Description

n-(9-Borabicyclo[3.3.1]Nonan-9-Yl)-9-Borabicyclo[3.3.1]Nonan-9-Amine is a highly versatile and reactive organoboron compound, specifically a borane-amine adduct, valued for its role as a selective reducing agent and catalyst precursor. Its primary commercial value lies in enabling precise synthetic transformations in advanced chemical manufacturing, offering chemists a powerful tool for complex molecule construction. This product is essential for research and production in the pharmaceutical, agrochemical, and specialty materials sectors, where high-purity intermediates are critical.

Application

• Asymmetric Synthesis Catalyst Precursor: Serves as a key starting material for generating chiral catalysts used in the production of enantiomerically pure pharmaceuticals and fine chemicals.
• Selective Reducing Agent: Used in organic synthesis for the chemoselective reduction of specific functional groups, such as carbonyls, while leaving other sensitive groups intact.
• Hydroboration Reactions: Acts as a boron source in hydroboration processes to create organoboranes, which are pivotal intermediates for cross-coupling reactions like Suzuki-Miyaura coupling.
• Pharmaceutical Intermediate Manufacturing: Employed in the synthesis of complex drug molecules, particularly in steps requiring controlled stereochemistry and high functional group tolerance.
• Agrochemical Active Ingredient Synthesis: Utilized in the development of advanced pesticides and herbicides where specific stereoisomers are required for optimal activity.
• Polymer & Material Science: Facilitates the creation of novel polymeric materials and coatings through controlled initiation or modification reactions.
• Academic & Industrial R&D: A fundamental reagent in discovery chemistry for developing new synthetic methodologies and exploring novel chemical spaces.

Basic Information

Product Name	n-(9-Borabicyclo[3.3.1]Nonan-9-Yl)-9-Borabicyclo[3.3.1]Nonan-9-Amine
CAS No.	74421-04-8
Molecular Formula	C16H30B2N
Molecular Weight	261.04 g/mol
Synonyms	9-BBN-amine adduct; 9-Borabicyclo[3.3.1]nonane amine complex; Bis(9-borabicyclo[3.3.1]nonyl)amine; Amine-Borane Adduct (9-BBN); n-BBN-9-BBN Amine; 9-BBN-NH2 Adduct; Borane-amine complex (9-BBN derived); Contact for additional trade names.
EINECS	Contact for details

Quality Control

Our n-(9-Borabicyclo[3.3.1]Nonan-9-Yl)-9-Borabicyclo[3.3.1]Nonan-9-Amine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes rigorous analytical testing, including NMR, HPLC, and titration methods, to confirm identity, potency, and impurity profiles. Certificates of Analysis (COA) detailing all specifications are provided with every shipment. We adhere to cGMP principles where applicable to support our customers in regulated industries.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic and easily oxidized nature, the container must be kept sealed and free from moisture and oxygen exposure. Keep away from heat, sparks, and open flame.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Assay (Titration)	≥ 97.0%
Purity (HPLC)	≥ 98.0%
Melting Point	Contact for details
Heavy Metals	< 10 ppm
Residue on Ignition	< 0.1%

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