5-Amino-1-methylquinolinium chloride
| 제품명 | 5-Amino-1-methylquinolinium chloride |
|---|---|
| 다른 이름 | 1-Methyl-5-aminoquinolinium chloride; 5-Amino-1-methylquinolin-1-ium chloride |
| CAS 번호 | Not assigned |
| 분자식 | C10H11ClN2 |
| 분자량 | 194.66 g/mol |
| 외관 | Yellow to orange crystalline powder |
| 분석법 (HPLC) | ≥98.0% |
| 용해도 | Soluble in water, methanol; slightly soluble in ethanol |
| 건조 손실 | ≤0.5% |
| 소각 잔류물 | ≤0.1% |
| 중금속 | ≤10 ppm |
| 패키지 | 25 kg fiber drum with double polyethylene bags |
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Synonyms: 5-Amino-1-methylquinolinium chloride, 1-Methyl-5-aminoquinolinium chloride, 5-Amino-1-methylquinolin-1-ium chloride, NSC 176327
In the evolving landscape of heterocyclic chemistry, 5-Amino-1-methylquinolinium chloride has emerged as a building block of considerable interest for pharmaceutical and agrochemical discovery programs. Its quinolinium core, functionalized with an amino group at the 5-position and a methyl group on the nitrogen, offers a versatile platform for derivatization, making it a valuable intermediate for researchers targeting kinase inhibitors, antimicrobial agents, and fluorescent probes.
5-Amino-1-methylquinolinium chloride is a quaternary ammonium salt derived from 5-aminoquinoline through N-methylation. The permanent positive charge on the nitrogen enhances water solubility and facilitates interactions with biological targets, while the amino group provides a handle for further functionalization via acylation, alkylation, or diazotization. This dual functionality makes it a strategic starting material for constructing complex molecular architectures.
LyvBio supplies 5-Amino-1-methylquinolinium chloride with a purity of ≥98% (HPLC), ensuring consistent performance in demanding synthetic routes. Each batch is rigorously tested to meet strict quality standards, supported by comprehensive documentation for seamless integration into your R&D and production workflows.
5-Amino-1-methylquinolinium chloride is a small molecule with the molecular formula C10H11ClN2 and a molecular weight of 194.66 g/mol. It appears as a yellow to orange crystalline powder that is readily soluble in polar solvents such as water and methanol. The compound’s structure combines a quinolinium cation with a chloride counterion, imparting unique electronic properties that are advantageous in various chemical transformations.
The presence of the amino group at the 5-position allows for selective reactions, enabling the introduction of diverse substituents without affecting the quinolinium core. This regioselectivity is particularly valuable in medicinal chemistry, where precise modifications can lead to improved potency and pharmacokinetic profiles.
| 매개변수 | 사양 |
|---|---|
| 분석법 (HPLC) | ≥98.0% |
| 외관 | Yellow to orange crystalline powder |
| 건조 손실 | ≤0.5% |
| 소각 잔류물 | ≤0.1% |
| 중금속 | ≤10 ppm |
| 용해도 | Soluble in water, methanol |