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| Product | Description | |
|---|---|---|
| Sodium Acid Pyrophosphate | Sodium Acid Pyrophosphate. Category PHOSPHATES. Pack Sizes Drums/ Bag |  |
| Sodium Acid Pyrophosphate | Sodium Acid Pyrophosphate. SUPPLIERS TO BUSINESS CUSTOMERS ONLY. |  North America & APAC |
| Sodium Acid Pyrophosphate (SAPP) | Sodium Acid Pyrophosphate (SAPP). Group: Phosphates. Pack Sizes: 25Kgs Cartons. |  |
| dGpCpp | dGpCpp, a pyrophosphate analog employed in biomedical research for studying RNA and DNA polymerase activity, possesses anti-proliferative action against cancerous cells and showcases potential benefits in certain viral infections. Notably, the compound serves as an inhibitor of protein synthesis through the stimulation of mRNA degradation and the targeting of elongation factors. Synonyms: (dGMPCPP); 2'-Deoxyguanosine-5'-[(α,β)-methyleno]triphosphate, Sodium salt. Grades: ≥ 95% by HPLC. CAS No. 941569-34-2. Molecular formula: C11H18N5O12P3 (free acid). Mole weight: 505.21 (free acid). |  |
| Disodium pytophosphate | Disodium pyrophosphate or sodium acid pyrophosphate is an inorganic compound consisting of sodium cations and pyrophosphate anion. It is a white, water-soluble solid that serves as a buffering and chelating agent, with many applications in the food industry. When crystallised from water, it forms a hexahydrate, but it dehydrates above room temperature. Pyrophosphate is a polyvalent anion with a high affinity for polyvalent cations, e.g. Ca2+.Disodium pyrophosphate is produced by heating sodium dihydrogen phosphate:2 NaH2PO4 → Na2H2P2O7 + H2O. Group: Electrolytes. Alternative Names: DISODIUM PYROPHOSPHATE; disodium pytophosphate; DI-SODIUM DIHYDROGEN PYROPHOSPHATE; Diphosphoric acid disodium salt; DSPP; SODIUM ACID PYROPHOSPHATE; SODIUM DIHYDROGEN PYROPHOSPHATE; SAPP. CAS No. 7758-16-9. Product ID: disodium [hydroxy(oxido)phosphoryl] hydrogen phosphate. Molecular formula: 221.94. Mole weight: H2Na2O7P2. OP(=O)([O-])OP(=O)(O)[O-]. [Na+]. [Na+]. GYQBBRRVRKFJRG-UHFFFAOYSA-L. |  |
| Disodium pytophosphate | Disodium pyrophosphate or sodium acid pyrophosphate is an inorganic compound consisting of sodium cations and pyrophosphate anion. It is a white, water-soluble solid that serves as a buffering and chelating agent, with many applications in the food industry. When crystallised from water, it forms a hexahydrate, but it dehydrates above room temperature. Pyrophosphate is a polyvalent anion with a high affinity for polyvalent cations, e.g. Ca2+.Disodium pyrophosphate is produced by heating sodium dihydrogen phosphate:2 NaH2PO4 → Na2H2P2O7 + H2O. Group: Metal & ceramic materials. Alternative Names: DISODIUM PYROPHOSPHATE;disodium pytophosphate;DI-SODIUM DIHYDROGEN PYROPHOSPHATE;Diphosphoric acid disodium salt;DSPP;SODIUM ACID PYROPHOSPHATE;SODIUM DIHYDROGEN PYROPHOSPHATE;SAPP. CAS No. 7758-16-9. Molecular formula: H2Na2O7P2. Mole weight: 221.94. Appearance: White powder. Purity: N/A. IUPACName: disodium [hydroxy(oxido)phosphoryl] hydrogen phosphate. Canonical SMILES: OP(=O)([O-])OP(=O)(O)[O-]. [Na+]. [Na+]. Density: 2.311 g/cm³ (25ºC). ECNumber: 231-835-0. Catalog: ACM7758169. |  |
| Disodium pytophosphate | Disodium pytophosphate. Synonyms: Di sodium pytophospha; Two sodium pyrophosphatetwo hydrogen ; Amyl oid PrecursorProtein β , Secreted; ANTI-DSPP (N-TERM) antibodyproducedinrabbit; DChe micalbookentinsialophosphoprotein; sodium pyrophosphatedibasicpractica lgrade; sodium PYROPHOSPHATEDIBASI CBIOULTR; FoodGrade sodium AcidPyro phosphate. CAS No. 7758-16-9. Product ID: CDC10-0120. Molecular formula: H2Na2O7P2. Category: Cosmetic Chelating Chemicals. Product Keywords: Cosmetic Ingredients; Cosmetic Chelating Chemicals; Disodium pytophosphate; CDC10-0120; 7758-16-9; H2Na2O7P2; DisodiuMpytophospha; TwosodiuMpyrophosphatetwohydrogen; AmyloidPrecursorProteinβ, Secreted; ANTI-DSPP(N-TERM)antibodyproducedinrabbit; DChemicalbookentinsialophosphoprotei n; sodium pyrophosphatedibasicpracticalgrade; SODIUMPYROPHOSPHATEDIBASICBIOULTR; FoodGradeSodiumAcidPyrophosphate; 231-835-0; 7758-16-9. Purity: 0.98. Color: White to off-white. EC Number: 231-835-0. Physical State: Powder. Solubility: H2O: 0.1 M at 20 °C, clear, colorless. Storage: -70°C. Melting Point: decomposes 220°C [MER06]. Density: 1.86 g/mL. |  |
| GTPαS | GTPαS can be accomplished by 50-thiophosphorylation of 7-methylguanosine in (MeO)3PO in the presence of 2,6-lutidine,12 followed by addition of tributylammonium pyrophosphate and subsequent hydrolysis of the trimetaphosphate-like intermediate. Synonyms: Guanosine-5'-(α-thio)-triphosphate, Sodium salt; (1 : 1 Mixture of R; and S; isomers). Grades: ≥ 95 % by HPLC. CAS No. 81570-51-6. Molecular formula: C10H16N5O13P3S (free acid). Mole weight: 539.24 (free acid). | |
| Phytic acid sodium salt | Phytic acid sodium salt (myo-Inositol; hexakis dihydrogen phosphate; Inositol hexaphosphate) is an orally active compound derived from the seeds of legumes. Phytic acid sodium salt is a [PO4] 3 - storage depot and precursor for other inositol phosphates and pyrophosphates. phytic acid is hydrolyzed by phytases in a stepwise manner in the plant. Phytic acid sodium salt attenuates Aβ oligomers and upregulates autophagy protein. Phytic acid sodium salt can be used in cardiovascular disease, metabolic disease, nervous system disease and cancer research [1] [2] [3] [4] [5] [6] [7] [8] [9] [10]. Uses: Scientific research. Group: Natural products. Alternative Names: myo-Inositol, hexakis(dihydrogen phosphate) sodium salt; Inositol hexaphosphate sodium salt. CAS No. 14306-25-3. Pack Sizes: 500 mg; 1 g. Product ID: HY-N2581. |  |
| Risedronic acid sodium | Risedronic acid (Risedronate) sodium, a bisphosphonate, is a potent anti-resorption agent that inhibits osteoclast-mediated bone resorption and changes the bone metabolism. Risedronic acid sodium suppresses osteoblast differentiation and induced caspase- and isoprenoid depletion-dependent apoptosis. Risedronic acid sodium inhibits blood stages of Plasmodium falciparum ( IC 50 of 20.3 μM). Risedronic acid sodium inhibits the transfer of the farnesyl pyrophosphate group to parasite proteins [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Risedronate sodium. CAS No. 115436-72-1. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg; 1 g. Product ID: HY-B0119. | |
| Sodium Phosphate Monobasic | The hydrated forms of monobasic sodium phosphate occur as odorless, colorless or white, slightly deliquescent crystals. The anhydrous form occurs as a white crystalline powder or granules. Synonyms: Acid sodium phosphate; E339; Kalipol 32; monosodium orthophosphate; monosodium phosphate; natrii dihydrogenophosphas dihydricus; phosphoric acid, monosodium salt; primary sodium phosphate; sodium biphosphate; sodium dihydrogen orthophosphate; sodium dihydrogen phosphate. Product ID: PE-0557. Category: Buffering Agents; Emulsifying Agents; Sequestering Agents. Product Keywords: Excipients for Liquid Dosage Form; Emulsifier Excipients; PE-0557; Sodium Phosphate Monobasic; Buffering Agents; Emulsifying Agents; Sequestering Agents;. UNII: 3980JIH2SW. Grade: Pharmceutical Excipients. Administration route: Injections; infusions; ophthalmic, oral, topical, and vaginal. Dosage Form: Injections; infusions; ophthalmic, oral, topical, and vaginal preparations. Stability and Storage Conditions: Monobasic sodium phosphate is chemically stable, although it is slightly deliquescent. On heating at 100°C, the dihydrate loses all of its water of crystallization. On further heating, it melts with decomposition at 205°C, forming sodium hydrogen pyrophosphate, Na2H2P2O7. At 250°C it leaves a final residue of sodium metaphosphate, NaPO3. Aqueous solutions are stable and may be sterilized by autoclaving. Monobasic sodium phosphate sho | |
| Sodium pyrophosphate | Sodium pyrophosphate (Disodium pyrophosphate), a food additive, is an inorganic compound. Sodium pyrophosphate has potential hematotoxic and immunotoxic effects [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Disodium pyrophosphate; Sodium acid pyrophosphate; SAPP. CAS No. 7758-16-9. Pack Sizes: 100 mg; 250 mg; 500 mg; 1 g. Product ID: HY-W105970. | |
| Sodium Pyrophosphate | SODIUM PYROPHOSPHATE, DECAHYDRATE, ACS Reagent, crystal, (Synonym: Diphosphoric Acid, Tetrasodium Salt, Decahydrate), Formula: Na4P2O7.10H2O. CAS No. 13472-36-1. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Tetrasodium pyrophosphate | Synonyms: DIPHOSPHORIC ACID TETRASODIUM SALT; DIPHOSPHORIC ACID, TETRASODIUM SALT, DECAHYDRATE; DECAHYDRATE TETRASODIUM PYROPHOSPHATE; TETRA-SODIUM DIPHOSPHATE; TETRA-SODIUM DIPHOSPHATE-10-HYDRATE; TETRA-SODIUM DIPHOSPHATE DECAHYDRATE; TETRASODIUM PYROPHOSPHATE; SODIUM D. Grades: anhydrous, Technical. CAS No. 7722-88-5. Molecular formula: Na4P2O7. Mole weight: 265.90. | |
| Uridine-5'-diphosphate trisodium salt | Uridine-5'-diphosphate trisodium salt is an indispensable biochemical compound utilized extensively in the nucleic acid synthesis and glycogen metabolism research. Within the tapestry of scientific exploration, Uridine-5'-diphosphate trisodium salt emerges as a pivotal player, intimately intertwined with the intricate fabric of RNA metabolism assessment, viral replication elucidation and the research of afflictions such as cancer and neurological disorders. Synonyms: Uridine 5'-(trihydrogendiphosphate), trisodium salt; ((2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl diphosphate trisodium salt; Uridine 5'-(trisodium pyrophosphate); trisodium uridine 5'-diphosphate; Uridine, 5'-(trihydrogen diphosphate), sodium salt (1:3). Grades: ≥95%. CAS No. 19817-91-5. Molecular formula: C9H11N2Na3O12P2. Mole weight: 470.11. | |
| Diphosphoric acid sodium salt | Heterocyclic Organic Compound. Alternative Names: Sodium diphosphate, Diphosphoric acid, sodium salt, Pyrophosphoric acid, sodium salt, 7722-88-5 (Parent), NSC56751, EINECS 233-134-5, CID107877, 10042-91-8. CAS No. 10042-91-8. Molecular formula: H3NaO7P2. Mole weight: 199.956912 [g/mol]. Purity: 0.96. IUPACName: sodium phosphono hydrogen phosphate. Catalog: ACM10042918. | |
| EDA-XTP | EDA-XTP is a compelling inhibitorexcelinging at pinpointing and hindering the functionality of Xanthosine triphosphate pyrophosphatase (XTPase). This multifaceted compound exhibits remarkable effectiveness in studyting a diverse range of ailments associated with aberrant nucleotide metabolism, including gout, hyperuricemia and select forms of malignancy. Synonyms: 2'/3'-O-(2-Aminoethyl-carbamoyl)-Xanthosine-5'-triphosphate, Sodium salt. Grades: ≥ 95 % by HPLC. Molecular formula: C13H21N6O16P3(free acid). Mole weight: 610.26 (free acid). | |
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