Description

(E)-n-Methyl-4-(3-Pyridinyl)-3-Buten-1-Amine Fumarate is a high-purity, pharmacologically relevant organic salt, specifically the fumarate salt of a substituted butenylamine. This compound is a critical pharmaceutical intermediate and a key building block in advanced organic synthesis, valued for its defined stereochemistry and consistent quality. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of novel therapeutic agents and fine chemical production.

Application

• Pharmaceutical Intermediate: Serves as a key chiral precursor in the synthesis of active pharmaceutical ingredients (APIs) targeting neurological and other therapeutic areas.
• Medicinal Chemistry Research: Used as a building block for constructing compound libraries and exploring structure-activity relationships (SAR) in drug discovery programs.
• Chemical Synthesis: Acts as a versatile intermediate for the preparation of more complex molecules containing pyridinyl and amine functional groups.
• Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical analysis.
• Biochemical Research: Investigated for its potential interactions with biological systems and receptors in preclinical studies.

Basic Information

Product Name	(E)-n-Methyl-4-(3-Pyridinyl)-3-Buten-1-Amine Fumarate
CAS No.	183288-99-5
Molecular Formula	C14H18N2O4
Molecular Weight	278.31 g/mol
Synonyms	(E)-N-Methyl-4-(3-pyridinyl)-3-buten-1-amine fumarate; (E)-N-Methyl-4-(pyridin-3-yl)but-3-en-1-amine fumarate; (2E)-N-Methyl-4-(3-pyridinyl)-3-buten-1-amine (2E)-2-butenedioate; 3-Buten-1-amine, N-methyl-4-(3-pyridinyl)-, (2E)-, (2E)-2-butenedioate (1:1); (E)-N-Methyl-4-(3-pyridyl)-3-buten-1-amine fumarate; (E)-1-Methyl-4-(3-pyridinyl)-3-buten-1-amine fumarate; (E)-N-Methyl-4-(3-pyridyl)-3-butenylamine fumarate
EINECS	Contact for details

Quality Control

Our (E)-n-Methyl-4-(3-Pyridinyl)-3-Buten-1-Amine Fumarate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the stringent requirements for pharmaceutical research and development. A comprehensive Certificate of Analysis (COA) detailing purity, assay, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to maintain stability.

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%
Purity (HPLC, Area%)	≥99.0%
Water Content (KF)	≤0.5%
Residue on Ignition	≤0.1%
Heavy Metals	≤10 ppm

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