The largest database of trusted experimental protocols

3 protocols using 1 hexylamine

1

Functionalized Polystyrene Microparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols
Sodium p-styrenesulfonate hydrate (TCI, > 93.0%) (NaStS); copper(I) bromide 98% (Sigma-Aldrich, Seoul, South Korea) (CuIBr); 4-(bromomethyl)benzoic acid 97% (Alfa Aesar, Seoul, South Korea) (BMB); 2,2′-bipyridine (bpy) 99.5% (Junsei, Tokyo, Japan); 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (TCI, > 98.0%) (DMTMM); propiolic acid (TCI, > 97.0%) (PA); 1-hexylamine 99% (Sigma-Aldrich) (HA); and ninhydrin (TCI, > 98%) were used as received, without further purification. Silica gel 60 (Merck, 0.063-0.200 mm) was used for the column chromatography while tetrahydrofuran (Duksan, extra pure grade) (THF) was used to improve the purity of the polymer through solvent-precipitation. Deuterium oxide 99.9% D (Cambridge Isotope Laboratories, Inc., Seoul, South Korea) (D2O) was used as the NMR solvent. Polystyrene microparticles (5% w/v, 2.0–2.2 μm diameter) having surfaces functionalized with amine groups, were procured from Spherotech, IL, Illinois, USA.
+ Open protocol
+ Expand
2

Synthesis and Characterization of Functionalized Polymers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Dopamine hydrochloride (99%, DA), 2,3-dichloromaleic anhydride (97%), 1-hexylamine (99%), sodium citrate tribasic (≥99%), and fluorobenzene were purchased from Sigma-Aldrich (Sydney, Australia) and used as received without any further purification. Silver nitrate and triethylamine (TEA) were purchased from Univar (Sydney, Australia) and also used as received. 2,2′-azobis(isobutyronitrile) (AIBN, Sigma-Aldrich, 97%) was purified by recrystallization from cold methanol prior to use. Pentafluorostyrene (PFS, Oakwood Products, 99%) was passed through a column of activated basic alumina prior to use to remove inhibitor. 4-cyanopentanoic acid dithiobenzoate (CPADB) was synthesized as described in the literature [22 (link)]. 1-thio-β-ᴅ-glucose sodium salt (GluSNa) was prepared from 1-thio-β-ᴅ-glucose tetraacetate (AcO-GluSH) according to literature method [23 (link)]. All solvents were laboratory reagent grade and used as received without any further purification.
+ Open protocol
+ Expand
3

Synthesis of Alkylamine Derivatives

Check if the same lab product or an alternative is used in the 5 most similar protocols
Glyoxal (40 wt% in water), oxalic acid (98%, 144-62-7), and 1-octylamine (99+%, 111-86-4) were purchased from Acros Organics (Geel, Belgium). 1-Decylamine (98%, 2016-57-1) was purchased from TCI Europe (Zwijndrecht, Belgium). 1-Hexadecylamine (94%, 143-27-1) and 1-octadecylamine (≥85%, 124-30-1) were obtained from Merck (Heverlee, Belgium). 1-Hexylamine (99%, 111-26-2) and nitric acid (70 wt% in water, 7697-37-2) were bought from Sigma-Aldrich (Diegem, Belgium). 1-Dodecylamine (98%, 124-22-1) and 1-tetradecylamine (98%, 2016-42-4) were purchased from Janssen-Chemica (Beerse, Belgium). Acetic acid, glacial (100%, 64-19-7), hydrochloric acid (37 wt% in water, 7647-01-0) and formaldehyde (36 wt% in water, 50-00-0) were obtained from Fisher Scientific Limited (Loughborough, UK). Petroleum ether (bp 40–65 °C, technical grade) and acetonitrile (≥99.8%) were obtained from VWR (Heverlee, Belgium). Petroleum ether was distilled prior to use to remove high boiling residues. All other chemicals were used as received without further purification.
+ 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!