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Chemical Components and Synonyms

MET Fumarate:
IUPAC Name: N-Ethyl-N-methyl-1H-indole-3-ethanamine fumarate
Common Synonyms: Methyl-ethyltryptamine fumarate

CAS Number

MET Fumarate: This compound may not have a widely recognized CAS number due to its niche status in research.

Molecular Formula and Structure

MET Fumarate:
Molecular Formula: C13H18N2 · C4H4O4 (including the fumarate)
Structural Diagram:

   C10H6(N(CH2CH3)(CH3))CH2CH2 · C4H4O4

Purity and Grade

Purity: ≥ 98%
Grade: Research Grade

Physical and Chemical Properties

• Form: Powder (Fumarate Salt)
• Solubility: Soluble in water and organic solvents
• Molecular Weight: Approximately 308.35 g/mol (including the fumarate)

Safety and Handling Information

• Hazard Symbols: ⚠️
• Precautionary Statements:
  • Avoid inhalation, ingestion, and contact with skin and eyes outside of research protocols.
  • Use personal protective equipment (PPE) such as gloves and safety goggles during handling in a research setting.
• First-Aid Measures:
  • If inhaled, move to fresh air and seek medical attention if necessary.
  • In case of skin contact, rinse with plenty of water and soap.
  • If ingested in a non-research context, seek immediate medical help.

Usage and Applications

MET Fumarate is primarily used in research to investigate potential psychoactive effects and interactions with serotonin receptors. Studies may focus on its pharmacodynamics and pharmacokinetics.

Storage Conditions

Store in a cool, dry place away from direct sunlight. Keep the container tightly closed and store at room temperature.

Regulatory Information

This product complies with international chemical safety standards. Researchers must ensure compliance with local regulations concerning the use of MET in their studies.

Shipping Information

Clients are responsible for verifying the legal status of MET in their country before purchasing. Our packaging meets industry standards to ensure safe delivery, and we offer various shipping options for your convenience.

Technical Support and Contact Information

For any questions or technical support, please visit our Contact Us page.

FAQ

1. What is the form of MET in this product?

MET is provided in the fumarate salt form, as a powder, for research purposes.

2. What are the typical applications of MET Fumarate?

It is used in research to study potential psychoactive effects and serotonin receptor interactions.

3. How should I store MET Fumarate?

Store it in a cool, dry place away from direct sunlight, at room temperature.

4. Are there any shipping restrictions for MET Fumarate?

Yes, clients must verify the legal status of MET in their country before purchasing.

5. Who do I contact if I have questions about MET Fumarate?

For any inquiries, please visit our Contact Us page for assistance.

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Introduction

MET Fumarate, also known as Methionine Fumarate, is a compound of significant interest in the fields of biochemistry and nutrition. Methionine is an essential amino acid, and its fumarate salt is often used to enhance its stability and bioavailability. This article provides a comprehensive overview of MET Fumarate, including its chemical properties, biological significance, and research applications.

Chemical Properties

• IUPAC Name: (2S)-2-amino-4-(methylthio)butanoic acid fumarate
• Molecular Formula: C6H11NO2S (Methionine), C4H4O4 (Fumaric Acid)
• Molecular Weight: 149.21 g/mol (Methionine), 116.07 g/mol (Fumaric Acid)
• Chemical Structure: The structure includes the amino acid methionine bonded to fumaric acid, which is a dicarboxylic acid.

Biological Significance

Methionine is an essential amino acid, meaning it cannot be synthesized by the human body and must be obtained through diet. It plays several critical roles:

• Protein Synthesis: Methionine is a building block of proteins and is crucial for the initiation of protein synthesis.
• Methylation: It serves as a precursor to S-adenosylmethionine (SAMe), a vital methyl donor involved in numerous methylation reactions, including DNA methylation.
• Antioxidant Production: Methionine is a precursor to cysteine, which is a component of glutathione, one of the body’s most important antioxidants.

Research Applications

MET Fumarate is utilized in various research areas due to its biological importance:

• Nutritional Studies: Investigating the role of methionine in human and animal nutrition, including its effects on growth, metabolism, and health.
• Biochemical Research: Studying methionine’s involvement in methylation processes and its impact on gene expression and epigenetics.
• Medical Research: Exploring its potential therapeutic applications, such as in liver health, where methionine is known to support detoxification processes.

Advantages of Fumarate Salt Form

• Enhanced Stability: The fumarate salt form of methionine provides enhanced stability compared to the free amino acid, making it more suitable for various formulations.
• Improved Bioavailability: Fumarate salts generally exhibit better bioavailability, ensuring that a greater proportion of the administered dose is absorbed and utilized by the body.
• Ease of Handling: The fumarate form is often easier to handle and incorporate into various delivery systems, including supplements and pharmaceuticals.

Safety and Ethical Considerations

As with any compound used in research and supplementation, it is essential to adhere to safety guidelines and ethical standards. Proper dosing, monitoring, and reporting are crucial to ensure the reliability and reproducibility of research findings.

Conclusion

MET Fumarate, combining methionine with fumaric acid, offers a stable and bioavailable form of this essential amino acid. Its significance in protein synthesis, methylation, and antioxidant production makes it a valuable compound for research in nutrition, biochemistry, and medicine. As research continues, the full potential of MET Fumarate in various applications will become increasingly evident.