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D0787

Sigma-Aldrich

3-(Dimethylamino)benzoic acid

≥97% (HPLC), powder

Sinônimo(s):

3-Dimethylaminobenzoic acid

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About This Item

Fórmula linear:
(CH3)2NC6H4CO2H
Número CAS:
99-64-9
Peso molecular:
165.19
Beilstein:
2208586
Número CE:
202-775-2
Número MDL:
MFCD00002497
Código UNSPSC:
12352204
ID de substância PubChem:
57654065
NACRES:
NA.83

product name

3-(Dimethylamino)benzoic acid, ≥97% (HPLC)

Ensaio

≥97% (HPLC)

forma

powder

pf

148-150 °C (lit.)

solubilidade

methanol: 50 mg/mL, clear to very slightly hazy, yellow to brown

cadeia de caracteres SMILES

CN(C)c1cccc(c1)C(O)=O

InChI

1S/C9H11NO2/c1-10(2)8-5-3-4-7(6-8)9(11)12/h3-6H,1-2H3,(H,11,12)

chave InChI

NEGFNJRAUMCZMY-UHFFFAOYSA-N

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Aplicação

3-(Dimethylamino)benzoic acid has been used to analyse glucose content from the extraction of starch and soluble sugars.

Ações bioquímicas/fisiológicas

3-dimethylaminobenzoic acid (DMAB) can be used to quantity the activity of peroxidase and manganese peroxidase.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Belén Borrego et al.
Antiviral research, 142, 30-36 (2017-03-21)
Foot-and-mouth disease virus (FMDV) is the causative agent of a highly contagious disease and a major concern in animal health worldwide. We have previously reported the use of RNA transcripts mimicking structural domains in the non-coding regions of the FMDV
Maria Cristina Diez et al.
Environmental science and pollution research international, 25(22), 21440-21450 (2017-09-16)
A biopurification system based on the adsorption and degradation capacity of a biomixture to degrade a mixture of pesticides (atrazine, chlorpyrifos, iprodione; 50 mg kg-1 each) in repeated applications (0, 30, and 60 days) was evaluated. Tanks of 1 m3 packed with a biomixture
Lixiang Cheng et al.
Physiologia plantarum, 168(3), 675-693 (2019-07-26)
Potato tuberization is a complicated biological process regulated by multiple phytohormones, in particular cytokinins (CKs). The information available on the molecular mechanisms regulating tuber development by CKs remains largely unclear. Physiological results initially indicated that low 6-benzylaminopurine (BAP) concentration (3 mg l-1
Peroxidase-catalyzed oxidative coupling of paraphenylenediamine with 3-dimethylaminobenzoic acid: application in crude plant extracts
Nagaraja P, et al.
Journal of Agricultural and Food Chemistry, 57(12), 5173-5177 (2009)
Mikako Ogawa et al.
Nuclear medicine and biology, 37(3), 347-355 (2010-03-30)
The nicotinic acetylcholine receptor (nAChR) alpha7 subtype (alpha(7) nAChR) is one of the major nAChR subtypes in the brain. We synthesized C-11 labeled alpha(7) nAChR ligands, (R)-2-[(11)C]methylamino-benzoic acid 1-aza-bicyclo[2.2.2]oct-3-yl ester ([(11)C](R)-MeQAA) and its isomer (S)-[(11)C]MeQAA, for in vivo investigation with
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