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3 4 dhb

Manufactured by Merck Group
Sourced in United States

3,4-DHB is a chemical compound commonly used as a laboratory reagent. It is a dihydroxybenzoic acid derivative with the chemical formula C7H6O3. This compound is frequently utilized in various analytical and research applications within the scientific community.

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2 protocols using 3 4 dhb

1

Catechol-Functionalized Chitosan Synthesis

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Catechol-conjugated chitosan (CS-C) was synthesized using chitosan (Mw 100 kDa, 80% deacetylated; Sigma-Aldrich) and 3,4-dihydroxybenzaldehyde (3,4-DHB; Sigma-Aldrich) following previously published method by Clifford et al.26 The catechol was conjugated to the amine groups of chitosan by Schiff base reaction. Methanol was used to dissolve 3,4-DHB, NaBH4 (Sigma-Aldrich) as a reductant was used to reduce the C=N to C-N, and the degree of catechol substitution on the backbone of chitosan was determined by proton nuclear magnetic resonance. Stock solutions of CS-C (2 mg/mL, pH 6.5) were prepared for further use.
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2

Analytical Standards and Chemicals for LC-MS

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Analytical standards of MeP, EtP, n-PrP, n-BuP, 4-HB, and 3,4-DHB were purchased from Sigma-Aldrich (St. Louis, MO, USA). Chlorzoxazone was purchased from National Institutes for Food and Drug Control (NIFDC, Beijing, China). β-glucuronidase (100,000 U/mL) was supplied by Sigma-Aldrich (St. Louis, MO, USA). Acetonitrile, methanol, ethyl acetate, ammonium acetate, and formic acid were supplied by Thermo Fisher Scientific (Houston, TX, USA). All the chemicals were of LC-MS or HPLC grade. Ultra-pure water was obtained from the Milli-Q system (Millipore, Bedford, MA, USA).
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