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| Product | Description | |
|---|---|---|
| Sodium glycolate | 100g Pack Size. Group: Aroma Chemicals, Biochemicals, Buffers, Building Blocks, Flavours and Fragrance Materials, Organics. Formula: C2H3NaO3. CAS No. 2836-32-0. Prepack ID 65967917-100g. Molecular Weight 98.03. See USA prepack pricing. |  |
| Sodium Starch Glycolate | Sodium Starch Glycolate can be used in the synthesis of capsules for delivery of drugs or medicaments. Sodium Starch Glycolate is widely used in oral pharmaceuticals as a disintegrant in capsule and tablet formulations. Synonyms: Sodium carboxymethyl starch; Carboxymethyl Starch Sodium Salt; Covagel; Crayon B 300P; Deprogel; Emsize CMS 100; Emsize CMS 60; Explosol; Explotab; Polvitex Z; Polytex 60; Primojel; Sodium CM-starch; Vivastar P; USP Sodium Starch Glycolate Type Al; starch carboxymethylether, sodium salt. CAS No. 9063-38-1. Molecular formula: (C2H4NaO3)x. |  |
| Sodium Starch Glycolate | Sodium Starch Glycolate. CAS No: 9063-38-1 |  Sarchem Laboratories New Jersey NJ |
| Sodium Starch Glycolate | Sodium starch glycolate is a white or almost white free-flowing very hygroscopic powder. Synonyms: Carboxymethyl starch, sodium salt; carboxymethylamylum natricum; Explosol; Explotab; Glycolys; Primojel; starch carboxymethyl ether, sodium salt; Tablo; Vivastar P. CAS No. 9063-38-1. Product ID: PE-0643. Mole weight: 5×10^5~1×10^6. Category: Disintegrants; Suspending Agentss. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0643; Sodium Starch Glycolate; Disintegrants; Suspending Agentss; ; 9063-38-1. UNII: N/A. Chemical Name: Sodium carboxymethyl starch. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Oral capsules and tablets. Stability and Storage Conditions: Tablets prepared with sodium starch glycolate have good storage properties. Sodium starch glycolate is stable although very hygroscopic, and should be stored in a well-closed container in order to protect it from wide variations of humidity and temperature, which may cause caking. The physical properties of sodium starch glycolate remain unchanged for up to 5 years if it is stored at moderate temperatures and humidity. Source and Preparation: Sodium starch glycolate is a substituted derivative of potato starch. Typically, commercial products are also crosslinked using either sodium trimetaphosphate (Types A and B) or dehydration (Type C). Starch is carboxymethylated by reacting it with sodium chloroa |  |
| Sodium Starch Glycolate IP/BP/USP | Sodium Starch Glycolate IP/BP/USP. CAS No. 9063-38-1. |  |
| Sodium Starch Glycolate Type A | Sodium starch glycolate is a white or almost white free-flowing very hygroscopic powder. Synonyms: Carboxymethyl starch, sodium salt Type A. CAS No. 9063-38-1. Product ID: PE-0641. Mole weight: 5×10^5~1×10^6. Category: Disintegrants; Suspending Agentss. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0641; Sodium Starch Glycolate Type A; Disintegrants; Suspending Agentss; ; 9063-38-1. UNII: N/A. Chemical Name: Sodium carboxymethyl starch. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Oral capsules and tablets. Stability and Storage Conditions: Tablets prepared with sodium starch glycolate have good storage properties. Sodium starch glycolate is stable although very hygroscopic, and should be stored in a well-closed container in order to protect it from wide variations of humidity and temperature, which may cause caking. The physical properties of sodium starch glycolate remain unchanged for up to 3 years if it is stored at moderate temperatures and humidity. Source and Preparation: Sodium starch glycolate is a substituted derivative of potato starch. Typically, commercial products are also crosslinked using either sodium trimetaphosphate (Types A and B) or dehydration (Type C). Starch is carboxymethylated by reacting it with sodium chloroacetate in an alkaline, nonaqueous medium, typically denatured ethanol or methanol, followed by neutralization | |
| Sodium Starch Glycolate(Type B) | Sodium starch glycolate is a white or almost white free-flowing very hygroscopic powder. Synonyms: Carboxymethyl starch, sodium salt. CAS No. 9063-38-1. Product ID: PE-0642. Mole weight: 5×10^5~1×10^6. Category: Disintegrants; Suspending Agentss. Product Keywords: Excipients for Liquid Dosage Form; Suspending Agents; PE-0642; Sodium Starch Glycolate(Type B); Disintegrants; Suspending Agentss; ; 9063-38-1. UNII: N/A. Chemical Name: Sodium carboxymethyl starch. Grade: Pharmceutical Excipients. Administration route: Oral. Dosage Form: Oral capsules and tablets. Stability and Storage Conditions: Tablets prepared with sodium starch glycolate have good storage properties. Sodium starch glycolate is stable although very hygroscopic, and should be stored in a well-closed container in order to protect it from wide variations of humidity and temperature, which may cause caking. The physical properties of sodium starch glycolate remain unchanged for up to 4 years if it is stored at moderate temperatures and humidity. Source and Preparation: Sodium starch glycolate is a substituted derivative of potato starch. Typically, commercial products are also crosslinked using either sodium trimetaphosphate (Types A and B) or dehydration (Type C). Starch is carboxymethylated by reacting it with sodium chloroacetate in an alkaline, nonaqueous medium, typically denatured ethanol or methanol, followed by neutralization with | |
| Sodium Starch Glycolate USP-NF | Sodium Starch Glycolate USP-NF. |  CA, FL & NJ |
| Carboxymethylcellulose Sodium | Carboxymethylcellulose sodium occurs as a white to almost white, odorless, tasteless, granular powder. It is hygroscopic after drying. Synonyms: Akucell; Aqualon CMC; Aquasorb; Blanose; Carbose D; carmellosum natricum; Cel-O-Brandt; cellulose gum; Cethylose; CMC sodium; E466; Finnfix; Glykocellan; Nymcel ZSB; SCMC; sodium carboxymethylcellulose; sodium cellulose glycolate; Sunrose; Tylose CB; Tylose MGA; Walocel C; Xylo-Mucine. CAS No. 9004-32-4. Product ID: PE-0309. Mole weight: 90000~700000. Category: Coating Agents; Stabilizing Agents; Suspending Agents; Tablet and Capsule Disintegrant; Tablet Binder; Viscosity-increasing Agents; water-absorbing Agents. Product Keywords: Binder Excipients; Stabilizers; Suspending Agents; Excipients for Mucosal Drug Delivery Systems Materials; PE-0309; Carboxymethylcellulose Sodium; Coating Agents; Stabilizing Agents; Suspending Agents; Tablet and Capsule Disintegrant; Tablet Binder; Viscosity-increasing Agents; water-absorbing Agents; ; 9004-32-4. UNII: NA. Chemical Name: Cellulose, carboxymethyl ether, sodium salt. Grade: Pharmceutical Excipients. Administration route: Oral, subcutaneous, intramuscular, intraarticular, intrasynovial. Dosage Form: Dental preparations; intraarticular, intrabursal, intradermal, intralesional, and intrasynovial injections; oral drops, solutions, suspensions, syrups and tablets; topical preparations. Stability and Storage Conditions: C | |
| Carboxymethyl cellulose sodium - Viscosity 1400 - 2000cps | Carboxymethyl cellulose sodium is an esteemed compound boasting a mesmerizing viscosity spanning the range of 1400 to 2000cps. Within the realms of pharmaceutical preparations, particularly oral suspensions and ophthalmic solutions, it acts as a thickening compound, stabilizer and binder. Synonyms: Cellulose Glycolic Acid Sodium Salt; Sodium Tylose; Sodium Cellulose Glycolate; Sodium Carboxymethyl Cellulose. Molecular formula: (C6H7O2(OH)x(OCH2COONa)y)n. | |
| Glycolic Acid-13C Sodium Salt | Glycolic Acid-13C Sodium Salt is the isotope labelled analog of Glycolic Acid Sodium Salt; a compound that increases the glycolate oxidase activity in the liver when fed to rats. It also increases the lactate dehydrogenase activity in the liver and kidney. Group: Biochemicals. Grades: Highly Purified. CAS No. 1706469-52-4. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C13CH3NaO3, Molecular Weight: 99.03. US Biological Life Sciences. |  Worldwide |
| Sodium carboxyl methylstarch | Sodium carboxyl methylstarch. Group: Biochemicals. Alternative Names: Sodium Starch Glycolate. Grades: Highly Purified. CAS No. 9063-38-1. Pack Sizes: 50g, 100g, 250g, 500g, 1kg. US Biological Life Sciences. | Worldwide |
| Sodium carboxyl methylstarch | Sodium carboxyl methylstarch. Product ID: PE-0016. Molecular formula: C2H4O3·xNa·x. Category: Effervescents. Product Keywords: Pharmaceutical Excipients; Liquid Dosage Form; Solid Dosage Form; Disintegrants Excipients; Effervescents; Sodium carboxyl methylstarch; PE-0016; C2H4O3·xNa·x. Appearance: White to Off-White. Purity: 0.99. Synonym(s): Sodium carboxyl methylstarch;SODIUM STARCH GLYCOLATE;SODIUM STARCH GLYCOLLATE;PRIMOJEL(R). Solubility: Practically insoluble in methylene chloride. It gives a translucent suspension in water. Storage: Inert atmosphere,Room Temperature. Melting Point: >210°C (dec.). | |
| Stargel Type A | Stargel Type A. Sodium Starch Glycolate is the internally cross-linked sodium salt of carboxymethyl starch. It is a off-white, odorless, tasteless, and relatively free-flowing powder typically used in pharmaceutical applications. Dosage Form: Capsule, Orally Disintegrating Tablet, Tablet. Functionality: Cellulose Filling, Disintegrant, Dissolution Accelerator, Rapid Release Agent. Process: Direct Compression, Dry Granulation, Wet Granulation. |  Sigachi US Inc |
| 1,2-Ethanediol Disodium Salt | 1,2-Ethanediol Disodium Salt. Group: Biochemicals. Alternative Names: Disodium Ethylene Glycol; Ethylene Glycol Disodium Salt; Sodium Ehylene Glycoxide. Grades: Highly Purified. CAS No. 10604-71-4. Pack Sizes: 500mg. Molecular Formula: C2H4Na2O2, Molecular Weight: 106.03. US Biological Life Sciences. | Worldwide |
| 18:0 mPEG2000 PE sodium | 18:0 mPEG2000 PE sodium can be used for the preparation of stabilized nucleic acid-lipid particllipid particles (SNALPs). SNALPs represent some of the earliest and best functional siRNA-ABC nanoparticles described [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: DSPE-mPEG2000 sodium; 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[methoxy(polyethylene glycol)-2000] sodium. CAS No. 247925-28-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-112760. |  |
| 2,3,4-Tri-O-acetyl- β-D-glucuronic Acid Methyl Ester Propan-2-ol-D6 | 2,3,4-Tri-O-acetyl- β-D-glucuronic Acid Methyl Ester Propan-2-ol-D6 is an intermediate in the synthesis of Propylene Glycol-d6 1-Glucuronide (Mixture of Diastereomers) Sodium Salt (P835237). Isotope labelled Propylene Glycol 1-Glucuronide is a metabolite of propylene glycol, used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C16H18D6O11. US Biological Life Sciences. | Worldwide |
| 2-Deoxy-D-glucose-6-phosphate sodium salt | 2-Deoxy-D-glucose-6-phosphate sodium salt, an indispensable compound in the field of biomedicine, exhibits its vital role as a metabolic inhibitor by effectively impeding glycolysis through competitive inhibition of glucose uptake. With its remarkable ability to disrupt crucial energy processes in diseased cells, the compound shows immense potential in combating a wide range of illnesses such as cancers and viral infections. Synonyms: CID 16219287; 33068-19-8; DTXSID90585139; PUBCHEM_16219287; [(2,3,4-trihydroxy-6-oxohexyl)oxy]phosphonic acid sodium. CAS No. 33068-19-8. Molecular formula: C6H12O8P.Na. Mole weight: 266.12. | |
| (2R)-2-[6-(4-Chlorophenoxy)hexyl]-oxiranecarboxylic Acid Sodium Salt | (2R)-2-[6-(4-Chlorophenoxy)hexyl]-oxiranecarboxylic Acid Sodium Salt is a carnitine palmatoyltransferase 1 inhibitor. It is also a chemo-sensitizing agent that is able to induce apoptosis in HL60 cells when used with glycolytic inhibitors such as 2-deoxy-D-glucose (D239000) and lonidamine (L469458). Group: Biochemicals. Grades: Highly Purified. CAS No. 828934-41-4. Pack Sizes: 5mg, 10mg. Molecular Formula: C15H18ClNaO4, Molecular Weight: 320.74. US Biological Life Sciences. | Worldwide |
| 3-N-Glycolylneuraminyl-D-lactose sodium salt | 3-N-Glycolylneuraminyl-D-lactose sodium salt is a remarkable biomedical compound, tailored to the research of combating aberrant sialic acid metabolism linked to diverse ailments like metabolic disorders and select cancers. Synonyms: Neu5Gc-a-2-3-Gal-b-1-4-Glc. | |
| 6-N-Glycolylneuraminyl-D-lactose sodium salt | | |
| α-Galactosidase 110A from Bacteroides fragilis, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.-. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 67.9 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides fragilis. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 110A. Cat No: NATE-1405. |  |
| α-Galactosidase 110A from Bacteroides thetaiotaomicron, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >50% by SDS-PAGE. GLA. Mole weight: 65.1 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 110A. Cat No: NATE-1403. | |
| α-Galactosidase 27A from Clostridium cellulolyticum, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 44.0 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium cellulolyticum. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 27A. Cat No: NATE-1400. | |
| α-Galactosidase 4A from Bacillus halodurans, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 51.8 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacillus halodurans. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 27A. Cat No: NATE-1404. | |
| α-Galactosidase 95A from Bacteroides ovatus, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 91 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides ovatus. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 95A. Cat No: NATE-1406. | |
| α-Galactosidase 97A from Bacteroides thetaiotaomicron, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >50% by SDS-PAGE. GLA. Mole weight: 74.7 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 97A. Cat No: NATE-1402. | |
| α-Galactosidase 97B from Bacteroides thetaiotaomicron, Recombinant | Alpha-galactosidase is a glycoside hydrolase enzyme that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. It is encoded by the GLA gene. Two recombinant forms of alpha-galactosidase are called agalsidase alfa (INN) and agalsidase beta (INN). Group: Enzymes. Synonyms: Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase. Enzyme Commission Number: EC 3.2.1.22. CAS No. 9025-35-8. Purity: >90% by SDS-PAGE. GLA. Mole weight: 74.9 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Bacteroides thetaiotaomicron. Alpha-Galactosidase; Galactosidase; EC 3.2.1.22; GLA; GALA; melibiase; α-D-galactosidase; α-galactosidase A; α-galactoside galactohydrolase; α-Galactosidase 97B. Cat No: NATE-1401. | |
| beta-Nicotyrine | Beta-nicotyrine is a chemical substance found in plants. It is an alkaloid that has been shown to have carcinogenic potential, and can be used for analytical methods for the determination of nicotinamide in plant metabolism. Beta-nicotyrine can be extracted from rat liver microsomes with dispersive solid-phase extraction. This extraction process involves the use of glycol ether as an organic solvent and malonic acid as a reagent to extract beta-nicotyrine from rat liver microsomes. The resulting extract is then treated with hydroxide solution and analyzed by gas chromatography/mass spectrometry (GC/MS) using chemical ionization. The GC/MS system consists of a zirconium oxide column and sodium hydroxide solution as the eluent. Group: Other alkaloids. Alternative Names: 3-(1-Methyl-2-pyrrolyl)pyridine. CAS No. 487-19-4. Molecular formula: C10H10N2. Mole weight: 158.2 g/mol. Canonical SMILES: CN1C=CC=C1C2=CN=CC=C2. Catalog: ACM487194-1. |  |
| CARBOXYMETHYLCELLULOSE SODIUM SALT | OtherSolid;Slightly hygroscopic white or slightly yellowish or greyish odourless and tasteless, granular or fibrous powder. Group: Polymerspolysaccharide. Alternative Names: CARBOXYMETHYL CELLULOSE SODIUM; CARBOXYMETHYLCELLULOSE SODIUM SALT; CELLULOSE, CARBOXY METHYL, SODIUM SALT; CELLULOSE GLYCOLIC ACID SODIUM SALT; CMC 7HF; CMC 7LF; CMC 7MF; AQUACIDE I. CAS No. 9004-32-4. Molecular formula: 263.2g/mol. Mole weight: The polymers contain substituted anhydroglucose units with the following general formula:; C6H7O2(OR1)(OR2)(OR3), where R1, R2, R3each may be one of the following:??H;C8H16NaO8. CC(=O)O.C(C(C(C(C(C=O)O)O)O)O)O.[Na]. InChI=1S/C6H12O6. C2H4O2. Na/c7-1-3(9)5(11)6(12)4(10)2-8; 1-2(3)4; /h1, 3-6, 8-12H, 2H2; 1H3, (H, 3, 4). DPXJVFZANSGRMM-UHFFFAOYSA-N. |  |
| Carboxymethyl cellulose sodium - Viscosity 1000 - 1300 mPa.s | Viscosity 1000 - 1300 mPa.s - Carboxymethyl cellulose sodium (CMC-Na) is a multifaceted and crucial compound with high viscosity attributes, making it an exceptional choice for compound formulations. CMC-Na has profound impact on enhancing compound stability, controlling drug release and augmenting viscosity. Synonyms: CM Cellulose; Carmellose; Almelose; Glycolic acid cellulose ether. | |
| D-(+)-2-Phosphoglyceric Acid Sodium Hydrate | Enantiomerically pure metabolite of glycolysis / gluconeogenesis and also substrate for a number of important enzymes in central metabolism like enolase and phosphoglycerate mutase. Group: Biochemicals. Alternative Names: (R) -3-Hydroxy-2- (phosphonooxy) propanoic Acid Trisodium Salt. Grades: Highly Purified. CAS No. 70195-25-4. Pack Sizes: 5mg, 10mg. Molecular Formula: C?H?Na?O?P, Molecular Weight: 252. US Biological Life Sciences. | Worldwide |
| Dapagliflozin propanediol | Dapagliflozin propanediol is the salt of Dapagliflozin, which is a selective, orally active renal sodium-glucose cotransporter type 2 (SGLT2) inhibitor used for the treatment of type 2 diabetes mellitus (T2DM). Synonyms: Dapagliflozin propanediol anhydrous; D-Glucitol, 1,5-anhydro-1-C-[4-chloro-3-[(4-ethoxyphenyl)methyl]phenyl]-, (1S)-, compd. with (2S)-1,2-propanediol (1:1); Dapagliflozin S-propylene glycol; (2S,3R,4R,5S,6R)-2-(4-Chloro-3-(4-ethoxybenzyl)phenyl)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol, (2S)-propane-1,2-diol (1:1). Grades: ≥95%. CAS No. 1971128-01-4. Molecular formula: C21H25ClO6.C3H8O2. Mole weight: 484.97. | |
| DCA | DCA is a mitochondrial pyruvate dehydrogenase kinase (PDK) inhibitor that shifts pyruvate metabolism from glycolysis and lactate production to glucose oxidation in the mitochondria. DCA also induces apoptosis and reverses the KV1.5 channels downregulation in cancer. Synonyms: Sodium dichloroacetate; Sodium 2,2-dichloroacetate; Dichloroacetic acid sodium salt. CAS No. 2156-56-1. Molecular formula: C2HCl2NaO2. Mole weight: 150.92. | |
| D-Fructose-13C6 1,6-Bisphosphate Sodium Salt Hydrate | Fructose1,6-bisphosphate is an intermediate that lies within the glycolysis metabolic pathway and is also an pyruvate kinase allosteric activator. Synonyms: D-Fructose-13C6 1,6-Bis(dihydrogen phosphate); D-Fructose-13C6 1,6-Biphosphate; D-Fructose-13C6 1,6-Bisphosphate; D-Fructose-13C6 1,6-Diphosphate; Diphosphofructose-13C6; Esafosfan-13C6; Esafosfina-13C6; FDP-13C6; Fosfructose-13C6; Fructose-13C6 1,6-Bis(dihydrogen phosphate); Fructose-13C6 1,6-Bisphosphate; Fructose-13C6 1,6-Diphosphate; Harden-Young Ester-13C6. Molecular formula: [13C]6H14O12P2 xH2O xNa. Mole weight: 346.06. | |
| D-Fructose-13C6 1,6-Bisphosphate Sodium Salt Hydrate | Isotope labelled Fructose1,6-bisphosphate is an intermediate that lies within the glycolysis metabolic pathway and is also an allosteric activator of pyruvate kinase. Group: Biochemicals. Alternative Names: D-Fructose-13C6 1,6-Bis(dihydrogen phosphate); D-Fructose-13C6 1,6-Biphosphate; D-Fructose-13C6 1,6-Bisphosphate; D-Fructose-13C6 1,6-Diphosphate; Diphosphofructose-13C6; Esafosfan-13C6; Esafosfina-13C6; FDP-13C6; Fosfructose-13C6; Fructose-13C6 1,6-Bis(dihydrogen phosphate); Fructose-13C6 1,6-Bisphosphate; Fructose-13C6 1,6-Diphosphate; Harden-Young Ester-13C6. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| D-Fructose 1,6-Bisphosphate Sodium Salt Hydrate | Fructose1,6-bisphosphate is an intermediate that lies within the glycolysis metabolic pathway and is also an pyruvate kinase allosteric activator. Synonyms: D-Fructose, 1,6-bis(dihydrogen phosphate) Sodium Salt Hydrate;D-Fructose, 1,6-bis(dihydrogen phosphate) Sodium Salt Hydrate; D-Fructose 1,6-bisphosphate Sodium Salt Hydrate; D-Fructose 1,6-diphosphate Sodium Salt Hydrate; Diphosphofructose Sodium Salt Hydrate; Esafosfan Sodium Salt Hydrate; Esafosfina Sodium Salt Hydrate; FDP Sodium Salt Hydrate; Fosfructose Sodium Salt Hydrate; Fructose 1,6-bis(dihydrogen phosphate) Sodium Salt Hydrate; Fructose 1,6-bisphosphate Sodium Salt Hydrate; Fructose 1,6-diphosphate Sodium Salt Hydrate; Harden-Young ester Sodium Salt Hydrate. CAS No. 41012-14-0. Molecular formula: C6H14O12P2 xH2O xNa. Mole weight: 340.12. | |
| D-Fructose-1,6-diphosphate tetrasodium salt | D-Fructose-1,6-diphosphate tetrasodium salt is a crucial compound widely used in the pharmaceutical industry. It acts as a mediator in glycolysis, aiding glucose metabolism to produce energy. Additionally, it serves as a regulator in various biochemical pathways, making it valuable in treating metabolic disorders and enhancing cellular functions. Synonyms: D-Fructose, 1,6-bis(dihydrogen phosphate), tetrasodium salt; D-Fructose-1,6-diphosphate tetrasodium salt; D-fructose1,6-diphosphatesodiumsalt; tetrasodium; [(2R,3R,4S)-2,3,4-trihydroxy-5-oxo-6-phosphonatooxyhexyl] phosphate; D-Fructose, 1,6-bis(dihydrogen phosphate), trisodium salt; Sodium (3S,4R,5R)-6-((hydrogenphosphonato)oxy)-3,4,5-trihydroxy-2-oxohexyl phosphate; EINECS 245-884-0; 81028-91-3; Hexose diphosphate sodium salt; sodium fructose 1,6-bisphosphate; MFCD00135870; D-Fructose, 1,6-bis(dihydrogen phosphate), sodium salt (1:4); sodium (2R,3R,4S)-2,3,4-trihydroxy-5-oxohexane-1,6-diyl diphosphate. CAS No. 23784-19-2. Molecular formula: C6H10Na4O12P2. Mole weight: 428.04. | |
| D-Fructose-2,6-diphosphate sodium salt | D-Fructose-2,6-diphosphate sodium salt is a vital compound in biomedicine used as a metabolic regulator. It plays a crucial role in the regulation of glycolysis and gluconeogenesis. D-Fructose-2,6-diphosphate sodium salt is employed in researching enzyme mechanisms, drug development targeting metabolic disorders, and in studying the treatment of diseases like diabetes and cancer. Synonyms: D-Fructose-2,6-bisphosphate sodium salt. CAS No. 84364-89-6. Molecular formula: C6H13NaO12P2. Mole weight: 362.1. | |
| D-Fructose 6-Phosphate-13C6 Disodium Salt | Isotope labelled analogue of D-Fructose 6-Phosphate. β-D-form of D-Fructose 6-Phosphate is commonly found in cells within the glycolysis metabolic pathway produced by the isomerization of glucose 6-phosphate (G596805). Group: Biochemicals. Alternative Names: 6-(Dihydrogen phosphate) D-Fructose Sodium Salt; D-fructose 6-phosphate Disodium. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| D-Fructose 6-Phosphate-13C6 Disodium Salt | Isotope labelled analogue of D-Fructose 6-Phosphate. β-D-form of D-Fructose 6-Phosphate is commonly found in cells within the glycolysis metabolic pathway produced by the isomerization of glucose 6-phosphate. Synonyms: 6-(Dihydrogen phosphate) D-Fructose Sodium Salt; D-fructose 6-phosphate Disodium. Grades: 97%; 98% atom 13C. Molecular formula: [13C]6H11Na2O9P. Mole weight: 310.06. | |
| DSPE-PEG-NH2 | DSPE-PEG-NH2,1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-(polyethylene glycol) -amine (sodium salt) is a active targeting drug delivery material,it can be conjugated with peptides, antibodies, or proteins which contain NHS esters, carboxy groups on the surface. Synonyms: 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-(polyethylene glycol) -amine (sodium salt). Product ID: MSMN-055. Category: Raw Materials. | |
| Endoglycosidase F2 from Elizabethkingia miricola, Recombinant | An Endoglycosidase is an enzyme that releases oligosaccharides from glycoproteins or glycolipids. It may also cleave polysaccharide chains between residues that are not the terminal residue, although releasing oligosaccharides from conjugated protein and lipid molecules is more common. It breaks the glycosidic bonds between two sugar monomer in the polymer. It is different from exoglycosidase that it does not do so at the terminal residue. Hence, it is used to release long carbohydrates from conjugated molecules. If an exoglycosidase were used, every monomer in the polymer would have to be removed, one by one from the chain, taking a long time. An endoglycosidase cleaves, giving a polymeric product. Group: Enzymes. Synonyms: EC 3.2.1.96; Elizabethkingia miricola; Endo-β-N-acetylglucosaminidase F2; Endo F2; Endoglycosidase F2 from Chryseobacterium meningosepticum; Endoglycosidase F2 from Elizabethkingia meningoseptica; Endoglyco. Enzyme Commission Number: EC 3.2.1.96. CAS No. 37278-88-9. Endo-β-N-acetylglucosaminidase. Activity: 20 units/mg. Storage: -20°C. Form: Aseptically filled solution in 10 mM sodium acetate, 25 mM sodium chloride, pH 4.5. Source: E. coli. Species: Elizabethkingia miricola. EC 3.2.1.96; Elizabethkingia miricola; Endo-β-N-acetylglucosaminidase F2; Endo F2; Endoglycosidase F2 from Ch | |
| Endoglycosidase F3 from Elizabethkingia miricola, Recombinant | An Endoglycosidase is an enzyme that releases oligosaccharides from glycoproteins or glycolipids. It may also cleave polysaccharide chains between residues that are not the terminal residue, although releasing oligosaccharides from conjugated protein and lipid molecules is more common. It breaks the glycosidic bonds between two sugar monomer in the polymer. It is different from exoglycosidase that it does not do so at the terminal residue. Hence, it is used to release long carbohydrates from conjugated molecules. If an exoglycosidase were used, every monomer in the polymer would have to be removed, one by one from the chain, taking a long time. An endoglycosidase cleaves, giving a polymeric product. Group: Enzymes. Synonyms: Endoglycosidase F3; Elizabethkingia miricola; Endo-β-N-. Enzyme Commission Number: EC 3.2.1.96. CAS No. 231-791-2. Endo-β-N-acetylglucosaminidase. Activity: 30 U/mg. Storage: 2-8°C. Form: Aseptically filled solution in 20 mM Tris-HCl, pH 7.5. Source: E. coli. Species: Elizabethkingia miricola. Endoglycosidase F3; Elizabethkingia miricola; Endo-β-N-acetylglucosaminidase F3; Endoglycosidase F3 from Elizabethkingia (Chryseobacterium/Flavobacterium) meningosepticum; EC 3.2.1.96; 231-791-2; Endo F3. Pack: Supplied with 5× Reaction Buffer, 250 mM sodium acetate, pH 4.5. Cat No: NATE-0216. | |
| Fructose 1,6-bisphosphatase from Human, Recombinant | Fructose 1,6-bisphosphatase (FBPase; EC 3.1.3.11) is an enzyme in the liver that converts fructose-1,6-bisphosphate to fructose 6-phosphate in gluconeogenesis. Fructose bisphosphatase catalyses the reverse of the reaction which is catalysed by phosphofructokinase, which is involved in the process of glycolysis. These enzymes only catalyse the reaction in one direction each, and are regulated by metabolites such as fructose 2,6-bisphosphate so that high activity of one of the two enzymes is accompanied by low activity of the other. It is involved in many different metabolic pathways and found in most organisms. FBPase requires metal ions for catalysis (Mg2+ and Mn2+ being preferred) and the enzyme is potently inhibited by Li+. Group: Enzymes. Synonyms: Fructose-bisphosphatase; EC 3.1.3.11; FBPase; Hexose diphosphatase. Enzyme Commission Number: EC 3.1.3.11. Purity: > 90% (densitometry). FBPase. Mole weight: 36.8 kDa. Activity: 1525 pmol/min/ug. Storage: Stable for > 6 months at -80°C. Form: Liquid. Storage Buffer: 50 mM potassium phosphate pH-7.4, 50 mM sodium chloride, 0.5 mM ethylenediaminetetraaceticacid, and 2.5% glycerol. Source: E. coli. Species: Human. Fructose-bisphosphatase; EC 3.1.3.11; FBPase; Hexose diphosphatase. Cat No: NATE-1576. | |
| Glycolaldehyde diethyl acetal,stab.with ca 0.1%sodium carbonate | Glycolaldehyde diethyl acetal,stab.with ca 0.1%sodium carbonate. Group: Biochemicals. Grades: Highly Purified. CAS No. 621-63-6. Pack Sizes: 1g, 2g, 5g, 10g, 25g. Molecular Formula: C6H14O3. US Biological Life Sciences. | Worldwide |
| Glycolithocholic acid sodium | Glycolithocholic acid (Lithocholylglycine) sodium is the sodium salt of Glycolithocholic acid. Glycolithocholic acid is a glycine-conjugated secondary bile acid. Glycolithocholic acid can be used to diagnose ulcerative colitis (UC), non-alcoholic steatohepatitis (NASH) and primary sclerosing cholangitis (PSC) [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lithocholylglycine sodium. CAS No. 24404-83-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-116374A. | |
| Lactate-d3 (sodium) (60% in water) | Lactate-d 3 sodium (60% in water) is the deuterium labeled Lactate sodium (60% in water). Lactate sodium (60% in water) is the product of glycogenolysis and glycolysis. Lactate sodium (60% in water) functions in a variety of biochemical processes [1] [2]. Uses: Scientific research. Group: Isotope-labeled compounds. Alternative Names: Lactic acid-d3 sodium. CAS No. 1219802-24-0. Pack Sizes: 1 mg (5.20 M * 1.67 μL in Water); 5 mg (5.20 M * 8.36 μL in Water); 10 mg (5.20 M * 16.71 μL in Water). Product ID: HY-B2227BS1. | |
| Lactate (sodium) (60% in water) | Lactate (60% in water) (Lactic acid) sodium is the product of glycogenolysis and glycolysis [1]. Lactate sodium (60% in water) is an organic salt that is mainly used as a buffer and pH adjuster for injection solutions. Lactate sodium (60% in water) can be metabolized by the body into sodium bicarbonate, which in turn acts to increase the pH of the blood. Lactate sodium (60% in water) is used to improve metabolic acidosis and hypovolemic states. In terms of pharmaceutical preparations, Lactate sodium (60% in water) is often used in combination with sodium chloride, glucose, etc. to form normal saline or compound liquid intravenous injection [2] [3] [4] [5]. Lactate sodium (60% in water) also has antimicrobial activity, which can be used as a food preservative [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lactic acid sodium. CAS No. 72-17-3. Pack Sizes: 100 mg (5.34 M * 167 μL in Water); 250 mg (5.34 M * 418 μL in Water); 500 mg (5.34 M * 835 μL in Water); 1 g (5.34 M * 1.67 mL in Water). Product ID: HY-B2227B. | |
| Lacto-N-Biosidase, Recombinant | Lacto-N-Biosidase may be used during glycoprotein analysis to better study the structure and function of glycoprotein and glycolipid sugar chains. This product can be used for specific oligosaccharide hydrolysis of type-I chain oligosaccharides, producing lacto-N-biose (Gal β 1-3 GlcNAc) as a byproduct, but not oligosaccharide hydrolysis of type-II chain oligosaccharides. As a result, Lacto-N-Biosidase can be used to distinguish type-I versus type-II glycoprotein as well as glycolipid sugar chains. When used in conjunction with α -1,3/4-Fucosidase, Lacto-N-Biosidase can also help distinguish Sialyl-Lewis x and Sialyl-Lewis a structures. Applications: Specific hydrolysis of oligosaccharides with type-i sugar chains and production of byproduct lacto-n-biose (gal β 1-3 glcnac). Group: Enzymes. Synonyms: Oligosaccharide lacto-N-biosylhydrolase; Lacto-N-Biosidase. Lacto-N-Biosidase. Mole weight: 60 kDa (SDS-PAGE). Form: Solution in 50 mM sodium acetate buffer, pH 5.5, containing 0.05% Brij-58. Source: Streptomyces sp. 142. Oligosaccharide lacto-N-biosylhydrolase; Lacto-N-Biosidase. Cat No: NATE-0855. | |
| N-Acetylglucosamine endo-β-galactosidase 16C from Clostridium perfringens, Recombinant | Endo-β-Galactosidase is an enzyme that hydrolyzes internal β-galactosidic linkages of oligosaccharides in poly-N-acetyl-lactosamine structures. This enzyme resembles the Escherichia freundii enzyme due to its specificity towards bovine corneal keratan sulphate, milk oligosaccharides and the glycolipids lacto-N-neotetraosylceramide and lacto-N-tetraosylceramide. Group: Enzymes. Synonyms: β-Galactosidase bacterial; Keratanase; Endo-β-galactosidase; keratan sulfate endogalactosidase; keratan-sulfate 1,4-β-D-galactanohydrolase; EC 3.2.1.103. Enzyme Commission Number: EC 3.2.1.-. Purity: >90% by SDS-PAGE. Endo-β-galactosidase. Mole weight: 33.7 kDa. Storage: This enzyme is shipped at room temperature but should be stored at -20 °C. Form: 35 mM NaHepes buffer, pH 7.5, 750 mM NaCl, 200 mM imidazol, 3.5 mM CaCl2, 0.02% sodium azide and 25% (v/v) glycerol. Source: E. coli. Species: Clostridium perfringens. β-Galactosidase bacterial; Keratanase; Endo-β-galactosidase; keratan sulfate endogalactosidase; keratan-sulfate 1,4-β-D-galactanohydrolase; EC 3.2.1.-; N-Acetylglucosamine endo-β-galactosidase 16C. Cat No: NATE-1412. | |
| Native Human Glyceraldehyde-3-phosphate Dehydrogenase | Glyceraldehyde-3-phosphate dehydrogenase catalyzes the conversion of glyceraldehyde-3-phosphate to 1,3-bisphosphoglycerate as part of glycolysis. It has also been shown to have roles in initiation of apoptosis, transcription activation and the shuttling of ER to Golgi vesicles. Group: Enzymes. Synonyms: EC 1.2.1.12; GAPDH; glyceraldehyde-3-phosphate dehydrogenase (phosphorylating); triosephosphate dehydrogenase; dehydrogenase, glyceraldehyde phosphate; phosphoglyceraldehyde dehydrogenase; 3-phosphoglyceraldehyde dehydrogenase; NAD+-dependent glyceraldehyde phosphate dehydrogenase; glyceralde. Enzyme Commission Number: EC 1.2.1.12. CAS No. 9001-50-7. Glyceraldehyde-3-phosphate Dehydrogenase. Activity: 50-150 units/mg protein. Storage: -20°C. Form: Lyophilized powder containing sodium Citrate buffer salts. Source: Human erythrocytes. Species: Human. EC 1.2.1.12; GAPDH; glyceraldehyde-3-phosphate dehydrogenase (phosphorylating); triosephosphate dehydrogenase; dehydrogenase, glyceraldehyde phosphate; phosphoglyceraldehyde dehydrogenase; 3-phosphoglyceraldehyde dehydrogenase; NAD+-dependent glyceraldehyde phosphate dehydrogenase; glyceraldehyde phosphate dehydrogenase (NAD+); glyceraldehyde-3-phosphate dehydrogenase (NAD+); NADH-glyceraldehyde phosphate dehydrogenase; glyceraldehyde-3-P-dehydrogenase; 9001-50-7. Cat No: NATE-0280. | |
| O-Glycosidase from Streptococcus pneumoniae, Recombinant | O-Glycosidase releases unsubstituted Ser-and Thr-linked β-Gal-(1?3)-α-GalNAc (Core 1 type O-glycan) from glycoproteins. Substitutions of the disaccharide core with sialic acid, lactosamine (galactose-N-acetyl glucosamine), or fucose will block hydrolysis and prevent the liberation of the oligosaccharide from the protein. Pretreament with glycolytic enzymes to remove substituent saccharides from the O-glycan may be needed prior to cleavage using O-glycosidase. Group: Enzymes. Synonyms: endo-α-acetylgalactosaminidase; endo-α-N-acetyl-D-galactosaminidase; mucinaminylserine mucinaminidase; D-galactosyl-3-(N-acetyl-α-D-galacto. Enzyme Commission Number: EC 3.2.1.97. CAS No. 9032-92-2. O-Glycosidase. Storage: 2-8°C. Form: buffered aqueous solution; Solution in 50 mM sodium phosphate, pH 7.5. Source: E. coli. Species: Streptococcus pneumoniae. endo-α-acetylgalactosaminidase; endo-α-N-acetyl-D-galactosaminidase; mucinaminylserine mucinaminidase; D-galactosyl-3-(N-acetyl-α-D-galactosaminyl)-L-serine mucinaminohydrolase; endo-α-GalNAc-ase; glycopeptide α-N-acetylgalactosaminidase; D-galactosyl-N-acetyl-α-D-galactosamine D-galactosyl-N-acetyl-galactosaminohydrolase; 9032-92-2; EC 3.2.1.97. Pack: Supplied with 5× Reaction Buffer, 250 mM NaH2PO4 pH 5.0. Cat No: NATE-0497. | |
| Phenytoin Impurity D | An impurity of Phenytoin which is believed to protect against seizures by causing voltage-dependent block of voltage gated sodium channels. Synonyms: 5157-15-3; Diphenylglycoluril; 7,8-Diphenylglycoluril; 3a,6a-Diphenylglycoluril; GLYCOLURIL, 3a,6a-DIPHENYL-. Grades: > 95%. CAS No. 5157-15-3. Molecular formula: C16H14N4O2. Mole weight: 294.32. | |
| Polyethylene glycol carboxymethyl C11-15-alkyl ether sodium salts | Tertiary oil recovery agent, viscosity reductant. Group: Oil field. Alternative Names: PEG C11-15 Alkyl ether carboxylic acid, sodium salt. CAS No. 68603-23-6. Molecular formula: (C2H4O)nC13H26O3. Na-(C2H4O)nC17H34O3. Na. Catalog: ACM68603236. | |
| Polyethylene glycol carboxymethyl C12-15-alkyl ether sodium salts | Tertiary oil recovery agent, viscosity reductant. Group: Oil field. Alternative Names: PEG C12-15 Alkyl ether carboxylic acid, sodium salt. CAS No. 70632-06-3. Molecular formula: (C2H4O)nC14H28O3. Na-(C2H4O)nC17H34O3. Na. Catalog: ACM70632063. | |
| Polyethylene glycol mono-C6-10-alkyl ether sulfate sodium salt | Foaming agents, wetting agents. Group: Oil field. Alternative Names: C6-10 Alkyl ethoxylate sulfuric acid, sodium salt. CAS No. 73665-22-2. Molecular formula: (C2H4O)n. C6H14O4S. Na-(C2H4O)n. C10H22O4S. Na. Catalog: ACM73665222. | |
| Polyethylene glycol monooleyl ether sulfate sodium salt | Emulsifier. Group: Emulsifying agents. Alternative Names: Polyethylene glycol oleyl ether sulfate sodium salt. CAS No. 27233-34-7. Molecular formula: (C2H4O)n.C18H36O4S.Na. IUPACName: Disodium;1-octadec-9-enoxyoctadec-9-ene;sulfate. Canonical SMILES: CCCCCCCCC= CCCCCCCCCOCCCCCCCCC= CCCCCCCCC. [O-] S (= O) (= O) [O-]. [Na+]. [Na+]. Catalog: ACM27233347-1. | |
| Polyethylene glycol (MW:400) | Polyethylene glycol (MW:400). CAS No. 25322-68-3. Product ID: PE-0312. Molecular formula: CH2(OH)(CH2CH2O)nCH2OH. Mole weight: 380 - 420. Category: Humectants; Micro-drug Delivery Systems. Product Keywords: Pharmaceutical Excipients; Micro-drug Delivery Systems; Polyethylene glycol (MW:400); PE-0312; CH2(OH)(CH2CH2O)nCH2OH; 25322-68-3; 25322-68-3. Grade: Pharmaceutical Grade. Purity: ≥99%. Applications: Liposome and Micelle Formulations in Market. Product Description: 1,2-Distearoyl-sn-glycero-3-phosphoglycerol, sodium salt. | |
| Propylene Glycol 1-Glucuronide Sodium Salt (Mixture of Diastereomers) | Propylene Glycol 1-Glucuronide is a metabolite of propylene glycol. It can be used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds. Synonyms: (2S,3S,4S,5R,6R)-3,4,5-Trihydroxy-6-(2-hydroxypropoxy)tetrahydro-2H-pyran-2-carboxylic Acid Sodium Salt. Grades: 96%. Molecular formula: C9H15NaO8. Mole weight: 274.2. | |
| Propylene Glycol 2-α-Glucopyranosiduronic Acid Benzyl Ester 2,3,4-Triacetate | Propylene Glycol 2-α-Glucopyranosiduronic Acid Benzyl Ester 2,3,4-Triacetate is an impurity in the synthesis of Propylene Glycol 2-Glucuronide Sodium Salt, which is a metabolite of propylene glycol, used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg. Molecular Formula: C23H30O11, Molecular Weight: 482.48. US Biological Life Sciences. | Worldwide |
| Propylene Glycol 2-Glucopyranosiduronic Acid Methyl Ester 2,3,4-Triacetate | Propylene Glycol 2-Glucopyranosiduronic Acid Methyl Ester 2,3,4-Triacetate is an intermediate in the synthesis of Propylene Glycol 2-Glucuronide Sodium Salt, which is a metabolite of propylene glycol, used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 10mg. Molecular Formula: C16H24O11. US Biological Life Sciences. | Worldwide |
| Propylene Glycol 2-Glucuronide Sodium Salt (Mixture of Diastereomers) | Propylene Glycol 2-Glucuronide Sodium Salt is a metabolite of propylene glycol, which can be used in the synthesis of N-terminal kinase inhibitors with cellular activity. Acts as a solvent for various pharmaceutical compounds. Synonyms: (1S,2R,3R,5R)-2,3-Dihydroxy-5-((1-hydroxypropan-2-yl)oxy)cyclohexanecarboxylic Acid Sodium Salt. Grades: >85%. Molecular formula: C9H15NaO8. Mole weight: 274.2. | |
| Sodium Laureth Phosphate | Emulsifier; Dispersing agent. Group: Emulsifying agents. Alternative Names: Sodium polyethylene glycol lauryl ether phosphate. CAS No. 42612-52-2. Molecular formula: C14H30NaO5P. Mole weight: 332.35. IUPACName: Sodium;2-dodecoxyethyl hydrogen phosphate. Canonical SMILES: CCCCCCCCCCCCOCCOP(=O)(O)[O-].[Na+]. Catalog: ACM42612522. | |
| Sodium lauryl polyoxyethylene ether sulfate | Sodium laureth sulfate (SLES), an accepted contraction (Lauryl + Ether = Laureth) of sodium lauryl ether sulfate (SLES), is an anionic detergent and surfactant found in many personal care products (soaps, shampoos, toothpaste etc.). SLES is an inexpensive and very effective foaming agent. SLES, sodium lauryl sulfate (SLS), ammonium lauryl sulfate (ALS), and sodium pareth sulfate are surfactants that are used in many cosmetic products for their cleaning and emulsifying properties. They behave similarly to soap. Alternative Names: Poly(oxy-1,2-ethanediyl)-alpha-sulfo-omega-(dodecyloxy)-sodium salt;sulfate or polyoxyethene glycol ether;Sodium Poly(oxyethylene) Lauryl Ether Sulfate;Sodium laureth sulfate;Sodium laureth sulphate. CAS No. 9004-82-4. Molecular formula: C14H29NaO5S. Mole weight: 272.37. Appearance: Solid. Purity: ~70%. Catalog: ACM9004824. | |
| Sodium Oxamate | Sodium oxamate is an inhibitor of lactate dehydrogenase (LDH), a key regulator of glycolysis, reversibly catalyzing the conversion of pyruvate to lactate. Synonyms: Sodium 2-amino-2-oxoacetate; Oxamic acid sodium salt. Grades: ≥95%. CAS No. 565-73-1. Molecular formula: C2H2NO3·Na. Mole weight: 111. | |
| Sodium pyruvate | Sodium pyruvate is the end product of glycolysis and is used for further metabolic cycles to provide energy for cells. Synonyms: Propanoic acid, 2-oxo-, sodium salt (1:1); Pyruvic Acid Sodium Salt; Pyruvate Sodium; Propanoic acid, 2-oxo-, monosodium salt; Sodium 2-oxopropanoate; Sodium α-ketopropionate. Grades: ≥95%. CAS No. 113-24-6. Molecular formula: C3H3NaO3. Mole weight: 110.04. | |
| Sucrose-6-phosphate sodium | Sucrose-6-phosphate sodium, an exquisite biomedicine wonder, emerges as a paramount therapeutic resource for a myriad of entangled metabolic intricacies and scarce hereditary ailments. Displaying its virtuosity as a pivotal participant within the glycolytic pathway, this enigmatic marvel bestows profound energy sustenance. Harvested from sucrose, it unveils boundless therapeutic potentials, granting respite to those grappling with glycogen storage maladies, fructose intolerance, and sundry metabolic aberrations. Synonyms: b-D-Fructofuranosyl-6-O-phosphono-a-D-glucopyranoside. CAS No. 22372-29-8. Molecular formula: C12H23O14P. Mole weight: 422.28. | |
| Thymidine Phosphorylase from Escherichia coli, Recombinant | An enzyme that catalyzes the reversible conversion of thymidine to thymine. Thymidine phosphorylase is part of the pyrimidine nucleoside salvage pathway. This pathway allows pyrimidine bases to be recycled for nucleotide biosynthesis, while the pentose 1-phosphates are converted to intermediates of the pentose phosphate shunt and glycolysis. The E. coli thymidine phosphorylase shares 40% sequence homology with the human sequence, which has been found to be identical to the angiogenic agent platelet-derived endothelial growth factor. The purified E. coli enzyme has been shown to stimulate blood vessel growth in chick chorioallantoic membrane assays. Applications: ...hosphate deoxy-D-ribosyltransferase; EC 2.4.2.4; 9030-23-3. Enzyme Commission Number: EC 2.4.2.4. CAS No. 9030-23-3. Thymidine Phosphorylase. Activity: Type I, > 900 units/mL, aseptically filled; Type II, > 500 units/mL. Storage: 2-8°C. Form: buffered aqueous solution, Solution in 0.5 M potassium phosphate containing 2 mM uracil, 0.02% sodium azide and bovine serum albumin. Source: E. coli. Species: Escherichia coli. thymidine phosphorylase; pyrimidine phosphorylase; thymidine-orthophosphate deoxyribosyltransferase; animal growth regulators, blood platelet-derived endothelial cell growth factors; blood platelet-derived endothelial cell growth factor; deoxythymidi | |
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