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| Product | Description | |
|---|---|---|
| Sodium borohydride | 100g Pack Size. Group: Building Blocks, Inorganic Chemicals. Formula: H4BNa. CAS No. 16940-66-2. Prepack ID 19526770-100g. Molecular Weight 37.83. See USA prepack pricing. |  |
| Sodium borohydride | 25g Pack Size. Group: Building Blocks, Inorganic Chemicals. Formula: H4BNa. CAS No. 16940-66-2. Prepack ID 19526770-25g. Molecular Weight 37.83. See USA prepack pricing. | |
| Sodium borohydride | Sodium borohydride. Group: Biochemicals. Grades: Highly Purified. CAS No. 16940-66-2. Pack Sizes: 25g, 50g, 100g, 250g, 500g. US Biological Life Sciences. |  Worldwide |
| Sodium Borohydride | SODIUM BOROHYDRIDE, 98% pure, powder, (Synonym: Sodium Tetrahydridoborate), Formula: NaBH4. CAS No. 16940-66-2. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Sodium Borohydride-d4 | Labeled Sodium Borohydride used as a reagent used to prepare α,α-dideutero- β-amino acids. Sodium Borohydride-d4 is also used to prepare amine-stabilized, deuterated borane-THF. Group: Biochemicals. Alternative Names: Sodium Borodeuteride; Sodium Tetrahydro-d4-borate; Sodium tetradeuterioborate; Sodium tetradeuteroborate; Sodium tetrahydroborate-d4. Grades: Highly Purified. CAS No. 15681-89-7. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| Sodium borohydride (Granular) | 25g Pack Size. Group: Building Blocks, Inorganic Chemicals. Formula: H4BNa. CAS No. 16940-66-2. Prepack ID 90028203-25g. Molecular Weight 37.83. See USA prepack pricing. | |
| Sodium Tris (1, 1, 1, 3, 3, 3-hexafluoroisopropoxy) borohydride | Sodium Tris (1, 1, 1, 3, 3, 3-hexafluoroisopropoxy) borohydride. Group: Biochemicals. Grades: Highly Purified. CAS No. 139494-68-1. Pack Sizes: 2g, 5g, 10g, 25g, 50g. US Biological Life Sciences. | Worldwide |
| Sodium Tris(1,1,1,3,3,3-hexafluoroisopropoxy)borohydride | Sodium Tris(1,1,1,3,3,3-hexafluoroisopropoxy)borohydride is a reducing agent and weakly coordinating anionic salt, used in the preparation of ionic liquids. Group: Heterocyclic organic compound. Alternative Names: (T-4) ?-tris (1, ?1, ?1, ?3, ?3, ?3-hexafluoro-2-propanolato) ?hydro-Borate (1-) ? sodium. CAS No. 139494-68-1. Molecular formula: C9H4BF18NaO3. Mole weight: 535.9. Purity: >98.0%(V). IUPACName: sodium;tris(1,1,1,3,3,3-hexafluoropropan-2-yloxy)boron(1-). Canonical SMILES: [B-] (OC (C (F) (F)F)C (F) (F)F) (OC (C (F) (F)F)C (F) (F)F)OC (C (F) (F)F)C (F) (F)F. [Na+]. Catalog: ACM139494681. |  |
| 2-Picoline | 2-Picoline is used as a reagent in the synthesis of 2-Picolineborane, a non-toxic alternative to sodium borohydride for the labelling of oligosaccharides. Group: Biochemicals. Grades: Highly Purified. CAS No. 109-06-8. Pack Sizes: 1g, 10g. Molecular Formula: C6H7N, Molecular Weight: 93.13. US Biological Life Sciences. | Worldwide |
| 2-Picoline-d7 | 2-Picoline-d7 is the isotope labelled analog of 2-Picoline; a reagent used in the synthesis of 2-Picolineborane which is a non-toxic alternative to sodium borohydride for the labelling of oligosaccharides. Group: Biochemicals. Grades: Highly Purified. CAS No. 93951-93-0. Pack Sizes: 100mg, 250mg. Molecular Formula: C6D7N, Molecular Weight: 100.17. US Biological Life Sciences. | Worldwide |
| BODIPY FL hydrazide | BODIPY FL Hydrazide is a green-fluorescent dye, BODIPY FL Hydrazide is reactive with aldehyde/ketone on polysaccharides and glycoproteins, yielding a reversible Schiff base product that can be transformed to a stable linkage using a reducing agent like sodium borohydride or sodium cyanoborohydride. (λ ex =495 nm, λ em =516 nm) [1] [2]. Uses: Scientific research. Group: Fluorescent dye. CAS No. 178388-71-1. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-114351. |  |
| Native Flavobacterium meningosepticum Glycerol kinase | The activity of glycerol kinase is found widely in nature. In microorganisms GK makes possible the utilization of glycerol as a carbon source. In mammals the enzyme represents a juncture of sugar and fat metabolism; The enzyme is important to the clinical chemist in the determination of glycerol. GK is also useful in the assay of glyceraldehydes and dihydroxyacetone following their quantitative reduction to glycerol with sodium borohydride. Applications: Useful for the measurement of triglyceride. Group: Enzymes. Synonyms: glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Enzyme Commission Number: EC 2.7.1.30. GK. Mole weight: 150 kDa (TSK G3000SWXL) 50 kDa (SDS-PAGE). Activity: More than 70 U/mg solid. Appearance: White to light grayish white amorphous powder, lyophilized. Storage: Storage at -20°C in the presence of a desiccant is recommended. Form: Freeze dried powder. Source: Flavobacterium meningosepticum. glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Cat No: NATE-1155. |  |
| Native Microorganism Glycerol Kinase | The activity of glycerol kinase is found widely in nature. In microorganisms GK makes possible the utilization of glycerol as a carbon source. In mammals the enzyme represents a juncture of sugar and fat metabolism; The enzyme is important to the clinical chemist in the determination of glycerol. GK is also useful in the assay of glyceraldehydes and dihydroxyacetone following their quantitative reduction to glycerol with sodium borohydride. Applications: This enzyme is useful for enzymatic determination of glycerol and triglyceride when coupled with glycerol-3-phosphate dehydrogenase, glycerol-3-phosphate oxidase or pyruvate kinase and lactate dehydrogenase, lipoprotein lipase in clinical analysis. Group: Enzymes. Synonyms: glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Enzyme Commission Number: EC 2.7.1.30. CAS No. 9030-66-4. GK. Mole weight: approx. 220 kDa (by gel filtration). Activity: Grade? 30 U/mg-solid or more. Stability: Stable at-20°C. Appearance: White amorphous powder, lyophilized. Form: Freeze dried powder. Source: Microorganism. glycerokinase; GK; ATP: glycerol-3-phosphotransferase; glycerol kinase phosphorylating; glyceric kinase; EC 2.7.1.30. Cat No: DIA-149. | |
| Native Streptococcus faecalis L-Tyrosine Decarboxylase Apoenzyme | In enzymology, a tyrosine decarboxylase (EC 4.1.1.25) is an enzyme that catalyzes the chemical reaction:L-tyrosine<-> tyramine + CO2. Hence, this enzyme has one substrate, L-tyrosine, and two products, tyramine and carbon dioxide. This enzyme belongs to the family of lyases, specifically the carboxy-lyases, which cleave carbon-carbon bonds. This enzyme participates in tyrosine metabolism and alkaloid biosynthesis. It employs one cofactor, pyridoxal phosphate. Applications: L-tyrosine decarboxylase apoenzyme from strept oc occus faecalis has been used in a study to purify and characterize tyrosine decarboxylase and aromatic-l-amino-acid decarboxylase. l-tyrosine decarboxylase apoenzyme from strept oc occus faecalis has also been used in a study to investigate the stereospecificity of sodium borohydride reduction of tyrosine decarboxylase. Group: Enzymes. Synonyms: tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarb. Enzyme Commission Number: EC 4.1.1.25. CAS No. 9002-9-9. L-Tyrosine Decarboxylase. Activity: <0.005 unit/mg solid (without pyridoxal 5-phosphate),> 0.05 unit/mg solid (with excess pyridoxal 5-phosphate). Storage: -20°C. Source: Streptococcus faecalis. tyrosine decarboxylase; EC 4.1.1.25; L-tyrosine decarboxylase; L-(-)-tyrosine apodecarboxylase; L-tyrosine carboxy-lyase; 9002-09-9. Cat No: NATE-0420. | |
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