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| Product | Description | |
|---|---|---|
| Ammonium carbonate | Ammonium carbonate. Group: Biochemicals. Grades: Highly Purified. CAS No. 506-87-6. Pack Sizes: 500g, 1kg, 2kg, 5kg, 10kg. Molecular Formula: CH8N2O3. US Biological Life Sciences. |  Worldwide |
| 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. |  |
| Ammonium Carbonate | AMMONIUM CARBONATE, ACS Reagent, powder, Formula: (NH4)2CO3 (approx.). CAS No. 506-87-6. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Ammonium Carbonate | Ammonium Carbonate. Grade: ACS FCC. CAS: 506-87-6. Packing: Various. |  New Jersey NJ |
| Ammonium Carbonate | Ammonium Carbonate. Grades: 99.99% Extremely High (>=99%). CAS No. 506-87-6. Pack Sizes: Gram Quantities: 500 gm , 1 kg. Order Number: 1051. |  www.prochemonline.com |
| Ammonium Carbonate | Ammonium Carbonate. Grades: ACS. CAS No. 506-87-6. Pack Sizes: Kilogram Quanitites: 1 kg , 5 kg. Order Number: 1050-2. | www.prochemonline.com |
| Ammonium Carbonate Carbamate | Ammonium Carbonate Carbamate is used in the study of amino acids and has important implications in biochemical studies. Group: Biochemicals. Grades: Highly Purified. CAS No. 8000-73-5. Pack Sizes: 100mg, 250mg. Molecular Formula: C2H11N3O5, Molecular Weight: 157.13. US Biological Life Sciences. | Worldwide |
| Ammonium Carbonate ≥37% (NH3) | Ammonium Carbonate ≥37% (NH3). Group: Biochemicals. Grades: Reagent Grade. Pack Sizes: 1Kg, 5Kg, 25Kg. US Biological Life Sciences. | Worldwide |
| Ammonium carbonate pure Food grade | Heterocyclic Organic Compound. CAS No. 10361-29-2. Molecular formula: CH2O3?H3N. Mole weight: 79.0545. Catalog: ACM10361292. | |
| Ammonium Carbonate, Reagent Grade, 500 g | Formula: (NH4)2CO3. F. W: 96. 09. Characteristics: Hard crystals, lumps. Notes: Water soluble; decomposes in hot water. Storage Code: Green; general chemical storage. Grades: chem-grade reagent. CAS No. 506-87-6. Product ID: 843752. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Ammonium carbonate/scandium carbonate | Ammonium carbonate/scandium carbonate. Group: Electrolytes. Alternative Names: AMMONIUM CARBONATE/SCANDIUM CARBONATE; AMMONIUM CARBONATE/SCANDIUM CARBONATE DO; Ammonium carbonate / scandium carbonatemonohydratedoublesalt. CAS No. 312623-99-7. Product ID: AMMONIUM CARBONATE/SCANDIUM CARBONATE. Molecular formula: 366.02434. Mole weight: C4< / sub>H8< / sub>N2< / sub>O12< / sub>Sc2< / sub>. 96%. | |
| Ammonium Carbonate USP | Ammonium Carbonate USP. CAS No. 8000-73-5. Molecular formula: (NH4)2CO3. |  |
| Ammonium bicarbonate | Ammonium bicarbonate. Group: Biochemicals. Alternative Names: Ammonium hydrogen carbonate. Grades: Highly Purified. CAS No. 1066-33-7. Pack Sizes: 2kg, 5kg. US Biological Life Sciences. | Worldwide |
| Ammonium bicarbonate | Heterocyclic Organic Compound. Alternative Names: acidammoniumcarbonate; ammoniumbicarbonate(1:1); monoammoniumcarbonate; AMMONIUM BICARBONATE;AMMONIUM ACID CARBONATE;AMMONIUM HYDROGEN CARBONATE;AMMONIUM CARBONATE, ACIDIC;AMMONIUM CARBONATE TS. CAS No. 1066-33-7. Molecular formula: CH5NO3. Mole weight: 79.06. Density: 1,586 g/cm³. Catalog: ACM1066337. | |
| Ammonium Bicarbonate | Ammonium bicarbonate appears as a white crystalline solid having the odor of ammonia. Soluble in water. The primary hazard is the threat to the environment. Immediate steps should be taken to limit spread to the environment. Used to make other ammonium compounds, in food processing, and for other uses.;DryPowder; Liquid;White crystals or crystalline powder;COLOURLESS OR WHITE CRYSTALS WITH CHARACTERISTIC ODOUR. Group: Glass additivespolymers. Product ID: azanium; hydrogen carbonate. Molecular formula: 79.056g/mol. Mole weight: CH5NO3;CH5NO3;NH4HCO3;NH4HCO3;CH5NO3. C(=O)(O)[O-].[NH4+]. InChI=1S/CH2O3.H3N/c2-1(3)4;/h(H2, 2, 3, 4);1H3. ATRRKUHOCOJYRX-UHFFFAOYSA-N. | |
| Ammonium Bicarbonate | AMMONIUM BICARBONATE, Reagent, powder, (Synonym: Ammonium Hydrogen Carbonate), Formula: NH4HCO3. CAS No. 1066-33-7. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Ammonium hydrogen carbonate | 1kg Pack Size. Group: Biochemicals, Buffers. Formula: NH4HCO3. CAS No. 1066-33-7. Prepack ID 19327456-1kg. Molecular Weight 79.06. See USA prepack pricing. |  |
| Ammonium Hydrogen Carbonate EP | Ammonium Hydrogen Carbonate EP. CAS No. 1066-33-7. Molecular formula: NH4HCO3. | |
| Ammonium zirconium(IV) carbonate solution | Ammonium zirconium(IV) carbonate solution. Group: Electrolytes. | |
| Tributylmethylammonium methyl carbonate solution | Tributylmethylammonium methyl carbonate can be used in the preparation of counter-cation anionic monomers by reacting with 2-acrylamido-2- methylpropanesulfonic acid and acrylic acid. Uses: Cas: 274257-37-3, mf: c15h33no3, mw: 275.43. Group: Electrolytes. Alternative Names: Methyltributyl Ammonium methylcarbonate. CAS No. 274257-37-3. Product ID: methyl carbonate; tributyl(methyl)azanium. Molecular formula: 275.43. Mole weight: Linear Formula (CH3CH2CH2CH2)3N(Cl)CH3. CCCC[N+](C)(CCCC)CCCC.COC(=O)[O-]. 1S/C13H30N.C2H4O3/c1-5-8-11-14(4, 12-9-6-2)13-10-7-3; 1-5-2(3)4/h5-13H2, 1-4H3; 1H3, (H, 3, 4)/q+1; /p-1. ZKWSMHMGQLTZGI-UHFFFAOYSA-M. ~50%inmethanol:water(2:3). | |
| Immobilized Endoproteinase Glu-C on F7m | Endoproteinase Glu-C hydrolyzes peptide and ester linkages specifically at the carboxyl end of glutamic acid (-Glu/-X; in ammonium carbonate pH 7. 8, or ammonium acetate pH 4. 0, buffer A) or of glutamic and aspartic acid (-Glu/-X and -Asp/-X; in phosphate buffer pH 7. 8, buffer B). F7m: 1. 0 mg endoproteinase Glu-C immobilized on matrix F7m per CR-column. 900 units immobilized per CR-column. Nr. 7 Storage buffer: 50 mM Tris/HCl at pH 7. 5, 5 mM EDTA. Nr. 31 Reaction buffer A: 25 mM ammonium acetate, pH 4. 0 (see above)Nr. 32 Washing buffer A: 25 mM ammonium acetate, pH 4. 0, 1 M NaClNr. 62 Reaction buffer B: 50 mM phosphate buffer, pH 7. 8 (see above)Nr. 63 Washing buffer B: 50 mM phosphate buffer, pH 7. 8, 1 M NaCl. Group: Enzymes. Synonyms: EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase. Enzyme Commission Number: EC 3. 4. 21. 19. Storage: 4 °C. Source: Staphylococcus aureus. EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase; Immobilized Endoproteinase Glu-C. Cat No: NATE-1763. |  |
| Immobilized Endoproteinase Glu-C on G3m | Endoproteinase Glu-C hydrolyzes peptide and ester linkages specifically at the carboxyl end of glutamic acid (-Glu/-X; in ammonium carbonate pH 7. 8, or ammonium acetate pH 4. 0, buffer A) or of glutamic and aspartic acid (-Glu/-X and -Asp/-X; in phosphate buffer pH 7. 8, buffer B). G3m: 25 ug (22 units) endoproteinase Glu-C per CR-column immobilized on dextran. This CR-column cuts at least 12 ug tubulin or 5 ug BSA per application in phosphate buffer. Nr. 7 Storage buffer: 50 mM Tris/HCl at pH 7. 5, 5 mM EDTA. Nr. 31 Reaction buffer: 25 mM NH4-acetate, pH 4. 0 (see above)Nr. 32 Washing buffer: 25 mM NH4-acetate, pH 4. 0, 1 M NaClNr. 62 Reaction buffer: 50 mM phosphate buffer, pH 7. 8 (see above)Nr. 63 Washing buffer: 50 mM phosphate buffer, pH 7. 8, 1 M NaCl. Group: Enzymes. Synonyms: EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase. Enzyme Commission Number: EC 3. 4. 21. 19. Storage: 4 °C. Source: Staphylococcus aureus. EC 3. 4. 21. 19; Staph aureus V8 Protease; Protease, Staph aureus (Endoproteinase Glu-C); Glutamyl endopeptidase; V8 proteinase, endoproteinase Glu-C; staphylococcal serine proteinase; Immobilized Endoproteinase Glu-C. Cat No: NATE-1764. | |
| 18:0 PEG2000 PE CF | PEG Lipids. Alternative Names: 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[poly(ethylene glycol)2000-N'-carboxyfluorescein] (ammonium salt); 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[carbonyl-aminopoly(ethylene glycol)-2000-N'-(carboxyfluorescein)] (ammonium salt). CAS No. 1092697-61-4. Molecular formula: C153H279N4O60P. Mole weight: 3165.86. Appearance: Powder. Purity: >99%. Catalog: ACM1092697614. | |
| 1-Bromohexadecane | 1-Bromohexadecane is used in the preparation of soluble carbon nano-onions by covalent functionalization with hexadecyl chains. It is also used to synthesize [2- (methacryloyloxy) ethyl] dimethylhexadecyl Ammonium bromide monomer, required for the synthesis of novel methacrylate based adsorbents. Group: Biochemicals. Grades: Highly Purified. CAS No. 112-82-3. Pack Sizes: 1g, 5 g. Molecular Formula: C16H33Br, Molecular Weight: 305.339999999999. US Biological Life Sciences. | Worldwide |
| 2-[3-[2-[Diethyl (methyl)azaniumyl]ethoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxyethyl-diethyl-methylazanium diiodide | Heterocyclic Organic Compound. Alternative Names: 2-[3-[2-[diethyl (methyl)azaniumyl]ethoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxyethyl-diethyl-methylazanium diiodide; 2,2-[(2,4-diphenylcyclobutane-1,3-diyl)bis(carbonyloxy)]bis(N,N-diethyl-N-methylethanaminium) diiodide; Ammonium,diethyl(2-hydroxyet. CAS No. 10066-72-5. Molecular formula: C32H48I2N2O4. Mole weight: 778.543 g/mol. Purity: 0.96. IUPACName: 2-[3-[2-[diethyl (methyl)azaniumyl]ethoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxyethyl-diethyl-methylazanium; diiodide. Canonical SMILES: CC[N+] (C) (CC)CCOC (=O)C1C (C (C1C2=CC=CC=C2)C (=O)OCC[N+] (C) (CC)CC)C3=CC=CC=C3. [I-]. [I-]. Catalog: ACM10066725. | |
| 2-(Dibutylcarbamoyloxy)ethyl-ethyl-dimethylazanium | Heterocyclic Organic Compound. Alternative Names: Dibutoline, Dibuline, 124129-33-5, AC1L1VWB, 532-49-0 (sulfate), 2-(dibutylcarbamoyloxy)ethyl-ethyl-dimethylazanium, 2-[(dibutylcarbamoyl)oxy]-N-ethyl-N,N-dimethylethanaminium, (Ethyl(2-hydroxyethyl)dimethylammonium)sulfate bis(dibutylcarbamate), 2-(((Dibutylamino)carbonyl)oxy)-N-ethyl-N,N-dimethylethanaminium, Ammonium, ethyl(2-hydroxyethyl)dimethyl-, dibutylcarbamate (ester), Ethanaminium, 2-(((dibutylamino)carbonyl)oxy)-N-ethyl-N,N-dimethyl-, 124129-34-6, 21962-82-3. CAS No. 124129-33-5. Molecular formula: C15H33N2O2+. Mole weight: 273.435 g/mol. Purity: 0.96. IUPACName: 2-(dibutylcarbamoyloxy)ethyl-ethyl-dimethylazanium. Canonical SMILES: CCCCN(CCCC)C(=O)OCC[N+](C)(C)CC. Catalog: ACM124129335. | |
| 2-(Diphenylcarbamoyloxy)ethyl-triethylazanium iodide | Heterocyclic Organic Compound. Alternative Names: Triethyl(2-hydroxyethyl)ammoniumiodide, diphenylcarbamate (6CI,7CI); Ethanaminium, 2-[[(diphenylamino)carbonyl]oxy]-N, N, N-triethyl-, iodide (9CI); Triaethyl-(2-diphenylcarbamoyloxy-aethyl)-ammonium,Jodid; Ethanaminium, 2-[[(diphenylamino)carbonyl]oxy]-N, N, N-t. CAS No. 101710-53-6. Molecular formula: C21H29IN2O2. Mole weight: 468.372 g/mol. Purity: 0.96. IUPACName: N,N-diphenylcarbamate;triethyl(2-hydroxyethyl)azanium;iodide. Catalog: ACM101710536. | |
| 5-[3-[5-[Diethyl (methyl) azaniumyl]pentoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxypentyl-diethyl-methylazanium diiodide | Heterocyclic Organic Compound. Alternative Names: Ammonium,diethyl(5-hydroxypentyl)methyl-,iodide,ester with (cis-1,2,trans-1,3,trans-1,4)-2,4-diphenyl-1,3-cyclobutanedicarboxylic acid (2:1); 5,5-[(2,4-diphenylcyclobutane-1,3-diyl)bis(carbonyloxy)]bis(N,N-diethyl-N-methylpentan-1-aminium) diiodide; 5-[3-. CAS No. 10066-76-9. Molecular formula: C38H60I2N2O4. Mole weight: 862.703 g/mol. Purity: 0.96. IUPACName: 5-[3-[5-[diethyl (methyl) azaniumyl]pentoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxypentyl-diethyl-methylazanium; diiodide. Canonical SMILES: CC[N+] (C) (CC)CCCCCOC (=O)C1C (C (C1C2=CC=CC=C2)C (=O)OCCCCC[N+] (C) (CC)CC)C3=CC=CC=C3. [I-]. [I-]. Catalog: ACM10066769. | |
| 7-[3-[7-[Diethyl (methyl) azaniumyl]heptoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxyheptyl-diethyl-methylazanium diiodide | Heterocyclic Organic Compound. Alternative Names: Ammonium,diethyl(7-hydroxyheptyl)methyl-,iodide,ester with (cis-1,2,trans-1,3,trans-1,4)-2,4-diphenyl-1,3-cyclobutanedicarboxylic acid (2:1); 7,7-[(2,4-diphenylcyclobutane-1,3-diyl)bis(carbonyloxy)]bis(N,N-diethyl-N-methylheptan-1-aminium) diiodide; 7-[3-. CAS No. 10066-77-0. Molecular formula: C42H68I2N2O4. Mole weight: 918.809 g/mol. Purity: 0.96. IUPACName: 7-[3-[7-[diethyl (methyl) azaniumyl]heptoxycarbonyl]-2, 4-diphenylcyclobutanecarbonyl]oxyheptyl-diethyl-methylazanium; diiodide. Canonical SMILES: CC[N+] (C) (CC)CCCCCCCOC (=O)C1C (C (C1C2=CC=CC=C2)C (=O)OCCCCCCC[N+] (C) (CC)CC)C3=CC=CC=C3. [I-]. [I-]. Catalog: ACM10066770. | |
| 7-Epi Clindamycin 2-Phosphate Ammonium Salt | Clindamycin impurity. Synonyms: Methyl 7-Chloro-6,7,8-trideoxy-6-[[[(2S,4R)-1-methyl-4-propyl-2-pyrrolidinyl]carbonyl]amino]-1-thio-D-erythro-α-D-galactooctopyranoside 2-(Dihydrogen Phosphate) Monoammonium Salt. Molecular formula: C18H37ClN3O8PS. Mole weight: 521.99. |  |
| Allyloxycarbonyl-D-phenylalanine dicyclohexyl ammonium salt | Synonyms: Aloc-D-Phe-OH DCHA; (2R)-3-phenyl-2-{[(prop-2-en-1-yloxy)carbonyl]amino}propanoic acid. dicyclohexylamine; Allyloxycarbonyl-D-Phenylalanine dicyclohexylamine. Grades: ≥ 99% (HPLC). CAS No. 152507-71-6. Molecular formula: C13H15NO4·C12H23N. Mole weight: 430.59. | |
| Ammonium cerium(IV) sulfate dihydrate | Ammonium cerium(IV) sulfate dihydrate. Uses: Cerium ammonium sulfate can be used in preparation of cerium iv oxidimetric solutions,it is also applied as industrial antioxidant and etching agent for the integrated circuit, is also raw material for polishing powder, special glass and ceramics. in steels, cerium degasifies and can help reduce sulfides and oxides, and it is a precipitation hardening agent in stainless steel. cerium alloys are used in permanent magnets, and in tungsten electrodes for gas tungsten arc welding. it is also used in carbon-arc lighting, especially in the motion picture industry. Group: Electrolytes. Alternative Names: Cerium(IV) ammonium sulfate dihydrate. CAS No. 10378-47-9. Molecular formula: 632.55. Mole weight: CeH20N4O18S4. 99%+. | |
| Ammonium cerium(IV) sulfate dihydrate | Cerium Ammonium Sulfate can be used in preparation of cerium IV oxidimetric solutions,it is also applied as industrial antioxidant and etching agent for the integrated circuit, is also raw material for polishing powder, special glass and ceramics. In steels, Cerium degasifies and can help reduce Sulfides and Oxides, and it is a precipitation hardening agent in stainless steel. Cerium alloys are used in permanent magnets, and in Tungsten electrodes for gas Tungsten arc welding. It is also used in carbon-arc lighting, especially in the motion picture industry. Group: Metal & ceramic materials. Alternative Names: Cerium(IV) ammonium sulfate dihydrate. CAS No. 10378-47-9. Molecular formula: CeH20N4O18S4. Mole weight: 632.55. Appearance: Yellow crystalline powder. Purity: 99%+. Catalog: ACM10378479-2. | |
| 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). | |
| Ammonium Persulfate | Ammonium Persulfate is used as a reagent in the low temperature synthesis of carbon-encapsulated spherical Fe7S8 nanocrystals as high-performance anode for lithium-ion batteries. Group: Biochemicals. Grades: Highly Purified. CAS No. 7727-54-0. Pack Sizes: 10g, 25g. Molecular Formula: H8N2O8S2. US Biological Life Sciences. | Worldwide |
| AR-23 | AR-23 is a melittin-related peptide from the skin of the Japanese frog, Rana tagoi, with antimicrobial and cytolytic properties. Synonyms: AR-23; AMMONIUM, (m-HYDROXYPHENYL)TRIMETHYL-, METHYLSULFATE, BENZYLCARBAMATE; Benzylcarbamic ester of 3-oxyphenyltrimethylammonium methylsulfate; 64051-16-7; Ammonium, (3-(N-benzylcarbamoyloxy)phenyl)trimethyl-, methylsulfate; Carbamic acid, N-benzyl-, 3-(trimethylammonio)phenyl ester, methylsulfate; DTXSID50214190; LS-18471; [3-(benzylcarbamoyloxy)phenyl]-trimethylazanium;methyl sulfate; Benzenaminium, N,N,N-trimethyl-3-[[[(phenylmethyl)amino]carbonyl]oxy]-, methyl sulfate. CAS No. 64051-16-7. Molecular formula: C18H24N2O6S. Mole weight: 396.5. | |
| Cabergoline N-Oxide | The N-oxide of Cabergoline , a dopamine D2-receptor agonist. Group: Biochemicals. Alternative Names: (3-{{ [6aR, 9R, 10aR) -7-Allyl-4, 6, 6a, 7, 8, 9, 10, 10a-octahydroindolo [4, 3-fg]quinolin-9yl]carbonyl} [ethylamino) carbonyl]amino}propyl) (dimethyl) ammoniumolate. Grades: Highly Purified. Pack Sizes: 500ug, 1mg. US Biological Life Sciences. | Worldwide |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- [bis (4-fluorophenyl] phosphino] ferrocenyl] ethyldi-tert-butylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (bis (4-fluorophenyl) phosphinoferrocenyl]ethyl (di-t-butylphosphine) }nickel (II) is used for: 1.Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. 4.Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-37-3. Mole weight: 774.69. Catalog: ACM2049086373. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldicyclohexylphosphine] nickel (II) | Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-35-1. Mole weight: 802.88. Catalog: ACM2049086351. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldiphenylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (dicyclohexylphosphino) ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is useful in these fields: Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-36-2. Mole weight: 790.79. Catalog: ACM2049086362. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) has the following various uses:1.Versatile, air-stable, low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-34-0. Mole weight: 738.71. Catalog: ACM2049086340. | |
| Cilastatin Ammonium Salt | Cilastatin Ammonium Salt is the ammonium salt of Cilastatin, which is a dipeptidase inhibitor of renal enzyme dehydropeptidase-I and leukotriene D4 peptidase. It inhibits metabolism of LTD4 to LTE4 and the hydrolysis of β-lactam antibiotics. It reduces toxic accumulation of cyclosporin A in kidney proximal tubule epithelial cells. It can be combined intravenously with imipenem in order to protect it from dehydropeptidase. It suppresses both host and target metabolism of the broad-spectrum antibiotic imipenem, improving its efficacy. It usually confers antibiotic resistance to certain bacteria because itself does not have antibiotic activity. It has nephroprotective effects. Synonyms: (2Z)-7-[[(2R)-2-amino-2-carboxyethyl]thio]-2-[[[(1S)-2,2-dimethylcyclopropyl]carbonyl]amino]-2-heptenoic Acid Ammonium Salt; MK-791 Ammonium Salt. Grades: > 95%. CAS No. 877674-82-3. Molecular formula: C16H29N3O5S. Mole weight: 375.48. | |
| Clindamycin B 2-Phosphate Ammonium Salt | Clindamycin B 2-Phosphate Ammonium Salt is the principal degradation product of Clindamycin 2-phosphate in bulk drug and formulations. Synonyms: Methyl 7-Chloro-6,7,8-trideoxy-6-[[[(2S,4R)-4-ethyl-1-methyl-2-pyrrolidinyl] carbonyl]amino]-1-thio-L-threo-α-D-galactooctopyranoside 2-(Dihydrogen Phosphate) Monoammonium Salt; (2S-trans)-Methyl-7-Chloro-6,7,8-trideoxy-6-[[(4-ethyl-1-methyl-2-pyrrolidiny. Grades: > 95%. CAS No. 54887-31-9. Molecular formula: C17H35ClN3O8PS. Mole weight: 507.97. | |
| Demecarium Bromide | Demecarium Bromide is an acetylcholinesterase inhibitor and veterinary medicine used to treat elevated intraocular pressure associated with primary glaucoma. Group: Biochemicals. Alternative Names: 3, 3'-[1, 10-decanediylbis[ (methylimino) carbonyloxy]]bis[N, N, N-trimethylbenzenaminium Bromide; (m-Hydroxyphenyl) trimethylammonium Bromide Decamethylenebis [methylcarbamate]; (m-hydroxyphenyl) trimethylammonium Bromide Decamethylenebis [methylcarbamate]; 3, 3'-[1, 10-Decanediylbis[ (methylimino) carbonyloxy]]bis[N, N, N-trimethylbenzenaminium Dibromide; Decamethylenebis(m-dimethylaminophenyl-N-methylcarbamate) dimethobromide; Decamethylenebis[N-methylcarbamic Acid m-Dimethylaminophenyl ester] Bromomethylate; Demekarium Bromide; Demekastigmine Bromide; Frumtosnil; Humorsol; N, N'-Bis [3-tri methyl Ammonium phenoxycarbonyl] -N, N'-di methyl deca methyl enediamine Dibromide; Tonilen; Tosmicil; Tosmilen; Tosmilene; Visumatic; Visumiotic. Grades: Highly Purified. CAS No. 56-94-0. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| DSPE-PEG(2000) Cyanur | PEG Lipids. Alternative Names: 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[cyanur(polyethylene glycol)-2000] (ammonium salt); Cyanur-PEG 2000-DSPE; 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[carbonyl-amino(polyethylene glycol)-2000-N'-(6-(2,4-dichloro-1,3,5-triazinyl)] (ammonium salt). CAS No. 1246304-74-4. Molecular formula: C135H265Cl2N6O54P. Mole weight: 2938.47. Appearance: Powder. Purity: >99%. Catalog: ACM1246304744. | |
| DSPE-PEG(5000) Folate | PEG Lipids. Alternative Names: 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[folate(polyethylene glycol)-5000] (ammonium salt); 1,2-Distearoyl-sn-glycero-3-phosphoethanolamine-N-[carbonyl-amino(polyethylene glycol)-5000-N'-(folyl)] (ammonium salt). CAS No. 1236288-25-7. Molecular formula: C287H558N11O127P. Mole weight: 6226.55. Appearance: Powder. IUPACName: azane; 5- [2- [2- [2- [2, 3-di (octadecanoyloxy) propoxy-hydroxyphosphoryl] oxyethylcarbamoyloxy] ethoxy] ethylamino] -2- [ [4- [ (2-imino-4-oxo-4aH-pteridin-6-yl) methylamino] benzoyl] amino] -5-oxopentanoic acid. Canonical SMILES: CCCCCCCCCCCCCCCCCC (=O)OCC (COP (=O) (O)OCCNC (=O)OCCOCCNC (=O)CCC (C (=O)O)NC (=O)C1=CC=C (C=C1)NCC2=NC3C (=O)NC (=N)N=C3N=C2)OC (=O)CCCCCCCCCCCCCCCCC. N. Catalog: ACM1236288257-1. | |
| Epalrestat Impurity 16 | Epalrestat Impurity 16. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 76046-54-3 (free acid); ammonium 2, 2'- (disulfannebis (carbonothioyl)bis (azanediyl))diacetate. Molecular Formula: C6H6N2O4S4·2NH4. Mole Weight: 334.46. Catalog: APB05550. |  |
| Farnesyl pyrophosphate ammonium | Farnesyl pyrophosphate ammonium salt, a 15-carbon isoprenoid, is a metabolic intermediate of the mevalonate (MVA) pathway. Farnesyl pyrophosphate ammonium salt is a TRPM2 (TRP Channel) agonist, and activates TRPM2 opening for ion influx. Farnesyl pyrophosphate ammonium salt is a key branch substrate for cholesterol synthesis, ubiquinones synthesis, protein farnesylation decoration, and geranyl-geranyl pyrophosphate (GGPP) synthesis [1]. Uses: Scientific research. Group: Natural products. Alternative Names: Farnesyl diphosphate ammonium. CAS No. 116057-57-9. Pack Sizes: 1 mg; 5 mg; 10 mg. Product ID: HY-113037C. |  |
| Fmoc-4-sulfomethyl-Phe(Tce)-OH | Fmoc-4-sulfomethyl-Phe(Tce)-OH is a stable sulfonyl tyrosine analog derivative suitable for Fmoc-SPPS. Lateral trichloroethyl (Tce) is cleaved by hydrogenolysis (H2/Pd) in the presence of ammonium formate. Synonyms: L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-[[(2,2,2-trichloroethoxy)sulfonyl]methyl]-; N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-[[(2,2,2-trichloroethoxy)sulfonyl]methyl]-L-phenylalanine; (S) -2- ( ( ( (9H-fluoren-9-yl) methoxy) carbonyl) amino) -3- (4- ( ( (2, 2, 2-trichloroethoxy) sulfonyl) methyl) phenyl) propanoic acid. Grades: 95%. CAS No. 1146758-11-3. Molecular formula: C27H24Cl3NO7S. Mole weight: 612.91. | |
| Methoxy-dimethyl-[2-(9H-xanthene-9-carbonyloxy)ethyl]azanium iodide | Heterocyclic Organic Compound. Alternative Names: CID59511, LS-17775, Dimethyl(2-hydroxyethyl)methoxyammonium iodide 9-xanthenecarboxylate, N-Methoxy-N-methyl-beta-aminoethyl 9-xanthenecarboxylate methiodide, AMMONIUM, DIMETHYL(2-HYDROXYETHYL)METHOXY-, IODIDE, 9-XANTHENECARBOXYLATE, 102571-27-7. CAS No. 102571-27-7. Molecular formula: C19H22INO4. Mole weight: 455.287 g/mol. Purity: 0.96. IUPACName: methoxy-dimethyl-[2-(9H-xanthene-9-carbonyloxy)ethyl]azanium iodide. Canonical SMILES: C[N+] (C) (CCOC (=O)C1C2=CC=CC=C2OC3=CC=CC=C13)OC. [I-]. Catalog: ACM102571277. | |
| Nα-Boc-Nε-allyloxycarbonyl-D-lysine dicyclohexyl ammonium salt | Synonyms: Boc-D-Lys(Aloc)-OH DCHA; Dicyclohexylamine (R)-6-(((allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)hexanoate. Grades: ≥ 99.9% (HPLC, Chiral purity). CAS No. 327156-94-5. Molecular formula: C27H49N3O6. Mole weight: 511.7. | |
| Nα-Boc-Nε-allyloxycarbonyl-L-lysine dicyclohexyl ammonium salt | Synonyms: Boc-L-Lys(Aloc)-OH DCHA; Dicyclohexylamine (S)-6-(((allyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)hexanoate; N-a-Boc-N-e-allyloxycarbonyl-L-lysine dicyclohexylaminesalt; (2S)-2-{[(tert-butoxy)carbonyl]amino}-6-{[(prop-2-en-1-yloxy)carbonyl]amino}hexanoic acid. Grades: ≥ 99% (HPLC). CAS No. 110637-52-0. Molecular formula: C15H26N2O6·C12H23N. Mole weight: 511.69. | |
| Nα-Z-Nδ-Boc-L-ornithine dicyclohexyl ammonium salt | Synonyms: Z-L-Orn(Boc)-OH DCHA; Dicyclohexylamine (S)-2-(((Benzyloxy)Carbonyl)Amino)-5-((Tert-Butoxycarbonyl)Amino)Pentanoate. Grades: ≥ 99% (HPLC). CAS No. 13665-13-9. Molecular formula: C18H26N2O6·C12H23N. Mole weight: 547.71. | |
| Native Almonds Mandelonitrile Lyase | In enzymology, a mandelonitrile lyase is an enzyme that catalyzes the chemical reaction:mandelonitrile<-> hydrogen cyanide + benzaldehyde. Hence, this enzyme has one substrate, mandelonitrile, and two products, hydrogen cyanide and benzaldehyde. This enzyme belongs to the family of lyases, specifically the aldehyde-lyases, which cleave carbon-carbon bonds. This enzyme participates in cyanoamino acid metabolism. It has 2 cofactors:flavin, and flavoprotein. Mandelonitrile lyase is a cyanogenic enzyme. Applications: Mandelonitrile lyase from almonds has been used in a study to assess the apoplastic antioxidant system in prunus. it has also been used in a study to investigate screening for new hydroxynitrilases from plants. Group: Enzymes. Synonyms: mandelonitrile lyase; EC 4.1.2.10; (R)-oxynit. Enzyme Commission Number: EC 4.1.2.10. CAS No. 9024-43-5. PhaMDL. Activity: 80-240 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 50 mM imidazole, 2.8 M (NH4)2SO4, pH 6.0. Source: Almonds. mandelonitrile lyase; EC 4.1.2.10; (R)-oxynitrilase; oxynitrilase; D-oxynitrilase; D-α-hydroxynitrile lyase; mandelonitrile benzaldehyde-lyase; PaHNL; AtHNL; PhaMDL; (R)-HNL; (R)-PeHNL; (R)-hydroxynitrile lyase; R-selective hydroxynitrile lyase; R-selective HNL; (R)-(+)-mandelonitrile lyase; 9024-43-5. Cat No: NATE-0557. | |
| Native Baker's yeast (S. cerevisiae) Pyruvate Decarboxylase | Pyruvate decarboxylase (PDC) is a homotetrameric enzyme that catalyses the decarboxylation of pyruvic acid to acetaldehyde and carbon dioxide in the cytoplasm. Pyruvate decarboxylase depends on cofactors thiamine pyrophosphate (TPP) and magnesium. PDC contains a β-α-β structure, yielding parallel β-sheets. Applications: Pyruvate decarboxylase (pdc) is used to study residues involved in thiamine pyrophosphate (tpp) binding. it is used to study the regulation of fermentation pathways in plant species. Group: Enzymes. Synonyms: Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Enzyme Commission Number: EC 4.1.1.1. CAS No. 9001-4-1. PDC. Activity: 5.0-20.0 units/mg protein (biuret). Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 3.2 M (NH4)2SO4 pH 6.5, stabilized with 5% glycerol, 5 mM potassium phosphate, 1 mM magnesium acetate, 0.5 mM EDTA, and 25 μM c ocarboxylase. Source: Baker's yeast (S. cerevisiae). Pyruvate decarboxylase; EC 4.1.1.1; α-carboxylase (ambiguous); pyruvic decarboxylase; α-ketoacid carboxylase; 2-oxo-acid carboxy-lyase; 9001-04-1; 2-Oxo-acid carboxy-lyase; PDC. Cat No: NATE-0510. | |
| Native Bovine L-Glutamic Dehydrogenase | L-glutamic dehydrogenase catalyzes the conversion of glutamate to α-ketoglutarate. Mammalian forms of this enzyme, including this bovine form, can use either NADP (H) or NAD (H) as coenzymes. L-glutamic dehydrogenase plays a unique role in mammalian metabolism. The reverse reaction catalyzed by this enzyme is the only pathway by which ammonia can become bound to the α-carbon atom of an α-carboxylic acid and thus, is the only source of de novo amino acid synthesis in mammalian species. Group: Enzymes. Synonyms: glutamic dehydrogenase; glutamate dehydrogenase [NAD (P)]; 9029-12-3; glutamate dehydrogenase [NAD (P)+]; EC 1.4.1.3; L-GLDH; L-Glutamate:NAD[P]+ Oxidoreductase (deaminating). Enzyme Commission Number: EC 1.4.1.3. CAS No. 9029-12-3. GLDH. Activity: Type I, > 40 units/mg protein; Type II, > 20 units/mg protein; Type III, > 35 units/mg protein. Storage: 2-8°C. Form: Type I, ammonium sulfate suspension, Suspension in 2.0 M (NH4)2SO4 solution; Type II, lyophilized powder, Contains primarily Citrate buffer salt; Type III, aqueous glycerol solution, Solution in 50% glycerol, pH 7.3. Source: Bovine liver. Species: Bovine. glutamic dehydrogenase; glutamate dehydrogenase [NAD (P)]; 9029-12-3; glutamate dehydrogenase [NAD (P)+]; EC 1.4.1.3; L-GLDH; L-Glutamate:NAD[P]+ Oxidoreductase (deaminating). Cat No: NATE-0392. | |
| Native Corn Phospho (enol)pyruvate Carboxylase | Phospho (enol)pyruvate carboxylase is a ubiquitous, highly regulated oligomeric, cytosolic enzyme in plants. Phospho (enol)pyruvate Carboxylase from corn was found to be highly susceptible to trypsin digestion. Phospho (enol)pyruvate carboxylase is a ubiquitous, highly regulated oligomeric, cytosolic enzyme in plants. Applications: Phospho (enol)pyruvate carboxylase has been used in a study to assess activity of carbon metabolism enzymes in wheat plants treated with kartolin-4 and exposed to water stress. it has also been used in a study to investigate the specific density of leaf as a characteristic of the photosynthetic apparatus. Group: Enzymes. Synonyms: phosphopyruvate (phosphate) carboxylase; PEP carboxylase; phosphoenolpyruvic carboxylase; PEPC; PEPCase; phosphate:oxaloacetate carboxy-lyase (phosphorylating); EC 4.. Enzyme Commission Number: EC 4.1.1.31. CAS No. 9067-77-0. PEPC. Activity: > 1 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension; Suspension in 2.4 M (NH4)2SO4 solution containing 10 mM phosphate buffer, pH 7.0, 1 mM biotin, 5 mM dithiothreitol and 1 mM phenylmethylsulfonyl fluoride. Source: Corn. phosphopyruvate (phosphate) carboxylase; PEP carboxylase; phosphoenolpyruvic carboxylase; PEPC; PEPCase; phosphate:oxaloacetate carboxy-lyase (phosphorylating); EC 4.1.1.31; 9067-77-0. Cat No: NATE-0543. | |
| Native Escherichia coli Penicillin Amidase | The biosynthesis of Penicillin amidase in E. coli by hydrophobic protein chromatography is an inducible reaction which is regulated by metabolized carbon source (e.g. polyols, carboxylic acid etc.). It is also influenced by catabolite repression. It catalyzes the formation of amide bonds through an acyl-enzyme intermediate. Penicillin amidase is a periplasmic 80k heterodimer with a and b chains (209 and 566 amino acids, respectively). it is widely distributed among microorganisms, including bacteria, yeast and filamentous fungi. among all the sources, the enzyme produced by e. coli is most well-characterized and common for industrial application. Applications: Penicillin...; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase; EC 3.5.1.11; 9014-06-6. Enzyme Commission Number: EC 3.5.1.11. CAS No. 9014-6-6. Penicillin Amidase. Mole weight: Mr ~70 kDa. Activity: Type I, 5-10 units/mg protein; Type II, > 10 units/mg protein (E1%/280). Storage: 2-8°C. Form: Type II, ammonium sulfate suspension, Suspension in 0.1 M phosphate, pH 7.5 and 3 M ammonium sulfate. Source: Escherichia coli. penicillin amidase; penicillin acylase; benzylpenicillin acylase; novozym 217; semacylase; α-acylamino-β-lactam acylhydrolase; ampicillin acylase; EC 3.5.1.11; 9014-06-6. Cat No: NATE-0541. | |
| Pectate Lyase from Caulobacter crescentus, Recombinant | Pectate lyase (EC 4.2.2.2) is an enzyme involved in the maceration and soft rotting of plant tissue. Pectate lyase is responsible for the eliminative cleavage of pectate, yielding oligosaccharides with 4-deoxy-α-D-mann-4-enuronosyl groups at their non-reducing ends. The protein is maximally expressed late in pollen development. It has been suggested that the pollen expression of pectate lyase genes might relate to a requirement for pectin degradation during pollen tube growth. This enzyme belongs to the family of lyases, specifically those carbon-oxygen lyases acting on polysaccharides. Group: Enzymes. Synonyms: (1->4)-alpha-D-galacturonan lyase; polygalactur...se. Mole weight: 58857.2 Da. Activity: 283 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Caulobacter crescentus CB15. (1->4)-alpha-D-galacturonan lyase; polygalacturonic transeliminase; pectic acid transeliminase; polygalacturonate lyase; endopectin methyltranseliminase; pectate transeliminase; endogalacturonate transeliminase; pectic acid lyase; pectic lyase; alpha-1,4-D-endopolygalacturonic acid lyase; PGA lyase; PPase-N; endo-alpha-1,4-polygalacturonic acid lyase; polygalacturonic acid lyase; pectin trans-eliminase; Polygalacturonic acid trans-eliminase; Pectate lyase; EC 4.2.2.2. Cat No: NATE-1222. | |
| Pectate Lyase from Clostridium acetobutylicum, Recombinant | Pectate lyase (EC 4.2.2.2) is an enzyme involved in the maceration and soft rotting of plant tissue. Pectate lyase is responsible for the eliminative cleavage of pectate, yielding oligosaccharides with 4-deoxy-α-D-mann-4-enuronosyl groups at their non-reducing ends. The protein is maximally expressed late in pollen development. It has been suggested that the pollen expression of pectate lyase genes might relate to a requirement for pectin degradation during pollen tube growth. This enzyme belongs to the family of lyases, specifically those carbon-oxygen lyases acting on polysaccharides. Group: Enzymes. Synonyms: (1->4)-alpha-D-galacturonan lyase; polygalact...eight: 26628.7 Da. Activity: 3.2 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Clostridium acetobutylicum ATCC 824. (1->4)-alpha-D-galacturonan lyase; polygalacturonic transeliminase; pectic acid transeliminase; polygalacturonate lyase; endopectin methyltranseliminase; pectate transeliminase; endogalacturonate transeliminase; pectic acid lyase; pectic lyase; alpha-1,4-D-endopolygalacturonic acid lyase; PGA lyase; PPase-N; endo-alpha-1,4-polygalacturonic acid lyase; polygalacturonic acid lyase; pectin trans-eliminase; Polygalacturonic acid trans-eliminase; Pectate lyase; EC 4.2.2.2. Cat No: NATE-1223. | |
| Tetraethylphosphonium Tetrafluoroborate | Tetraethylphosphonium Tetrafluoroborate is a transition metal salt that is a quaternary ammonium compound. It is used as a catalyst in organic synthesis, specifically for the formation of carbon-carbon bonds. Group: Heterocyclic organic compound. Alternative Names: CTK2F2252; TETRAETHYLPHOSPHONium TETRAFLUOROBORATE; AKOS015832946; TL8004711; TR-022505; TETRAETHYLPHOSPHANIUM TETRAFLUOROBORATE; T1747. CAS No. 665-49-6. Molecular formula: C8H20BF4P. Mole weight: 234.02. IUPACName: tetraethylphosphanium; tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.CC[P+](CC)(CC)CC. Catalog: ACM665496. | |
| Tetramethylammonium hydroxide pentahydrate | Tetramethylammonium hydroxide pentahydrate is a clathrate hydrate, which shows high proton conductivity. It can readily uptake carbon dioxide. It is a promising candidate for energy devices, gas separation, and gas storage applications. age under Argon! Group: Ammonium salts. Alternative Names: TMAH Pentahydrate. CAS No. 10424-65-4. Molecular formula: C4H23NO6. Mole weight: 181.23. Purity: ≥97%. IUPACName: tetramethylazanium; hydroxide; pentahydrate. Catalog: ACM10424654-1. | |
| Zinc Stannate | Zinc Hydroxystannate and Zinc Stannate are active smoke suppressants as well as flameretardants. Their superior performance is because of their dual phase mechanism. In addition to exhibiting vapor phase action, similar to Antimony Trioxide, they also exhibit condensed phase action during which they act as excellent char promoters. The condensed phase action of Zinc Hydroxystannate and Zinc Stannate enhances the formation of a thermally stable carbonaceous layer at the expense of aromatic, volatile and flammable products. These products exhibit synergy with Zinc Borate, Ammonium Octamolybdate and Antimony Trioxide. Uses: Zinc hydroxystannate and zinc stannate are effective in halogen free and halogen containing systems. although generally, there is little difference in the effectiveness of zinc hydroxystannate and zinc stannate, the latter is the preferred additive for polymers that are processed at temperatures above 200oc. Group: Heterocyclic organic compound. Alternative Names: ZnSnO3. CAS No. 12036-37-2. Molecular formula: ZnSnO3. Mole weight: 232.06. Appearance: White powder. Density: g/cm³. Catalog: ACM12036372. | |
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