Description

1-Methyloctahydro-1,6-Naphthyridin-2(1H)-One Hydrochloride is a high-purity, specialized organic salt of significant interest in advanced pharmaceutical research and development. This compound serves as a critical building block (intermediate) for the synthesis of complex molecules, particularly those targeting neurological and therapeutic applications. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in the production of active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Intermediate: A key synthetic precursor in the development of novel drug candidates, particularly for central nervous system (CNS) targets.
• Active Pharmaceutical Ingredient (API) Synthesis: Used in multi-step synthetic routes to construct complex nitrogen-containing heterocycles found in modern therapeutics.
• Medicinal Chemistry Research: Employed as a scaffold or building block for structure-activity relationship (SAR) studies and library synthesis in drug discovery.
• Biochemical Research: May be used as a reference standard or tool compound in pharmacological and biochemical assays.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects under cGMP conditions.

Basic Information

Product Name	1-Methyloctahydro-1,6-Naphthyridin-2(1H)-One Hydrochloride
CAS No.	848410-29-7
Molecular Formula	C9H15N2O·HCl
Molecular Weight	202.69 g/mol
Synonyms	1-Methyl-1,2,3,4,6,7,8,9-Octahydro-1,6-Naphthyridin-2-one Hydrochloride; 1-Methyl-1,2,3,4,6,7,8,9-octahydro-1,6-naphthyridin-2-one HCl; 1-Methyloctahydro-1,6-naphthyridin-2(1H)-one hydrochloride; 1,2,3,4,6,7,8,9-Octahydro-1-methyl-1,6-naphthyridin-2-one hydrochloride; 1-Methyl-1,2,3,4,6,7,8,9-octahydro-1,6-naphthyridin-2-one monohydrochloride
EINECS	Contact for details

Quality Control

Our production of 1-Methyloctahydro-1,6-Naphthyridin-2(1H)-One Hydrochloride adheres to stringent quality management protocols. The material is manufactured and tested to meet exacting standards suitable for pharmaceutical R&D applications. Certificates of Analysis (COA) are provided with each batch, detailing purity, identity, and impurity profiles. We support development with custom synthesis and can scale production under controlled conditions to meet specific project requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%; Any single impurity ≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.