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| Product | Description | |
|---|---|---|
| Carbon Dioxide (Carbonate) Ion Selective Electrode Solutions | Carbon Dioxide (Carbonate) Ion Selective Electrode Solutions. Group: Electrolytes. |  |
| 5H-1,2-Oxathiole-4-carbonylchloride,5-oxo-,2,2-dioxide(9ci) | Heterocyclic Organic Compound. CAS No. 103625-58-7. Catalog: ACM103625587. |  |
| Carbon nanotube/Titanium Dioxide | Carbon nanotube/Titanium Dioxide. Group: Carbon nano materials. | |
| 1,1,1,3,3,3-Hexafluoro-2-methyl-2-propanol | 1,1,1,3,3,3-Hexafluoro-2-methyl-2-propanol is used as an activator for the chemical fixation of carbon dioxide onto epoxides. Also used as a reagent in the synthesis of highly substituted furfuryl alcohols and amines. Group: Biochemicals. Grades: Highly Purified. CAS No. 1515-14-6. Pack Sizes: 1g, 5g. Molecular Formula: C4H4F6O, Molecular Weight: 182.06. US Biological Life Sciences. |  Worldwide |
| 1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidenegold(I) hydroxide, min. 97% | Catalyst used for the carboxylation of C-H bonds. Catalyst used for the hydrofluorination of alkynes. Gold-catalyzed synthesis of sulfinate derivatives Effective catalyst for the carboxylation/cyclization of propargylamines with carbon dioxide. Catalyst used for the polymerization of racemic β-butyrolactones. Catalyst used for the intermolecular mono and dihydroamination of activated alkenes. Group: Gold catalysts. Alternative Names: MFCD22666054;1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidenegold(I) hydroxide;1240328-73-7. CAS No. 1240328-73-7. Molecular formula: C27H38AuN2O. Mole weight: 603.581g/mol. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]imidazole;gold;hydrate. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN ([C]2)C3=C (C=CC=C3C (C)C)C (C)C. O. [Au]. Catalog: ACM1240328737. | |
| 1-Hexanol | 1-Hexanol. Synonyms: Hexyl alcohol. CAS No. 111-27-3. Product ID: CDC10-0165. Molecular formula: CH3(CH2)5OH. Category: Flavoring Chemical Agents. Product Keywords: Cosmetic Ingredients; Flavoring Chemical Agents; 1-Hexanol; CDC10-0165; 111-27-3; CH3(CH2)5OH; Hexyl alcohol; 203-852-3; MFCD00002982; 111-27-3. Purity: ≥99%. EC Number: 203-852-3. Physical State: Liquid. Solubility: Ethanol: soluble(lit.). Quality Level: 100. Storage: no restrictions. Application: 1-Hexanol has been used as an odorant to study olfactory responses and to thin the dielectric layer of poly(4-vinylphenol) (PVP). Boiling Point: 156-157 °C (lit.). Melting Point: -52 °C (lit.). Density: 0.814 g/mL at 25 °C (lit.). Product Description: 1-Hexanol is a linear primary alcohol. It is formed as an intermediate during the catalytic transformation of cellulose. The ability of 1,1,3,3-tetramethylguanidine (TMG) in 1-hexanol solvent system to capture carbon dioxide has been assessed. The solubility of light fullerenes in 1-hexanol as a function of temperature and pressure was studied. |  |
| 1-Hexyl-3-methylimidazolium bis(trifluormethylsulfonyl)imide | 1-Hexyl-3-methylimidazolium bis(trifluormethylsulfonyl)imide is a 1-alkyl-3-methylimidazolium based ionic liquid. The solubility of gases such as oxygen and methane in HMIM TFS can be improved in the presence of carbon dioxide. Group: Electrolytes. Alternative Names: HMIMBTI,HMIMTFS. CAS No. 382150-50-7. Product ID: bis(trifluoromethylsulfonyl)azanide; 1-hexyl-3-methylimidazol-3-ium. Molecular formula: 447.41. Mole weight: C12H19F6N3O4S2. CCCCCCN1C=C[N+] (=C1)C. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. 1S/C10H19N2. C2F6NO4S2/c1-3-4-5-6-7-12-9-8-11 (2)10-12; 3-1 (4, 5)14 (10, 11)9-15 (12, 13)2 (6, 7)8/h8-10H, 3-7H2, 1-2H3; /q+1; -1. RCNFOZUBFOFJKZ-UHFFFAOYSA-N. 98%. | |
| 1-Nonadecanol | 1-Nonadecanol is one of the compositions of supercritical carbon dioxide (SC-CO 2 ) essential oil of Heracleum thomsonii. 1-Nonadecanol is also an important aroma compound in Neotinea ustulata [1] [2]. Uses: Scientific research. Group: Natural products. CAS No. 1454-84-8. Pack Sizes: 1 g; 5 g; 25 g. Product ID: HY-W004297. |  |
| (±)-1-Octen-3-ol | (±)-1-Octen-3-ol, is one of the volatiles responsible for mold`s odor. It can be used in combination with carbon dioxide to attract insects in order to kill them. In animal study, 1-Octen-3-ol has been shown to interfere with dopamine transport in the brain of fruit flies, so it might be an environmental agent involved in parkinsonism. Group: Biochemicals. Grades: Highly Purified. CAS No. 3391-86-4. Pack Sizes: 10g, 25 g. Molecular Formula: C8H16O. US Biological Life Sciences. | Worldwide |
| 1-Pentadecanol | 1-Pentadecanol. Synonyms: Pentadecyl alcohol. CAS No. 629-76-5. Pack Sizes: 5 g in glass bottle. Product ID: CDC10-0200. Molecular formula: CH3(CH2)14OH. Category: Fragrance Agents. Product Keywords: Cosmetic Ingredients; Fragrance Agents; 1-Pentadecanol; CDC10-0200; 629-76-5; CH3(CH2)14OH; Pentadecyl alcohol; 211-107-9; MFCD00004759; 629-76-5. Purity: 0.99. EC Number: 211-107-9. Solubility: Ethanol: soluble(lit.). Quality Level: 100. Storage: no restrictions. Application: 1-Pentadecanol may be employed as starting reagent for the asymmetric synthesis of jaspine B. Boiling Point: 269-271 °C. Melting Point: 41-44 °C (lit.). Density: 0.814 g/mL at 25 °C (lit.). Product Description: 1-Pentadecanol is a linear alcohol. Vapor-phase composition of 1-pentadecanol in supercritical carbon dioxide at 323.15K has been evaluated by a flow-type apparatus. Molar heat capacities of 1-pentadecanol has been evaluated between 300K and 370K. | |
| (1R,2R)-(-)-[1,2-Cyclohexanediamino-N,N'-bis(3,5-di-t-butylsalicylidene)]aluminum(III) chloride, 98% | Aluminum salen complexes as catalysts for the kinetic resolution of terminal epoxides via carbon dioxide coupling. Efficient synthesis of bio-renewable polyesters and cyclic carbonates through tandem catalysis. Catalyst used for the asymmetric hydrocyanation of nitroolefins. Catalyst used in the reaction of epoxides with heterocumulenes. Group: Heterocyclic organic compound. CAS No. 250611-13-3. Molecular formula: C36H52AlClN2O2. Mole weight: 607.26. Purity: 0.96. IUPACName: aluminum; 2, 4-ditert-butyl-6- [ [ [ (1R, 2R) -2- [ (3, 5-ditert-butyl-6-oxocyclohexa-2, 4-dien-1-ylidene) methylamino] cyclohexyl] amino] methylidene] cyclohexa-2, 4-dien-1-one; trichloride. Canonical SMILES: CC (C) (C)C1=CC (=CNC2CCCCC2NC=C3C=C (C=C (C3=O)C (C) (C)C)C (C) (C)C)C (=O)C (=C1)C (C) (C)C. [Al+3]. [Cl-]. [Cl-]. [Cl-]. ECNumber: 607-518-1. Catalog: ACM250611133. | |
| 2-(3-methoxypropyl)-2H-thieno[3,2-e][1,2]thiazine-6-sulfonamide 1,1-dioxide | An impurity of Brinzolamide, a potent carbonic anhydrase inhibitor used to lower intraocular pressure in patients with open-angle glaucoma or ocular hypertension. Synonyms: 2-(3-METHOXYPROPYL)-2H-THIENO[3,2-E][1,2]THIAZINE-6-SULFONAMIDE 1,1-DIOXIDE; 2-(3-methoxypropyl)-1,1-dioxothieno[3,2-e]thiazine-6-sulfonamide; B0464-284943; 2-(3-METHOXYPROPYL)-2H-THIENO[3,2-E][1,2]THIAZINE-6-SULFONAMIDE1,1-DIOXIDE. CAS No. 171273-35-1. Molecular formula: C10H14N2O5S3. Mole weight: 338.42. |  |
| 2 5-Bis(Hexyloxy)Terephthalaldehyde | 2 5-Bis(Hexyloxy)Terephthalaldehyde. Uses: 1) gas (such as carbon dioxide) and pollutant air adsorption 2) as fe-based lewis acid catalyst. Group: Aldehyde cof linkers-2d-aldehyder cof linkers. CAS No.: | |
| 2-Amino-2-methyl-1-propanol | 2-Amino-2-methyl-1-propanol (AMP) is a neutralizer, buffer and surfactant. 2-Amino-2-methyl-1-propanol inhibits gelatinous product formation. 2-Amino-2-methyl-1-propanol is used for carbon dioxide absorption [1] [2] [3] [4]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 124-68-5. Pack Sizes: 10 mM * 1 mL; 100 g; 250 g. Product ID: HY-W013027. | |
| 2-Amino-4-chlorobenzonitrile | 2-Amino-4-chlorobenzonitrile was used in the preparation of several organic compounds including that of amidato divalent lanthanide complexes which can be used as a catalyst in the formation of quinazoline-2,4(1H,3H)-diones from carbon dioxide and 2-aminobenzonitriles. Group: Biochemicals. Grades: Highly Purified. CAS No. 38487-86-4. Pack Sizes: 1g, 2.5g. Molecular Formula: C7H5ClN2, Molecular Weight: 152.58. US Biological Life Sciences. | Worldwide |
| 2-Desaminosulfonyl 3-Aminosulfonyl Dorzolamide | 2-Desaminosulfonyl 3-Aminosulfonyl Dorzolamide is a useful synthetic compound. Also, it is derived from (4R,6S)-5,6-Dihydro-6-methyl-4H-thieno[2,3-b]thiopyran-4-ol 7,7-Dioxide (T344510), which is an analog of topically-active carbonic anhydrase inhibitor MK-507, commonly known Dorzolamide (D535100). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2mg. Molecular Formula: C10H16N2O4S3. US Biological Life Sciences. | Worldwide |
| 2-Desaminosulfonyl 3-Aminosulfonyl N-Acetyl Dorzolamide | 2-Desaminosulfonyl 3-Aminosulfonyl N-Acetyl Dorzolamide is an intermediate in the synthesis of 2-Desaminosulfonyl 3-Aminosulfonyl Dorzolamide (D288235), which is derived from (4R,6S)-5,6-Dihydro-6-methyl-4H-thieno[2,3-b]thiopyran-4-ol 7,7-Dioxide (T344510), which is an analog of topically-active carbonic anhydrase inhibitor MK-507, commonly known Dorzolamide (D535100). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C12H18N2O5S3. US Biological Life Sciences. | Worldwide |
| 2-?Methyl-?1,?4-?oxathiane 4,?4-?Dioxide | 2-?Methyl-?1,?4-?oxathiane 4,?4-?Dioxide is a six-membered cyclic sulfone used as a reactant in the hydrogen-deuterium exchange reaction at the α-carbon of the sulfone. Group: Biochemicals. Grades: Highly Purified. CAS No. 26475-39-8. Pack Sizes: 25mg, 50mg. Molecular Formula: C5H10O3S, Molecular Weight: 150.199999999999. US Biological Life Sciences. | Worldwide |
| 2-(Methylamino)ethanol | 2-(Methylamino)ethanol (N-Methylethanolamine) is an alkaloid that can be isolated from lentil seeds. 2-(Methylamino)ethanol is used as an organic building block in chemical synthesis and as a solvent for removing carbon dioxide from gas streams [1]. Uses: Scientific research. Group: Natural products. Alternative Names: N-Methylethanolamine. CAS No. 109-83-1. Pack Sizes: 10 mM * 1 mL; 500 g. Product ID: HY-Y1783. | |
| 2-oxoglutarate dioxygenase (ethylene-forming) | This is one of two simultaneous reactions catalysed by the enzyme, which is responsible for ethylene production in bacteria of the Pseudomonas syringae group. In the other reaction [EC 1.14.11.34, 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate-forming)] the enzyme catalyses the mono-oxygenation of both 2-oxoglutarate and L-arginine, forming succinate, carbon dioxide and L-hydroxyarginine, which is subsequently cleaved into guanidine and (S)-1-pyrroline-5-carboxylate.The enzymes catalyse two cycles of the ethylene-forming reaction for each cycle of the succinate-forming reaction, so that the stoichiometry of the products ethylene and succinate is 2:1. Group: Enzymes. Synonyms: ethylene-forming enzyme; EFE. Enzyme Commission Number: EC 1.13.12.19. 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-0611; 2-oxoglutarate dioxygenase (ethylene-forming); EC 1.13.12.19; ethylene-forming enzyme; EFE. Cat No: EXWM-0611. |  |
| 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate-forming) | This is one of two simultaneous reactions catalysed by the enzyme, which is responsible for ethylene production in bacteria of the Pseudomonas syringae group.In the other reaction [EC 1.13.12.19, 2-oxoglutarate dioxygenase (ethylene-forming)] the enzyme catalyses the dioxygenation of 2-oxoglutarate forming ethylene and three molecules of carbon dioxide.The enzyme catalyses two cycles of the ethylene-forming reaction for each cycle of the succinate-forming reaction, so that the stoichiometry of the products ethylene and succinate is 2:1. Group: Enzymes. Synonyms: ethylene-forming enzyme; EFE. Enzyme Commission Number: EC 1.14.11.34. 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-0652; 2-oxoglutarate/L-arginine monooxygenase/decarboxylase (succinate-forming); EC 1.14.11.34; ethylene-forming enzyme; EFE. Cat No: EXWM-0652. | |
| 4,4'-Dihydroxybiphenyl -3,3'-dicarboxylic acid | 4,4'-Dihydroxybiphenyl -3,3'-dicarboxylic acid. Uses: 1) gas (such as carbon dioxide) and pollutant adsorption 2) good drug carrier, which is able to decompose in stomach and release the drug content. Group: Mof&cof-ligand. | |
| 4,4'-Di-tert-butyl-2,2'-bipyridine | Ligand for the iridium-catalyzed borylation of arenes Ligand for the iridium-catalyzed synthesis of arylboronic acids and aryl trifluoroborates Ligand for the nickel-catalyzed hydroxycarboxylation of 1,2-dienes by reaction carbon dioxide and oxygen Ligand for the iridium-catalyzed meta borylation followed by halogenation of 1,3-disubstituted arenes Ligand for the iridium-catalyzed silyl-directed ortho-borylation of arenes Ligand for the iridium-catalyzed silane borylation followed by aryl borylation Ligand for the iridium-catalyzed microwave-accelerated borylation of aromatic C-H bonds Ligand for the iridium-catalyzed silyl-directed borylation of indoles Ligand for the nickel-catalyzed synthesis of functionalized dialkyl ketones from carboxylic acids and alkyl halides Ligand for the iron-catalyzed arylation of heterocycles. Group: Polymer/macromolecule. Alternative Names: BBBPY; 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. CAS No. 72914-19-3. Molecular formula: C18H24N2. Mole weight: 268.4. Appearance: White solid. Purity: 0.98. IUPACName: 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. Canonical SMILES: CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. Catalog: ACM72914193-2. | |
| 4,6-Diphenylthieno[2,4-d]-1,3-dioxol-2-one-5,5-dioxide | 4,6-Diphenylthieno[2,4-d]-1,3-dioxol-2-one-5,5-dioxide. Group: Biochemicals. Alternative Names: TDO-carbonate; Steglich's reagent. Grades: Highly Purified. CAS No. 54714-11-3. Pack Sizes: 2g, 5g. US Biological Life Sciences. | Worldwide |
| 4-Chlorophenoxyacetic acid (4-CPA) | 4-Chlorophenoxyacetic acid (4-CPA) is a widely used herbicide for weed control in agriculture. 4-Chlorophenoxyacetic acid can be degraded in aqueous media through an electrochemical oxidation process. The end products of 4-Chlorophenoxyacetic acid degradation are harmless, such as carbon dioxide, water, and chloride ions [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 4-CPA; p-Chlorophenoxyacetic acid. CAS No. 122-88-3. Pack Sizes: 25 g. Product ID: HY-19698. | |
| 4-Desethylamino 4-oxobrinzolamide | 4-Desethylamino 4-oxobrinzolamide is an impurity of Brinzolamide (B677600), a carbonic anhydrase inhibitor and a antiglaucoma agent. Group: Biochemicals. Alternative Names: 3,4-Dihydro-2-(3-methoxypropyl)-4-oxo-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-Dioxide. Grades: Highly Purified. CAS No. 154127-41-0. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| (5-formylfuran-3-yl)methyl phosphate synthase | The enzyme catalyses the reaction in the direction of producing (5-formylfuran-3-yl)methyl phosphate, an intermediate in the biosynthesis of methanofuran. The sequence of events starts with the removal of a phosphate group, followed by aldol condensation and cyclization. Methanofuran is a carbon-carrier cofactor involved in the first step of the methanogenic reduction of carbon dioxide by methanogenic archaea. Group: Enzymes. Synonyms: mfnB (gene name); 4-HFC-P synthase; 4-(hydroxymethyl)-2-furaldehyde phosphate synthase. Enzyme Commission Number: EC 4.2.3.153. 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-5168; (5-formylfuran-3-yl)methyl phosphate synthase; EC 4.2.3.153; mfnB (gene name); 4-HFC-P synthase; 4-(hydroxymethyl)-2-furaldehyde phosphate synthase. Cat No: EXWM-5168. | |
| (Acetato-κ O) [[2, 2'-[ (1R, 2R) -1, 2-cyclohexanediylbis[ (nitrilo-κ N) methylidyne]]bis[4, 6-bis (1, 1-dimethylethyl) phenolato-κ O]] (2-) ]cobalt | A cobalt complex used as a chiral selector of PVC membrane electrode. A highly active catalysts for the copolymerization of propylene oxide and carbon dioxide. (R,R)-(-)-N,N?-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediamine (B431500) derivative, a ligand used in the preparation of Jacobsen's catalyst. Group: Biochemicals. Alternative Names: (Acetato-κ O) [[2, 2'-[1, 2-cyclohexanediylbis[ (nitrilo-κ N) methylidyne]]bis[4, 6-bis (1, 1-dimethylethyl) phenolato-κ O]] (2-) ]-, [SP-5-13-(1R-trans)]-cobalt. Grades: Highly Purified. CAS No. 201870-82-8. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| acetoacetate decarboxylase | Acetoacetate decarboxylase (AAD or ADC) is an enzyme involved in both the ketone body production pathway in humans and other mammals, and solventogenesis in bacteria. Acetoacetate decarboxylase plays a key role in solvent production by catalyzing the decarboxylation of acetoacetate, yielding acetone and carbon dioxide. This enzyme has been of particular interest because it is a classic example of how pKa values of ionizable groups in the enzyme active site can be significantly perturbed. Specifically, the pKa value of lysine 115 in the active site is unusually low, allowing for the formation of a Schiff base intermediate and catalysis. Group: Enzymes. Synonyms: acetoacetic acid decarboxylase; acetoacetate carboxy-lyase. Enzyme Commission Number: EC 4.1.1.4. CAS No. 9025-03-0. 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-4784; acetoacetate decarboxylase; EC 4.1.1.4; 9025-03-0; acetoacetic acid decarboxylase; acetoacetate carboxy-lyase. Cat No: EXWM-4784. | |
| Ammonium carbonate | Ammonium carbonate is a salt with the chemical formula (NH4)2CO3. Commercial samples labelled ammonium carbonate no longer contain this compound, but a mixture that has similar ammonia content. Since it readily degrades to gaseous ammonia and carbon dioxide upon heating, it is used as a leavening agent and also as smelling salt. It is also known as bakers ammonia and was a predecessor to the more modern leavening agents baking soda and baking powder. It is a component of what was formerly known as sal volatile and salt of hartshorn. Group: Electrolytes. Alternative Names: crystalammonia; diammoniumcarbonate; hartshorn; HARTSHORN SALT; AMMONIU BICARBONATE. CAS No. 506-87-6. Product ID: azane; carbonic acid. Molecular formula: 96.09. Mole weight: CH8N2O3. C(=O)([O-])[O-].[NH4+].[NH4+]. ATRRKUHOCOJYRX-UHFFFAOYSA-N. 96%. | |
| Ammonium carbonate | Ammonium carbonate is a salt with the chemical formula (NH4)2CO3. Commercial samples labelled ammonium carbonate no longer contain this compound, but a mixture that has similar ammonia content. Since it readily degrades to gaseous ammonia and carbon dioxide upon heating, it is used as a leavening agent and also as smelling salt. It is also known as bakers ammonia and was a predecessor to the more modern leavening agents baking soda and baking powder. It is a component of what was formerly known as sal volatile and salt of hartshorn. Group: Metal & ceramic materials. Alternative Names: crystalammonia; diammoniumcarbonate; hartshorn; HARTSHORN SALT;AMMONIU BICARBONATE. CAS No. 506-87-6. Molecular formula: CH8N2O3. Mole weight: 96.09. Appearance: White powder. Purity: 0.96. IUPACName: azane; carbonic acid. Canonical SMILES: C(=O)([O-])[O-].[NH4+].[NH4+]. Density: 2.7. ECNumber: 208-058-0. Catalog: ACM506876. | |
| Bio-Clean for septic tanks | Bio-Clean is the safest way to keep your septic system running as is it non-poisonous! Bio-Clean changes the waste particles into water, carbon dioxide and mineral ash which run harmlessly out of your waste system. These elements are then available for plant life. Bio-Clean is a blend of natural bacteria and enzymes. Uses: Floor Drains, Bathtubs, Grease Traps. Pack Sizes: 2 Lb Container, 25 Lb Pail. |  USA |
| Biotin (D-Biotin, Vitamin H, Coenzyme R, Bioepiderm) | Biotin is used as a growth factor in mammalian cell culture as well as having numerous immunological purification roles in avidin/streptavidin-biotin binding mechanisms. Biotin, also known as vitamin H or B7, is a water-soluble B-complex vitamin which is composed of an ureido (tetra hydroimidizalone) ring fused with a tetrahydrothiophene ring. A valeric acid substituent is attached to one of the carbon atoms of the tetrahydrothiophene ring. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids. It plays a role in the citric acid cycle, which is the process by which biochemical energy is generated during aerobic respiration. Biotin not only assists in various metabolic reactions, but also helps to transfer carbon dioxide. Biotin is also helpful in maintaining a steady blood sugar level. Biotin is often recommended for strengt Group: Biochemicals. Alternative Names: (3aS,4S,6aR)-Hexahydro-2-oxo-1H-thieno[3,4-d]imidazole-4-pentanoic Acid; (+)-Biotin; Vitamin B7; Coenzyme R; D(+)-Biotin; Factor S; Lutavit H2; Meribin; NSC 63865; Rovimix H2. Grades: Molecular Biology Grade. CAS No. 58-85-5. Pack Sizes: 1g, 5g, 10g, 25g. Molecular Formula: C??H??N?O?S, Molecular Weight: 244.31. US Biological Life Sciences. | Worldwide |
| Biotin (Glucose Oxidase) | Biotin is used as a growth factor in mammalian cell culture as well as having numerous immunological purification roles in avidin/streptavidin-biotin binding mechanisms. Biotin, also known as vitamin H or B7, is a water-soluble B-complex vitamin which is composed of an ureido (tetra hydroimidizalone) ring fused with a tetrahydrothiophene ring. A valeric acid substituent is attached to one of the carbon atoms of the tetrahydrothiophene ring. Biotin is a cofactor in the metabolism of fatty acids and leucine, and it plays a role in gluconeogenesis. Biotin is necessary for cell growth, the production of fatty acids, and the metabolism of fats and amino acids. It plays a role in the citric acid cycle, which is the process by which biochemical energy is generated during aerobic respiration. Biotin not only assists in various metabolic reactions, but also helps to transfer carbon dioxide. Biotin is also helpful in maintaining a steady blood sugar level. Biotin is often recommended for strengt Group: Biochemicals. Alternative Names: Vitamin H, Coenzyme R, Bioepiderm. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Bismuth(III) carbonate basic | Bismuth(III) carbonate basic. Uses: Bismuth subcarbonate [(bio)2co3] is used to make other bismuth compounds, cosmetics, enamel, and ceramic glazes. its major use is as an opaque substance placed in the digestive tract to show up on x-rays. Group: Ceramic materials. Alternative Names: 2,4-dioxa-1,5-dibismapentane-1,3,5-trione; bismuth oxycarbonate; 5892-10-4; DSSTox_CID_26518; AN-20030; Bismuth(III) carbonate basic; Bismuth subcarbonate [USAN:USP:JAN]; 1,3,5-trioxo-2,4-dioxa-1,5-dibismapentane; Bismuth subcarbonate (JAN/USP); Dibismuth carbonate dioxide. CAS No. 5892-10-4. Product ID: bis(oxobismuthanyl) carbonate. Molecular formula: 509.967g/mol. Mole weight: (BiO)2CO3;CBi2O5. C(=O)(O[Bi]=O)O[Bi]=O. InChI=1S/CH2O3.2Bi.2O/c2-1(3)4; ; ; ; /h(H2, 2, 3, 4); ; ; ; /q; 2*+1; ; /p-2. MGLUJXPJRXTKJM-UHFFFAOYSA-L. | |
| Brinzolamide-d5 | Carbonic anhydrase inhibitor. Antiglaucoma agent. Group: Biochemicals. Alternative Names: (4R)-(Ethylamino-d5)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-dioxide; AL-4682-d5; Azopt-d5. Grades: Highly Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Brinzolamide Hydrochloride | Carbonic anhydrase inhibitor. Antiglaucoma agent. Group: Biochemicals. Alternative Names: (4R)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide 1,1-Dioxide Hydrochloride; AL-4682 Hydrochloride; Azopt Hydrochloride. Grades: Highly Purified. CAS No. 150937-43-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| carbamoyl-phosphate synthase (ammonia) | The enzyme catalyses the first committed step in the urea cycle. The reaction proceeds via three separate chemical reactions: phosphorylation of hydrogencarbonate to carboxyphosphate; a nucleophilic attack of ammonia on carboxyphosphate yielding carbamate; and the phosphorylation of carbamate forming carbamoyl phosphate. Two moles of ATP are utilized for the synthesis of one molecule of carbamyl phosphate, making the reaction essentially irreversible. The enzyme requires the allosteric activator N-acetyl-L-glutamate. cf. EC 6.3.5.5, carbamoyl-phosphate synthase (glutamine-hydrolysing). Group: Enzymes. Synonyms: carbon-dioxide-ammonia ligase; carbamoylphosphate synthase; carbamylphosphate synthetase; carbamoylphosphate synthase (ammonia); carbamoylphosphate synthetase; carbamylphosphate s. Enzyme Commission Number: EC 6.3.4.16. CAS No. 9026-23-7. 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-5785; carbamoyl-phosphate synthase (ammonia); EC 6.3.4.16; 9026-23-7; carbon-dioxide-ammonia ligase; carbamoylphosphate synthase; carbamylphosphate synthetase; carbamoylphosphate synthase (ammonia); carbamoylphosphate synthetase; carbamylphosphate synthetase I; CPSI (gene name); carbon-dioxide:ammonia ligase (ADP-forming, carbamate-phosphorylating). Cat No: EXWM-5785. | |
| carbamoyl-phosphate synthase (glutamine-hydrolysing) | The product carbamoyl phosphate is an intermediate in the biosynthesis of arginine and the pyrimidine nucleotides. The enzyme from Escherichia coli has three separate active sites, which are connected by a molecular tunnel that is almost 100 ? in length. The amidotransferase domain within the small subunit of the enzyme hydrolyses glutamine to ammonia via a thioester intermediate. The ammonia migrates through the interior of the protein, where it reacts with carboxyphosphate to produce the carbamate intermediate. The carboxyphosphate intermediate is formed by the phosphorylation of hydrogencarbonate by ATP at a site contained within the N-terminal half of the large ... (gene name); CAD (gene name); hydrogen-carbonate:L-glutamine amido-ligase (ADP-forming, carbamate-phosphorylating). Enzyme Commission Number: EC 6.3.5.5. CAS No. 37233-48-0. 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-5808; carbamoyl-phosphate synthase (glutamine-hydrolysing); EC 6.3.5.5; 37233-48-0; carbamoyl-phosphate synthetase (glutamine-hydrolysing); carbamyl phosphate synthetase (glutamine); carbamoylphosphate synthetase II; glutamine-dependent carbamyl phosphate synthetase; carbamoyl phosphate synthetase; CPS; carbon-dioxide:L-glutamine amido-ligase (ADP-forming, carbam | |
| Carbonic anhydrase, Bovine erythrocytes | Carbonic anhydrase, Bovine erythrocytes (EC 4.2.1.1) is ubiquitous zinc-containing metalloenzyme present in prokaryotes and eukaryotes. Carbonic anhydrase can catalyze reversible conversion of carbon dioxide to bicarbonate and protons. Carbonic anhydrase can be used for the research of cancer, glaucoma, obesity and epilepsy [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: EC 4.2.1.1. CAS No. 9001-03-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-P1775. | |
| Carbonic anhydrase from E. coli, recombinant | The carbonic anhydrases (or carbonate dehydratases) form a family of enzymes that catalyze the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa), a reversible reaction that occurs relatively slowly in the absence of a catalyst. The active site of most carbonic anhydrases contains a zinc ion; they are therefore classified as metalloenzymes. Group: Enzymes. Synonyms: Carbonate dehydratase; CAN; yadF. Enzyme Commission Number: EC 4.2.1.1. Purity: > 95% by SDS-PAGE. Carbonic Anhydrase. Mole weight: This protein is fused with 6x His tag at N terminus and the protein has a calculated MW of 27 kDa (240aa). Activity: >1,000 pmol/min/ug. Storage: Can be stored at 4°C short term (1-2 weeks). For long term storage, aliquot and store at -70°C. Avoid repeated freezing and thawing cycles. Form: Liquid. Source: E. coli. Species: E. coli. carbonic anhydrases; carbonate dehydratases; EC 4.2.1.1; anhydrase; carbonate anhydrase; carbonic acid anhydrase; carboxyanhydrase; carbonic anhydrase A; carbonate hydro-lyase; CA; CAN; yadF. Cat No: NATE-1669. | |
| Carbonic Anhydrase II from Bovine, Recombinant | The carbonic anhydrases (or carbonate dehydratases) form a family of enzymes that catalyze the rapid interconversion of carbon dioxide and water to bicarbonate and protons (or vice versa), a reversible reaction that occurs relatively slowly in the absence of a catalyst. The active site of most carbonic anhydrases contains a zinc ion; they are therefore classified as metalloenzymes. Carbonic anhydrase is a zinc-containing enzyme that catalyzes the reversible conversion of carbon dioxide to bicarbonate. one of its main physiological roles is to maintain the acid-base balance in blood and other tissues. lack of carbonic anhydrase results in carbonic anhydrase type ii defi...ns: Carbonic anhydrase is used to create carbon dioxide capture systems and to research various purification techniques. carbonic anhydrase is also used to study acid-base regulation in fish and carbonic anhydrase type ii deficiency syndrome. bovine carbonic anhydrase ii (ca II), has been widely used as a model protein in the investigation of the protein folding process. Group: Enzymes. Synonyms: carbonic anhydrases; carbonate dehydratases; EC 4.2.1.1; anhydrase; carbonate anhydrase; carbonic acid anhydrase; carboxyanhydrase; carbonic anhydrase A; carbonate hydro-lyase. Enzyme Commission Number: EC 4.2.1.1. CAS No. 9001-03-0. Purity: >90% by SDS-PAGE. Carbonic Anhydras | |
| Carbonic Anhydrase II from Human, Recombinant | Carbonic anhydrase is a zinc metalloenzyme that has a molecular weight of approximately 30 kDa Da. The enzyme catalyzes the hydRation of carbon dioxide to carbonic acid. It is involved in vital processes such as pH and CO2 homeostasis, transport of bicarbonate and CO2, biosynthetic reactions, bone resorption, calcification, and tumorigenicity. Therefore, this enzyme is an important target for inhibitors with clinical applications in various pathologies such as glaucoma, epilepsy and Parkinsons disease. Applications: Human carbonic anhydrase isozyme ii has been used to assess its gene fusion abilities for efficient expression and recovery of recombinant proteins. human ...viduals. the enzyme has also been used in the study of natural phenolic inhibitors of ca ii. Group: Enzymes. Synonyms: Carbonic Anhydrase II; carbonate dehydRatase; carbonic anhydrase; anhydrase; carbonate anhydrase; carbonic acid anhydrase; carboxyanhydrase; carbonic anhydrase A; carbonate hydro-lyase; EC 4.2.1.1; CA-II; CA2; Carbonic Anhydrase 2. Enzyme Commission Number: EC 4.2.1.1. CAS No. 9001-03-0. Carbonic Anhydrase. Activity: > 80%, > 3 ,000 W-A units/mg protein. Form: powder. Source: E. coli. Species: Human. Carbonic Anhydrase II; carbonate dehydRatase; carbonic anhydrase; anhydrase; carbonate anhydrase; carbonic acid anhydrase; carboxyanhydrase; carbonic anhyd | |
| Carbonic anhydrase (isoenzyme) | Carbonic anhydrase isoenzyme is the isoenzyme of Carbonic anhydrase (HY-P1775). Carbonic anhydrase isoenzyme is ubiquitous zinc-containing metalloenzyme present in prokaryotes and eukaryotes. Carbonic anhydrase isoenzyme catalyzes reversible conversion of carbon dioxide to bicarbonate and protons, and can be used for the research of cancer, glaucoma, obesity and epilepsy [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9001-03-0. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-P1775A. | |
| Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I) | Catalyst for the aziridination of olefins. Mild catalyst, superior to CuCl, in the methylenetriphenylphosphorane methyleneation of aldehydes and ketones. Copper(I) catalyzed alkylation of aryl and alkenylsilanes. Copper-catalyzed formal methylative and hydrogenative carboxylation of alkynes with carbon dioxide. Regioselective copper-catalyzed carboxylation of allylboronates with carbon dioxide. Carboxylation of organoboronic esters with potassium methyl carbonate under copper catalysis. Catalytic anti-Markovnikov hydrobromination of alkynes. Copper-catalyzed borylative cross-coupling of allenes and imines. Group: Heterocyclic organic compound. CAS No. 578743-87-0. Molecular formula: C27H36ClCuN2. Mole weight: 487.6. Purity: >98.0%(T). IUPACName: Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I). Catalog: ACM578743870. | |
| Chlorotricarbonyl(4,4'-di-t-butyl-2,2'-bipyridine)rhenium(I), 99% | This catalyst is used for the reduction of carbon dioxide. Group: Rhenium catalysts. Alternative Names: MFCD29037182; Chlorotricarbonyl(4, 4'-di-t-butyl-2, 2'-bipyridine)rhenium(I); 165612-19-1. CAS No. 165612-19-1. Molecular formula: C21H24ClN2O3Re. Mole weight: 574.091g/mol. IUPACName: 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine;carbon monoxide;chlororhenium. Canonical SMILES: CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. Cl[Re]. Catalog: ACM165612191. | |
| Cocoa Extract / Butter - CO2 | The cocoa bean contains caffeine, theobromine, and a variety of important fatty acids, among other nutrients. Caffeine, a well-known stimulant and pick-me-up, has been shown to offer numerous skin advantages. Furthermore, the high quantity of fatty acids in this oil makes it extremely moisturising for the skin. Production Process Cocoa beans are pressed and then completely defatted by supercritical CO2-extraction. The obtained high quality cocao butter is the raw material for the second step, in which the aroma components of the cocoa butter are enriched by counter current column extraction with natural carbon dioxide. Uses: Personal Care, Cosmetics, Aromatherapy, Flavoring. Group: Plant Extracts. INCI Names: Theobroma Cacao (Cocoa) Extract. Grades: INDUSTRIAL GRADE. CAS No. 8002-31-1; 84649-99-0. Pack Sizes: 25 kgs Jerrycan, 200 kg Drums. Product ID: CC-001. Olfactive Profile: Chocolate, bitter, cocoa, caramelic. EC No: 283-480-6. Origin: Indonesia. |  New Jersey |
| cyanase | This enzyme, which is found in bacteria and plants, is used to decompose cyanate, which can be used as the sole source of nitrogen. Reaction (1) can be considered as the reverse of 'carbamate = cyanate + H2O', where this is assisted by reaction with bicarbonate and carbon dioxide (see mechanism above), and hence is classified in sub-subclass 4.2.1. Bicarbonate functions as a recycling substrate. Group: Enzymes. Synonyms: cyanate lyase; cyanate hydrolase; cyanate aminohydrolase; cyanate C-N-lyase; cyanate hydratase. Enzyme Commission Number: EC 4.2.1.104. CAS No. 37289-24-0. 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-4943; cyanase; EC 4.2.1.104; 37289-24-0; cyanate lyase; cyanate hydrolase; cyanate aminohydrolase; cyanate C-N-lyase; cyanate hydratase. Cat No: EXWM-4943. | |
| Dichloro (p-cymene)triphenylphosphineruthenium (II) dichloromethane adduct, min. 98% | Ruthenium catalyst used for the hydrogenation of carbon dioxide. Ruthenium catalyst used for a selective monoarylation reaction in water. Group: Ruthenium catalysts. Alternative Names: 52490-94-5; Dichloro (p-cymene) (triphenylphosphane)ruthenium (II); MFCD28144560; Dichloro (p-cymene)triphenylphosphineruthenium (II) dichloromethane adduct. CAS No. 52490-94-5. Molecular formula: C29H31Cl4PRu. Mole weight: 653.411g/mol. IUPACName: dichloromethane;dichlororuthenium;1-methyl-4-propan-2-ylbenzene;triphenylphosphane. Canonical SMILES: CC1=CC=C (C=C1)C (C)C. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C (Cl)Cl. Cl[Ru]Cl. Catalog: ACM52490945. | |
| Diethylpyrocarbonate (DEPC) | DEPC is a strong nuclease inhibitor, utilizing a mechanism which modifies His and Tyr residues in proteins. Used as a RNase and DNase inhibitor for Molecular Biology solutions. DEPC is a chemical use to inactivate RNase enzymes and is sensitive to moisture and pH. It decomposes at 155°C, to ethanol and carbon dioxide in aqueous solution. DEPC is also sensitive to ammonia, which causes decomposition to urethane, a possible carcinogen. Group: Biochemicals. Alternative Names: Diethyloxydiformate; Ethyloxyformic acid anhydride; Diethyl dicarbonate; DEP; DEPC; EC 216-542-8. Grades: Molecular Biology Grade. CAS No. 1609-47-8. Pack Sizes: 25g, 50g, 100g. US Biological Life Sciences. | Worldwide |
| Diethyl Pyrocarbonate (DEPC) 99+% (GC) | DEPC is a strong nuclease inhibitor, utilizing a mechanism which modifies His and Tyr residues in proteins. Used as a RNase and DNase inhibitor for Molecular Biology solutions. DEPC is a chemical use to inactivate RNase enzymes and is sensitive to moisture and pH. It decomposes at 155°C, to ethanol and carbon dioxide in aqueous solution. DEPC is also sensitive to ammonia, which causes decomposition to urethane, a possible carcinogen. Group: Biochemicals. Alternative Names: Diethyloxydiformate; Ethyloxyformic acid anhydride; Diethyl dicarbonate; DEP; DEPC; EC 216-542-8. Grades: Molecular Biology Grade. CAS No. 1609-47-8. Pack Sizes: 5g, 25g, 100g, 250g. Molecular Formula: C6H10O5, Molecular Weight: 162.14. US Biological Life Sciences. | Worldwide |
| D(+)-Raffinose Pentahydrate | Raffinose is a trisaccharide composed of galactose, glucose, and fructose. It can be found in beans, cabbage, brussels sprouts, broccoli, asparagus, other vegetables, and whole grains. Raffinose can be hydrolyzed to D-galactose and sucrose by the enzyme α-galactosidase (α-GAL), an enzyme not found in the human digestive tract. α-GAL also hydrolyzes other α-galactosides such as stachyose, verbascose, and galactinol, if present. The enzyme does not cleave β-linked galactose, as in lactose.The raffinose family of oligosaccharides (RFOs) are alpha-galactosyl derivatives of sucrose, and the most common are the trisaccharide raffinose, the tetrasaccharide stachyose, and the pentasaccharide verbascose. RFOs are almost ubiquitous in the plant kingdom, being found in a large variety of seeds from many different families, and they rank second only to sucrose in abundance as soluble carbohydrates.Humans and other monogastric animals (pigs and poultry) do not possess the α-GAL enzyme to break down RFOs and these oligosaccharides pass undigested through the stomach and upper intestine. In the lower intestine, they are fermented by gas-producing bacteria that do possess the α-GAL enzyme and make carbon dioxide, methane or hydrogenleading to the flatulence commonly associated with eating beans and other vegetables. α-GAL is present in digestive aids such as the product Beano.Pr | |
| Ethanolamine | Used as buffer; removal of carbon dioxide and hydrogen sulfide from gas mixtures. Group: Biochemicals. Alternative Names: 1-Amino-2-hydroxyethane; 2-Amino-1-ethanol; 2-Aminoethanol; 2-Aminoethyl alcohol; 2-Ethanolamine; 2-Hydroxyethanamine; 2-Hydroxyethylamine; Aminoethanol; Colamine; ETA; Envision Conditioner PDD 9020; Ethanolamine; Ethylolamine; Glycinol; Kolamin; MEA; MEA (alcohol); MEA 90; MEA-LCI; Mealan; Monoethanolamine; Olamine; R 100; R 100 (amine); Seramine; β-Aminoethanol; β-Aminoethyl alcohol; β-Ethanolamine; β-Hydroxyethylamine; 2-Aminoethanol. Grades: Reagent Grade. CAS No. 141-43-5. Pack Sizes: 250ml, 1L, 2.5L, 4L. Molecular Formula: C?H?NO, Molecular Weight: 61.08. US Biological Life Sciences. | Worldwide |
| Ethanolamine hydrochloride | Ethanolamine hydrochloride, is an organic compound used in various industrial applications. It is a white or colorless solid that is soluble in water and has a faint odor. One of the major uses of Ethanolamine hydrochloride is in the production of detergents and surfactants. Used as a raw material in the manufacture of compounds such as ethylenediaminetetraacetic acid (EDTA) and diethanolamine, which are commonly used in household and industrial cleaning products. Ethanolamine hydrochloride is also used in the synthesis of pharmaceuticals, agrochemicals and rubber processing agents. It acts as a buffer in certain chemical reactions, helping to adjust pH and maintain stability. Ethanolamine hydrochloride can be used for gas purification and metal corrosion inhibitor. Its ability to react with acid gases such as carbon dioxide and sulfur dioxide makes it useful for removing impurities from natural gas and other industrial gases. Overall, Ethanolamine hydrochloride is a multifunctional compound with many potential industrial applications. Its ability to act as a buffer, chelating agent, and corrosion inhibitor makes it an important tool in a variety of industries. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: 2-Aminoethanol hydrochloride. CAS No. 2002-24-6. Pack Sizes: 25 g; 50 g. Product ID: HY-W035903. | |
| Formate dehydrogenase | Formate dehydrogenase is an enzyme ubiquitous in prokaryotes and eukaryotes that catalyzes the reversible oxidation of formate to carbon dioxide. According to its metal content, structure and catalytic strategy, Formate dehydrogenase can be divided into two categories, non-metallic and metal-containing, which are often used in biochemical research [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 9028-85-7. Pack Sizes: 50 U; 100 U. Product ID: HY-P2907. | |
| Formate Dehydrogenase (Crude Enzyme) | Formate Dehydrogenases are a set of enzymes that catalyse the oxidation of formate to carbon dioxide, donating the electrons to a second substrate, such as NAD + in formate:NAD + oxidoreductase (EC 1. 2. 1. 2) or to a cytochrome in formate:ferricytochrome-b1 oxidoreductase (EC 1. 2. 2. 1). This product with the indicated enzyme activity was briefly purified from engineered E. coli. Applications: Synthesis; biotechnology; medicine; analysis. Group: Enzymes. Synonyms: formate-NAD oxidoreductase; FDH I; FDH II; N-FDH; formic hydrogen-lyase; formate hydrogenlyase; hydrogenlyase; NAD-linked formate dehydrogenase; NAD-dependent formate dehydrogenase; formate dehydrogenase (NAD); NAD-formate dehydrogenase; formate benzyl-viologen oxidoreductase; formic acid dehydrogenase. Enzyme Commission Number: EC 1.2.1.2. CAS No. 9028-85-7. FDH. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. formate-NAD oxidoreductase; FDH I; FDH II; N-FDH; formic hydrogen-lyase; formate hydrogenlyase; hydrogenlyase; NAD-linked formate dehydrogenase; NAD-dependent formate dehydrogenase; formate dehydrogenase (NAD); NAD-formate dehydrogenase; formate benzyl-viologen oxidoreductase; formic acid dehydrogenase. Pack: 100ml. Cat No: NATE-1799. | |
| Graphene Oxide (GO) TEM Support Films | Graphene Oxide (GO) support film is available as Single Layer (0.6~1nm) or Double Layer (1~1.5nm) measured by EELS. It is hydrophilic and naturally placed over the ultra-flat Silicon Dioxide Substrate, Lacey Carbon (300 Mesh Copper TEM Grids) or Holy Silicon Nitride Membranes with typically 50-70% coverage. Available in package of 5, 10 or 25 pieces. A. 300 Mesh Copper TEM grid with Lacey Carbon film; B. 00nm-thick 2μm Diameter Holey Silicon Nitride Membrane on 200μm-thick Silicon Substrate; C. 5x5mm 675μm-thick Silicon Die with 200nm Thermal Oxide. Uses: 1) catalyst2) supercapacitors3) solar energy4) graphene semiconductor chips5) conductive graphene film6) graphene computer memory7) biomaterials8) transparent conductive coatings. Group: Graphenes. | |
| Graphene Oxide (GO) TEM Support Films | Graphene Oxide (GO) support film is available as Single Layer (0.6~1nm) or Double Layer (1~1.5nm) measured by EELS. It is hydrophilic and naturally placed over the ultra-flat Silicon Dioxide Substrate, Lacey Carbon (300 Mesh Copper TEM Grids) or Holy Silicon Nitride Membranes with typically 50-70% coverage. Available in package of 5, 10 or 25 pieces. A. 300 Mesh Copper TEM grid with Lacey Carbon film; B. 00nm-thick 2μm Diameter Holey Silicon Nitride Membrane on 200μm-thick Silicon Substrate; C. 5x5mm 675μm-thick Silicon Die with 200nm Thermal Oxide. Uses: 1) catalyst2) supercapacitors3) solar energy4) graphene semiconductor chips5) conductive graphene film6) graphene computer memory7) biomaterials8) transparent conductive coatings. Group: other nano materials. | |
| Hemoglobin | Hemoglobin is a iron-containing protein in red blood cells with oxygen binding properties. Hemoglobin is an inducer of HO-1. Hemoglobin consits of heme, which binds to oxygen. Hemoglobin also transports other gases, such as carbon dioxide, nitric oxide, hydrogen sulfide and sulfide. Hemoglobin absorbs unneeded oxygen in tissues, as an antioxidant [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 9008-02-0. Pack Sizes: 250 mg; 500 mg; 1 g. Product ID: HY-P2995. | |
| Hydrochlorothiazide-13c1,d2 (6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-13c1,d2-7-sulfonamide 1,1-Dioxide) | A labeled carbonic anhydrase inhibitor. Group: Biochemicals. Alternative Names: 6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-13c1,d2-7-sulfonamide 1,1-Dioxide. Grades: Highly Purified. Pack Sizes: 2.5mg. US Biological Life Sciences. | Worldwide |
| Hydrochlorothiazide (6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-Dioxide) | A carbonic anhydrase inhibitor. Group: Biochemicals. Alternative Names: 6-Chloro-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-Dioxide. Grades: Highly Purified. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| Lactobacillus Helveticus Freeze Dried Powder | Lactobacillus helveticus is a lactic-acid producing, rod-shaped bacterium of the genus Lactobacillus. It is most commonly used in the production of American Swiss cheese and Emmental cheese, but is also sometimes used in making other styles of cheese, such as Cheddar, Parmesan, Romano, provolone, and mozzarella. The primary function of L. helveticus culture is to prevent bitterness and produce nutty flavors in the final cheese. In Emmental cheese production, L. helveticus is used in conjunction with a Propionibacterium culture, which is responsible for developing the holes (known as "eyes") through production of carbon dioxide gas. Group: Probiotics. Synonyms: Lactobacillus Helveticus Freeze Dried Powder; Lactobacillus Helveticus. Activity: 10 billion CFU/g or more. Stability: 24 Months. Appearance: White To Light Yellow-Colored, Free-Flowing Powder. Storage: Recommend storage at refrigeration (4 °C) or frozen temperature (-18 °C) in original, sealed package until processed. Form: Powder. Oral Health Formula. Cat No: PRBT-020. | |
| Lithium carbonate | Lithium Carbonate is a water insoluble Lithium source that can easily be converted to other Lithium compounds, such as the oxide by heating (calcination). Carbonate compounds also give off carbon dioxide when treated with dilute acids. Lithium Carbonate is generally immediately available in most volumes. Uses: A neuroprotective effect of lithium carbonate in amyotrophic lateral sclerosis (als). Synonyms: Camcolit; Candamide; Carbolith; Carbolithium; Carbolitium; Carbonic acid lithium salt (Li2CO3); Ceglution; CP 15467-61. Grades: 99%. CAS No. 554-13-2. Molecular formula: Li2CO3. Mole weight: 73.89. | |
| Lithium Carbonate | Lithium Carbonate is a water insoluble Lithium source that can easily be converted to other Lithium compounds, such as the oxide by heating (calcination). Carbonate compounds also give off carbon dioxide when treated with dilute acids. Lithium Carbonate is generally immediately available in most volumes. Alternative Names: Quilonum retard. CAS No. 554-13-2. Molecular formula: Li2CO3. Mole weight: 73.9. Appearance: White powder. Purity: 99%+. IUPACName: Dilithium;carbonate. Canonical SMILES: [Li+].[Li+].C(=O)([O-])[O-]. Density: 2.11 g/mL at 25 °C (lit.). ECNumber: 209-062-5;233-818-3. Catalog: ACM554132. | |
| Lithium Carbonate | Lithium Carbonate is a water insoluble Lithium source that can easily be converted to other Lithium compounds, such as the oxide by heating (calcination). Carbonate compounds also give off carbon dioxide when treated with dilute acids. Lithium Carbonate is generally immediately available in most volumes. Group: Electrolyteselectrode materials phosphors - phosphor materials battery materials. Alternative Names: Quilonum retard. CAS No. 554-13-2. Product ID: Dilithium; carbonate. Molecular formula: 73.9. Mole weight: Li2CO3. [Li+].[Li+].C(=O)([O-])[O-]. InChI=1S/CH2O3.2Li/c2-1(3)4;/h(H2, 2, 3, 4);/q;2*+1/p-2. XGZVUEUWXADBQD-UHFFFAOYSA-L. 99%+. | |
| Lithium Hydroxide, Monohydrate, ACS | Used for the production of alkyd resins, lithium greases, lithium soaps, lithium stearate and lithium salts. It finds application as a carbon dioxide adsorbent in breathing gas purification systems for spacecrafts, submarines and rebreathers; as a storage-battery electrolyte; as a heat transfer medium and as a catalyst for polymerization reaction. It is also used in ceramics and some portland cement formulations. Group: Biochemicals. Grades: ACS Grade. CAS No. 1310-66-3. Pack Sizes: 100g, 250g, 1Kg, 5Kg. Molecular Formula: LiOH·H2O, Molecular Formula: 41.96. US Biological Life Sciences. | Worldwide |
| Lutetium (III) oxide | Lutetium oxide (Lu2O3), the oxide found in monazite ore, is a white solid. It is hygroscopic and also absorbs carbon dioxide, making it useful to remove CO2 in closed atmospheres. Alternative Names: Cassiopeium oxide. CAS No. 12032-20-1. Molecular formula: Lu2O3. Mole weight: 397.93. Appearance: White powder. Purity: 0.99. Density: 9.42 g/mL at 25 °C (lit.). Catalog: ACM12032201. | |
| Magnesium Carbonate | Magnesite appears as white, yellowish, grayish-white or brown crystalline solid or crystalline powder. Density: 3-3.1 g cm-3. An important ore for magnesium. Used in the manufacture of materials capable of withstanding very high temperatures. Sometimes used to produce carbon dioxide.;DryPowder; Liquid; OtherSolid; PelletsLargeCrystals;Odourless, light, white friable masses or as a bulky white powder;WHITE POWDER.;White, odorless, crystalline powder.;White, odorless, crystalline powder. Group: Polymers. Product ID: magnesium; carbonate. Molecular formula: 84.31g/mol. Mole weight: MgCO3? nH2O;MgCO3;MgCO3;CMgO3. C(=O)([O-])[O-].[Mg+2]. InChI=1S/CH2O3.Mg/c2-1(3)4;/h(H2, 2, 3, 4);/q;+2/p-2. ZLNQQNXFFQJAID-UHFFFAOYSA-L. | |
| Magnesium Oxide | Two forms of magnesium oxide exist: a bulky form termed light magnesium oxide and a dense form termed heavy magnesium oxide. Both forms of magnesium oxide occur as fine, white, odorless powders. Synonyms: Calcined magnesia; calcinated magnesite; Descote; E530; Magcal; Magchem 100; Maglite; magnesia; magnesia monoxide; magnesiausta; magnesii oxidum leve; magnesii oxidum ponderosum; Magnyox; Marmag; Oxymag; periclase. CAS No. 1309-48-4. Product ID: PE-0534. Molecular formula: MgO. Mole weight: 40.3. Category: Anticaking Agents; Emulsifying Agents; Glidant; Tablet and Capsule Diluent. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0534; Magnesium Oxide; Anticaking Agents; Emulsifying Agents; Glidant; Tablet and Capsule Diluent; MgO; 1309-48-4. UNII: 3A3U0GI71G. Chemical Name: Magnesium oxide. Grade: Pharmceutical Excipients. Administration route: Oral and buccal. Dosage Form: Oral capsules, tablets, and buccal. Stability and Storage Conditions: Magnesium oxide is stable at normal temperatures and pressures.However, it forms magnesium hydroxide in the presence of water.Magnesium oxide is hygroscopic and rapidly absorbs water and carbon dioxide on exposure to the air, the light form more readily than the heavy form. The bulk material should be stored in an airtight container in a cool, dry place. Source and Preparation: Magnesium oxide occurs naturally as the mineral periclase. It can be | |
| Medicinal Charcoal | Medicinal Charcoal. Synonyms: Medicinal Charcoal; Actirated Charcoal; Carbo Medecinalis; Decoloriging Carbon. Product ID: PE0362. Category: Adsorbentss. Product Keywords: Pharmaceutical Excipients; Excipients for Solid Dosage Form; Filler Excipients; Absorbent; Medicinal Charcoal; PE0362. Grade: Pharmceutical Excipients. Stability and Storage Conditions: The efficacy of this product will be reduced by moisture, so it should be stored in a dry place. And it should be stored separately from smelly medicines to avoid odor. Source and Preparation: This product is a solid porous carbonaceous material prepared by carbonizing or activating organic matter. Raw materials include sawn wood, peat, coal, fiber residue, coconut shell and petroleum coke. Adding or not adding inorganic salts to activated gas streams such as steam or carbon dioxide at high temperature to carbonize and activate the above raw materials. Carbon-containing substances can also be treated with chemical active agents such as phosphoric acid or zinc chloride, and carbonized and mixed at elevated temperatures. Then wash off the active agent with water. Safety: FAO/WHO stipulates that only "food grade plant activated carbon" can be used as a food additive. | |
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