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| Product | Description | |
|---|---|---|
| 3-Benzyloxy-5-hydroxyphenylpropenoic Acid 3-Sulfate Methyl Ester Triethylamine | 3-Benzyloxy-5-hydroxyphenylpropenoic Acid 3-Sulfate Methyl Ester Triethylamine. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| 4,6-O-Benzylidene Lactosamine 6-Sulfate Pentaacetate Triethylamine Salt | An intermediate in the preparation of α1,3-L-Fucosyltransferase acceptors. Synonyms: 2-(Acetylamino)-2-deoxy-4-O-(4,6-O-benzylidene-di-o-acetyl-β-D-galactopyranosyl)-tri-O-acetyl-D-glucose 6-(Hydrogen Sulfate) Triethylamine Salt. Molecular formula: C35H51N2O18S. Mole weight: 819.85. |  |
| 4-Amino-3-benzyl-1H-pyrazolo[3,4-d]pyrimidine 1-β-D-Ribofuranosyl 5'-(3-Thio-triphosphate) Triethylamine Salt | Used in the synthesis of nucleotide analogues containing a phosphorothiolate moiety at the terminal position of the phospate chain. Molecular formula: C17H22N5O12P3S x(C6H15N). Mole weight: 613.37. | |
| 4-Amino-3-benzyl-1H-pyrazolo[3,4-d]pyrimidine 1-β-D-Ribofuranosyl 5'-Triphosphate Triethylamine Salt | An inhibitor scaffold as a new allele specific kinase substrate. Uses: An inhibitor scaffolds as new allele specific kinase substrates. Synonyms: 1-[5-O-[Hydroxy[[hydroxy (phosphonooxy) phosphinyl]oxy]phosphinyl]-β -D-ribofuranosyl]-3- (phenylmethyl) -1H-pyrazolo[3, 4-d]pyrimidin-4-amine Triethylamine Salt. CAS No. 476371-80-9. Molecular formula: C17H22N5O13P3 x(C6H15N). Mole weight: 597.30. | |
| 4- (tert-Butyldi methyl silyloxy methyl ) -5- (6-O-triethylsilyl-1, 6-dihydroxyhexyl) -1, 3-dibenzyl-2-imidazolidinone Benzyl Ether | Used in the preparation of Selenobiotin (S248000). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 5- (tert-Butyldi methyl silyloxy methyl ) -1, 3-dibenzyl-2-oxo-4-imidazolidine- (6-triethylsilyloxy-hexanoic Acid) Benzyl Ester | Used in the preparation of Selenobiotin (S248000). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzyltriethylammonium Borohydride | Reducing reagent. Group: Biochemicals. Alternative Names: N,N,N-Triethyl-benzenemethanaminium Tetrahydroborate. Grades: Highly Purified. CAS No. 85874-45-9. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Benzyltriethylammonium bromide | Metal Plating, Electropolishing, Metal Reprocessing, Phase transfer media, Batteries Fuel Cells, Nanomaterials, Industrial Solvents, Nuclear Fuel Red Waste, Enzymatic Catalysis, Lubricants Heat Transfer and Solar Energy Conversion. Group: Bromine series. Alternative Names: N-Benzyl-N,N,N-triethylammonium bromide. CAS No. 5197-95-5. Molecular formula: C13H22BrN. Mole weight: 272.22. Purity: 0.99. IUPACName: benzyl(triethyl)azanium;bromide. Canonical SMILES: CC[N+](CC)(CC)CC1=CC=CC=C1.[Br-]. ECNumber: 225-986-1. Catalog: ACM5197955-1. |  |
| Benzyltriethylammonium chloride | Metal Plating, Electropolishing, Metal Reprocessing, Phase transfer media, Batteries Fuel Cells, Nanomaterials, Industrial Solvents, Nuclear Fuel Red Waste, Enzymatic Catalysis, Lubricants Heat Transfer and Solar Energy Conversion. Group: Ammonium ionic liquids. Alternative Names: BTEAC. CAS No. 56-37-1. Molecular formula: C13H22ClN. Mole weight: 227.77. Purity: 0.99. IUPACName: benzyl(triethyl)azanium;chloride. Canonical SMILES: CC[N+](CC)(CC)CC1=CC=CC=C1.[Cl-]. ECNumber: 200-270-1. Catalog: ACM56371-4. | |
| Benzyltriethylammonium Chloride | Hydrochloride salt of benzyltriethylammonium which acts as a phase-transfer catalyst in chemical reactions. Group: Biochemicals. Alternative Names: N, N, N-Triethyl Benzene methanaminium Chloride; Benzyltriethylmmmonium Chloride; N, N, N-Triethyl Benzene methanaminium Chloride; Benzyltriethylammonium Chloride; BAC-TE; N,N,N-Triethyl-N-benzylammonium Chloride; TEBA; TEBAC; Triethylbenzylammonium Chloride. Grades: Highly Purified. CAS No. 56-37-1. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Benzyltriethylammonium Tetrafluoroborate | Benzyltriethylammonium Tetrafluoroborate is used as a key intermediate in the preparation of Ammonium-based Ionic Liquids-based ionic liquids. Group: Heterocyclic organic compound. Alternative Names: N-Benzyl-N,N-diethylethanaminium tetrafluoroborate; Triethyl-(phenylmethyl)ammonium tetrafluoroborate; Benzyl Triethylammonium Tetrafluoroborate. CAS No. 77794-93-5. Molecular formula: C13H22N BF 4?. Mole weight: 192.328681. Catalog: ACM77794935. | |
| N6-Benzyladenosine 5'-triphosphate triethylammonium salt | N6-Benzyladenosine 5'-triphosphate triethylammonium salt, a pivotal compound in biomedicine, exhibits its indispensability in advanced research within the biomedical industry due to its high purity and stability. Functioning as a potential modulator for a diverse array of enzymes participating in intricate cellular signaling pathways, this compound plays a crucial role in exploring the complexities of cancer, cardiovascular, and neurological diseases. Furthermore, it aids in the identification of potential therapeutic targets. Synonyms: N6-Benzyl-D-adenosine triphosphate triethylammonium salt. Molecular formula: C19H26N5O11P3·C18H48N3. Mole weight: 899.95. | |
| Benzyl Benzoate | Benzyl benzoate is a clear, colorless, oily liquid with a slightly aromatic odor. It produces a sharp, burning sensation on the tongue. At temperatures below 17°C it exists as clear, colorless crystals. Synonyms: Benzoic acid benzyl ester; benzylbenzenecarboxylate; benzylis benzoas; benzyl phenylformate; phenylmethyl benzoate. CAS No. 120-51-4. Product ID: PE-0586. Molecular formula: C14H12O2. Mole weight: 212.24. Category: Plasticizer; Solubilizing Agents; Solvent; therapeutic Agents. Product Keywords: Excipients for Liquid Dosage Form; Solubilizer Excipients; PE-0586; Benzyl Benzoate; Plasticizer; Solubilizing Agents; Solvent; therapeutic Agents; C14H12O2; 120-51-4. UNII: N863NB338G. Chemical Name: Benzoic acid phenylmethyl ester. Grade: Pharmceutical Excipients. Administration route: IM injections and oral. Dosage Form: IM injections and oral capsules. Stability and Storage Conditions: Benzyl benzoate is stable when stored in tight, well-filled, lightresistant containers. Exposure to excessive heat (above 40°C) should be avoided. Source and Preparation: Benzyl benzoate is a constituent of Peru balsam and occurs naturally in certain plant species. Commercially, benzyl benzoate is produced synthetically by the dry esterification of sodium benzoate and benzoyl chloride in the presence of triethylamine or by the reaction of sodium benzylate with benzaldehyde. Applications: Benzyl benzoate is used as a solubilizing age |  |
| γ-(6-Aminohexyl)-N6-Benzyl-ATP - ATTO-647N | γ-(6-Aminohexyl)-N6-Benzyl-ATP - ATTO-647N is a fluorescent dye used for cell imaging and analysis in the biomedical industry. It is commonly employed in molecular biology and drug discovery research. This product finds extensive applications in studying ATP-dependent biological processes, including DNA replication, transcription and signal transduction pathways. with superior brightness and photostability, it facilitates high-resolution imaging and accurate quantification of cellular activities related to ATP metabolism. Synonyms: γ-(6-Aminohexyl)-N; -benzyl-adenosine-5'-triphosphate, labeled with ATTO 647N, Triethylammonium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C23H35N6O13P3- ATTO 647N (free acid). Mole weight: 1324.34 (free acid). | |
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