95745-99-6

Usage

Chemical class

Organic compound

Structure

Long hydrophobic carbon chain attached to a benzene ring

Primary use

Corrosion inhibitor in metalworking fluids and lubricants

Industrial applications

Water or moisture resistance

Additional uses

Additive in metalworking fluids for improved lubrication, surfactant and emulsifier in personal care products and cosmetics

Safety concerns

Potential toxicity and adverse health effects; proper safety precautions required during handling and use

Upstream product

• 1493-27-2 ortho-nitrofluorobenzene 
• 95-54-5 1,2-diamino-benzene 
• 112-89-0 1-Bromooctadecane 
• 95808-72-3 N-(2-Nitrophenyl)-1-octadecanamine 

Downstream Products

• 405167-22-8 4,6-Dinitro-N,N'-bis-(2-octadecylamino-phenyl)-benzene-1,3-diamine 

Relevant academic research and scientific papers

Supramolecular Chemistry-Based One-Pot High-Efficiency Separation of Solubilizer-Free Pure Semiconducting Single-Walled Carbon Nanotubes: Molecular Strategy and Mechanism

Single-walled carbon nanotubes (SWCNTs) have the potential to revolutionize nanoscale electronics and power sources; however, their low purity and high separation cost limit their use in practical applications. Here we present a supramolecular chemistry-based one-pot, less expensive, scalable, and highly efficient separation of a solubilizer/adsorbent-free pure semiconducting SWCNT (sc-SWCNT) using flavin/isoalloxazine analogues with different substituents. On the basis of both experimental and computational simulations (DFT study), we have revealed the molecular requirements of the solubilizers as well as provided a possible mechanism for such a highly efficient selective sc-SWCNT separation. The present sorting method is very simple (one-pot) and gives a promising sc-SWCNT separation methodology. Thus, the study provides insight for the molecular design of an sc-SWCNT solubilizer with a high (n,m)-chiral selectivity, which benefits many areas including semiconducting nanoelectronics, thermoelectric, bio and energy materials, and devices using solubilizer-free very pure sc-SWCNTs.

The structure of a tetraazapentacene molecular monolayer

Langmuir molecular monolayers of a unique tetraazapentacene zwitterionic amphiphile were found to form stripe-like domains that responded strongly to an applied magnetic field. These stripe domains were transferred as Langmuir-Blodgett (LB) films to glass

Benzimidazole derivative, hair growth promoter and external composition for skin using the same

A benzimidazole derivative or a salt thereof expressed by the following Formula (I): wherein one of A and B is a hydrocarbon group of C10-30expressed by R1and the other is —(CH2)n—NR2R3; R