CAS 1219804-47-3 Terbutryn-[d5] - Isotope / BOC Sciences

General Information
Catalog: BLP-004583
CAS: 1219804-47-3
Molecular Formula: C10H14D5N5S
Molecular Weight: 246.39

General Information

Catalog: BLP-004583

CAS: 1219804-47-3

Molecular Formula: C10H14D5N5S

Molecular Weight: 246.39

Chemical Structure

Description	Terbutryn-[d5] is a labelled analogue of Terbutryn. Terbutryn is a chemical compound with a triazine ring as a basic structure. It is used as a herbicide. It also acts as an inhibitor of photosynthesis. It is absorbed by the roots and foliage.
Synonyms	4-N-tert-butyl-6-methylsulfanyl-2-N-(1,1,2,2,2-pentadeuterioethyl)-1,3,5-triazine-2,4-diamine
IUPAC Name	2-N-tert-butyl-6-methylsulfanyl-4-N-(1,1,2,2,2-pentadeuterioethyl)-1,3,5-triazine-2,4-diamine
Related CAS	886-50-0 (unlabelled)
Canonical SMILES	CCNC1=NC(=NC(=N1)SC)NC(C)(C)C
InChI	InChI=1S/C10H19N5S/c1-6-11-7-12-8(15-10(2,3)4)14-9(13-7)16-5/h6H2,1-5H3,(H2,11,12,13,14,15)/i1D3,6D2
InChI Key	IROINLKCQGIITA-YRYIGFSMSA-N
Purity	>98%
Appearance	Colorless Crystalline

Terbutryn-[d5], an isotopically labeled herbicide, finds its primary applications in research and environmental studies. Here are key applications of Terbutryn-[d5] presented with a high degree of perplexity and burstiness:

Environmental Research: Widely employed in environmental studies, Terbutryn-[d5] plays a crucial role in monitoring the herbicide's fate and behavior across diverse ecosystems. Through the utilization of this labeled compound, researchers can meticulously track its degradation pathways and comprehend its implications on soil, water, and biota. This knowledge is indispensable for evaluating ecological risks and devising effective strategies for pollution abatement.

Analytical Chemistry: Within the realm of analytical chemistry, Terbutryn-[d5] stands as an invaluable internal standard for quantifying terbutryn levels within environmental samples. Its distinctive isotopic label enables precise calibration and correction in mass spectrometry-based methodologies, bolstering the reliability and accuracy of analytical outcomes. This results in robust data that underpins environmental assessments and regulatory compliance efforts.

Herbicide Resistance Studies: Delving into herbicide resistance mechanisms within weeds and crops, Terbutryn-[d5] emerges as a pivotal tool in research endeavors aimed at understanding how certain species metabolize or withstand the herbicide. By unraveling these resistance pathways, scientists can devise management strategies to combat resistant weed populations, ensuring the sustainability of agricultural practices.

Pharmaceutical Research: While primarily recognized as an herbicide with isotopic labeling, Terbutryn-[d5] also finds applications in pharmaceutical research for exploring metabolic pathways and interactions in model organisms. Researchers harness its capabilities to trace the biotransformation and excretion processes of similar compounds in biological systems, offering profound insights into drug metabolism and the potential environmental ramifications of pharmaceutical residues.