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Mono-isobutyl phthalate-[ring-1,2-13C2,dicarboxyl-13C2]

General Information
Catalog: BLP-009482
Molecular Formula: C8[13C]4H14O4
Molecular Weight: 226.21
Chemical Structure
Mono-isobutyl phthalate-[ring-1,2-13C2,dicarboxyl-13C2]
Description Mono-isobutyl phthalate-[ring-1,2-13C2,dicarboxyl-13C2] is a 13C labelled analogue of Monoisobutyl phthalic acid, which is a phthalate metabolite that is in human semen and in meconium.
Synonyms Isobutyl hydrogen phthalate-ring-1,2-13C2-dicarboxyl-13C2; Monoisobutyl phthalic acid-ring-1,2-13C2-dicarboxyl-13C2
Related CAS 30833-53-5 (unlabelled)
InChI InChI=1S/C12H14O4/c1-8(2)7-16-12(15)10-6-4-3-5-9(10)11(13)14/h3-6,8H,7H2,1-2H3,(H,13,14)/i9+1,10+1,11+1,12+1
InChI Key RZJSUWQGFCHNFS-BMHINFNASA-N
Purity 98% by CP; 99% atom 13C

Mono-isobutyl phthalate-[ring-1,2-13C2,dicarboxyl-13C2], a uniquely labeled isotopic compound, plays a pivotal role in cutting-edge research applications. Here are key applications presented with high perplexity and burstiness:

Metabolic Tracing: This isotopically labeled phthalate serves as a powerful tool in metabolic tracing studies, enabling researchers to map out the biotransformation and metabolic pathways of phthalates within biological systems. By leveraging this compound as a tracer, scientists delve deep into the distribution and elimination patterns of phthalates in tissues and organs, shedding light on their impact on human health and the environment.

Environmental Monitoring: Mono-isobutyl phthalate-[ring-1,2-13C2,dicarboxyl-13C2] finds utility in environmental studies aimed at tracking the presence and movement of phthalate pollutants. By introducing this precisely labeled compound into environmental samples, researchers can trace its journey through diverse mediums like water, soil, and air. This aids in deciphering the persistence and degradation dynamics of phthalates, facilitating the formulation of robust environmental management strategies.

Toxicological Research: Within the realm of toxicology, this compound serves as a valuable asset for investigating the mechanisms underlying toxicity and adverse effects linked to phthalate exposure. The utilization of the labeled version allows for meticulous tracking of the compound within cellular and animal models, contributing crucial insights for risk assessments and regulatory frameworks concerning phthalate exposure-related health hazards.

Analytical Method Development: The isotopic labeling of Mono-isobutyl phthalate enables the refinement and validation of analytical methodologies in chemical and biochemical research. Through the application of mass spectrometry techniques, researchers can precisely quantify and detect phthalate compounds with exceptional sensitivity and specificity. This advancement is pivotal for enhancing analytical capacities and ensuring accurate detection within intricate matrices.

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