Product Summary
LGD3303, LGD-3303 SARM, CAS 917891-35-1, SARM raw powder, research chemical) Item Specification Product Name LGD-3303 CAS No. 917891-35-1 IUPAC Name 9-Chloro-2-ethyl-1-methyl-3-(2,2,2-trifluoroethyl)-6H-pyrrolo[3,2-f]quinolin-7-one Molecular Formula C₁₆H₁₄ClF₃N₂O Molecular Weight 342.74 g/mol Purity ...
Dietary Supplement Powder SARM Powder LGD 3303 muscle tissue reducing fat sarms
Basic Properties
Trading Properties
LGD 3303 SARM powder
,muscle tissue dietary supplement
,fat reducing SARMs powder
LGD3303, LGD-3303 SARM, CAS 917891-35-1, SARM raw powder, research chemical)
| Item | Specification |
|---|---|
| Product Name | LGD-3303 |
| CAS No. | 917891-35-1 |
| IUPAC Name | 9-Chloro-2-ethyl-1-methyl-3-(2,2,2-trifluoroethyl)-6H-pyrrolo[3,2-f]quinolin-7-one |
| Molecular Formula | C₁₆H₁₄ClF₃N₂O |
| Molecular Weight | 342.74 g/mol |
| Purity | ≥98% HPLC Tested |
| Appearance | Pale Yellow to Off-White Crystalline Powder |
| Solubility | Soluble in DMSO, Slightly soluble in Methanol & Chloroform |
| Storage | -20℃ Sealed, Avoid Light & Moisture |
| Available Package | 5mg,10mg,50mg,100mg,500mg,1g bulk powder |
| Certificate | COA, HPLC, NMR, MSDS Available |
| Usage | Only for Laboratory Research Purpose, Not for Human Consumption / Clinical Use |
2. Core Research Properties & Mechanism
High Tissue Selectivity: Oral available SARM with brain penetrability; nearly no cross-binding with glucocorticoid, mineralocorticoid and progesterone receptors. At effective muscle-building dose (1mg/kg oral daily), LGD-3303 fully prevents muscle weight loss without obvious prostate proliferation in animal trials.
Potent Anabolic Effect on Muscle: Stimulates protein synthesis effectively to boost lean muscle mass; verified to raise levator ani muscle weight significantly in castrated rat models at elevated dosage.
Outstanding Bone Metabolism Promotion: Improves bone mineral density (BMD), bone mineral content & bone formation rate, widely studied for anti-osteoporosis related pharmacology research.
Good Oral Bioavailability: No aromatization, stable chemical property for oral administration research trials.
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