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线性分子式:
(HO)2C6H3CO2H
化学文摘社编号:
分子量:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-139-5
Beilstein/REAXYS Number:
2209117
MDL number:
产品名称
2,3-二羟基苯甲酸, 99%
InChI key
GLDQAMYCGOIJDV-UHFFFAOYSA-N
InChI
1S/C7H6O4/c8-5-3-1-2-4(6(5)9)7(10)11/h1-3,8-9H,(H,10,11)
SMILES string
OC(=O)c1cccc(O)c1O
assay
99%
mp
204-206 °C (lit.)
solubility
methanol: soluble 50 mg/mL, clear to faintly hazy, orange
functional group
carboxylic acid
Quality Level
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Application
以 2,3-二羟基苯甲酸为对象,在碱性介质中,用电化学、分光光度法和磁学方法研究了锰与脂肪族和芳香族多羟基配体的配合物 。用于从 创伤弧菌(一种人类病原体 )的低铁培养物中分离新铁载体 vulnibactin。作为共晶形成剂,研究了位置异构对吡拉西坦共晶形成及理化属性的影响 。
Biochem/physiol Actions
在大鼠高血容量输注模型中发现 2,3-二羟基苯甲酸是口服有效的铁螯合药物 。其为牛种布氏杆菌 产生的单儿茶酚铁载体 。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
N Okujo et al.
Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine, 7(2), 109-116 (1994-04-01)
A new siderophore named vulnibactin has been isolated from low iron cultures of Vibrio vulnificus, a human pathogen. The structure was established as N-[3-(2,3-dihydroxybenzamido)propyl]-1,3-bis[2-(2-hydroxy-phenyl)- trans-5 - methyl-2-oxazoline-4-carboxamido]propane by a combination of acid hydrolysis, nuclear magnetic resonance spectroscopy and positive fast
Nao Yamakawa et al.
Nature communications, 9(1), 4647-4647 (2018-11-09)
The emergence of zebrafish Danio rerio as a versatile model organism provides the unique opportunity to monitor the functions of glycosylation throughout vertebrate embryogenesis, providing insights into human diseases caused by glycosylation defects. Using a combination of chemical modifications, enzymatic
Xiangmin Liao et al.
Journal of pharmaceutical sciences, 99(1), 246-254 (2009-06-09)
The effect of position isomerism on the co-crystals formation and physicochemical properties was evaluated. Piracetam was used as the model compound. Six position isomers, 2,3-, 2,4-, 2,5-, 2,6-, 3,4-, and 3,5-dihydroxybenzoic acid (DHBA), were used as the co-crystal formers. Co-crystals
Anna Nilsson et al.
Scientific reports, 7(1), 6352-6352 (2017-07-27)
Knowledge about the region-specific absorption profiles from the gastrointestinal tract of orally administered drugs is a critical factor guiding dosage form selection in drug development. We have used a novel approach to study three well-characterized permeability and absorption marker drugs
The identification of 2, 3-dihydroxybenzoic acid as a potentially useful iron-chelating drug.
J H Graziano et al.
The Journal of pharmacology and experimental therapeutics, 190(3), 570-575 (1974-09-01)
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