33788-00-0

Basic information

• Product Name: 6-AMINOUNDECANE
• Synonyms: 1-Pentylhexylamine;6-Undecanamine;6-AMINOUNDECANE;NISTC33788000
• CAS NO: 33788-00-0
• Molecular Formula: C₁₁H₂₅N
• Molecular Weight: 171.32
• Product Categories: alkyl
• Mol File: 33788-00-0.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 158°C/28mmHg(lit.)
• Flash Point: 92.8°C
• Appearance: /
• Density: 0.799g/cm³
• Vapor Pressure: 0.0664mmHg at 25°C
• Refractive Index: 1.4340 to 1.4380
• PKA: 11.13±0.35(Predicted)
• CAS DataBase Reference: 6-AMINOUNDECANE(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINOUNDECANE(33788-00-0)
• EPA Substance Registry System: 6-AMINOUNDECANE(33788-00-0)

Safety Data

• RIDADR: UN 2735 8/PG II
• HazardClass: 8
• PackingGroup: II
• Hazardous Substances Data: 33788-00-0(Hazardous Substances Data)

Usage

General Description

6-Aminoundecane is a chemical compound with the molecular formula C11H25N. It is a long-chain primary amine, also known as 1-aminoundecane, and is commonly used as an intermediate in the production of various industrial chemicals and surfactants. Its primary function is as a building block in the synthesis of emulsifiers, corrosion inhibitors, and lubricants. 6-Aminoundecane is a water-soluble compound and is known for its mild odor. It is generally used in the chemical industry for its properties as a dispersing agent and surfactant, as well as for its ability to modify the surface tension of liquids.

InChI:InChI=1/C11H25N/c1-3-5-7-9-11(12)10-8-6-4-2/h11H,3-10,12H2,1-2H3

Upstream product

• 32504-26-0 6-(hydroxyimino)undecane 
• 1158270-35-9 N-(1-pentylhexyl)phthalimide 
• 927-49-1 dipentyl ketone 

Downstream Products

• 1157351-13-7 C₁₇H₂₉N 

Relevant articles and documents

RETRACTED ARTICLE: Step-Growth Annulative ?-Extension Polymerization for Synthesis of Cove-Type Graphene Nanoribbons

Graphene nanoribbons (GNRs), nanometer-wide strips of graphene, are attracting significant attention in materials science as candidates for next-generation carbon materials. As their physical properties mainly depend on their structures, the precise synthesis of structurally well-defined GNRs is highly desirable to control their properties. Herein, we report a step-growth annulative ?-extension polymerization that allows for the rapid and modular synthesis of cove-type GNRs with pyrene and/or coronene diimide repeating units. The structures and photophysical properties of the separated GNRs were confirmed by various spectroscopic analyses. In addition, gas-blow-assisted uniform on-surface self-assembly of the GNRs was accomplished.

Non-fullerene acceptor engineering with three-dimensional thiophene/selenophene-annulated perylene diimides for high performance polymer solar cells

We report two new propeller-shaped perylene diimide (PDI) acceptors based on tetraphenylethylene (TPE) as the core and flanked with S/Se-fused PDIs, named as TPE-PDI4-S and TPE-PDI4-Se. Compared to the sulfur-annulated counterpart, T

N -Annulated perylene diimide derivatives as non-fullerene acceptors for solution-processed solar cells with an open-circuit voltage of up to 1.14 v

Three different non-fullerene small molecular acceptors containing N-annulated perylene diimide, named di-PNR, TPA-PNR and EDOT-PNR, were successfully designed and synthesized for photovoltaic applications. Introducing an electron donating unit such as tr