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| Product | Description | |
|---|---|---|
| Copper formate | Copper formate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: COPPER (II) FORMATE;CUPRIC FORMATE;COPPER FORMATE;cupricdiformate;formicacid,copper(2+)salt;formicacid,copper(2+)salt(1:1);formicacid,copper(2++)salt;copper diformate. Product Category: Organic Copper. Appearance: Blue crystalline powder. Sinks and mixes with water. CAS No. 544-19-4. Molecular formula: C2H2CuO4. Mole weight: 153.58. Purity: 0.96. IUPACName: copper diformate. Density: 1831. Product ID: ACM544194. Alfa Chemistry ISO 9001:2015 Certified. |  |
| grixazone synthase | A type 3 multi copper protein. The enzyme, isolated from the bacterium Streptomyces griseus, catalyses an 8 electron oxidation. Activation of the enzyme requires a copper chaperone (GriE). It also acts on 3-amino-4-hydroxybenzaldehyde, giving grixazone A. The second aldehyde group is presumably lost as formate. The enzyme also catalyses the reaction of EC 1.10.3.4 o-aminophenol oxidase. Group: Enzymes. Synonyms: GriF. Enzyme Commission Number: EC 1.10.3.15. 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-0481; grixazone synthase; EC 1.10.3.15; GriF. Cat No: EXWM-0481. |  |
| 17-ODYA | 17-ODYA is a CYP450 ω-hydroxylase inhibitor. 17-ODYA is also a potent inhibitor (IC 50 <100 nM) of the formation of 20-hydroxyeicosatetraenoic acid (20-HETE), epoxyeicosatrienoic acids and dihydroxyeicosatrienoic acids by rat renal cortical microsomes incubated with arachidonic acid. 17-ODYA completely attenuates the isoproterenol (ISO)-induced apoptosis, and necrosis in cultured cardiomyocytes [1] [2] [3]. 17-ODYA is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups. Uses: Scientific research. Group: Signaling pathways. CAS No. 34450-18-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg. Product ID: HY-101016. |  |
| 2-(Di-tert-butylphosphino)biphenyl | 2-(Di-tert-butylphosphino)biphenyl. Uses: Ligand used in the palladium-catalyzed synthesis of aromatic amines from aryl chlorides, bromides and triflates. ligand employed in a very active and general catalyst for suzuki coupling reactions using aryl chlorides, bromides and triflates. ligand used in palladium-catalyzed synthesis of oxindoles from α-chloroacetanilides. effective ligand used in palladium-catalyzed arylation of thiazoles. used in the formation of 2-benzylindolines via sequential palladium-catalyzed n-arylation/cyclization/c-arylation. selective in the palladium-catalyzed arylation of silyl enol ethers formed from copper-catalyzed reduction of enones. Additional or Alternative Names: (2-Biphenylyl)-Di-Tert-Butylphosphine. Product Category: Organic Phosphine Compounds. Appearance: Solid. CAS No. 224311-51-7. Molecular formula: C20H27P. Mole weight: 298.4. Purity: 0.98. IUPACName: ditert-butyl-(2-phenylphenyl)phosphane. Canonical SMILES: CC(C)(C)P(C1=CC=CC=C1C2=CC=CC=C2)C(C)(C)C. Density: 1 g/cm3. Product ID: ACM224311517-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| AF488 azide | AF488 is a fluorescent dye. AF488 is a fluorophore pH-insensitive over a broad pH range (from 4 to 10). It has an absorption maximum at 495 nm and an emission maximum at 519 nm in the green spectrum region. The dye is hydrophilic and can be used to introduce the fluorescent label into various molecules, including proteins and antibodies. Conjugates of molecules with AF488 have high brightness and photostability and are commonly used in flow cytometry and microscopy. This allows the detection of biological objects with high sensitivity at a longer imaging time.,AF488 azide interacts with alkynyl derivatives of biomolecules in Click Chemistry reactions either in the presence of copper (I) catalyst (with terminal alkynes) or without catalyst (with cyclooctynes), leading to the formation of stable adducts. Grades: NMR 1H, HPLC-MS (95%). CAS No. 1679326-36-3 (with azidohexyl group). Molecular formula: C36H56N8O10S2. Mole weight: 825.01. |  |
| Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I) | Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I). Uses: Copper-catalyzed coupling of imidazoles and pyrazoles with 1,1-dibromo-1-alkenes: a distinct approach for direct nalkynylation of heteroarenes. synthesis of benzoindoloquinolizines via a cu(I)-mediated c-n bond formation. efficient synthesis of 1,4-disubstituted triazolyl n-carboxamides via a simple and convenient mcr using basic alumina as a solid support. cu(I) complexes with diethoxyphosphoryl-1,10-phenanthrolines in catalysis of c-c and c-heteroatom bond formation. Additional or Alternative Names: Bromocopper;1,10-phenanthroline;triphenylphosphane. Appearance: Powder. CAS No. 25753-84-8. Molecular formula: C30H23BrCuN2P. Mole weight: 585.9. Purity: 0.98. Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1.[Cu]Br. Product ID: ACM25753848-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Disulfiram | Disulfiram (Tetraethylthiuram disulfide) is a specific inhibitor of aldehyde-dehydrogenase (ALDH1) , used for the treatment of chronic alcoholism by producing an acute sensitivity to alcohol. Disulfiram inhibits gasdermin D (GSDMD) pore formation in liposomes and inflammasome-mediated pyroptosis and IL-1β secretion in human and mouse cells. Disulfiram, a copper ion carrier,?with?Cu 2+ increases intracellular ROS levels and induces cuproptosis [1] [2] [3] [4] [5] [6]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Tetraethylthiuram disulfide; TETD. CAS No. 97-77-8. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B0240. | |
| Ditiocarb sodium | Ditiocarb sodium (Sodium diethyldithiocarbamate) is a copper reagent. The reaction with Cu 2+ solution resulted in the formation of a complex, which increased the copper displacement precipitation rate. Ditiocarb sodium can reduce HIV infection and can be used in adjuvant immune research of high-risk breast cancer [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Sodium diethyldithiocarbamate. CAS No. 148-18-5. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1637. | |
| Electrolytic Copper with added Impurities | Electrolytic Copper with added Impurities. Uses: For analytical and research use. Group: Physical properties; metal alloys; physical properties. Catalog: APS007775. Format: Neat. Shipping: Room Temperature. |  |
| Laccase, Microorganisms | Laccase, Microorganisms (Denilite IIS) is a multi-copper oxidase (MCOs), which widely exists in microorganisms, plants and fungi, and can catalyze the oxidation of one electron of various phenolic compounds. Laccase can promote the oxidative coupling of single lignin, which plays an important role in the formation and biodegradation of lignin, and also has the potential to cross-link food polymers [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Denilite IIS. CAS No. 80498-15-3. Pack Sizes: 100 mg; 500 mg; 1 g. Product ID: HY-P2890. | |
| Native Laccase from White rot fungi | Laccase (Laccase E.C. 1. 10. 3. 2) is a glucoproteinase containing copper. It can catalyze phenols and its derivatives, aromatic amine and its derivatives, carboxylic acids and its derivatives, steroid hormone, biochrome, organometallic compounds and non-phenols substrate. Applications: For indigo-dye-fading technique of jean processing by using laccase and catalysis enzymes in jean-washing industry, for selectively catalyze lignin-degradation and pulp bleaching by using laccase combined medium and xylanase. it is also a new environment friendly technique in wastepaper deinking process. for chlorophenols organic compounds degradation of wastewater treatment (which in line with ph requirements of laccase). for baking. for extract sugar. it can raise color value remaining. for others using as fiberboard adhesive, hair dyeing, lacquer dyeing film formation, crosslinking agent and biological measurement. Group: Enzymes. Synonyms: Laccases; EC 1.10. CAS No. 80498-15-3. Laccase. Activity: 10,000u/ml. Stability: 6 months at 5°C, activity remain ≥90%. Increase dosage after shelf life. Appearance: Liquid. Storage: Should be stored in a cool place to avoid effect of high temperature. Source: White rot fungi. Laccases; EC 1.10.3.2; 80498-15-3; urishiol oxidase; urushiol oxidase; p-diphenol oxidase; benzenediol:oxygen oxidoreductase. Cat No: NATE-1021. | |
| Sodium diethylcarbamodithioate trihydrate | Sodium diethylcarbamodithioate (Ditiocarb sodium) trihydrate is a copper reagent. The reaction with Cu 2+ solution resulted in the formation of a complex, which increased the copper displacement precipitation rate. Sodium diethylcarbamodithioate trihydrate can reduce HIV infection and can be used in adjuvant immune research of high-risk breast cancer [1] [2] [3]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Ditiocarb sodium trihydrate. CAS No. 20624-25-3. Pack Sizes: 100 mg; 250 mg. Product ID: HY-W009722. | |
| Sodium diethyldithiocarbamate,98% | Sodium diethyldithiocarbamate,98% (Ditiocarb sodium,98%) is a copper reagent. The reaction with Cu 2+ solution resulted in the formation of a complex, which increased the copper displacement precipitation rate. Sodium diethyldithiocarbamate can reduce HIV infection and can be used in adjuvant immune research of high-risk breast cancer [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Ditiocarb sodium,98%. CAS No. 148-18-5. Pack Sizes: 100 g; 500 g. Product ID: HY-B1637A. | |
| Soybean Oil | Soybean oil as the refined fixed oil obtained from the seeds of the soya plant Glycine max Merr. (Fabaceae); if an antoxidant is added, the name and quantity must be specified on the label. Synonyms: Aceite de soja; Calchem IVO-114; Lipex 107; Lipex 200; Shogun CT; soiae oleum raffinatum; soja bean oil; soyabean oil; soya bean oil. CAS No. 8001-22-7. Product ID: PE-0513. Category: Carrier Excipients. Product Keywords: Pharmaceutical Excipients; Other Materials; Soybean Oil; Carrier Excipients; Carrier Excipients; 8001-22-7; 8001-22-7. UNII: 241ATL177A. Chemical Name: Soybean oil. Grade: Pharmceutical Excipients. Administration route: IV, oral and topical. Dosage Form: IV injections, oral capsules, and topical preparations; chewable tablets; oral lozenges; topical bath additives. Stability and Storage Conditions: Soybean oil is a stable material if protected from atmospheric oxygen.The formation of undesirable flavors in soybean oil is accelerated by the presence of 0.01 ppm copper and 0.1 ppm iron, which act as catalysts for oxidation; this can be minimized by the addition of chelating agents. Prolonged storage of soybean oil emulsions, particularly at elevated temperatures, can result in the formation of free fatty acids, with a consequent reduction in the pH of the emulsion; degradation is minimized at pH 6-7. However, soybean oil emulsions are stable at room temperature if stored under nitrogen in a light-resistant |  |
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