SOLASONINE CAS#19121-58-5

CAS Number: 19121‑58‑5

Chemical Formula: C₄₅H₇₃NO₁₆

Synonyms: PURAPURI, NSC 82149, Solasonine, alpha‑Solasonine

Appearance: Fine, free‑flowing white crystalline powder, with uniform particle size distribution. The material shows no obvious lumps or visible foreign impurities under normal visual inspection, maintaining stable physical status under proper storage conditions.

Product Introduction: Solasonine is a naturally‑derived bioactive compound, also well‑known under alternative aliases including PURAPURI, NSC 82149 and alpha‑Solasonine. This high‑purity powder material is widely researched for its biological activities, frequently applied in pharmaceutical intermediate projects, lab‑scale trials and related formulation development work. Strict quality control is implemented throughout production to guarantee consistent batch quality to meet downstream research and manufacturing requirements.

MOQ (Minimum Order Quantity): The minimum ordering threshold is one full container load (1 FCL). We maintain stable production capacity and standardized export‑grade packaging to satisfy large‑volume commercial procurement demands from research institutions and manufacturing enterprises.

SOLASONINE CAS#19121‑58‑5

Solasonine is a natural steroidal glycoalkaloid widely distributed across multiple plant species belonging to the Solanum genus, including S. aviculare, S. sodomeum, S. verbascifolium and S. xanthocarpum. 

This bio‑active alkaloid can be recrystallized from 80% ethanol to form hydrous crystals containing 4.5 molecules of water, displaying a melting point of 245‑250 °C with decomposition upon heating. Its anhydrous crystalline form can be obtained by recrystallization from absolute methanol. It presents a specific rotation value of [α]₂₅ᴰ ‑68° when dissolved in ethanol. Multiple derivative salts can be prepared from this compound: hydrochloride with melting point at 265 °C, picrate melting at 199‑201 °C, picrolonate melting at 230 °C, as well as its acetyl derivative with melting point ranging from 135‑138 °C. When subjected to alkaline hydrolysis conditions, the molecule breaks down to produce solasodine aglycone, alongside one‑mole equivalent each of galactose, glucose and rhamnose sugar units. 

When mixed with concentrated sulfuric acid, its solution gradually develops a distinct crimson colour accompanied by brown fluorescence, which serves as a typical identification reaction for this substance. In terms of solubility performance, it dissolves readily in hot ethanol and hot dioxane, shows limited solubility in hot water and dilute acetic acid, while being practically insoluble in chloroform and diethyl ether. 

Industrially, this compound is mainly extracted from the fruit of Solanum aviculare Forst., a well‑documented plant species within the Solanaceae family, and undergoes strict purification procedures to meet research and intermediate‑grade material requirements.

SOLASONINE Chemical Properties

Melting point 

301-303℃

alpha 

D23 -88° (c = 1.01 in pyridine); D22 -74.5° (c = 0.51 in methanol)

density 

1.42

solubility 

DMSO : 100 mg/mL (113.11 mM; Need ultrasonic)

form 

powder

pka

12.78±0.70(Predicted)

color 

White-beige

InChIKey

QCTMYNGDIBTNSK-YQBIRKIONA-N

LogP

4.350 (est)

SOLASONINE Chemical Properties

Solasonine features stable and standardized physicochemical properties. Its melting point is 301–303℃. The specific rotation is D23 -88° (c = 1.01 in pyridine) and D22 -74.5° (c = 0.51 in methanol), with a density of 1.42. The product shows good solubility in DMSO, reaching 100 mg/mL (113.11 mM) with ultrasonic assistance required for full dissolution. It appears as white-beige powder form. The predicted pKa value is 12.78±0.70, and the estimated LogP value is 4.350. Its fixed InChIKey is QCTMYNGDIBTNSK-YQBIRKIONA-N for accurate chemical identification.

Product Application of SOLASONINE CAS#19121-58-5

α-Solasonine is a pure natural glycoalkaloid compound derived from Solanaceae plants. It has prominent biological activity and is commonly applied in biomedical research. Relevant studies prove that it can effectively inhibit Gli-mediated transcriptional activity, serving as a key experimental material for pharmacological research and new drug development.

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