4,4′-Diaminobenzophenone

Name: 4,4′-Diaminobenzophenone
Brand: ChemScene
Availability: InStock
Rating: 5 (1 reviews)

CAS No. 611-98-3
Cat. No. CS-W015006
Purity≥98%
MDL No.MFCD00038138

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HazMat Fee

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Each bottle is packed as an Excepted Quantity, with a maximum of 1g for items in class 6.1 packing group I or II, and up to 25g for all other hazardous materials.

If shipping is charged to your FedEx account, the HazMat fee will be billed directly by the courier. Otherwise, the fee will be included on your invoice. To help you avoid the HazMat fee, we can package a 5g order of a class 6.1 packing group I or II material as five separate 1g units, and a 100g order of any other dangerous good as four 25g units. This packaging adjustment will be made unless you instruct otherwise on your purchase order. Below, you will find the fee schedule from FedEx for handling hazardous materials.

Type	HazMat Fee
Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
Hazmat Ground shipping	$50.00+
Inaccessible (Haz class 6.1 or 9), Domestic	$68.00+
Accessible (Haz class 3, 4, 5 or 8), Domestic	$158.00+
Inaccessible (Haz class 6.1 or 9), International	$108.00+
Accessible (Haz class 3, 4, 5 or 8), International	$238.00+

An item is classified as a dangerous good if our website displays Hazardous Material (HazMat) information for it.

There is a HazMat shipping fee for each item that qualifies as a dangerous good. Please contact our quotation team via email to confirm the details.

*For research and further manufacturing use only, not for direct human use.

Structure of 611-98-3

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Description

4,4′-Diaminobenzophenone features two amino groups positioned para to the carbonyl linkage, enabling its integration into polyamides and conjugated polymers. The electron-rich diamine moiety enhances charge transport properties while maintaining structural rigidity. This compound serves as a key monomer for high-performance materials requiring thermal stability and electronic functionality.

Application

4,4′-Diaminobenzophenone serves as a key building block in the synthesis of advanced organic materials and pharmaceutical intermediates. Its dual aniline functionalities enable efficient coupling reactions, including amide and urea formation, while maintaining stability under standard reaction conditions. The molecule functions as a versatile scaffold for constructing conjugated systems, with demonstrated utility in dye chemistry and polymer development due to its excellent solubility and thermal resilience.

General Information

CAS No. 611-98-3
Cat. No. CS-W015006
Purity ≥98%
MDL No. MFCD00038138
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₁₃H₁₂N₂O
Molecular Weight 212.25
Synonym(s) None
SMILES NC1=CC=C(C(C2=CC=C(N)C=C2)=O)C=C1

Computational Chemistry Data

TPSA 69.11
LogP 2.082
H_Acceptors 3
H_Donors 2
Rotatable_Bonds 2

Safety Information

Download SDS

GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352

Quality Control

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Other Classifications

Building Blocks Functional Group Ketone

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Material Science Polymer Materials Macromolecular Monomer

Material Science Biomaterials/Biocompatible Materials Research Reagents Monomers, Macromonomers Diamine Monomers

Material Science Polymer/Macromolecule Reagents Monomers Diamine Monomers

Material Science Polymer/Macromolecule Reagents Polyimide Raw Materials Diamines

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4,4′-Diaminobenzophenone

CAS No. 611-98-3

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