CAS 102-32-9
:DOPAC
Descrizione:
DOPAC, o acido 3,4-diidrossifenilacetico, è un composto organico aromatico caratterizzato dai suoi due gruppi idrossilici attaccati a un anello fenilico e a un gruppo acido acetico. È un metabolita della dopamina, svolgendo un ruolo significativo nelle vie biochimiche del metabolismo delle catecolamine. DOPAC si trova tipicamente nei sistemi biologici, in particolare nel cervello, dove è coinvolto nella regolazione dei neurotrasmettitori. Il composto è un solido cristallino bianco a bianco sporco, solubile in acqua e solventi organici, il che facilita la sua attività biologica. DOPAC presenta proprietà antiossidanti ed è stato studiato per le sue potenziali implicazioni nelle malattie neurodegenerative e nei disturbi psichiatrici. La sua struttura chimica gli consente di partecipare a varie reazioni chimiche, rendendolo un argomento di interesse nella ricerca farmacologica e biochimica. I dati di sicurezza indicano che DOPAC deve essere maneggiato con cura, come molti composti organici, per evitare potenziali rischi per la salute.
Formula:C8H8O4
InChI:InChI=1S/C8H8O4/c9-6-2-1-5(3-7(6)10)4-8(11)12/h1-3,9-10H,4H2,(H,11,12)
InChI key:InChIKey=CFFZDZCDUFSOFZ-UHFFFAOYSA-N
SMILES:C(C(O)=O)C1=CC(O)=C(O)C=C1
Sinonimi:- (3,4-Dihydroxyphenyl)-Aceticaci
- (3,4-Dihydroxyphenyl)Acetate
- (3,4-Dihydroxyphenyl)acetic acid
- 2-(3,4-Dihydroxyphenyl)acetic acid
- 3,4-Dihydroxy-Benzeneaceticaci
- 3,4-Dihydroxybenzeneacetic acid
- 3,4-Dihydroxybenzeneaceticacid
- 3,4-Dihydroxyphenylessigsaure
- Acetic acid, (3,4-dihydroxyphenyl)-
- Acide 3,4-Dihydroxyphenylacetique
- Acido 3,4-Dihidroxifenilacetico
- Ba 2773
- Ba2773
- Benzeneacetic acid, 3,4-dihydroxy-
- Dihydroxyphenylacetic acid
- Dopac
- Dopacetic acid
- Homoprotocatechuic acid
- Vedi altri sinonimi
Ordinare per
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13 prodotti.
3,4-Dihydroxyphenylacetic acid, 98+%
CAS:<p>3,4-Dihydroxyphenylacetic acid is an important metabolite when studying the behavior of the dopaminergic system. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The origina</p>Formula:C8H8O4Purezza:98+%Colore e forma:White to cream to grey to pale brown to purple-grey, PowderPeso molecolare:168.153,4-Dihydroxyphenylacetic acid
CAS:3,4-Dihydroxyphenylacetic acid analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.Formula:C8H8O4Purezza:(HPLC) ≥95%Colore e forma:PowderPeso molecolare:168.15Benzeneacetic acid, 3,4-dihydroxy-
CAS:Formula:C8H8O4Purezza:98%Colore e forma:SolidPeso molecolare:168.14673,4-Dihydroxyphenylacetic acid
CAS:<p>3,4-Dihydroxyphenylacetic acid</p>Formula:C8H8O4Purezza:98%Colore e forma: off white. faint red solidPeso molecolare:168.15g/mol3,4-Dihydroxyphenylacetic acid
CAS:Formula:C8H8O4Purezza:≥ 98.0%Colore e forma:White to off-white, red, brown or purple crystalline powderPeso molecolare:168.153,4-Dihydroxybenzeneacetic acid
CAS:3,4-Dihydroxybenzeneacetic acidPurezza:≥98%Peso molecolare:168.15g/mol3,4-Dihydroxyphenylacetic Acid
CAS:Formula:C8H8O4Purezza:>98.0%(GC)Colore e forma:White to Gray to Red powder to crystalPeso molecolare:168.15Ref: 4Z-A-138034
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiesta3,4-Dihydroxybenzeneacetic acid
CAS:3,4-Dihydroxybenzeneacetic acid (3,4-Dihydroxyphenylacetic acid) is the main metabolite of dopamine.Formula:C8H8O4Purezza:99.19% - 99.31%Colore e forma:SolidPeso molecolare:168.153,4-Dihydroxyphenylacetic Acid
CAS:Prodotto controllato<p>Applications 3,4-Dihydroxyphenylacetic Acid is a metabolite of Dopamine (D533782).<br>References Johnson, S. et al.: J. Physiol., 450, 455 (1992)<br></p>Formula:C8H8O4Colore e forma:NeatPeso molecolare:168.153,4-Dihydroxyphenylacetic acid
CAS:<p>3,4-Dihydroxyphenylacetic acid (DOPAC) is a metabolite of dopamine and is found in the central nervous system. Dopamine is an important neurotransmitter that is involved in the regulation of movement, emotional responses, and hormone release. Dopamine is synthesized from tyrosine by tyrosine hydroxylase and then converted to L-3,4-dihydroxyphenylalanine by L-aromatic amino acid decarboxylase. DOPAC can be formed from dopamine by monoamine oxidases or catechol O-methyltransferases. The level of DOPAC in the brain has been shown to be increased following exposure to neurotoxins such as 6-hydroxy dopamine or 1-methyl 4-phenyl 1,2,3,6 tetrahydropyridine (MPTP). This increase may be due to decreased activity of monoamine oxidases. The level</p>Formula:C8H8O4Purezza:Min. 95%Colore e forma:Beige PowderPeso molecolare:168.15 g/mol3,4-dihydroxyphenylacetic acid
CAS:Formula:C8H8O4Purezza:95%Colore e forma:Solid, Crystalline PowderPeso molecolare:168.148











