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| Product | Description | |
|---|---|---|
| Potassium acetate | 1kg Pack Size. Group: Biochemicals, Buffers, Building Blocks, Salts. Formula: C2H3KO2. CAS No. 127-08-2. Prepack ID 90018486-1kg. Molecular Weight 98.14. See USA prepack pricing. |  |
| Potassium acetate | Potassium acetate. CAS No. 127-08-2. Pack Sizes: 25 kg. Product ID: CDC10-0227. Molecular formula: C2H3KO2. Category: Buffering Agents. Product Keywords: Cosmetic Ingredients; Buffering Agents; Potassium acetate; CDC10-0227; 127-08-2; C2H3KO2; 204-822-2; MFCD00012458; 127-08-2. Purity: 0.99. Color: Colourless crystals or white. EC Number: 204-822-2. Physical State: Powder. Solubility: H2O: 100 mg/mL. Quality Level: 200. Storage: Store at RT. Boiling Point: 117.1°C at 760 mmHg. Melting Point: 292°C. Density: 1.57 g/cm3. Product Description: Potassium acetate (KCH3COO) is the potassium salt of acetic acid. |  |
| Potassium acetate | Potassium acetate (KCH3COO) is the potassium salt of acetic acid. Group: Micro/nanoelectronics. Alternative Names: Acetic acid potassium. CAS No. 127-08-2. Molecular formula: C2H3KO2. Mole weight: 98.14. Appearance: White to light brown solid. Purity: 95%+. IUPACName: Potassium;acetate. Canonical SMILES: CC(=O)[O-].[K+]. Density: 1.57 g/cm³ at 25 °C (lit.). ECNumber: 204-822-2;204-822-2. Catalog: ACM127082. |  |
| Potassium acetate | Potassium acetate (KCH3COO) is the potassium salt of acetic acid. Group: Solution deposition precursors. Alternative Names: Acetic acid potassium. CAS No. 127-08-2. Pack Sizes: 25 kg. Product ID: Potassium; acetate. Molecular formula: 98.14. Mole weight: C2H3KO2. CC(=O)[O-].[K+]. InChI=1S/C2H4O2.K/c1-2(3)4;/h1H3, (H, 3, 4);/q;+1/p-1. SCVFZCLFOSHCOH-UHFFFAOYSA-M. 95%+. |  |
| Potassium Acetate | POTASSIUM ACETATE, 99% pure, crystal, Formula: KOOCCH3. CAS No. 127-08-2. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Potassium Acetate | POTASSIUM ACETATE, ACS Reagent, crystalline, Formula: KOOCCH3. CAS No. 127-08-2. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Potassium Acetate | Potassium Acetate. CAS: 127-08-2. Packing: Bag. |  New Jersey NJ |
| Potassium Acetate | Potassium Acetate. CAS No. 127-08-2. Molecular Formula CH3COOK. Chemical Reagents |  Cater Chemicals Corp. Illinois IL |
| Potassium Acetate | White crystalline solid. Uses: deicer, food preservative. Group: organic salt. CAS No. 127-08-2. |  |
| Potassium Acetate, ACS | Potassium Acetate is a competitive and false substrate which inhibits histone deacetylase 6 (HDAC-6), thus reducing the cytotoxicity and inflammatory responses caused by C. difficile toxin A. Group: Biochemicals. Alternative Names: Catacyst LB; Cryotech E 36; DPG 35; Dabco K 2008; Dabco K 2097; Dabco P 15; K 15; LCM 1; LK 25; P 15; PC 46; Pelcat 9648A; Polycat 46; Potassium ethanoate; Safeway KA-HOT; Potassium Salt Acetic Acid. Grades: ACS Grade. CAS No. 127-08-2. Pack Sizes: 500g, 1Kg, 2.5Kg, 5Kg, 10Kg. Molecular Formula: CH3CKO2, Molecular Weight: 98.14. US Biological Life Sciences. |  Worldwide |
| Potassium Acetate Anhydrous USP | Potassium Acetate Anhydrous USP. |  CA, FL & NJ |
| Potassium Acetate BP/USP | Potassium Acetate BP/USP. CAS No. 127-08-2. Molecular formula: C2H3O2K. |  |
| Potassium Acetate, crystal | Potassium Acetate, crystal. Grades: ACS. CAS No. 127-08-2. Pack Sizes: Gram Quantities: 6 x 500 gm, 2.5 kg, 4 x 2.5 kg , 12 kg. Order Number: 14473. |  www.prochemonline.com |
| Potassium acetate Molecular biology grade | 1kg Pack Size. Group: Biochemicals, Salts. Formula: C2H3KO2. CAS No. 127-08-2. Prepack ID 12389251-1kg. Molecular Weight 98.14. See USA prepack pricing. | |
| 1-Phenol-4-sulfonic acid acetate potassium salt | Heterocyclic Organic Compound. Alternative Names: 1-Phenol-4-sulfonic acid acetate potassium salt. CAS No. 110949-38-7. Molecular formula: C8H7KO5S. Mole weight: 254.30148. Purity: 0.96. IUPACName: potassium;4-acetyloxybenzenesulfonate. Canonical SMILES: CC(=O)OC1=CC=C(C=C1)S(=O)(=O)[O-]. [K+]. Catalog: ACM110949387. | |
| 5-[ (p-Sulfophenyl) azo]salicylic Acid Acetate Methyl Ester Potassium Salt | 5-[ (p-Sulfophenyl) azo]salicylic Acid Acetate Methyl Ester Potassium Salt is an intermediate in the preparation of Sulfasalazine (S699084) and its derivatives. Group: Biochemicals. Alternative Names: 2- (Acetyloxy) -5-[2- (4-sulfophenyl) diazenyl]benzoic Acid 1-Methyl Ester Potassium Salt. Grades: Highly Purified. CAS No. 34265-46-8. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Potassium dichloroacetate | Potassium dichloroacetate. Group: Solution deposition precursors. Alternative Names: Acetic acid, dichloro-, potassium salt. CAS No. 19559-59-2. Product ID: Potassium; 2,2-dichloroacetate. Molecular formula: 167.03. Mole weight: C2HCl2KO2. C(C(=O)[O-])(Cl)Cl.[K+]. InChI=1S/C2H2Cl2O2.K/c3-1(4)2(5)6; /h1H, (H, 5, 6); /q; +1/p-1. KDGSZJXXQWMOKP-UHFFFAOYSA-M. 95%+. | |
| 1-Acetyl-3-indoxyl-d5 Acetate | 1-Acetyl-3-indoxyl-d5 Acetate is an intermediate in the synthesis of 3-Indoxyl Sulfate-d4 Potassium Salt (I655102), which is a labelled uremic toxin that acts as a potent endogenous agonist for the human aryl hydrocarbon receptor (AHR). Studies suggest that it is a sensitive and early biomarker of nephrotoxicity. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 5mg. Molecular Formula: C12H6D5NO3, Molecular Weight: 222.25. US Biological Life Sciences. | Worldwide |
| A2793 | A2793 is a dual inhibitor of TWIK-related spinal cord potassium channel (TRESK/K2P18/KCNK18) and TASK-1 (KCNK3) with IC50 of 6.8 μM for mouse TRESK. Synonyms: Ethyl [(5-Chloroquinolin-8-yl)oxy]acetate. CAS No. 88349-90-0. Molecular formula: C13H12ClNO3. Mole weight: 265.69. |  |
| Acesulfame Potassium | Acesulfame Potassium. CAS No. 55589-62-3. Product ID: PE-0484. Molecular formula: C4H4KNO4S. Mole weight: 201.24. Category: Sweetening agent. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Acesulfame Potassium; Sweeteners Excipients; Sweetening agent; C4H4KNO4S; 55589-62-3; 55589-62-3. UNII: NA. Chemical Name: 6-Methyl-1, 2, 3-oxathiazin-4(3H)-one-2, 2-dioxide potassium salt. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Oral preparations. Stability and Storage Conditions: Acetylsul panpotassium has good stability. Stored in bulk at room temperature for many years without signs of decomposition. The sweetness of aqueous solution (pH 3.0 - 3.5, 20°C) did not decrease for about two years. Although some decomposition after storage at 40°C for several months, it has good stability at temperature rise. Neither sterilization nor pasteurization affected the sweetness of acetylsulpanpotassium. Bulk products should be stored in airtight containers in a dry place. Source and Preparation: Acetylsul panpotassium is synthesized from tert-butyl acetoacetate and fluorosulfonyl isocyanate. The resulting product is converted to fluorosulfonyl acetoacetamide and cyclized into dioxythiazone cyclization in the presence of potassium hydroxide. Because this compound is strongly acidic, it can directly form potassium salt. Another route for the synthesis of acetylsulfamide be | |
| K-Oxyma | Potassium salt of OxymaPure, suitable coupling choice when peptides are assembled in highly acid-labile solid-supports, avoiding premature release of the peptide from the resin. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: 2-Cyano-2-(hydroxyimino)acetic acid ethyl ester, potassium salt, Ethyl (hydroxyimino)cyanoacetate potassium salt. CAS No. 158014-03-0. |  Luxembourg Bio Technologies |
| Native Bacillus stearothermophilus Acetate Kinase | In molecular biology, acetate kinase (EC 2.7.2.1), which is predominantly found in micro-organisms, facilitates the production of acetyl-CoA by phosphorylating acetate in the presence of ATP and a divalent cation. Short-chain fatty acids (SCFAs) play a major role in carbon cycle and can be utilized as a source of carbon and energy by bacteria. The enzyme is important in the process of glycolysis, enzyme levels being increased in the presence of excess glucose. The growth of a bacterial mutant lacking acetate kinase has been shown to be inhibited by glucose, suggesting that the enzyme is involved in excretion of excess carbohydRate. A related enzyme, butyRate kinase, ... acetate kinase from creative enzymes. this [32p]-acetyl phosphate was used to label bldm, bldm d-54n or bldm d-54a loci during the study of the effect of bldm gene on streptomyces coelicolor development. Group: Enzymes. Synonyms: Acetate kinase (phosphorylating); Acetic kinase; Acetokinase; EC 2.7.2.1; 9027-42-3; Acetate kinase. Enzyme Commission Number: EC 2.7.2.1. CAS No. 9027-42-3. Acetate kinase. Activity: 400-1,200 units/mg solid. Storage: 2-8°C. Form: lyophilized powder. Contains potassium phosphate buffer. Source: Bacillus stearothermophilus. Acetate kinase (phosphorylating); Acetic kinase; Acetokinase; EC 2.7.2.1; 9027-42-3; Acetate kinase. Cat No: NATE-0016. |  |
| Native Bacillus stearothermophilus Phosphotransacetylase | Phosphotransacetylase converts CoA to acetyl CoA. This enzyme belongs to the family of transferases, specifically those acyltransferases transferring groups other than aminoacyl groups. This enzyme participates in 3 metabolic pathways:taurine and hypotaurine metabolism, pyruvate metabolism, and propanoate metabolism. Applications: Phosphotransacetylase, from bacillus stearothermophilus, is used to convert coa to acetyl coa. phosphotransacetylase (pta) is used to study transport systems for acetate. it is used to study metabolic pathways in various bacterium. Group: Enzymes. Synonyms: phosphate acetyltransferase; phosphotransacetylase; phosphoacylase; PTA; EC 2.3.1.8; 9029-91-8. Enzyme Commission Number: EC 2.3.1.8. CAS No. 9029-91-8. PTA. Activity: > 3,000 units/mg protein (biuret). Storage: -20°C. Form: Lyophilized powder containing potassium phosphate. Source: Bacillus stearothermophilus. phosphate acetyltransferase; phosphotransacetylase; phosphoacylase; PTA; EC 2.3.1.8; 9029-91-8. Cat No: NATE-0641. | |
| Native Baker's yeast (S. cerevisiae) Pyruvate Decarboxylase | Pyruvate decarboxylase (PDC) is a homotetrameric enzyme that catalyses the decarboxylation of pyruvic acid to acetaldehyde and carbon dioxide in the cytoplasm. Pyruvate decarboxylase depends on cofactors thiamine pyrophosphate (TPP) and magnesium. PDC contains a β-α-β structure, yielding parallel β-sheets. Applications: Pyruvate decarboxylase (pdc) is used to study residues involved in thiamine pyrophosphate (tpp) binding. it is used to study the regulation of fermentation pathways in plant species. Group: Enzymes. Synonyms: Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Enzyme Commission Number: EC 4.1.1.1. CAS No. 9001-4-1. PDC. Activity: 5.0-20.0 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.2 M (NH4)2SO4 pH 6.5, stabilized with 5% glycerol, 5 mM potassium phosphate, 1 mM magnesium acetate, 0.5 mM EDTA, and 25 μM c ocarboxylase. Source: Baker's yeast (S. cerevisiae). Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Cat No: NATE-0510. | |
| Native Baker's yeast (S. cerevisiae) S-Acetyl-coenzyme A synthetase | Acetyl-coenzyme A synthetase catalyzes the production of acetyl-CoA. It is involved in histone acetylation in the nucleus. It may be involved in the growth of nonfermentable carbon sources such as glycerol. Acetyl-coenzyme A synthetase is induced by acetate, acetaldehyde and ethanol. Applications: S-acetyl-coenzyme a synthetase may be used to study various metabolic pathways, such as glycolysis, gluconeogenesis, pyruvate metabolism and co fixation. it may also be used in gene expression studies. Group: Enzymes. Synonyms: acetyl-CoA synthetase; acetyl activating enzyme; acetate thiokinase; acyl-activating enzyme; acetyl coenzyme A synthetase; acetic thiokinase; acetyl CoA ligase; acetyl C. Enzyme Commission Number: EC 6.2.1.1. CAS No. 9012-31-1. ACS. Activity: > 3 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing stabilizers as potassium phosphate, sucrose, and reduced glutathione. Source: Baker's yeast (S. cerevisiae). acetyl-CoA synthetase; acetyl activating enzyme; acetate thiokinase; acyl-activating enzyme; acetyl coenzyme A synthetase; acetic thiokinase; acetyl CoA ligase; acetyl CoA synthase; acetyl-coenzyme A synthase; short chain fatty acyl-CoA synthetase; short-chain acyl-coenzyme A synthetase; ACS; EC 6.2.1.1; 9012-31-1. Pack: Package size based on protein content. Cat No: NATE-0026. | |
| Native Escherichia coli Acetate Kinase | In molecular biology, acetate kinase (EC 2.7.2.1), which is predominantly found in micro-organisms, facilitates the production of acetyl-CoA by phosphorylating acetate in the presence of ATP and a divalent cation. Short-chain fatty acids (SCFAs) play a major role in carbon cycle and can be utilized as a source of carbon and energy by bacteria. The enzyme is important in the process of glycolysis, enzyme levels being increased in the presence of excess glucose. The growth of a bacterial mutant lacking acetate kinase has been shown to be inhibited by glucose, suggesting that the enzyme is involved in excretion of excess carbohydRate. A related enzyme, butyRate kinase, facili...rom escherichia coli has been used as part of an atp-regenerating system to study the kinetics of agonist-stimulated transphosphatidylatio. Group: Enzymes. Synonyms: Acetate kinase (phosphorylating); Acetic kinase; Acetokinase; AK; EC 2.7.2.1; 9027-42-3; Acetate kinase. Enzyme Commission Number: EC 2.7.2.1. CAS No. 9027-42-3. Acetate kinase. Activity: > 150 units/mg protein (biuret). Storage: -20°C. Form: Lyophilized powder containing trehalose with small amounts of potassium phosphate, magnesium chloride, and dithiothreitol. Source: Escherichia coli. Acetate kinase (phosphorylating); Acetic kinase; Acetokinase; AK; EC 2.7.2.1; 9027-42-3; Acetate kinase. Cat No: NATE-0017. | |
| Native Escherichia coli L-Glutamine Synthetase | Glutamine synthetase (GS) (EC 6.3.1.2) is an enzyme that plays an essential role in the metabolism of nitrogen by catalyzing the condensation of glutamate and ammonia to form glutamine:Glutamate + ATP + NH3 ? Glutamine + ADP + phosphate. Glutamine Synthetase uses ammonia produced by Nitrate reduction, amino acid degradation, and photorespiration. The amide group of glutamate is a nitrogen source for the synthesis of glutamine pathway metabolites. Applications: L-glutamine synthetase may be used for the purification of proteases from escherichia coli. Group: Enzymes. Synonyms: glutamine synthetase; glutamylhydroxamic synthetase; L-glutamine synthetase; glutamate-ammonia ligase; L-Glutamate:ammonia ligase (ADP-forming); EC 6.3.1.2; GS; 9023-70-5. Enzyme Commission Number: EC 6.3.1.2. CAS No. 9023-70-5. Purity: affinity chromatography. GS. Activity: 400-2,000 units/mg protein. Storage: -20°C. Form: lyophilized powder; Contains potassium phosphate, sodium Citrate and magnesium acetate buffer salts. Source: Escherichia coli. glutamine synthetase; glutamylhydroxamic synthetase; L-glutamine synthetase; glutamate-ammonia ligase; L-Glutamate:ammonia ligase (ADP-forming); EC 6.3.1.2; GS; 9023-70-5. Cat No: NATE-0321. | |
| Native Flavobacterium heparinum 2-O-Sulfatase | Hydrolyses the terminal 2-O-sulphate on the unsaturated di-and oligo-saccharides produced by the action of lyases on sulphated glycosaminoglycans. Hydrolyses the terminal 2-o-sulphate on the unsaturated di-and oligo-saccharides produced by the action of lyases on sulphated glycosaminoglycans. Applications: 2-o-sulfatase from flavobacterium heparinum has been used in a study to determine that oversulfated chondroitin sulfate is a contaminant in heparin associated with adverse clinical events. 2-o-sulfatase from flavobacterium heparinum has also been used in a study to determine the structure of oligosaccharides prepared from acharan sulfate. Group: Enzymes. Synonyms: 2-O-Sulfatase. 2-O-Sulfatase. Activity: 10-40 (units/ml). Storage: -20°C. Form: Solution contains 10 mM tris-acetate, pH 7.3, 80 mM NaCl, 10 mM potassium phosphate, 0.2% BSA. Source: Flavobacterium heparinum. 2-O-Sulfatase. Cat No: NATE-0002. | |
| Native Pigeon Carnitine Acetyltransferase | Carnitine acetyltransferase maintains the cellular and mitochondrial levels of acetyl-CoA, a key cofactor required for oxidative metabolism, by catalyzing an equilibrium between acetyl-CoA and acetyl-L-carnitine, a storage form of activated acetate. Carnitine acetyltransferase also maintains the pool of acetyl-CoA required for neuronal and nonneuronal acetylcholine production. Protein determined by biuret. Group: Enzymes. Synonyms: acetyl-CoA-carnitine O-acetyltransferase; acetylcarnitine transferase; carnitine acetyl coenzyme A transferase; carnitine acetylase; carnitine acetyltransferase; carnitine-acetyl-CoA transferase; CATC; 9029-90-7; carnitine O-acetyltransferase; EC 2.3.1.7; CRAT; CAT. Enzyme Commission Number: EC 2.3.1.7. CAS No. 9029-90-7. CRAT. Activity: > 70 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension. Crystalline suspension in 3.2 M (NH4)2SO4 solution, 50 mM potassium phosphate, 1 mM dithiothreitol, pH 7.0. Source: Pigeon breast muscle. Species: Pigeon. acetyl-CoA-carnitine O-acetyltransferase; acetylcarnitine transferase; carnitine acetyl coenzyme A transferase; carnitine acetylase; carnitine acetyltransferase; carnitine-acetyl-CoA transferase; CATC; 9029-90-7; carnitine O-acetyltransferase; EC 2.3.1.7; CRAT; CAT. Cat No: NATE-0159. | |
| 17α-Ethoxymethyl 6-Dehydrotestosterone | 17α-Ethoxymethy 6-Dehydrotestosterone is an intermediate in the synthesis of 7 β-Acetylthio-17α-ethoxymethy Testosterone which is an impurity of Spironolactone (S683000), which is a synthetic 17-lactone steroid which is a renal competitive aldosterone antagonist in a class of pharmaceuticals called potassium-sparing diuretics, used primarily to treat ascites in patients with liver disease, low-renin hypertension, hypokalemia, and Conns syndrome. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg. Molecular Formula: C22H32O3. US Biological Life Sciences. | Worldwide |
| 17 β-Spiro[5-androsten-17,2'-oxiran]-3 β-ol | 17 β-Spiro[5-androsten-17,2'-oxiran]-3 β-ol is an intermediate in the synthesis of 7 β-Acetylthio-17α-ethoxymethy Testosterone which is an impurity of Spironolactone (S683000), which is a synthetic 17-lactone steroid which is a renal competitive aldosterone antagonist in a class of pharmaceuticals called potassium-sparing diuretics, used primarily to treat ascites in patients with liver disease, low-renin hypertension, hypokalemia, and Conns syndrome. Group: Biochemicals. Grades: Highly Purified. CAS No. 847-75-6. Pack Sizes: 25mg, 50mg. Molecular Formula: C20H30O2. US Biological Life Sciences. | Worldwide |
| 17-(Ethoxymethyl) Androst-5-ene-3 β,17 β-diol | 17-(Ethoxymethyl) Androst-6-ene-3 β,17 β-diol is an intermediate in the synthesis of 7 β-Acetylthio-17α-ethoxymethy Testosterone which is an impurity of Spironolactone (S683000), which is a synthetic 17-lactone steroid which is a renal competitive aldosterone antagonist in a class of pharmaceuticals called potassium-sparing diuretics, used primarily to treat ascites in patients with liver disease, low-renin hypertension, hypokalemia, and Conns syndrome. Group: Biochemicals. Grades: Highly Purified. CAS No. 855-49-2. Pack Sizes: 10mg, 25mg. Molecular Formula: C22H36O3. US Biological Life Sciences. | Worldwide |
| 1-Acetyl-3-indoxyl-d4 Sulfate | 3-Indoxyl Sulfate Potassium Salt (I655102) derivative. Used in the preparation of peptidomimetics. Group: Biochemicals. Alternative Names: 1-Acetyl-3-hydroxyindole-d4 Sulfate; N-Acetyl-3-hydroxyindole-d4 Sulfate; N-Acetylindol-3-ol-d4 Sulfate. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| 1-Acetyl-3-indoxyl Sulfate | 3-Indoxyl Sulfate Potassium Salt (I655100) derivative. Used in the preparation of peptidomimetics. Group: Biochemicals. Alternative Names: 1-Acetyl-3-hydroxyindole Sulfate; N-Acetyl-3-hydroxyindole Sulfate; N-Acetylindol-3-ol Sulfate. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| 2- (4- (Methylsulfonamido) phenoxy) acetic Acid | 2- (4- (Methylsulfonamido) phenoxy) acetic Acid is a metabolite of antiarrhythmic drug Dofetilide, which is a is a potassium channel blocker. Group: Biochemicals. Grades: Highly Purified. CAS No. 103790-20-1. Pack Sizes: 10mg, 25mg. Molecular Formula: C9H11NO5S. US Biological Life Sciences. | Worldwide |
| 2- (4- (Methylsulfonamido) phenoxy) acetic Acid-13C | 2- (4- (Methylsulfonamido) phenoxy) acetic Acid-13C is isotopically labelled analogue of 2- (4- (Methylsulfonamido) phenoxy) acetic Acid (M332215), which is a metabolite of antiarrhythmic drug Dofetilide (D525700), a potassium channel blocker. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C813CH11NO5S. US Biological Life Sciences. | Worldwide |
| 2-?[4-?[ (Methylsulfonyl) ?amino]?phenoxy]?-?acetic Acid Methyl Ester | 2-?[4-?[ (Methylsulfonyl) ?amino]?phenoxy]?-?acetic Acid Methyl Ester is an intermediate in the synthesis of 2- (4- (Methylsulfonamido) phenoxy) acetic Acid (M332215). 2- (4- (Methylsulfonamido) phenoxy) acetic Acid is a metabolite of antiarrhythmic drug Dofetilide (D525700), which is a is a potassium channel blocker. Group: Biochemicals. Grades: Highly Purified. CAS No. 1192366-04-3. Pack Sizes: 25mg, 50mg. Molecular Formula: C10H13NO5S, Molecular Weight: 259.279999999999. US Biological Life Sciences. | Worldwide |
| 2-?[4-?[ (Methylsulfonyl) ?amino]?phenoxy]?-?acetic Acid Methyl Ester-13C | 2-?[4-?[ (Methylsulfonyl) ?amino]?phenoxy]?-?acetic Acid Methyl Ester-13C is an intermediate in synthesizing 2- (4- (Methylsulfonamido) phenoxy) acetic Acid-13C (M332217), an isotopically labelled analogue of 2- (4- (Methylsulfonamido) phenoxy) acetic Acid (M332215), which is a metabolite of antiarrhythmic drug Dofetilide (D525700), a potassium channel blocker. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. Molecular Formula: C913CH13NO5S. US Biological Life Sciences. | Worldwide |
| (2Z) ? -2-? (4-Ethenyl-? 1, ? 5-? dihydro-? 3-? methyl-? 5-? oxo-? 2H-? pyrrol-? 2-? ylidene) ? acetamide | (2Z)-2-(4-Ethenyl-1,5-dihydro-3-methyl-5-oxo-2H-pyrrol-2-ylidene)acetamide is a Bilirubin (B385300) oxidation end product that results from the oxidative degradation of heme and hemoglobin. It is hypothesized to be associated with diseases such as subarachnoid hemorrhage induced cerebral vasospasm, in addition to altering potassium channel activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 1634653-34-1. Pack Sizes: 500ug, 5mg. Molecular Formula: C9H10N2O2, Molecular Weight: 178.19. US Biological Life Sciences. | Worldwide |
| 3-Indoleacetic acid potassium salt | 3-Indoleacetic acid potassium salt. Group: Biochemicals. Alternative Names: Heteroauxine potassium salt; Indole-3-acetic acid potassium salt. Grades: Highly Purified. CAS No. 2338-19-4. Pack Sizes: 100g, 250g, 500g, 1Kg, 2Kg. Molecular Formula: C10H8NO2·K. US Biological Life Sciences. | Worldwide |
| 4-Acetaminophen-d3 sulfate potassium salt | 2H Labeled Compounds. Alternative Names: N-[4-(Sulfooxy)phenyl]acetamide-d3 Monopotassium Salt;4-Hydroxyacetanilide-d3 Sulfate Potassium Salt;PCM-S-d3 Potassium Salt;Paracetamol-d3 Sulfate Potassium Salt;Potassium N-Acetyl-p-aminophenyl-d3 Sulfate;Acetaminophen-d3 sulphate potassium salt. CAS No. 1188263-45-7. Molecular formula: C8H5D3KNO5S. Mole weight: 272.33. Catalog: ACM1188263457. | |
| 4-Acetaminophen Sulfate, Potassium Salt | A metabolite of 4-Acetaminophen (Paracetamol) as blood platelet aggregation inhibitor. Group: Biochemicals. Alternative Names: N-[4- (Sulfooxy) phenyl]acetamide Monopotassium Salt; 4-Hydroxyacetanilide Sulfate Potassium Salt; PCM-S Potassium Salt; Paracetamol Sulfate Potassium Salt; Potassium N-Acetyl-p-aminophenyl Sulfate. Grades: Highly Purified. CAS No. 32113-41-0. Pack Sizes: 10mg, 25mg. Molecular Formula: C?H?KNO?S, Molecular Weight: 269.32. US Biological Life Sciences. | Worldwide |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside-6-sulfate potassium salt | 4-Methylumbelliferyl 2-acetamido-2-deoxy-a-D-glucopyranoside-6-sulfate potassium salt is an indispensable compound, serving as a pivotal substrate for precise detection and quantification of sulfatase enzyme efficacy. Synonyms: 4MU-a-N-sulpho-D-glucosaminide. CAS No. 154639-35-7. Molecular formula: C18H20KNO11S. Mole weight: 497.52. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-galactopyranoside-6-sulfate potassium salt | 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-galactopyranoside-6-sulfate potassium salt is a potent fluorescent substrate used in studying glycosidase enzymes. It is commonly utilized for detecting and measuring the activity of β-galactosidase in various biological samples. This compound finds applications in drug discovery, enzyme kinetics is and diagnosis of lysosomal storage diseases such as galactosialidosis. Synonyms: 4-METHYLUMBELLIFERYL 2-ACETAMIDO-2-DEOXY-BETA-D-GALACTOPYRANOSIDE 6-SULFATE POTASSIUM SALT; Potassium ((2R,3R,4R,5R,6S)-5-acetamido-3,4-dihydroxy-6-((4-methyl-2-oxo-2H-chromen-7-yl)oxy)tetrahydro-2H-pyran-2-yl)methyl sulfate; 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-galactopyranoside 6 sulphate potassium salt; 4-Methylumbelliferyl 2-Acetamido-2-deoxy- beta -D-galactopyranoside, 6-Sulfate, Potassium Salt; potassium [(2R,3R,4R,5R,6S)-5-acetamido-3,4-dihydroxy-6-[(4-methyl-2-oxo-2H-chromen-7-yl)oxy]oxan-2-yl]methyl sulfate. CAS No. 383160-14-3. Molecular formula: C18H20KNO11S. Mole weight: 497.52. | |
| 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate potassium salt | 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate potassium salt is a chemical compound used in the biomedical industry for various applications. It is commonly employed as a substrate to measure the activity of different enzymes involved in diseases like lysosomal storage disorders and mucopolysaccharidoses. Synonyms: MUGS; 4-Methylumbelliferyl 2-acetamido-2-deoxy-6-O-sulfo-b-D-glucopyranoside potassium salt; Potassium; [(2R,3S,4R,5R,6S)-5-acetamido-3,4-dihydroxy-6-(4-methyl-2-oxochromen-7-yl)oxyoxan-2-yl]methyl sulfate; 4-Methylumbelliferyl 6-Sulfo-2-acetamido-2-deoxy-beta-D-glucopyranoside Potassium Salt; 4-Methylumbelliferyl 2-acetamido-2-deoxy-b-D-galactopyranoside 6 sulphate potassium salt. CAS No. 210357-38-3. Molecular formula: C18H20KNO11S. Mole weight: 497.52. | |
| 4-Methylumbelliferyl 2-Acetamido-2-deoxy-β-D-galactopyranoside 6-Sulfate | 4-Methylumbelliferyl 2-Acetamido-2-deoxy-β-D-galactopyranoside 6-Sulfate is an intermediate in the synthesis of 4-Methylumbelliferyl 2-Acetamido-2-deoxy-β-D-galactopyranoside 6-Sulfate Potassium Salt. Synonyms: 7-[[2-(Acetylamino)-2-deoxy-6-O-sulfo-β-D-galactopyranosyl]oxy]-4-methyl-2H-1-benzopyran-2-one. CAS No. 99389-63-6. Molecular formula: C18H21NO11S. Mole weight: 459.42. | |
| 4-Nitrophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate potassium salt | 4-Nitrophenyl 2-acetamido-2-deoxy-b-D-glucopyranoside-6-sulfate potassium salt is a potent compound widely used in biomedical research. It acts as a substrate for sulfatase enzymes, allowing the study of enzymatic activities related to sulfatase deficiency diseases. This compound also serves as a valuable tool for investigating drug interactions and developing therapeutic strategies for treating diseases associated with impaired sulfatase activity, such as mucopolysaccharidoses. CAS No. 210418-06-7. Molecular formula: C14H17N2O11S.K. Mole weight: 460.46. | |
| 6-Sialyl-D-galactose Potassium Salt (α/β mixture) | 6-Sialyl-D-galactose Potassium Salt is a derived product of D-Galactose and N-Acetylneuraminic Acid also known as Sialic Acid. Synonyms: 6-O-(N-Acetyl-α-neuraminosyl)-α-D-galactopyranose Monopotassium Salt. CAS No. 82731-28-0. Molecular formula: C17H28KNO14. Mole weight: 509.5. | |
| Acecainide HCl | Acecainide, also known as N-acetylprocainamide and ASL 601, is a class III antiarrhythmic compound. It increases the duration of the action potential by decreasing the delayed outward potassium current, slightly decreasing the calcium current, and slightly depressing the inward rectifier potassium current. Acecainide can be given either intravenously or orally, and is eliminated primarily by renal excretion. Synonyms: 4'- ( (2- (Diethylamino) ethyl) carbamoyl) acetanilide monohydrochloride; Acecainide; N-acetylprocainamide, ASL 601; ASL-601; ASL601. CAS No. 34118-92-8. Molecular formula: C15H24ClN3O2. Mole weight: 313.82. | |
| ACES potassium salt | ACES potassium salt. Group: Biochemicals. Alternative Names: N-(2-Acetamido)-2-aminoethanesulfonic acid potassium salt. Grades: Highly Purified. CAS No. 336129-15-8. Pack Sizes: 50g, 100g, 250g. Molecular Formula: C4H9KN2O4S. US Biological Life Sciences. | Worldwide |
| Acesulfame Potassium EP Impurity A (Acetoacetamide) | Acesulfame Potassium EP Impurity A (Acetoacetamide). Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 5977-14-0 (keto form); 120166-77-0 (enol form); 3-hydroxybut-2-enamide compound with 3-oxobutanamide (1:1). Molecular Formula: C4H7NO2. Mole Weight: 101.10. Catalog: APB03130. |  |
| Acetaminophen Sulphate Potassium Salt | A metabolite of 4-Acetaminophen (Paracetamol) as blood platelet aggregation inhibitor. Synonyms: N-[4-(Sulfooxy)phenyl]acetamide Monopotassium Salt; 4-Hydroxyacetanilide Sulfate Potassium Salt; PCM-S Potassium Salt; Paracetamol Sulfate Potassium Salt; Potassium N-Acetyl-p-aminophenyl Sulfate. Grades: > 95%. CAS No. 32113-41-0. Molecular formula: C8H8NO5S.K. Mole weight: 269.32. | |
| Acetohexamide | Acetohexamide is a first-generation sulfonylurea agent used in research related to type 2 diabetes; it stimulates the pancreas to secrete insulin.Acetohexamide inhibits ATP-sensitive potassium channels in the β cells of the pancreas [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 968-81-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-B0881. |  |
| Acetylenedicarboxylic acid monopotassium salt | Acetylenedicarboxylic acid monopotassium salt (CAS# 928-04-1) is a useful research chemical. Synonyms: potassium;4-hydroxy-4-oxobut-2-ynoate. CAS No. 928-04-1. Molecular formula: C4HKO4. Mole weight: 152.15. | |
| Astemizole | Astemizole is a potent and orally active nonsedating-type histamine H1 receptor antagonist with IC50 value of 4 nM. It competitively binds to histamine H1 receptor sites in the uterus, gastrointestinal tract, bronchial muscle and blood vessels. It suppresses the formation of edema and pruritus caused by histamine. It has antipruritic and anticholinergic effects. It is also a potent blocker of ether-a-go-go-related gene (ERG) potassium channel blocker with IC50 value of 0.9 nM. It exhibits antimalarial activity in multidrug resistant strains in vitro with IC50 value of 227-734 nM. It has the potential for combination therapy with antivancer drugs in resistant leukemia. It is considerably less potent at muscarinic acetylcholine receptors with Ki value of 2.4 μM. It may be used as a potential antineoplastic agent for decreasing proliferation of various cancer cells. It may be used as a pharmacological chaperone to restore protein function for some mutated forms of hERG channels and correct folding defects. It was developed by Johnson & Johnson. Synonyms: 1-(p-Fluorobenzyl)-2-((1-(2-(p-methoxyphenyl)ethyl)piperid-4-yl)amino)benzim; Laridal; 1-[(4-Fluorophenyl)methyl]-N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine; Astemisan; Hismanal; Histamen; Paralergin; R 42512; Retolen; Waruzol. Grades: ≥99% by HPLC. CAS No. 68844-77-9. Molecular formula: C28H31FN4O. Mole weight: 458.57. | |
| AVE-0118 | AVE 0118 is a potassium channel blocker that has the potential for the treatment of sleep apnea syndrome. AVE 0118 functions without apparent effect on ventricular repolarization. Noteworthy, the atrial selective and dose-dependent prolongation of atrial refractoriness (ERP) by AVE 0118 has been claimed to be an inhibitory effect of sodium channel activity in an atrial-selective manner, and may therefore contribute to the anti-AF property of AVE0118. Synonyms: [1,1'-Biphenyl]-2-carboxamide, 2'-[[[2-(4-methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl]-; 2'-[[[2-(4-Methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl][1,1'-biphenyl]-2-carboxamide; [1,1'-Biphenyl]-2-carboxamide, 2'-[[[(4-methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl]-; 2'-[[2- (4-Methoxyphenyl) acetylamino]methyl]biphenyl-2-carboxylic acid (2-pyridin-3-yl-ethyl)amide; AVE 0118; AVE0118. Grades: ≥95%. CAS No. 498577-53-0. Molecular formula: C30H29N3O3. Mole weight: 479.57. | |
| AVE 0118 hydrochloride | AVE 0118 hydrochloride is a potassium channel blocker that has the potential for the treatment of sleep apnea syndrome. AVE 0118 functions without apparent effect on ventricular repolarization. Noteworthy, the atrial selective and dose-dependent prolongation of atrial refractoriness (ERP) by AVE 0118 has been claimed to be an inhibitory effect of sodium channel activity in an atrial-selective manner, and may therefore contribute to anti-AF property of AVE0118. Synonyms: Benzeneacetamide, 4-methoxy-N-[[2'-[[[2-(3-pyridinyl)ethyl]amino]carbonyl][1,1'-biphenyl]-2-yl]methyl]-, hydrochloride (1:1); 2'-[[[2-(4-Methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl][1,1'-biphenyl]-2-carboxamide hydrochloride; [1,1'-Biphenyl]-2-carboxamide, 2'-[[[(4-methoxyphenyl)acetyl]amino]methyl]-N-[2-(3-pyridinyl)ethyl]-, hydrochloride; 2'-[[2- (4-Methoxyphenyl) acetylamino]methyl]biphenyl-2-carboxylic acid (2-pyridin-3-yl-ethyl)amide hydrochloride; AVE 0118 hydrochloride; AVE0118 hydrochloride. Grades: 99%. CAS No. 2108821-80-1. Molecular formula: C30H29N3O3.HCl. Mole weight: 516.03. | |
| Benzeneacetic acid, potassium salt | Heterocyclic Organic Compound. Alternative Names: PHENYLACETIC ACID, Benzeneacetic acid, phenylacetate, Benzenacetic acid, alpha-Toluic acid, Acetic acid, phenyl-, 2-Phenylacetic acid, Phenylethanoic acid, Benzylformic acid, Ucephan, Phenyllacetic acid, Benzylcarboxylic acid, alpha-Tolylic acid, Benzeneacetiic acid, sodium phenylacetate. alpha.-Toluic acid, 2-Phenylethanoic acid, Phenylacetic acid (natural), PHENYL-ACETIC ACID. omega.-Phenylacetic acid. CAS No. 13005-36-2. Molecular formula: C8H7KO2. Mole weight: 174.24. Appearance: colorless transparent liquid. Purity: 0.96. IUPACName: 2-phenylacetic acid. Canonical SMILES: C1=CC=C(C=C1)CC(=O)[O-].[K+]. Density: 1.257g/cm³. ECNumber: 235-845-6. Catalog: ACM13005362. | |
| Bromamphenicol | It is produced by the strain of Streptomyces sp. 3022 in the presence of potassium bromide. It is a semisynthetic chloramphenicol analogue with dibromoacetamide instead of dichloroacetamide. It has weak antibacterial activity. Synonyms: N-[(1R,2R)-1-(Hydroxymethyl)-2-hydroxy-2-(4-nitrophenyl)ethyl]-2,2-dibromoacetamide; 2,2-Dibromo-N-[β-hydroxy-α-(hydroxymethyl)-p-nitrophenethyl]-acetamide; Bromomycin. Grades: >99% by HPLC. CAS No. 16803-75-1. Molecular formula: C11H12Br2N2O5. Mole weight: 412.03. | |
| Carabersat | Carabersat, also called as SB 204269, an orally-effective anticonvulsant agent, is an ATP-sensitive potassium channel (K-ATP) opener with potential effect to treat epilepsy. Synonyms: N-[(3R,4S)-6-acetyl-3-hydroxy-2,2-dimethyl-3,4-dihydrochromen-4-yl]-4-fluorobenzamide; Carabersat; Sb 204269-eo; SB-204269; SB 204269; SB204269. Grades: 95%. CAS No. 184653-84-7. Molecular formula: C20H20FNO4. Mole weight: 357.38. | |
| Cholesterol myristate | Cholesterol myristate is a natural steroid present in traditional Chinese medicine. Cholesterol myristate binds to several ion channels such as the nicotinic acetylcholine receptor , GABAA receptor , and the inward-rectifier potassium ion channel. Uses: Scientific research. Group: Natural products. Alternative Names: Cholesteryl myristate; Cholesteryl tetradecanoate. CAS No. 1989-52-2. Pack Sizes: 500 mg; 1 g. Product ID: HY-N2338. | |
| diaminobutyrate-2-oxoglutarate transaminase | A pyridoxal-phosphate protein that requires potassium for activity.In the proteobacterium Acinetobacter baumannii, this enzyme is cotranscribed with the neighbouring ddc gene that also encodes EC 4.1.1.86, diaminobutyrate decarboxylase. Differs from EC 2.6.1.46, diaminobutyrate-pyruvate transaminase, which has pyruvate as the amino-group acceptor. This is the first enzyme in the ectoine-biosynthesis pathway, the other enzymes involved being EC 2.3.1.178, diaminobutyrate acetyltransferase and EC 4.2.1.108, ectoine synthase. Group: Enzymes. Synonyms: L-2,4-diaminobutyrate:2-ketoglutarate 4-aminotransferase; 2,4-diaminobutyrate 4-aminotransferase; diaminobutyrate aminotransferase; DABA aminotransferase; DAB aminotransferase; EctB; diaminibutyric acid aminotransferase; L-2,4-diamin. Enzyme Commission Number: EC 2.6.1.76. CAS No. 196622-96-5. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2916; diaminobutyrate-2-oxoglutarate transaminase; EC 2.6.1.76; 196622-96-5; L-2,4-diaminobutyrate:2-ketoglutarate 4-aminotransferase; 2,4-diaminobutyrate 4-aminotransferase; diaminobutyrate aminotransferase; DABA aminotransferase; DAB aminotransferase; EctB; diaminibutyric acid aminotransferase; L-2,4-diaminobutyrate:2-oxoglutarate 4-aminotransferase. Cat No: EXWM-2916. | |
| Diclofenac EP Impurity D | Diclofenac EP Impurity D is an impurity of Diclofenac, which is a non-selective COX inhibitor used as a non-steroidal anti-inflammatory drug (NSAID). Synonyms: Diclofenac sodium EP impurity D; Diclofenac potassium EP impurity D; [2-[(2-bromo-6-chlorophenyl)amino]phenyl]acetic acid; Benzeneacetic acid, 2-[(2-bromo-6-chlorophenyl)amino]-; 2-[(2-Bromo-6-chlorophenyl)amino]benzeneacetic acid; Diclofenac Impurity D; Diclofenac related compound D [USP]; Diclofenac bromo analog. Grades: ≥95%. CAS No. 127792-23-8. Molecular formula: C14H11BrClNO2. Mole weight: 340.60. | |
| Diclofenac Potassium | Diclofenac potassium is a nonsteroidal anti-inflammatory drug (NSAID) taken to reduce inflammation and as an analgesic reducing pain in certain conditions. It is a competitive inhibitor of cyclooxygenase (COX) that suppresses the production of prostaglandins. Diclofenac potassium induces apoptosis of neural stem cells (NSCs) via the activation of the caspase cascade. Uses: Nsaid. Synonyms: 2-[(2,6-Dichlorophenyl)amino]benzeneacetic Acid Potassium Salt; [o-(2,6-Dichloroanilino)phenyl]acetic Acid Monopotassium Salt; 2-[(2,6-Dichlorophenyl)amino]benzeneacetic Acid Monopotassium Salt; Caflam; Cataflam; K-fenak; Potassium diclofenac. Grades: >98%. CAS No. 15307-81-0. Molecular formula: C14H10Cl2KNO2. Mole weight: 334.24. | |
| Dicyclomine hydrochloride | Dicyclomine is an M1 and M2 muscarinic acetylcholine receptor antagonist. It inhibits inositol phosphate accumulation induced by the non-selective acetylcholine agonist carbamoylcholine (carbacho) in guinea pig cortex. Dicyclomine inhibits potassium-induced contraction of ileum, colon, and duodenum in anesthetized rats. Formulations containing dicyclomine have been used to treat functional and irritable bowel syndrome and to relieve muscle spasms in the gastrointestinal tract. Uses: Parasympatholytics. Synonyms: Dicycloverine; Dicyclomine HCl; Bentyl. Grades: ≥98%. CAS No. 67-92-5. Molecular formula: C19H35NO2·HCl. Mole weight: 346. | |
| Difluoro methyl thioacetic Acid Potassium Salt | Difluoro methyl thioacetic Acid Potassium Salt is a reagent used in the preparation of oxacephem antibiotics. Group: Biochemicals. Alternative Names: (Difluoromethylthio) acetic Acid; 2-[ (Difluoromethyl) thio]acetic Acid Potassium Salt. Grades: Highly Purified. CAS No. 83494-32-0. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| EMD 66684 | EMD 66684 is a potent and selective non-peptide angiotensin AT1 receptor antagonist (IC50 = 0.7 and >10000 nM for AT1 and AT2 receptors, respectively). It inhibits isolated rabbit aorta contractions induced by angiotensin II (IC50 = 0.2 nM) and lowers blood pressure in hypertensive rats. Synonyms: 5H-Imidazo[4,5-c]pyridine-5-acetamide, 2-butyl-3,4-dihydro-N,N-dimethyl-4-oxo-3-[[2'-(2H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-, potassium salt (1:1); Potassium 5-(4'-((2-butyl-5-(2-(dimethylamino)-2-oxoethyl)-4-oxo-4,5-dihydro-3H-imidazo[4,5-c]pyridin-3-yl)methyl)-[1,1'-biphenyl]-2-yl)tetrazol-1-ide; 5H-Imidazo[4,5-c]pyridine-5-acetamide, 2-butyl-3,4-dihydro-N,N-dimethyl-4-oxo-3-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]-, potassium salt; EMD-66684; EMD66684. Grades: ≥95%. CAS No. 187683-79-0. Molecular formula: C28H29KN8O2. Mole weight: 548.69. | |
| GIBBERELLIC ACID POTASSIUM SALT | GIBBERELLIC ACID POTASSIUM SALT. Synonyms: 10-dicarboxylicacid, 2, 4a, 7-trihydroxy-1-methyl-8-methylene-, 1, 4a-lactone, monopotassiumsalt, (Gibb-3-ene-1; gibberellicacid, monopotassiumsalt; gibberellicacidpotassiumplantcell * culture; gibberellina3potassiumsalt; gibberellins, potassiumsalt; gibrofit; k-ga; GIBBERELLIC ACID POTASSIUM SALT. CAS No. 125-67-7. Pack Sizes: 1 kg. Product ID: CDF4-0054. Category: Enzyme Preparations. Product Keywords: Food Ingredients; Enzyme Preparations; GIBBERELLIC ACID POTASSIUM SALT; CDF4-0054; 125-67-7; 204-749-6; 125-67-7. Purity: 0.99. Color: White. EC Number: 204-749-6. Physical State: Powder. Product Description: White crystalline powder, odorless. Del- iquescent, sol in water, alc, acetone. A salt of gib- berellic acid. | |
| Iptakalim hydrochloride | Iptakalim hydrochloride, a lipophilic para-amino compound, is a novel ATP-sensitive potassium channel (K ATP ) opener, as well as an α 4 β 2 -containing nicotinic acetylcholine receptor (nAChR) antagonist [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 642407-63-4. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-108069. | |
| Linopirdine | Linopirdine is an enhancer of the release of several neurotransmitters, affecting neurotransmission and being used as a cognitive enhancer for the treatment of neurological disorders including Alzheimer's disease, Parkinsonism, and depression. It increases acetylcholine release in rat hippocampal CA1 neurons by blocking M-type (Kv7.2/7.3; KCNQ2/3) K+ current with an IC50 value of 2.4 μM. Uses: Potassium channel blockers. Synonyms: 2H-Indol-2-one, 1,3-dihydro-1-phenyl-3,3-bis(4-pyridinylmethyl)-; 1,3-Dihydro-1-phenyl-3,3-bis(4-pyridinylmethyl)-2H-indol-2-one; DuP 996; 1-Phenyl-3,3-bis(4-pyridinylmethyl)-1,3-dihydro-2H-indol-2-one; 1-Phenyl-3,3-bis(pyridin-4-ylmethyl)-1,3-dihydro-2H-indol-2-one. Grades: ≥98%. CAS No. 105431-72-9. Molecular formula: C26H21N3O. Mole weight: 391.46. | |
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