N propylamine
N-propylamine is a chemical compound used in various laboratory applications. It functions as a building block for the synthesis of other organic compounds. The core function of N-propylamine is to serve as a reagent or intermediate in chemical reactions and formulations. Further details on its intended use are not available.
Lab products found in correlation
12 protocols using n propylamine
Functionalized Nanomaterials Synthesis Protocols
Synthesis and Characterization of Dental Composites
Facile Synthesis of CuO Nanoparticles
Synthesis and Characterization of Thermoresponsive Polymers
N-n-propylacrylamide (NNPAM) was synthesized via a Schotten–Baumann reaction published by Hirano et al. [21 ]. For this reaction, acryloylchloride (Sigma-Aldrich Chemie GmbH, Munich, Germany; purity 98%), n-propylamine (Fluka, Sigma-Aldrich Chemie GmbH, Munich, Germany; purity 99%), triethylamine (Grüssing GmbH Analytika, Filsum, Germany; purity 99%) and methylenchloride (p.a.) were used as received. The obtained monomer NNPAM was washed with NaHCO (10 wt %) and dried over MgSO . After filtration, the solvent was evaporated and the product was distilled in vacuum (115 C, 10 mbar).
Synthesis of Metal Oxide Nanoparticles
Preparation of Arsenic Sulfide Solutions
Synthesis and Characterization of Siloxane-Based Antimicrobials
Trimethylvinylsilane (Me3SiVi, 97%), used for the in vitro tests of antimicrobial activity and for the synthesis of Me3SiCH2CH2SCH2COOH, was purchased from Sigma Aldrich and used as received. Poly(vinylsilsesquioxane) terminated with trimethylsilyl groups (LPSQ) was obtained as previously reported [50 (link)].
Silver Nanoparticle Synthesis Protocol
Synthesis of Semiconductor Nanocrystals
(99%), di-n-propylamine (99%), diethylamine (>99.5%),
phenethylamine
(≥99%), n-dodecylamine (≥99%), n-octylamine (+99%), n-pentylamine (+99%), n-propylamine (+98%), Cd(OAc)2·2H2O (>98%), trin-octylphosphine (TOP) (97%), and
oleylamine
(or cis-9-octadecenylamine, technical grade, 70%) were obtained from
Sigma-Aldrich. Selenourea (99.9%, metal basis) was obtained from Alpha
Aesar. All were used as received and stored under N2. Toluene
was obtained from Sigma-Aldrich (CHROMASOLV for HPLC, ≥99.9%).
Transmission electron microscopy (TEM) sample grids (Cu with holey
carbon film) were obtained from Ted Pella, Inc.
All synthetic
procedures were conducted under dry N2, except the final
washing steps, which were conducted in the ambient atmosphere. The
reaction mixtures were not stirred. The synthetic products were generally
stored as reaction mixtures, after addition of TOP (see below).
Electrode Material Synthesis and Characterization
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