Log In Sign up
The largest database of trusted experimental protocols

2 ethylhexylamine

Manufactured by Merck Group
Visit Supplier

2-ethylhexylamine is a chemical compound used in various industrial applications. It is a colorless liquid with a characteristic amine odor. The core function of 2-ethylhexylamine is as a chemical intermediate in the synthesis of other compounds.

Automatically generated - may contain errors

Lab products found in correlation

Propylamine hydrochloride, by Merck Group (1 mentions) Formaldehyde, by Avantor (1 mentions) Butylamine, by Merck Group (1 mentions) Alpha ftir, by Bruker (1 mentions) La no3 3 6h2o, by Merck Group (1 mentions) Y no3 3 6h2o, by Merck Group (1 mentions) Topspin 4, by Bruker (1 mentions) Optima8300 dv icp oes spectrometer, by PerkinElmer (1 mentions) Avance 3 300 mhz spectrometer, by Bruker (1 mentions) Pentaerythritol triacrylate, by Merck Group (1 mentions) Tetrahydrofuran thf, by Thermo Fisher Scientific (1 mentions) Benzyl acrylate, by Merck Group (1 mentions) N butylamine, by Merck Group (1 mentions) N hexane, by Thermo Fisher Scientific (1 mentions) 2 ethylhexyl acrylate, by Merck Group (1 mentions) Trimethylolpropane triacrylate, by Merck Group (1 mentions) Dibutylamine, by Merck Group (1 mentions) N octylamine, by Merck Group (1 mentions)

2 protocols using 2 ethylhexylamine

1

Lanthanoid Complexes Synthesis and Characterization

Check if the same lab product or an alternative is used in the 5 most similar protocols
Formaldehyde (36%) was purchased
from VWR; phosphorous acid (99%) and hexylamine (98%) from Fluka Chemical
Co.; 2-ethylhexylamine (98%), La(NO3)3·6H2O, and propylamine hydrochloride from Sigma-Aldrich; ethylamine
hydrochloride (98%), butylamine (99%), and Y(NO3)3·6H2O (99.8%) from Merck; and Lu(NO3)3·H2O from abcr and amylamine (98%) from TCI
chemicals. All of the chemicals were reagent grade and used without
further purification. NMR measurements and titrations were performed
on a Bruker Avance III 300 MHz-spectrometer, and NMR data was processed
with Bruker TopSpin 4.0.8. IR spectra were measured by Bruker Alpha
FT-IR. Elemental analyses were done by an Elementar Vario EL III-analysator.
Lanthanoid concentrations were determined by a Perkin Elmer Optima
8300 DV ICP-OES- spectrometer.
Virtanen E.J., Perämäki S., Helttunen K., Väisänen A, & Moilanen J.O. (2021). Alkyl-Substituted Aminobis(phosphonates)—Efficient Precipitating Agents for Rare Earth Elements, Thorium, and Uranium in Aqueous Solutions. ACS Omega, 6(37), 23977-23987.
+ Open protocol
+ Expand
2

Synthesis of Acrylate and Amine Monomers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Material Benzylalcohol (≥99%), benzylacrylate (≥99%, contains hydroquinone monomethyl ether (MEHQ) as inhibitor), bisphenol A glycerolate (1 glycerol/phenol) diacrylate (contains 250-500ppm MEHQ as inhibitor), n-butylamine (≥99%), dibutylamine (≥99%), N,Ndiisopropylethylamine (DIPEA, ≥99%) 2-ethylhexylacrylate (98%, contains MEHQ as inhibitor), 2-ethylhexylamine (98%), N-methylbutylamine (≥98%), pentaerythritol triacrylate (PTA, technical grade, contains 600ppm MEHQ as inhibitor), trimethylolpropane triacrylate (TMPTA, technical grade, contains 300-400ppm MEHQ as inhibitor), n-octylamine (99%), were purchased from Sigma-Aldrich. Tetrahydrofuran (THF), and n-hexane were purchased from Acros Organics.
4,4′-methylenebis(cyclohexylamine) (MBCA, >98%) was purchased from TCI. Jeffamine D2000 was kindly provided by Huntsman, and Priamine 1074 was kindly provided by Croda. All reagents were used without further purification unless stated otherwise.
Taplan C., Guerre M, & Du Prez F.E. (2021). Covalent Adaptable Networks Using β-Amino Esters as Thermally Reversible Building Blocks. Journal of the American Chemical Society, 143(24).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!