CAS 102-32-9
:DOPAC
Description:
DOPAC, or 3,4-Dihydroxyphenylacetic acid, is an aromatic organic compound characterized by its two hydroxyl groups attached to a phenyl ring and an acetic acid moiety. It is a metabolite of dopamine, playing a significant role in the biochemical pathways of catecholamine metabolism. DOPAC is typically found in biological systems, particularly in the brain, where it is involved in neurotransmitter regulation. The compound is a white to off-white crystalline solid, soluble in water and organic solvents, which facilitates its biological activity. DOPAC exhibits antioxidant properties and has been studied for its potential implications in neurodegenerative diseases and psychiatric disorders. Its chemical structure allows it to participate in various chemical reactions, making it a subject of interest in pharmacological and biochemical research. Safety data indicates that DOPAC should be handled with care, as with many organic compounds, to avoid potential health hazards.
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
Synonyms:- (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
- See more synonyms
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Found 13 products.
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:C8H8O4Purity:98+%Color and Shape:White to cream to grey to pale brown to purple-grey, PowderMolecular weight: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:C8H8O4Purity:(HPLC) ≥95%Color and Shape:PowderMolecular weight:168.15Benzeneacetic acid, 3,4-dihydroxy-
CAS:Formula:C8H8O4Purity:98%Color and Shape:SolidMolecular weight:168.14673,4-Dihydroxyphenylacetic acid
CAS:<p>3,4-Dihydroxyphenylacetic acid</p>Formula:C8H8O4Purity:98%Color and Shape: off white. faint red solidMolecular weight:168.15g/mol3,4-Dihydroxyphenylacetic acid
CAS:Formula:C8H8O4Purity:≥ 98.0%Color and Shape:White to off-white, red, brown or purple crystalline powderMolecular weight:168.153,4-Dihydroxybenzeneacetic acid
CAS:3,4-Dihydroxybenzeneacetic acidPurity:≥98%Molecular weight:168.15g/mol3,4-Dihydroxyphenylacetic Acid
CAS:Formula:C8H8O4Purity:>98.0%(GC)Color and Shape:White to Gray to Red powder to crystalMolecular weight:168.153,4-Dihydroxybenzeneacetic acid
CAS:<p>3,4-Dihydroxybenzeneacetic acid (3,4-Dihydroxyphenylacetic acid) is the main metabolite of dopamine.</p>Formula:C8H8O4Purity:99.19% - 99.31%Color and Shape:SolidMolecular weight:168.153,4-Dihydroxyphenylacetic Acid
CAS:Controlled Product<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:C8H8O4Color and Shape:NeatMolecular weight: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:C8H8O4Purity:Min. 95%Color and Shape:Beige PowderMolecular weight:168.15 g/mol3,4-dihydroxyphenylacetic acid
CAS:Formula:C8H8O4Purity:95%Color and Shape:Solid, Crystalline PowderMolecular weight:168.148











