2 bromoethylamine hydrobromide
2-bromoethylamine hydrobromide is a chemical compound commonly used as a laboratory reagent. It is a colorless crystalline solid that is soluble in water and alcohol. The compound is often utilized in organic synthesis reactions and is a versatile building block in the preparation of various derivatives.
Lab products found in correlation
9 protocols using 2 bromoethylamine hydrobromide
Antibody Characterization and Modification
Synthesis of Imidazole-based Compounds
Lipid-Polymer Hybrid Nanoparticle Synthesis
Synthesis and Characterization of Ionic Liquids
Peptide Synthesis Reagents and Solvents
(TIS), 2-bromoethylamine
hydrobromide, Chloroform-d1, sodium borohydride,
dimethyl sulfoxide-d6, bromoacetic acid, N,N′-diisopropylcarbodiimide (DIC), 4-bromobenzyl
bromide, methanol-d4, and H-Rink Amide
ChemMatrix were purchased from Sigma-Aldrich. Ditert-butyl dicarbonate and (benzotriazol-1-yloxy)tripyrrolidinophosphonium
hexafluorophosphate (PyBOP) were purchased from Novabiochem. Solvents
for peptide synthesis (analytical grade) were purchased from Sigma-Aldrich
(dimethylformamide) and J. T. Baker (diethyl ether). Trifluoroacetic
acid (TFA) and N,N-diisopropylethylamine
(DIEA) were purchased from Iris Biotech. Ethyl acetate and acetic
acid were purchased from J. T. Baker. Chloroform and dimethyl sulfoxide
were purchased from Chempur. Se powder and ethyl alcohol were purchased
from POCH. Amino acids were purchased from PeptideWeb. 4-Methoxybenzyl
chloride was purchased from TCI. Solvents for LC-MS and HPLC measurements
were as follows: acetonitrile (MeCN), formic acid (HCOOH), and water
were purchased from chemsolve and J. T. Baker. The solvent (HPLC grade)
for the irradiation experiments and UV–vis measurement was
methanol (MeOH), which was purchased from J. T. Baker. The solvent
for GC-MS measurement was dichloromethane (DCM), which was purchased
from Chemsolve.
Polymer-Based Biomaterial Synthesis
Ferulic Acid-Crosslinked Gelatin Hydrogels
Inactivation of Rabies Virus for Immunization
hydrobromide (Sigma-Aldrich) as previously described [16 (link)]. The compound was dissolved in 0.5 M sodium hydroxide (NaOH) at the
concentration of 0.6 M and was converted to binary ethylenimine (BEI) by incubation at
37°C for 1 hr. The BEI was then added to the virus stock at a final concentration of 0.03
M, incubated for 18 hr at 37°C, and neutralized by adding sodium thiosulfate
(Sigma-Aldrich) to a final concentration of 2%. The inactivated virus was then mixed
thoroughly with aluminum hydroxide adjuvant (60% virus: 40% adjuvant).
Electrochemical Sensing of Biomolecules
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