Description

6-(2,2-Dimethyl-Propionylamino)-Nicotinic Acid is a high-purity, advanced pharmaceutical intermediate with a distinct molecular structure. This compound is valued for its role as a critical building block in the synthesis of complex active pharmaceutical ingredients (APIs), particularly in research and development for novel therapeutic agents. It is primarily sought by pharmaceutical manufacturers, biotechnology R&D laboratories, and fine chemical synthesis companies engaged in developing next-generation medications.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of complex drug molecules and active pharmaceutical ingredients (APIs).
• Biotechnology Research: Used in medicinal chemistry for the design, discovery, and optimization of new chemical entities with potential therapeutic activity.
• Organic Synthesis Building Block: Serves as a versatile reagent for constructing heterocyclic compounds and introducing specific functional groups in complex organic molecules.
• Contract Manufacturing (CMO/CDMO): Supplied to contract development and manufacturing organizations for use in custom synthesis projects and scale-up production.
• Academic & Institutional Research: Utilized in university and institutional laboratories for chemical research and the study of reaction mechanisms.

Basic Information

Product Name	6-(2,2-Dimethyl-Propionylamino)-Nicotinic Acid
CAS No.	898561-66-5
Molecular Formula	C11H14N2O3
Molecular Weight	222.24 g/mol
Synonyms	6-(2,2-Dimethylpropanamido)nicotinic acid; 6-Pivalamidonicotinic acid; 6-[(2,2-Dimethylpropanoyl)amino]pyridine-3-carboxylic acid; Nicotinic acid, 6-[(2,2-dimethyl-1-oxopropyl)amino]-; Pivalic acid (6-carboxy-3-pyridyl)amide; 898561-66-5; 6-(Pivaloylamino)nicotinic acid
EINECS	Contact for details

Quality Control

Our 6-(2,2-Dimethyl-Propionylamino)-Nicotinic Acid is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets the high-purity standards required for pharmaceutical R&D and synthesis. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing purity, identity, and impurity profiles. Our quality commitment aligns with cGMP principles where applicable, ensuring reliable and consistent material for your critical processes.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). The material may be hygroscopic (moisture-sensitive); therefore, the container must be kept tightly sealed to prevent absorption of atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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