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Hydrochloric acid (hcl)

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Hydrochloric acid is a clear, colorless, and highly corrosive liquid chemical. It is a commonly used laboratory reagent with a strong acidic pH. Hydrochloric acid is primarily used for adjusting the acidity or pH of solutions, as well as for various analytical and synthetic procedures in chemical laboratories.

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827 protocols using hydrochloric acid (hcl)

1

Analytical Reagents and Solvents Characterization

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Certified reference components and general chemical reagents were obtained from Cayman Chemical (Michigan, USA). Solvents used for GC-MS and HPLC-PDA were of analytical grade.
Methanol, acetonitrile and hydrochloric acid (37 %) were obtained from Fisher Chemical (Fisher Bioblock, Belgium). Water was purified by a Milli-Q system obtained from Merck Millipore (Darmstadt, Germany). Triethylammonium (TEA) phosphate 1 M was purchased from Sigma (Zwijndrecht, Belgium) and was diluted 1/40 immediately before use. The external standard diphenylamine was obtained from VWR International (Leuven, Belgium). N-methyl-N-(trimethylsilyl) trifluoroacetamide (MSTFA) and N-methyl-bis(trifluoroacetamide) (MBTFA) were purchased from Machery-Nagel (Germany). NMR analysis and associated sample preparation: deuterated solvents for NMR were purchased from Euriso Top (St. Aubain, France).
Tetramethylsilane was of NMR grade and was acquired from Acros Organics (Geel, Belgium).
Dichloromethane was purchased from Sigma-Aldrich and was of HPLC grade. hydrochloric acid and sodium hydroxide were purchased from Acros Organics (Geel, Belgium) and were of ACS grade. Ultrapure water was obtained from a Millipore Synergy UV apparatus (Billerica MA, USA).
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2

Wool-Based Emulsion Protocol

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Clean
sheep’s wool was obtained from
Wingham Wool Work. Sunflower oil was obtained from Tesco and used
as the DP for the primary emulsion. Urea ≥ 98%, sodium metabisulfite
≥ 99%, tris(hydromethyl)aminomethane ≥ 99.8%, sodium
dodecyl sulfate (SDS) ≥ 95%, hydrochloric acid (HCl, 35%),
and sodium hydroxide (NaOH, 98%) were purchased from Fisher Scientific,
UK. HCl and NaOH were diluted to 0.1 M as stock solution for pH adjustments;
low-molecular-weight chitosan, acetic acid ≥ 99%, fluorescein
isothiocyanate (FITC) ≥ 90%, methanol ≥ 99.9%, nile
red ≥ 98%, hydrochloric acid 32%, and GTA solution grade II
25 wt % in H2O were obtained from Sigma-Aldrich UK and
used without further purification.
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3

Synthesis and Characterization of Polyaniline

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Polyaniline was prepared by oxidation
of aniline hydrochloride (10% in water at pH about 1) with the chemical
method described elsewhere, modified in our laboratory.
The
polymeric material (polyaniline) was characterized with physical and
chemical methods: FTIR, EPR, elemental analysis, and electrical conductivity
measurements, giving results similar to the values measured for materials
previously prepared in our laboratory.21 (link),22 (link),45 (link)Chemicals and solvents:
Hydrochloric
acid (HCl) (Stanlab, pure p.a.)—600 mL of 1
M solution prepared from concentrated hydrochloric acid (36%)—50
mL of 36% HCl dissolved in 550 mL of H2O.
Aniline
hydrochloride (C6H8NCl) (Fisher Scientific,
pure p.a.)—6.9 g of aniline hydrochloride dissolved in 300
mL of 1 M hydrochloric acid.
Ammonium persulfate [(NH4)2S2O8] (Chempur, pure p.a.)—11.4
g of ammonium persulfate
was dissolved in 200 mL of 1 M hydrochloric acid.
Ammonium hydroxide
(NH4OH) solution 25% (POCh, pure
p.a.)—500 mL of 1 M solution prepared from concentrated ammonium
hydroxide (25%)—37 mL of 25% ammonium hydroxide dissolved in
463 mL of H2O.
Chloroform (CHCl3) (Chempur,
pure p.a.)—75 mL.
p-Toluenesulfonic
acid (CH3C6H4SO3H) (Aldrich,
p.a.)—1.4 g of p-toluenesulfonic acid was
dissolved in 75 mL of Chloroform.
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4

Quantitative LC-MS Analysis of Analytes

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The list of analytical standards of all target analytes and their deuterated analogues, along with their acronym, CAS number and supplier, can be found in Supplementary Information Tables S6 andS7, respectively. LC-MS water, methanol (MeOH), acetone, hexanes, hydrochloric acid, formic acid, HPLC grade methyl tert-butyl ether (MtBE), pesticide grade isooctane, sulfuric acid, ammonium hydroxide, and hydrochloric acid were all purchased from Fisher Scientific (U.S.A.).
Ultrapure water was prepared using a MilliQ water purification system purchased from Millipore Corporation (Billerica, MA, USA). Oasis HLB, Oasis WAX and glass Oasis HLB glass cartridges were all purchased from Waters (MA, U.S.A.).
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5

Curcumin and 5-FU Delivery Polymer

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® a co-polymer of polyvinyl caprolactame-polyvinyl acetate-polyethylene was donated by BASF (Ludwigshafen, Germany). Curcumin (CRC, >94%), 5-fluorouracil (5-FU, >99%), cis-platin (CPT, >99%)) and sodium fluorescein (FlNa) were purchased from Sigma-Aldrich, UK. Padgett Dermatome and dermatome blades were purchased from Integra Life TM Sciences Corporation (PA, USA), KH2PO4 , Na 2 HPO 4 .12H 2 O, NaCl, KCl, NaOH, HCl, acetonitrile, acetic acid, methanol, ethanol, phosphoric acid and hydrochloric acid were purchased from Fisher Scientific (Loughborough, UK).
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6

Quantifying Advanced Glycation in Bone

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Advanced glycation end-product content of the femur diaphysis was measured using a fluorimetric assay, and was expressed relative to hydroxy-proline (OH-proline) content measured by a colorimetric OH-proline assay. Femurs were flushed of marrow, acid-hydrolyzed for 3 h at 124 °C with 6 N HCL (Fisher Scientific), dried overnight and reconstituted with 0.001 N HCL. The hydrolysate was used for determination of OH-proline and AGE content. For OH-proline, an OH-proline (Sigma-Aldrich) standard curve was prepared. Chloramine T and Erlich's reagent (Sigma-Aldrich) were used for the colorimetric assay; standards and samples were read at 558 nm using disposable cuvettes. For AGE content, a quinine (Fisher) standard curve was prepared; and, fluorescence was measured at an excitation wavelength of 360 nm and an emission wavelength of 460 nm (Tang et al., 2007 (link)).
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7

Mild Steel Corrosion in Hydrochloric Acid

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The working electrode (WE) in this experiment was mild steel and the composition is given in our earlier publications29 (link),30 (link). For weight loss measurement, the steel was cut into sheets with dimensions of 2.5 cm × 2 cm × 0.1 cm from a large strip. The WE were then polished with emery sheets in a range of grits (#320 to 1200) before being sonicated in 50% ethanol, dried, and stored in a desiccator. All corrosion experiments were carried out in 1 M HCl (Fisher Scientific, India), which was generated from HCl stock (37%, reagent grade).
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8

PES UF Membrane Characterization and Vanillin Rejection

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Commercial PES UF membrane UH004 P with nominal molecular weight cut-off (NMWCO) of 4 kDa obtained from Microdyn-Nadir GmbH, Wiesbaden, Germany, was utilized as a base membrane for both membrane surface modification and fouling experiment. The model compound utilized in rejection study was Polyethylene glycol (PEG, CAS: 25322-68-3) with molecular weight of 4 kD purchased from Fluka AG (Buchs, Switzerland). Vanillin with a purity of 99% (Mw. 152.15 g/mol, CAS: 121-33-5) and hydrochloric acid with European Pharmacopoeia quality standard (HCl, 37.0%, CAS: 7647-01-0), were provided by Acros Organics (Geel, Belgium) and VWR chemicals, respectively. Methanol (J. T. Baker, the Netherlands, CAS: 67-56-1) was used as the solvent for extraction of vanillin from the surface of the membrane. Ultra-pure deionized water (DI, 0.5–1 μ S/cm at 25 C) was obtained from CENTRA-R 60/120 system (Elga purification system, Veolia Water, Bucks, UK) and was used for all experiments and preparation of solutions.
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9

Synthesis and Characterization of Iron-Humate Complexes

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Iron(II) chloride tetrahydrate (99+%), iron(III) chloride hexahydrate (99+%) and ammonium hydroxide (25% solution in water), hydrochloric acid (37%), and sodium hydroxide (98%) were purchased in Acros Organics™, Geel, Belgium. Sodium chloride (99+%), albumin from human serum (99+%) and glucose (99.5+%) were purchased from SigmaAldrich, St. Louis, MO, USA. All chemicals were used without further purification.
Commercially available potassium humate from leonardite (a highly oxidized variety of lignites) (Powhumus®, Humintech GmbH, Grevenbroich, Germany) was used. Its basic properties, such as elemental and functional group analyses, 13C NMR spectroscopy, and size exclusion chromatography have been reported earlier elsewhere [26 (link)].
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10

Synthesis of Rhodamine-Doped Silica Nanoparticles

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All chemicals were used without further purification. Sigma‐Aldrich: (3‐aminopropyl) trimethoxysilane (APTMS, 99 %), sodium silicate solution (27 %), Rhodamine 6G, RhCl3 (98 %), hydroxylamine hydrochloride (>98 %); Alfa Aesar: HAuCl4 ⋅ 3H2O (99.99 % metal basis); Merck: hydrochloric acid (37 %); and Acros Organics: trisodium citrate dihydrate (99 %). Water was purified with Milli‐Q system (18.2 MΩ) before use. Argon (99.999 %), hydrogen (99.999 %), oxygen (99.999 %), and nitric oxide (10 % NO in He), quality>4.5 (>99.995 %) were purchased from Linde Gas.
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