which not only could serve as molecular signatures for diagnosis but also shed light on the
S A Ponomarenko et al.
Faraday discussions, 174, 313-339 (2014-10-04)
This contribution describes recent progress in the design, synthesis and properties of solution-processible star-shaped oligomers and their application in organic photovoltaics. Even though alternative chemistry has been used to design such oligomers, the most successful approach is based on a
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