Description

2-(1H-Pyrrolo[2,3-C]Pyridin-3-Yl)Acetic Acid Hydrochloride is a high-purity pharmaceutical intermediate and building block of significant importance in modern organic synthesis. This compound serves as a critical precursor in the research and development of novel therapeutic agents, particularly within the fields of oncology and neurology. It is primarily utilized by pharmaceutical R&D laboratories, contract research organizations (CROs), and fine chemical manufacturers seeking reliable, high-quality raw materials for advanced drug discovery programs.

Application

• Pharmaceutical Intermediate: A key building block for the synthesis of complex drug candidates, especially kinase inhibitors and other targeted therapies.
• Active Pharmaceutical Ingredient (API) Development: Used in the research and scale-up phases for developing new active pharmaceutical ingredients.
• Biochemical Research: Employed as a reagent in proteomics and molecular biology research to study enzyme interactions and signaling pathways.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects under cGMP conditions.
• Academic Research: Utilized in university and institutional laboratories for medicinal chemistry and heterocyclic compound research.
• Library Synthesis: Valuable for creating diverse compound libraries for high-throughput screening in drug discovery.

Basic Information

Product Name	2-(1H-Pyrrolo[2,3-C]Pyridin-3-Yl)Acetic Acid Hydrochloride
CAS No.	933717-12-5
Molecular Formula	C9H9ClN2O2
Molecular Weight	212.63 g/mol
Synonyms	2-(1H-Pyrrolo[2,3-c]pyridin-3-yl)acetic acid hydrochloride; 1H-Pyrrolo[2,3-c]pyridine-3-acetic acid hydrochloride; 3-Carboxymethyl-1H-pyrrolo[2,3-c]pyridine hydrochloride; 933717-12-5; Pyrrolopyridine-3-acetic acid hydrochloride; 2-(1H-Pyrrolo[2,3-c]pyridin-3-yl)ethanoic acid hydrochloride
EINECS	Contact for details

Quality Control

Our 2-(1H-Pyrrolo[2,3-C]Pyridin-3-Yl)Acetic Acid Hydrochloride is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. All materials are subjected to rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to confirm identity and purity. A comprehensive Certificate of Analysis (COA) detailing purity, impurities, and residual solvents is provided with each shipment. We support development under cGMP guidelines for pharmaceutical applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Residual Solvents (GC)	Complies with ICH Q3C guidelines

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