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Sodium borohydride

Sodium borohydride is a powerful reducing agent commonly used in organic synthesis and biochemical research.
It is employed in the reduction of carbonyl compounds, halides, and other functional groups.
Sodium borohydride is known for its high reactivity and selectivity, making it a valuable tool for chemists and biologists alike.
It is important to handle this compound with care due to its flammable nature.
PubCompare.ai offers a convenient way to optimize your sodium borohydrie research, helping you locate the best protocols and products from literature, pre-prints, and patents to enhance reproducibility and accuracy.

Most cited protocols related to «Sodium borohydride»

Complete series through the brains of 4 CRFR1-GFP mice were prepared for concurrent localization of GFP and CRFR1 mRNA. Combining immunoperoxidase labeling with isotopic in situ hybridization required minor modifications of the constituent methods (Chan et al., 1993 (link)). Immunostaining was carried out first, and the protocols modified as follows: (1) normal tissue pretreatments in hydrogen peroxide and sodium borohydride were omitted, (2) blocking sera were replaced in the immunostaining procedure with 2% bovine serum albumin and 2% heparin sulfate, (3) nickel enhancement steps were eliminated, and (4) Nissl counterstaining was omitted.
Publication 2008
Brain Heparin Immunoperoxidase Techniques In Situ Hybridization Mice, Laboratory Nickel Peroxide, Hydrogen RNA, Messenger Serum Serum Albumin, Bovine sodium borohydride Sulfates, Inorganic Tissues
OS were extracted from human milk obtained from the milk banks in San Jose, CA and Austin, TX. The extraction method was the same as in our previous publication.27 (link), 45 (link) Sodium borohydride (98%) and 2,5-dihydroxybenzoic acid (DHB) were purchased from Sigma-Aldrich (St. Louis, MO). Nonporous graphitized carbon cartridges (GCC, 150mg bed weight, 4mL cartridge volume) were bought from Alltech (Deerfield, IL). Standard HMOs were purchased from Dextra Laboratories (Earley Gate, UK). α(1-2)-Fucosidase was from EMD Calbiochem (La Jolla, CA). β(1-3)-Galactosidase was from New England Biolab (Beverly, MA). β(1-4)-Galactosidase was from ProZyme (San Leandro, CA). α(1-3,4)-Fucosidase was from Sigma-Aldrich (St. Louis, MO). All other reagents were of analytical or HPLC grade.
Publication 2010
2,3-dihydroxybenzoic acid austin Carbon Fucosidase Galactosidase High-Performance Liquid Chromatographies Milk, Human sodium borohydride

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Publication 2015

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Publication 2018
Acetate Acetic Acid Acetone Adenosine Monophosphate Ammonium C.I. 42655 Chlorine Chloroform Cytidine Monophosphate Deoxycholic Acid dinitrophenylhydrazine Dithiothreitol DNA Fingerprinting Edetic Acid Ethanol ethyl acetate Glucose Guanidine hen egg lysozyme Hexanes High-Performance Liquid Chromatographies Hydrochloric acid Hypochlorite Inferior Colliculus Iron Methanol Mucosa, Gastric Pepsin A Peroxide, Hydrogen Phenol Phosphates Pigs Salmo salar Serum Albumin, Bovine Sodium sodium borohydride Sodium Carboxymethylcellulose Sodium Chloride Sodium Hydroxide Streptomycin Sulfate Sulfate, Sodium Dodecyl Sulfates, Inorganic Thymidine Monophosphate Trichloroacetic Acid triphosphate Tromethamine Urea
The OS used in this study are from pooled human milk provided by milk banks in San Jose, CA and Austin, TX. HMOs were isolated from the milk using a previously described procedure involving defatting, chloroform/methanol extraction, ethanol precipitation, and evaporation.6 (link) A sample enrichment step with solid phase extraction (SPE) employing graphitized carbon cartridge (GCC) was used before the analysis. GCC (150 mg bed weight, 4mL volume) were purchased from Alltech (Deerfield, IL). Sodium borohydride (98%) and 2, 5-dihydroxybenzoic acid (DHB) were obtained from Sigma–Aldrich (St. Louis, MO). Standard HMOs were purchased from Dextra Laboratories (Earley Gate, UK). α(1–2)-Fucosidase was obtained from EMD CALBIOCHEM (La Jolla, CA), β(1–3)-galactosidase and α(2–3)-neuraminidase from New England Biolab (Beverly, MA), β(1–4)-galactosidase from ProZyme (San Leandro, CA), and α(1–3,4)-fucosidase from Sigma–Aldrich (St. Louis, MO). The non-selective sialidase was purified and provided by Prof. David Mills from the Department of Viticulture and Enology in UC Davis. All reagents are of analytical or HPLC grade.
Publication 2011
2,3-dihydroxybenzoic acid austin Carbon Chloroform Ethanol Fucosidase Galactosidase High-Performance Liquid Chromatographies Methanol Milk Milk, Human Neuraminidase sodium borohydride Solid Phase Extraction

Most recents protocols related to «Sodium borohydride»

The UF adhesive (100 g) and sodium borohydride (x g) were mixed with the aid of a magnetic stirrer spun at 250 rpm for 20 min to obtain a sodium borohydride-modified UF adhesive (denoted as BMU-x, where x denotes the added mass of sodium borohydride).
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Publication 2024
The effects of the concentration of the reducing agent (NaBH4) on the degradation of crystal violet and methylene blue were investigated. To determine the optimum concentration of reducing agent for the best catalytic degradation, various concentrations of reducing agent were tested from 0.01 to 0.20 M. The catalyst dose was fixed at 0.025 gm/25 mL for crystal violet and 0.075 gm/25 mL for methylene blue, while the initial concentrations of crystal violet and methylene blue were fixed at 20 ppm and 15 ppm, respectively. Prior to conducting these experiments, other parameters were optimized and applied.
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Publication 2024
Ammonium chloride, urea, sodium borohydride, formaldehyde, formic acid, and sodium hydroxide (AR, Xilong Science Co., Ltd., Shantou, China) were used as raw materials. Flour was obtained from Beijing Guchuan Flour Company, Beijing, China. The eucalyptus veneer (480 mm × 480 mm × 1.7 mm; moisture content: 8–12%) used to prepare the plywood was purchased from Guilin Liding Plywood Factory, Guilin, China.
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Publication 2024
Resins were prepared with a flat vulcanizer (XLB-D, Huzhou Shunli Rubber Machinery Co., Ltd., Huzhou, China). Sodium borohydride and the UF resin were mixed using the aid of a magnetic stirrer (79-1, Jiangsu Zhongda Industry Co., Ltd., Changzhou, China). The strength of the samples was measured by a universal mechanical testing machine (MWW-10A, specification 10 kN, Jinan Xinguang Testing Machine Manufacturing Co., Ltd., Jinan, China). FTIR spectra were recorded using a Spectrum One spectrometer (Perkin-Elmer, Waltham, MA, USA). TG was performed using a synchronous thermal analyzer (STA-449C, Netzsch, Selb, Germany).
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Publication 2024
Zabrus tenebrioides is one of the main pests of wheat crops worldwide and is really difficult to control. This species is widespread both in our country and in the Palaearctic region. The species are usually dark black-brown in color, large, bloated and strongly built and can be easily distinguished from other Carabidae genera when viewed from the front due to the peculiar structure of their pronotum [21] .
The specimens were collected in Eskişehir, a province in the central Anatolian region of Turkey [22] . The chitin was gathered from the elytra, mandible and antennae (body parts which have the most chitin polymer) of Z. tenebrioides, air dried and powdered.
Cobalt (II) chloride hexahydrate (> 97%), sodium hydroxide pellets (> 98%) and sodium borohydride powder (> 98%) were purchased from Acros Organics and Sigma-Aldrich, respectively. All chemicals used in this study were of analytical grade without further processing.
Publication 2024

Top products related to «Sodium borohydride»

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Sodium borohydride is a reducing agent commonly used in organic synthesis and analytical chemistry. It is a white, crystalline solid that reacts with water to produce hydrogen gas. Sodium borohydride is frequently employed in the reduction of carbonyl compounds, such as aldehydes and ketones, to alcohols. Its primary function is to facilitate chemical transformations in a laboratory setting.
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Silver nitrate is a chemical compound with the formula AgNO3. It is a colorless, water-soluble salt that is used in various laboratory applications.
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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.
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Sodium borohydride (NaBH4) is a white, crystalline, water-soluble reducing agent commonly used in organic synthesis and chemical analysis. It is a versatile reagent that can selectively reduce various functional groups, such as aldehydes, ketones, and nitriles, to alcohols. NaBH4 is stable at room temperature and is widely utilized in chemical laboratories as a reducing agent for a variety of chemical transformations.
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L-ascorbic acid is a chemical compound commonly known as vitamin C. It is a white, crystalline solid that is soluble in water and has a slight acidic taste. L-ascorbic acid is an essential nutrient required for various metabolic processes in the body and acts as an antioxidant, protecting cells from damage caused by free radicals.
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Hydrochloric acid is a commonly used laboratory reagent. It is a clear, colorless, and highly corrosive liquid with a pungent odor. Hydrochloric acid is an aqueous solution of hydrogen chloride gas.
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Ascorbic acid is a chemical compound commonly known as Vitamin C. It is a water-soluble vitamin that plays a role in various physiological processes. As a laboratory product, ascorbic acid is used as a reducing agent, antioxidant, and pH regulator in various applications.
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Ethanol is a clear, colorless liquid chemical compound commonly used in laboratory settings. It is a key component in various scientific applications, serving as a solvent, disinfectant, and fuel source. Ethanol has a molecular formula of C2H6O and a range of industrial and research uses.
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Gold(III) chloride trihydrate is an inorganic compound with the chemical formula AuCl3·3H2O. It is a yellow crystalline solid that is used as a precursor in the synthesis of other gold compounds. The compound has a melting point of 170°C and is soluble in water and various organic solvents.
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Sodium borohydride is a white crystalline solid that is commonly used as a reducing agent in organic synthesis. It is a mild, chemoselective reducing agent that can selectively reduce certain functional groups without affecting others. The main function of sodium borohydride is to facilitate chemical reactions by donating hydrogen atoms to reactants.

More about "Sodium borohydride"

Sodium borohydride (NaBH4) is a powerful reducing agent widely used in organic synthesis and biochemical research.
It is known for its ability to reduce a variety of functional groups, including carbonyl compounds, halides, and others.
This versatile compound is valued by chemists and biologists alike for its high reactivity and selectivity, making it a valuable tool in their work.
NaBH4 is commonly employed in the reduction of aldehydes, ketones, and esters to alcohols, as well as the reduction of halides to alkanes.
It is also used in the synthesis of various organic compounds, such as pharmaceuticals and natural products.
In biochemical applications, sodium borohydride is utilized for the reduction of proteins, peptides, and other biomolecules, often in conjunction with agents like silver nitrate, sodium hydroxide, L-ascorbic acid, hydrochloric acid, and ascorbic acid.
It's important to handle sodium borohydride with care due to its flammable nature.
Proper safety precautions, such as the use of personal protective equipment (PPE) and appropriate storage and disposal methods, are crucial when working with this compound.
PubCompare.ai offers a convenient solution for optimizing your sodium borohydride research.
By leveraging AI-driven comparisons, the platform helps you locate the best protocols and products from literature, preprints, and patents, enhancing the reproducibility and accuracy of your experiments.
Explore the power of PubCompare.ai today to streamline your sodium borohydride-related research and unlock new possibilities in your field.