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| Product | Description | |
|---|---|---|
| Bis(8-quinolinolato)copper(II) | Bis(8-quinolinolato)copper(II). Uses: Fungicide and mildew-proofing of fabrics, analysis for copper. Group: Magnetic metal complexes. Alternative Names: Fennotox 45; Cuprinol Dispersion AQ; Oxyquinoleate de cuivre [French]; 8-Quinolinol, copper(II) chelate; Bis(quinolin-8-olato)copper (IUPAC); Oxine copper; Copper, bis(8-quinolinolato-N(sup 1),O(sup 8))-; Dokirin; Copper(II) Bis(8-hydroxyquinolinate); Cupric 8-hydroxyquinolate. CAS No. 10380-28-6. Product ID: copper; quinolin-8-olate. Molecular formula: 351.852g/mol. Mole weight: C18H12CuN2O2;C18H12CuN2O2. C1=CC2=C(C(=C1)[O-])N=CC=C2. C1=CC2=C(C(=C1)[O-])N=CC=C2. [Cu+2]. InChI=1S/2C9H7NO. Cu/c2*11-8-5-1-3-7-4-2-6-10-9(7)8; /h2*1-6, 11H; /q; ; +2/p-2. YXLXNENXOJSQEI-UHFFFAOYSA-L. |  |
| Bis(8-quinolinolato)copper(II) | Fungicide and mildew-proofing of fabrics, analysis for copper. Group: Organic copper. Alternative Names: Fennotox 45; Cuprinol Dispersion AQ; Oxyquinoleate de cuivre [French]; 8-Quinolinol, copper(II) chelate; Bis(quinolin-8-olato)copper (IUPAC); Oxine copper; Copper, bis(8-quinolinolato-N(sup 1),O(sup 8))-; Dokirin; Copper(II) Bis(8-hydroxyquinolinate); Cupric 8-hydroxyquinolate. CAS No. 10380-28-6. Molecular formula: C18H12CuN2O2;C18H12CuN2O2. Mole weight: 351.852g/mol. IUPACName: copper;quinolin-8-olate. Canonical SMILES: C1=CC2=C(C(=C1)[O-])N=CC=C2. C1=CC2=C(C(=C1)[O-])N=CC=C2. [Cu+2]. Density: Relative density (water = 1): 1.63. ECNumber: 233-841-9. Catalog: ACM10380286. |  |
| Gluconic acid copper(II) salt, 98% | copper gluconate is cited as having skin-conditioning and skinprotecting functions. Group: Metal & ceramic materials. Alternative Names: Chelates of copper gluconate; KS-00000WNP; DB11246; D-Gluconicacidcopper(II)salt; HSDB 261; Copper gluconate (USP); Copper gluconate [USP]; Copper(II) (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate; AN-45570; SCHEMBL23076. CAS No. 527-09-3. Molecular formula: C12H22CuO14. Mole weight: 453.84g/mol. IUPACName: copper;(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate. Canonical SMILES: C(C(C(C(C(C(=O)[O-])O)O)O)O)O. C(C(C(C(C(C(=O)[O-])O)O)O)O)O. [Cu+2]. ECNumber: 208-408-2. Catalog: ACM527093. | |
| Gluconic acid copper(II) salt, 98% | Gluconic acid copper(II) salt, 98%. Uses: Copper gluconate is cited as having skin-conditioning and skinprotecting functions. Group: Electrolytes. Alternative Names: Chelates of copper gluconate; KS-00000WNP; DB11246; D-Gluconicacidcopper(II)salt; HSDB 261; Copper gluconate (USP); Copper gluconate [USP]; Copper(II) (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate; AN-45570; SCHEMBL23076. CAS No. 527-09-3. Product ID: copper; (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate. Molecular formula: 453.84g/mol. Mole weight: C12H22CuO14. C(C(C(C(C(C(=O)[O-])O)O)O)O)O. C(C(C(C(C(C(=O)[O-])O)O)O)O)O. [Cu+2]. InChI=1S/2C6H12O7. Cu/c2*7-1-2(8)3(9)4(10)5(11)6(12)13; /h2*2-5, 7-11H, 1H2, (H, 12, 13); /q; ; +2/p-2/t2*2-, 3-, 4+, 5-; /m11. /s1. OCUCCJIRFHNWBP-IYEMJOQQSA-L. | |
| SOD1 Inhibitor, LCS-1 (4,5-dichloro-2-(3-methylphenyl)-3(2H)-pyridazinone, 4,5-dichloro-2-m-tolylpyridazin-3(2H)-one, Superoxide Dismutase 1 Inhibitor, Lung Cancer Screen 1) | A 2-phenylpyridazin-3(2H)-one based non-copper chelater that selectively inhibits the activity of Superoxide dismutase 1 (Cu/Zn-SOD) (IC50=1.07uM). Cells over-expressing SOD1 show reduced sensitivity to LCS-1. Shown to preferably inhibit the growth of a variety of human lung adenocarinoma cell lines with EGFR and KRAS mutations (IC50=200nM). Prevents serum-induced activation of the ERK and PI 3-kinase/AKT signaling thereby affecting cell growth and survival. Apparent half-life of this compound is reported to be 6.6min in human liver microsomes. Group: Biochemicals. Grades: Highly Purified. CAS No. 41931-13-9. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| 2,2'-Bipyridyl | 2,2'-Bipyridyl also known as 2,2'-bipyridine, is a symmetrical bipyridine commonly used as a neutral ligand for chelating with metal ions. A study of its impact on Petunia hybrida flowers showed that it caused inhibition of senescence. We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information. Uses: Ligand for copper in greener oxidation of alcohols under aerobic conditions. 2,2'-bipyridyl has been used in the preparation of copper(II)-bipyridine-naringenin complex. it may be used in the preparation of 2,2'-bipyridyl hydrobromide. bidentate ligand employed in transition metal catalysis and aluminum initiated polymerization (inorganic syntheses). ligand for copper in greener oxidation of alcohols under aerobic conditions. copper(I)/tempo-catalyzed aerobic oxidation of primary alcohols to aldehydes with ambient air. Group: Ligands for functional metal complexespolymerization reagents. Alternative Names: 2,2'-Dipyridyl, 2,2'-Dipyridine, 2,2'-Bipyridine. CAS No. 366-18-7. Pack Sizes: Packaging 25, 100, 500 g in poly bottle 2.5, 10 g in glass bottle 12 kg in poly drum 1 kg in poly bottle. Product ID: 2-pyridin-2-ylpyridine. Molecular formula: 156.18. Mole weight: C10H8N2. c1ccc(nc1)-c2ccccn2. 1S/C10H8N2/c1-3-7-11-9 (5-1)10-6-2-4-8-12-10/h1-8H. ROFVEXUMMXZLPA-UHFFFAO | |
| 8-Hydroxyquinoline | 8-Hydroxyquinoline (8-Quinolinol) is a lipophilic metal chelator that can be used as a fungicide.8-Hydroxyquinoline shows the MIC range of 27.56-55.11 μM (4-8 μg/mL) against the clinical isolates of Neisseria gonorrhoeae. 8-Hydroxyquinoline can bind to copper form complexes and transport copper into cells. 8-Hydroxyquinoline increases in the number of micronucleated polychromatic erythrocytes and can also make hair depigmented in mice [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 8-Quinolinol. CAS No. 148-24-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g. Product ID: HY-B1005. |  |
| Allylthiourea | Allylthiourea can selectively inhibit the oxidation of ammonia. Allylthiourea is commonly used to inhibit nitrification by targeting ammonia monooxygenase and chelating copper in the active site to suppress its activity. Allylthiourea also exhibits anticancer activity, showing cytotoxicity against the MCF-7 cell line with an IC 50 of 5.22 mM. Allylthiourea can be utilized in research related to micropollutant biodegradability and cancer studies [1] [2] [3] [4]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Thiosinamine; N-Allylthiourea. CAS No. 109-57-9. Pack Sizes: 10 mM * 1 mL; 25 g; 50 g. Product ID: HY-B0543. | |
| Ammonium citrate dibasic | Ammonium citrate dibasic. Synonyms: Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate. CAS No. 3012-65-5. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0097. Molecular formula: C6H14N2O7. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ammonium citrate dibasic; CDC10-0097; 3012-65-5; C6H14N2O7; Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate; 221-146-3; MFCD00013068; 3012-65-5. Purity: 0.98. Color: White. EC Number: 221-146-3. Physical State: Solid. Solubility: H2O: 1 M at 20 °C, clear, colorless. Quality Level: 200. Storage: Store at 5°C to 30°C. Application: Ammonium citrate dibasic can be used as both carbon and nitrogen precursor to synthesize nitrogen-doped fluorescent carbon nanoparticles (CNPs) for the development of sensitive and selective sensors for picric acid detection. Solution form of ammonium citrate can also be used in leaching experiments to extract copper nanoparticles from waste printed circuit boards (WPCBs). Boiling Point: 100 °C(lit.). Melting Point: 185 °C (dec.)(lit.). Density: 1.22 g/mL at 20 °C. |  |
| Ammonium citrate dibasic | Ammonium citrate dibasic. Synonyms: Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate. CAS No. 7585-39-9. Pack Sizes: 100, 500 g in poly bottle. Product ID: CDC10-0099. Molecular formula: C42H70O35. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Ammonium citrate dibasic; CDC10-0099; 7585-39-9; C42H70O35; Ammonium hydrogencitrate, Citric acid ammonium salt, Diammonium hydrogen citrate; 221-146-3; MFCD00013068; 7585-39-9. Purity: 0.98. Color: White. EC Number: 221-146-3. Physical State: Solid. Solubility: 1 M NaOH: 50 mg/mL. Quality Level: 200. Application: Ammonium citrate dibasic can be used as both carbon and nitrogen precursor to synthesize nitrogen-doped fluorescent carbon nanoparticles (CNPs) for the development of sensitive and selective sensors for picric acid detection. Solution form of ammonium citrate can also be used in leaching experiments to extract copper nanoparticles from waste printed circuit boards (WPCBs). Boiling Point: 844.96°C (rough estimate). Melting Point: 290-300 °C (dec.) (lit.). Density: 1.2296 g/cm3(rough estimate). | |
| BLT-1 | BLT-1, a thiosemicarbazone copper chelator, is a selective scavenger receptor B, type 1 (SR-BI) inhibitor. BLT-1 inhibits the transfer of lipids between high-density lipoproteins (HDL) and cells mediated by SR-BI. BLT-1 is a potent HCV entry inhibitor. Group: Inhibitors. Alternative Names: [(2-hexylcyclopentylidene)amino]thiourea, 2-hexyl-1-cyclopentanone thiosemicarbazone, Block lipid transport-1, BLT1, Probes1_000008, Probes1_000093, Probes2_000390, Probes2_000409, AC1Q2VV0, Ambcb5234221, BLT-1, MolPort-003-180-025, MIT 9952-53, 33M20, EN300-68381, 321673-30-7. CAS No. 321673-30-7. Molecular formula: C12H23N3S. Mole weight: 241.4. Appearance: Solid. Purity: 0.96. IUPACName: [(E)-(2-hexylcyclopentylidene)amino]thiourea. Canonical SMILES: CCCCCCC1CCCC1=NNC(=S)N. Catalog: ACM321673307. | |
| BTTAA | CuAAC Click Reaction. Group: Copper-chelating ligands. CAS No. 1334179-85-9. Molecular formula: C19H30N10O2. Mole weight: 430.5. Appearance: Solid. Purity: 95%+ (HPLC). IUPACName: 2-[4-[[Bis[(1-tert-butyltriazol-4-yl)methyl]amino]methyl]triazol-1-yl]acetic acid. Canonical SMILES: CC (C) (C)N1C=C (N=N1)CN (CC2=CN (N=N2)CC (=O)O)CC3=CN (N=N3)C (C) (C)C. Density: 1.32±0.1 g/cm3(Predicted). Catalog: CCR1334179859. | |
| BTTES | CuAAC Click Reaction. Group: Copper-chelating ligands. CAS No. 2101505-88-6. Molecular formula: C20H34N10O3. Mole weight: 494.6. Appearance: Solid. Purity: 95%+ (HPLC). IUPACName: 3-[4-[[Bis[(1-tert-butyltriazol-4-yl)methyl]amino]methyl]triazol-1-yl]propane-1-sulfonic acid. Canonical SMILES: CC (C) (C)N1C=C (N=N1)CN (CC2=CN (N=N2)CCCS (=O) (=O)O)CC3=CN (N=N3)C (C) (C)C. Catalog: CCR2101505886. | |
| BTTP | CuAAC Click Reaction. Group: Copper-chelating ligands. CAS No. 1341215-17-5. Molecular formula: C20H34N10O. Mole weight: 430.6. Appearance: Solid. Purity: 95%+ (HPLC). IUPACName: 3-[4-[[Bis[(1-tert-butyltriazol-4-yl)methyl]amino]methyl]triazol-1-yl]propan-1-ol. Canonical SMILES: CC (C) (C)N1C=C (N=N1)CN (CC2=CN (N=N2)CCCO)CC3=CN (N=N3)C (C) (C)C. Catalog: CCR1341215175. | |
| Cuprizone | Cuprizone is a copper chelating agent that forms a deep blue copper ketone complex with copper (II). The copper ketone reaction can be used in colorimetric tests for the presence of trace copper. Cuprizone can be used to induce some schizophrenia-like behavior in mice. Cuprizone acts on copper enzymes, including SOD1, cytochrome oxidase, and DβH, thereby causing oxidative stress and increasing DA levels in certain brain regions such as the medial prefrontal cortex (PFC) [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 370-81-0. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g; 5 g; 10 g. Product ID: HY-W115718. | |
| DL-Penicillamine | DL-Penicillamine [(±)-Penicillamine] is a copper chelating agent. DL-Penicillamine has antidotal effects in thallotoxicosis rats when co-treated with Prussian blue (HY-106594A). DL-Penicillamine can cause pyridoxine deficiency and then induce optic axial neuritis. DL-Penicillamine can also depress primary immune response [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: (±)-Penicillamine. CAS No. 52-66-4. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W017457. | |
| Ethylenediamine-N,N'-diacetic acid | Ethylenediaminediacetic acid is an ethylenediamine derivative in which two of the four amine protons of ethylenediamine are replaced by carboxymethyl groups. It has a role as a chelator and a bacterial xenobiotic metabolite. It is an ethylenediamine derivative, a glycine derivative, a polyamino carboxylic acid and an amino dicarboxylic acid. It is a conjugate acid of an ethylenediaminediacetate(1-). Uses: Ethylenediamine-n,n'-diacetic acid (edda) is a chelating agent that can be used to synthesize: binary and ternary copper(II) complexes with potent proteasome inhibitory properties. pd(edda) complexes which can coordinate with amino acids, peptides, or dna units. Group: Heterocyclic organic compound. Alternative Names: N,N'-Ethylenediglycine. CAS No. 5657-17-0. Molecular formula: C6H12N2O4. Mole weight: 176.17. Appearance: White powder. Purity: 0.98. IUPACName: 2-[2- (Carboxymethylamino) ethylamino]acetic acid. Canonical SMILES: C(CNCC(=O)O)NCC(=O)O. Density: 1.31 g/mL. ECNumber: 227-105-6. Catalog: ACM5657170-1. | |
| Gly-Gly-Gly | Triglycine (Gly-Gly-Gly) is used as a model peptide for studies of physicochemical parameters and molecular associations of small peptides. Triglycine is used as a copper chelator. Group: Amino acids. Alternative Names: Glycyl-glycyl-glycine, Triglycine. CAS No. 556-33-2. Molecular formula: NH2CH2CONHCH2CONHCH2COOH. Mole weight: 189.17. Canonical SMILES: NCC(=O)NCC(=O)NCC(O)=O. ECNumber: 209-122-0. Catalog: ACM556332. | |
| Penicillamine | Penicillamine (D-(-)-Penicillamine) is a penicillin metabolic degradation product, can be used as a heavy metal chelator. Penicillamine reduces free copper and reduces oxidative stress. Penicillamine has effect of seizures through nitric oxide/NMDA pathways. Penicillamine is a potential immune modulator. Penicillamine can be used for the research of Wilson disease, rheumatoid arthritis, and cystinuria [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: D-(-)-Penicillamine. CAS No. 52-67-5. Pack Sizes: 10 mM * 1 mL; 1 g; 5 g. Product ID: HY-B0300. | |
| Silver diethyldithiocarbamate | Silver diethyldithiocarbamate (SDDC) is an organic compound consisting of silver ions complexed with the ligand diethyldithiocarbamate. SDDC is mainly used as a reagent in analytical chemistry to detect the presence of copper, iron and other heavy metals in various materials. It acts as a chelating agent, binding to metal ions and forming stable complexes that can be easily analyzed using techniques such as UV-Vis spectroscopy. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Silver(1+) diethyldithiocarbamate. CAS No. 1470-61-7. Pack Sizes: 5 g; 10 g. Product ID: HY-W034674. | |
| 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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