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| Product | Description | |
|---|---|---|
| Copper glycinate | 5g Pack Size. Group: Building Blocks, Catalysts, Organics. Formula: C4H8CuN2O4. CAS No. 13479-54-4. Prepack ID 90027957-5g. Molecular Weight 211.66. See USA prepack pricing. |  |
| Copper Glycinate | Copper Glycinate. CAS No. 13479-54-4. Molecular formula: C4H8CuN2O4. |  |
| Copper2-[[(1R,2R)-2-[bis(2-oxido-2-oxoethyl)amino]cyclohexyl]-(2-oxido-2-oxoethyl)amino]acetate | Heterocyclic Organic Compound. Alternative Names: 19332-78-6, EINECS 242-968-9, AC1L3EUQ, 12295-59-9, 14705-97-6, copper 2-[[(1R,2R)-2-[bis(2-oxido-2-oxoethyl)amino]cyclohexyl]-(2-oxido-2-oxoethyl)amino]acetate, Cuprate(2-), ( (N, N-1, 2-cyclohexanediylbis (N- (carboxymethyl)glycinato)) (4-)-N, N, O, O, ON, ON)-, (OC-6-21-(trans))-, Cuprate(2-), ((rel-N,N-(1R,2R)-1,2-cyclohexanediylbis(N-((carboxy-kappaO)methyl)glycinato-kappaN,kappaO))(4-))-, (OC-6-21)-, Cuprate(2-), [[N,N-1,2-cyclohexanediylbis[ N-(carboxymethyl)glycinato]](4-)-N, N, O, O, O#N ,O#N#]-, [OC-6-21-(trans)]-, trans- ( (N, N-Cyclohexane-1, 2-diylbis (N- (carboxymethyl)glycinato)) (4-)-N, N, O, O, ON, ON)cuprate (2-). CAS No. 12295-59-9. Molecular formula: C14H18CuN2O8-2. Mole weight: 405.847 g/mol. Purity: 0.96. IUPACName: copper; 2-[[ (1R, 2R) -2-[bis (carboxylatomethyl) amino]cyclohexyl]- (carboxylatomethyl) amino]acetate. Canonical SMILES: C1CCC (C (C1)N (CC (=O)[O-])CC (=O)[O-])N (CC (=O)[O-])CC (=O)[O-]. [Cu+2]. ECNumber: 242-968-9. Catalog: ACM12295599. |  |
| 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. | |
| factor-independent urate hydroxylase | This enzyme was previously thought to be a copper protein, but it is now known that the enzymes from soy bean (Glycine max), the mould Aspergillus flavus and Bacillus subtilis contains no copper nor any other transition-metal ion. The 5-hydroxyisourate formed decomposes spontaneously to form allantoin and CO2, although there is an enzyme-catalysed pathway in which EC 3.5.2.17, hydroxyisourate hydrolase, catalyses the first step. The enzyme is different from EC 1.14.13.113 (FAD-dependent urate hydroxylase). Group: Enzymes. Synonyms: uric acid oxidase; uricase; uricase II; urate oxidase. Enzyme Commission Number: EC 1.7.3.3. CAS No. 9002-12-4. UO. 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-1626; factor-independent urate hydroxylase; EC 1.7.3.3; 9002-12-4; uric acid oxidase; uricase; uricase II; urate oxidase. Cat No: EXWM-1626. |  |
| Fmoc-Pra-OH | Fmoc-Pra-OH is a Glycine (HY-Y0966) derivative [1]. Fmoc-Pra-OH 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: Peptides. CAS No. 198561-07-8. Pack Sizes: 5 g; 10 g; 25 g; 100 g. Product ID: HY-W011210. |  |
| 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. | |
| 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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