LGD-4033 (Ligandrol) Capsules

LGD-4033 (Ligandrol) Capsules

$55.00

Description

LGD-4033 (Ligandrol) Capsules: Premium Industrial Grade Chemical Supply

 

Product Details Table

 

Attribute Specification
Brand BioSynLab Research Compounds
Product Name LGD-4033 (Ligandrol)
Synonyms Ligandrol, VK5211, Anabolicum
CAS Number 1165910-22-4
Molecular Formula C₁₄H₁₂F₆N₂O
Molecular Weight 338.25 g/mol
Chemical Class Selective Androgen Receptor Modulator (SARM)
Purity ≥99.0% (HPLC Verified)
Dosage Form Hard Gelatin Capsules
Unit Dose 5mg, 10mg, or 15mg (custom available)
Capsule Size Size 3 (5mg), Size 1 (10mg), Size 0 (15mg)
Capsule Color White opaque (5mg), Gray/White (10mg), Gray (15mg)
Fill Weight 120-250mg (API + excipients)
Excipients Microcrystalline cellulose, Magnesium stearate, Silicon dioxide
Packaging HDPE bottles (30, 60, 90 count) or blister packs
Storage 2-25°C, Desiccated, Light Protected
Shelf Life 24 months (sealed container)
Documentation COA, HPLC, NMR, MS, MSDS, Stability Data
Shipping Ambient Temperature, Discrete
Origin EU/GMP Certified Laboratory

LGD-4033 (Ligandrol) Capsules | High-Potency Selective Androgen Receptor Modulator | BioSynLab

BioSynLab presents pharmaceutical-grade LGD-4033 (Ligandrol) in precision-dosed capsule formulation for advanced androgen receptor research and high-potency anabolic studies. Recognized as one of the most potent non-steroidal SARMs in preclinical literature, Ligandrol serves as a critical research tool for investigating androgen receptor super-agonismmaximum anabolic/androgenic separation, and therapeutic applications in severe muscle wasting conditions and hormone replacement research.

Chemical Architecture & Superior Potency

LGD-4033 (Ligandrol, VK5211) is a non-steroidal selective androgen receptor modulator featuring a unique quinoline-based scaffold that confers exceptional receptor affinity:

Structural Features:

  • Quinoline Core: Fused bicyclic aromatic system providing planar conformation for optimal AR binding
  • Trifluoromethyl Groups: Dual CF₃ substituents enhancing metabolic stability and lipophilicity
  • Pyrrolidine Ring: Five-membered nitrogen heterocycle contributing to binding specificity
  • Amide Linkage: Critical pharmacophore for hydrogen bonding with AR ligand-binding domain

Mechanism of Action:

  • High-Affinity AR Agonist: Ki ~1 nM (highest affinity among commercial SARMs)
  • Tissue Selectivity: Anabolic effects in muscle and bone with minimal androgenic activity in prostate and seminal vesicles
  • Superior Potency: Significantly more potent than MK-2866 (Ostarine) and other first-generation SARMs
  • Oral Bioavailability: Excellent systemic exposure with single daily dosing

Physicochemical Properties:

  • Molecular weight: 338.25 g/mol (lower than MK-2866, enabling higher potency)
  • Calculated LogP: 3.6 (optimal lipophilicity for tissue penetration)
  • pKa: Non-ionizable (neutral molecule at physiological pH)
  • Melting point: 105-110°C (crystalline solid)
  • Chirality: Single enantiomer (chiral center at pyrrolidine)

Capsule Formulation & Pharmaceutical Engineering

Our LGD-4033 capsules utilize precision formulation technology optimized for high-potency delivery:

Excipient Composition:

  • Active Pharmaceutical Ingredient: LGD-4033 – 5mg, 10mg, or 15mg
  • Diluent: Microcrystalline cellulose (Avicel PH-102) – 80-200mg
  • Glidant: Silicon dioxide (Aerosil) – 1-3mg
  • Lubricant: Magnesium stearate – 1-2mg

Capsule Specifications:

Strength Capsule Size Fill Weight Color Code
5mg Size 3 ~120mg White opaque
10mg Size 1 ~180mg Gray/White
15mg Size 0 ~230mg Gray

Quality Attributes:

  • Content uniformity: RSD <5% (tight specifications for high potency)
  • Weight variation: Meets USP <905> criteria
  • Disintegration: <25 minutes (USP <701>)
  • Dissolution: >85% in 30 minutes (rapid release profile)

Packaging Options:

  • HDPE bottles: 30, 60, 90 count with desiccant canister and cotton filler
  • Blister packs: 10 capsules per sheet, child-resistantunit-dose
  • Bulk packaging: 500, 1000 count for institutional research programs

Analytical Characterization & Quality Verification

Each BioSynLab LGD-4033 batch undergoes comprehensive analytical profiling:

Chromatographic Analysis:

  • HPLC-UV (220nm): ≥99.0% purity by area normalization
  • Chiral HPLC: Enantiomeric purity >99% ee (single enantiomer)
  • Related substances: <1.0% total impurities, <0.3% single impurity
  • Residual solvents: Meets ICH Q3C (methanol, ethanol, acetonitrile, hexane, toluene)

Mass Spectrometry:

  • LC-MS/MS: [M+H]⁺ at m/z 339.1, characteristic fragmentation pattern
  • High-Resolution MS: Exact mass confirmation <3 ppm deviation (C₁₄H₁₃F₆N₂O⁺: 339.0967)

Nuclear Magnetic Resonance (NMR):

  • ¹H NMR (600MHz, DMSO-d₆):
    • Quinoline aromatic: δ 7.2-8.4 (m, 6H)
    • Pyrrolidine CH: δ 4.85 (m, 1H)
    • Pyrrolidine CH₂: δ 2.1-2.6 (m, 4H)
    • Amide NH: δ 8.72 (br s, 1H)
  • ¹⁹F NMR: Two distinct signals at δ -62.1 and -63.8 ppm (non-equivalent CF₃ groups)
  • ¹³C NMR (150MHz): 14 distinct carbon signals (symmetry-reduced)
  • FTIR: Amide N-H (3300 cm⁻¹), C=O (1680 cm⁻¹), C-F (1120, 1160 cm⁻¹), aromatic (1600 cm⁻¹)

Physical Testing:

  • Water content: <0.3% (Karl Fischer, coulometric)
  • Heavy metals: <5 ppm (ICP-MS, industrial standard)
  • Specific rotation: [α]²⁰D = +8° to +12° (c=1, methanol)
  • Residue on ignition: <0.1%

Research Applications & Scientific Significance

LGD-4033 capsules serve critical functions in multiple research disciplines:

Androgen Receptor Pharmacology:

  • Ultra-high affinity binding studies (sub-nanomolar Ki determination)
  • Crystal structure investigations (AR LBD co-crystallization)
  • Coactivator recruitment (SRC-1, GRIP1, p/CIP)
  • Coregulator profiling (NCoR, SMRT interactions)

Musculoskeletal Research:

  • Severe muscle atrophy models (cancer cachexia, COPD, HIV)
  • Hip fracture recovery studies (elderly populations)
  • Glucocorticoid-induced myopathy (steroid muscle wasting)
  • Sarcopenia interventions (age-related muscle loss)

Bone Health Research:

  • Osteoporosis models (ovariectomy, glucocorticoid-induced)
  • Bone mineral density enhancement studies
  • Fracture healing acceleration
  • Osteoblast/osteoclast activity modulation

Comparative SARM Research:

  • Potency comparisons (LGD-4033 vs. MK-2866 vs. RAD-140)
  • Selectivity profiling (prostate vs. muscle activity ratios)
  • Dose-response modeling (low-dose efficacy studies)
  • Combination studies (SARM + other anabolics)

Metabolic Studies:

  • Body recomposition analysis (muscle gain + fat loss)
  • Insulin sensitivity (glucose disposal rate)
  • Lipid metabolism (HDL/LDL effects)
  • Energy homeostasis (basal metabolic rate)

Clinical Translation Research:

  • Phase I/II modeling (dose escalation studies)
  • Pharmacokinetic profiling (t½ ~24-36 hours, QD dosing)
  • Safety pharmacology (hepatic, renal, cardiovascular)
  • Therapeutic index determination

Global Distribution & Discrete Procurement

BioSynLab provides secure, compliant distribution:

Packaging Specifications:

  • Primary: Hard gelatin capsules in HDPE bottles or blister packs
  • Secondary: Tamper-evident sealsdesiccant chambersoxygen absorbers
  • Tertiary: Discrete unmarked shipping containerscustoms documentation

Shipping Options:

  • Standard: Ambient temperature, 5-7 days
  • Express: Tracked courier, 2-3 days (DHL, FedEx, UPS)
  • Discrete: No product identifiers, generic return addresses, commercial invoices

Service Coverage:

United Kingdom: London, Manchester, Birmingham, Leeds, Glasgow, Liverpool, Sheffield, Bristol, Edinburgh, Cardiff, Belfast, Nottingham, Leicester, Coventry, Brighton.

European Union: Berlin, Hamburg, Munich, Cologne, Frankfurt, Amsterdam, Rotterdam, Paris, Lyon, Barcelona, Madrid, Rome, Milan, Vienna, Brussels, Prague, Warsaw, Budapest, Stockholm, Copenhagen, Oslo, Helsinki, Lisbon, Dublin, Zurich.

North America: New York, Los Angeles, Chicago, Houston, Philadelphia, San Antonio, San Diego, Dallas, San Jose, Austin, Jacksonville, Fort Worth, Columbus, Charlotte, San Francisco, Indianapolis, Seattle, Denver, Washington D.C., Boston, Toronto, Vancouver, Montreal.