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Product Usage: This PRODUCT IS INTENDED AS A RESEARCH CHEMICAL ONLY. This designation allows the use of research chemicals strictly for in vitro testing and laboratory experimentation only. All product information available on this website is for educational purposes only. Bodily introduction of any kind into humans or animals is strictly forbidden by law. This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused or mislabeled as a drug, food or cosmetic.
Clenbuterol Tablets (40mcg) X 100 Tabs

For research use only. Not for human consumption.

Clenbuterol Tablets (40mcg) X 100 Tabs

Price:

$150.00

Select Quantity:

10 in stock

Peptide Compounds
Overview

General Information

Product Name: Clenbuterol Hydrochloride Tablets Strength: 40 micrograms per tablet Form: Oral tablet Category: β2‑Adrenergic Agonist (Research Chemical) Intended Use: Laboratory and scientific research only

Description

Clenbuterol 40 mcg tablets are a research‑grade adrenergic agonist compound commonly referenced in scientific literature for their effects on bronchodilation, metabolic stimulation, and smooth‑muscle relaxation. These tablets are manufactured for controlled research environments, ensuring consistency and reliability for analytical studies.

Key Features

  • High‑purity research compound
  • Consistent 40 mcg tablet strength
  • Stable oral tablet format for precise measurement
  • Suitable for biochemical, pharmacological, and receptor‑binding research
  • Manufactured under controlled laboratory standards

Research Applications

Clenbuterol is frequently studied for:

  • β2‑adrenergic receptor activation
  • Thermogenic and metabolic pathway modulation
  • Smooth‑muscle relaxation mechanisms
  • Bronchodilation effects in preclinical models
  • Cellular energy signaling interactions

Physical Characteristics

  • Appearance: Small, typically white or off‑white tablets
  • Texture: Firm‑pressed, smooth surface
  • Packaging: Sealed, labeled research‑use containers

Storage & Stability

  • Store in a cool, dry environment
  • Protect from light and moisture
  • Keep sealed until use
  • Maintain in secure laboratory conditions

Regulatory Notice

This product is not intended for human or veterinary consumption. It is supplied strictly for laboratory, analytical, and scientific research. No claims are made regarding safety or efficacy outside controlled research settings.

Biochemical
Characteristics

Biochemical Characteristics of Clenbuterol (40 mcg Tablets)

Molecular Identity

  • Chemical Name: Clenbuterol Hydrochloride
  • Molecular Formula: C₁₂H₁₈Cl₂N₂O · HCl
  • Molecular Weight: ~277.2 g/mol (base), ~313.2 g/mol (hydrochloride salt)
  • Chemical Class: Sympathomimetic amine
  • Functional Group Profile:
    • Aromatic ring
    • Secondary amine
    • Chlorinated phenyl structure
    • β‑hydroxyamine configuration typical of β‑agonists

Receptor Pharmacology

  • Primary Target: β₂‑adrenergic receptors
  • Secondary Activity: Minimal β₁‑adrenergic interaction
  • Mechanism: Clenbuterol binds to β₂ receptors → activates adenylate cyclase → increases cyclic AMP (cAMP) → triggers downstream signaling affecting smooth muscle, metabolic pathways, and thermogenic processes.

Physicochemical Properties

  • Appearance: White crystalline powder compressed into tablets
  • Solubility:
    • Highly soluble in water due to hydrochloride salt form
    • Soluble in ethanol
  • Stability:
    • Stable under dry, cool conditions
    • Sensitive to prolonged heat and moisture
  • pKa: ~9.6 (amine group)
  • LogP: ~2.3 (moderate lipophilicity enabling membrane permeability)

Biological Activity (Research Context Only)

  • β₂‑agonism: Promotes smooth‑muscle relaxation in preclinical models
  • cAMP Elevation: Enhances intracellular signaling linked to metabolic activation
  • Thermogenic Modulation: Influences mitochondrial activity and energy expenditure pathways
  • Cellular Effects:
    • Increased lipolytic signaling
    • Enhanced adrenergic responsiveness
    • Modulation of calcium flux in smooth muscle cells

Pharmacokinetic Characteristics (Research Literature)

  • Absorption: Rapid in oral form
  • Distribution: Moderate lipophilicity allows tissue penetration
  • Metabolism: Limited hepatic metabolism; significant portion remains unmetabolized
  • Elimination: Primarily renal excretion
  • Half‑Life: Long elimination half‑life reported in research models (varies by species)

Tablet‑Specific Characteristics

  • Strength: 40 mcg per tablet
  • Matrix: Inert excipients for stability and compression
  • Purpose: Precise measurement for controlled laboratory studies

Regulatory & Safety Note

Clenbuterol is a research‑only compound. These biochemical characteristics are provided strictly for scientific, analytical, and academic reference.

Research Applications

Research Applications Clenbuterol is frequently examined in scientific contexts for:

  • Adrenergic receptor activity
  • Thermogenic and metabolic pathway modulation
  • Smooth‑muscle relaxation mechanisms
  • Bronchodilation effects in preclinical models
Chemical Properties

Chemical Properties of Clenbuterol (40 mcg Tablets)

1. Chemical Identity

  • Chemical Name: Clenbuterol Hydrochloride
  • IUPAC Name: 4‑Amino‑α‑[tert‑butylamino]methyl‑3,5‑dichlorobenzyl alcohol hydrochloride
  • Chemical Class: Sympathomimetic amine (β₂‑adrenergic agonist)
  • Molecular Formula: C₁₂H₁₈Cl₂N₂O · HCl
  • Molecular Weight:
    • Base: ~277.2 g/mol
    • Hydrochloride salt: ~313.2 g/mol

2. Structural Characteristics

  • Functional Groups:
    • Aromatic phenyl ring
    • Two chlorine substituents (3,5‑dichloro pattern)
    • Secondary amine
    • β‑hydroxyamine configuration
  • Stereochemistry:
    • Contains a chiral β‑carbon
    • Exists as a racemic mixture in most research formulations

3. Physical Properties

  • Appearance: White crystalline powder compressed into tablets
  • Odor: Odorless
  • Melting Point: ~174–175°C (hydrochloride form)
  • Boiling Point: Not applicable (solid compound; decomposes before boiling)
  • Density: ~1.3 g/cm³ (approximate crystalline density)

4. Solubility Profile

  • Water: Highly soluble due to hydrochloride salt
  • Ethanol: Moderately soluble
  • Organic Solvents: Limited solubility in non‑polar solvents
  • pKa: ~9.6 (amine group), indicating basicity

5. Stability & Reactivity

  • Thermal Stability:
    • Stable under cool, dry conditions
    • Degrades under high heat or prolonged exposure to moisture
  • Light Sensitivity:
    • Sensitive to UV light; store protected from light
  • Oxidation:
    • Low oxidative reactivity but should be kept away from strong oxidizers
  • Chemical Compatibility:
    • Stable with common tablet excipients
    • Non‑reactive with typical laboratory solvents

6. Chemical Behavior

  • Ionization:
    • Forms stable hydrochloride salt, improving solubility and handling
  • Lipophilicity (LogP): ~2.3
    • Moderate membrane permeability
  • Hydrogen Bonding:
    • Capable of both donating and accepting hydrogen bonds
    • Contributes to receptor binding affinity

7. Tablet‑Specific Chemical Considerations

  • Strength: 40 mcg active compound per tablet
  • Matrix: Inert excipients (binders, fillers) chosen for stability and compression
  • Chemical Uniformity:
    • Designed for consistent analytical measurement
    • Ensures reproducibility in controlled research environments

Regulatory Note

Clenbuterol is a research‑only compound. These chemical properties are provided strictly for scientific, analytical, and laboratory reference.

COA /HPLC / MS
3rd Party Testing

3rd Party Tested by Freedom Diagnostics Testing @ Freedom Diagnostics Testing – Reliable. Accountable. Accessible.

Storage

Storage & Handling

  • Store in a cool, dry environment away from light
  • Maintain in secure, controlled laboratory conditions
  • Handle only with appropriate research PPE

Important Notice This compound is not approved for human consumption. It is provided strictly for laboratory, analytical, and scientific research. No claims are made regarding safety, efficacy, or use outside controlled research settings.

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