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3,5-Diiodo-L-thyronine (T2)

CAS
1041-01-6
Molecular wt
525.08
Compound class
Iodothyronine / Thyroid Hormone Metabolite
Batch
KC-35T-01
Made
2025-12-04
Reports
1 on file
Everything shipping from this page today came off this batch. The code is printed on your label, and one certificate covers the whole batch.

3,5-Diiodo-L-thyronine (T2)

3,5-Diiodo-L-Thyronine (T2)

250mcg Per Dry-Fill Capsule

60ct

15mg

Dry fill for transport.

3,5-Diiodo-L-Thyronine (T2) is sold for laboratory research use only. Terms of sale apply. Not for human consumption, nor medical, veterinary, or household uses. Please familiarize yourself with our Terms and Conditions prior to ordering.

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Description

3,5-Diiodo-L-thyronine (T2) Research Standard

3,5-Diiodo-L-thyronine (T2) is an endogenous metabolite of thyroid hormones. While historically considered a degradation product of triiodothyronine (T3), it is now recognized in laboratory research as a biologically active iodothyronine that exerts distinct, rapid metabolic effects. Unlike the classical genomic actions of T3/T4, T2 is primarily investigated for its non-genomic interactions, particularly its direct influence on mitochondrial bioenergetics, oxidative phosphorylation, and lipid metabolism. It serves as a specialized tool for researchers studying the modulation of energy balance and metabolic rate at the mitochondrial level.

Physical & Handling Properties

Property Specification
Physical Appearance White to off-white powder

Mechanism of Action & Research Context

T2 is researched for its unique ability to modulate cellular energy expenditure, often independent of nuclear thyroid hormone receptors.

  • Mitochondrial Interaction: Research indicates that T2 interacts directly with the cytochrome c oxidase (COX) complex within the mitochondria. By binding to subunit Va of the COX complex, T2 can abolish the allosteric inhibition of respiration normally induced by ATP, thereby stimulating oxygen consumption.

  • Thermogenesis & Metabolism: T2 is studied for its role in stimulating fatty acid oxidation and mitochondrial uncoupling in skeletal muscle and liver tissues. This makes it a frequent subject in obesity and hepatic steatosis models, where researchers investigate its potential to enhance metabolic rate and lipid catabolism.

  • Non-Genomic Signaling: Unlike T3, T2 effects are often observed rapidly (within hours), suggesting non-genomic pathways that do not rely on protein synthesis, distinguishing it from the classical thyroid hormone receptor (TR) pathway.

Research Applications

T2 is a critical reagent for endocrine and metabolic research.

Primary fields of in vitro and laboratory investigation include:

  • Mitochondrial Bioenergetics: Utilizing isolated mitochondria or cell-line models to measure the effect of T2 on COX activity and oxidative phosphorylation rates.

  • Lipid Metabolism Research: Evaluating the inhibitory effects of T2 on de novo lipogenesis and its role in enhancing fatty acid beta-oxidation.

  • Comparative Pharmacology: Benchmarking T2 against T3 to differentiate between genomic (nuclear-mediated) and non-genomic (mitochondrial-mediated) thyroid hormone responses.

  • Metabolic Syndrome Models: Using cell-based models of insulin resistance or hepatic steatosis to explore the therapeutic potential of T2 in modulating energy balance.

Storage & Handling Guidelines

Store at controlled room temperature. Keep tightly closed.

Storage guidance is a house recommendation. Analytical documentation is per-lot release testing.

Related Research Compounds

Research Use Disclaimer

Research Use Only Disclaimer: This product is labeled and sold “For Research Use Only – NOT FOR HUMAN CONSUMPTION.” It is not a drug, dietary supplement, food, cosmetic, or medical device, and it is not approved by the FDA or any other regulator for human or veterinary use. It is supplied to approved account holders as a research chemical for laboratory use and must be handled in accordance with applicable law.

Compound Class Iodothyronine / Thyroid Hormone Metabolite
CAS Number 1041-01-6
Other Names -(4-Hydroxyphenyl)-3,5-diiodo-L-tyrosine; 3-[4-(p-Hydroxyphenoxy)-3,5-diiodophenyl]-L-alanine; L-T2
IUPAC Name 2-amino-3-[4-(4-hydroxyphenoxy)-3,5-diiodophenyl]propanoic acid
Molecular Formula C15H13I2NO4
Molecular Weight 525.08
Capsule Concentration 250mcg

Currently shipping from batch KC-35T-01.