464139
6-Methoxysalicylic acid
98%
Sinônimo(s):
2-Hydroxy-6-methoxybenzoic acid
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About This Item
Fórmula linear:
CH3OC6H3(OH)CO2H
Número CAS:
Peso molecular:
168.15
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
98%
Formulário
solid
pf
134-138 °C (lit.)
grupo funcional
carboxylic acid
cadeia de caracteres SMILES
COc1cccc(O)c1C(O)=O
InChI
1S/C8H8O4/c1-12-6-4-2-3-5(9)7(6)8(10)11/h2-4,9H,1H3,(H,10,11)
chave InChI
AAUQLHHARJUJEH-UHFFFAOYSA-N
Descrição geral
6-Methoxysalicylic acid has been reported to exhibit significant analgesic effects.[1]
Aplicação
6-Methoxysalicylic acid has been used to fabricate a dummy template molecule required for the preparation of dummy molecularly imprinted polymers (DMIPs). These polymers are useful for the simultaneous selective removal and enrichment of ginkgolic acids (GAs) during the processing of Ginkgo biloba leaves.[2] It may be employed as internal standard for the determination of acetylsalicylic acid (aspirin, ASA) and its major metabolite, salicylic acid (SA), in animal plasma by LC/MS/MS.[3]
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Francisco Palacios-Espinosa et al.
Journal of ethnopharmacology, 118(3), 448-454 (2008-06-28)
Brickellia veronicifolia (Kunth) Gray (Asteraceae) (BV) is broadly commercialized for treating gastrointestinal diseases (stomach aches, biliary colics and dyspepsia), arthritis, diabetes and painful inflammatory complaints. In order to complete the preclinical pharmacological profile of BV, first the antinociceptive effect of
Xiangrong Xu et al.
Biomedical chromatography : BMC, 23(9), 973-979 (2009-04-10)
A simple and sensitive analytical method using liquid chromatography-tandem mass spectrometry (LC/MS/MS) for determination of acetylsalicylic acid (aspirin, ASA) and its major metabolite, salicylic acid (SA), in animal plasma has been developed and validated. Both ASA and SA in plasma
Ecem Evrim Çelik et al.
Food research international (Ottawa, Ont.), 108, 286-294 (2018-05-08)
The interactions of coffee and bread crust melanoidins with hydroxycinnamic and hydroxybenzoic acids (HCA/HBA) containing different numbers of -OH and -OCH₃ groups localized at different positions on the aromatic ring were investigated. By doing so, mechanism of the interactions was
Wenhua Ji et al.
Journal of chromatography. A, 1368, 44-51 (2014-12-03)
Dummy molecularly imprinted polymers (DMIPs) for simultaneously selective removal and enrichment of ginkgolic acids (GAs) during the processing of Ginkgo biloba leaves have been prepared. Two dummy template molecule with similar structural skeleton to GAs, 6-methoxysalicylic acid (MOSA, DT-1) and
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