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(±)-4-Hydroxy-3-methoxymandelic acid-[d3]

General Information
Catalog: BLP-007930
Molecular Formula: C9H7D3O5
Molecular Weight: 201.19
Chemical Structure
(±)-4-Hydroxy-3-methoxymandelic acid-[d3]
Description (+/-)-4-Hydroxy-3-methoxymandelic acid-[d3] is the labelled analogue of VMA, which is an impurity of Epinephrine. Epinephrine is a natural neurotransmitter that is released from the adrenal medulla and activates adrenoceptors.
Synonyms (+/-)-4-Hydroxy-3-methoxymandelic Acid-D3 (ring-D3); VMA-D3; α,4-Dihydroxy-3-methoxybenzeneacetic Acid-d3; (+/-)-Vanilmandelic Acid-d3; [4-Hydroxy-3-methoxyphenyl]glycolic Acid-d3; HMMA-d3; Vanilinmandelic Acid-d3; DL-Vanillomandelic Acid-d3
IUPAC Name 2-hydroxy-2-(4-hydroxy-3-methoxyphenyl-2,5,6-d3)acetic acid
Related CAS 55-10-7 (unlabelled)
Purity 98%; 98% atom D
Solubility Slightly soluble in Ethyl Acetate (Heated), Methanol
Appearance Light Orange Solid
Storage Store at 2-8°C

(±)-4-Hydroxy-3-methoxymandelic acid-[d3] is a deuterated compound, primarily used in analytical and research settings, particularly in metabolic studies. Here are some key applications of (±)-4-Hydroxy-3-methoxymandelic acid-[d3]:

Isotope Dilution Mass Spectrometry: In the field of analytical chemistry, (±)-4-Hydroxy-3-methoxymandelic acid-[d3] serves as an internal standard in isotope dilution mass spectrometry (IDMS) techniques. This compound allows for precise quantification of 4-Hydroxy-3-methoxymandelic acid levels in biological samples by correcting for potential variability in sample processing and analysis. Its deuterated nature provides a clear distinction in mass spectrometric analysis, improving accuracy and reliability.

Metabolic Pathway Tracing: Researchers use (±)-4-Hydroxy-3-methoxymandelic acid-[d3] in metabolic pathway studies to investigate biochemical processes involving catecholamine metabolism. By incorporating the labeled compound into experiments, scientists can track its incorporation and transformation through different metabolic routes. This helps in understanding the dynamics of catecholamine metabolism and assessing the effects of various physiological and pathological conditions.

Pharmacokinetic Studies: In the pharmaceutical industry, (±)-4-Hydroxy-3-methoxymandelic acid-[d3] is utilized in pharmacokinetic studies to examine the absorption, distribution, metabolism, and excretion (ADME) of drugs impacting catecholamine pathways. The compound allows researchers to monitor the drug's effects on catecholamine metabolism by providing detailed insights into metabolite kinetics. This information is crucial for developing effective and safe therapeutic agents.

Biomarker Research: In clinical research, (±)-4-Hydroxy-3-methoxymandelic acid-[d3] is employed to study disease biomarkers associated with catecholamine metabolite levels, particularly in conditions like pheochromocytoma or neuroblastoma. By using this deuterated compound as a reference in assays, scientists can improve the precision of biomarker quantification. This contributes to better disease diagnosis, management, and therapeutic strategies.

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