Size 100mg Price 435 0 Purity 90 H NMR Formula C13H17NO5 Molecular Weight 267 28 Molecule Name tco nhs ester
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Size 100mg Price 245 0 Purity 95 HPLC H NMR Formula C23H18N2O5 Molecular Weight 402 4 Molecule Name dbco nhs ester
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Size 100mg Price 225 0 Purity 95 HPLC H NMR Formula C18H16N2O Molecular Weight 276 33 Molecule Name dbco amine
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Image Search Results

Journal: Acta biomaterialia
Article Title: Fabrication of magnetic and fluorescent chitin and dibutyrylchitin sub-micron particles by oil-in-water emulsification
doi: 10.1016/j.actbio.2016.08.057
Figure Lengend Snippet: DBC and chitin characterization. Solid state 13 C-NMR of chitin (A), 1 H-NMR of DBC in chloroform-d (B) and FTIR of chitin and DBC (C).
Article Snippet: 1
Techniques: Nuclear Magnetic Resonance

Journal: Medical Gas Research
Article Title: Effects of nitric oxide donor N,N’-di-sec-butyl-N,N’-dinitroso-1,4-phenylenediamine on the expression of interferon-gamma in tumor infiltrating lymphocytes
doi: 10.4103/2045-9912.273954
Figure Lengend Snippet: Synthesis and characterization of BNN6. Note: (A) N,N'-di-sec-butyl-N,N'-dinitroso-1,4-phenylenediamine (BNN6) was synthesized by N,N'-di-sec-butylaminop-phenylenediamine (BPA) and NaNO 2 in hydrochloric acid solution. (B) Each peak of BNN6 was found in hydrogen nuclear magnetic resonance ( 1 H NMR). (C) With the 279.18 Da, in accordance with the molecular structure of BNN6 (301.16 is BNN6 plus one unit of sodium, 249.18 is BNN6 minus one unit of nitric oxide (NO), and 220.15 is the reactant BPA). The blue ray response of the synthesized BNN6 was confirmed through the color change of the solution (A, digital photo). The yellow solution of BNN6 became red after 45 seconds of irradiation by blue-ray.
Article Snippet: The structure of BNN6 was detected by
Techniques: Synthesized, Nuclear Magnetic Resonance, Irradiation

Journal: Tissue Engineering and Regenerative Medicine
Article Title: In Vitro Anti-Inflammation and Chondrogenic Differentiation Effects of Inclusion Nanocomplexes of Hyaluronic Acid-Beta Cyclodextrin and Simvastatin
doi: 10.1007/s13770-018-0119-9
Figure Lengend Snippet: A Chemical structure of HA-β-CD. B 1 H-NMR spectrum of HA-β-CD measured in D 2 O
Article Snippet: The synthesized HA-β-CD was characterized with 1
Techniques: Nuclear Magnetic Resonance

Journal: International Journal of Molecular Sciences
Article Title: Water Soluble Usnic Acid-Polyacrylamide Complexes with Enhanced Antimicrobial Activity against Staphylococcus epidermidis
doi: 10.3390/ijms14047356
Figure Lengend Snippet: 1 H-NMR spectra of usnic acid ( a ), pAcDED T=0 /UA 70/30 complex ( b ) and pAcDED T=0 ( c ).
Article Snippet:
Techniques: Nuclear Magnetic Resonance

Journal: Nanomaterials
Article Title: Well-Defined Thermo-Responsive Copolymers Based on Oligo(Ethylene Glycol) Methacrylate and Pentafluorostyrene for the Removal of Organic Dyes from Water
doi: 10.3390/nano10091779
Figure Lengend Snippet: ( a ) Molar monomer conversions versus time. ( b ) GPC chromatograms of the reaction mixtures at different times; ( c ) molar mass and Ð evolutions versus weight conversion for the CPPTC-mediated RAFT copolymerizations of OEGMA and PFS; and ( d ) 1 H NMR spectrum (0–5 ppm region) of purified PFG24 in CDCl 3 .
Article Snippet:
Techniques: Gel Permeation Chromatography, Nuclear Magnetic Resonance, Purification

Journal: Nanomaterials
Article Title: Well-Defined Thermo-Responsive Copolymers Based on Oligo(Ethylene Glycol) Methacrylate and Pentafluorostyrene for the Removal of Organic Dyes from Water
doi: 10.3390/nano10091779
Figure Lengend Snippet: Self-assembly of OEGMA-based copolymers in water (5 mg/mL): ( a ) 1 H NMR spectra of PFG24 in CDCl 3 and D 2 O, in the region between 2.5 and 4.5 ppm; ( b ) DLS size distribution of PFG24 particles in aqueous solution (2.5 mg/mL) at temperatures across the LCST ; ( c ) temperature-dependent change of D h as measured by DLS; and ( d ) TEM micrographs at 20 (left side) and 60 °C (right side).
Article Snippet:
Techniques: Nuclear Magnetic Resonance, Transmission Electron Microscopy