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| Product | Description | |
|---|---|---|
| Ammonium ionophore I | function tested, ?95.0% (Nonactin, HPLC). Group: Ionophores potentiometric for ise. |  |
| Ammonium Ion Selective Electrode Solutions | Ammonium Ion Selective Electrode Solutions. Group: Electrolytes. |  |
| Ammonium Ion Selective Electrode Solutions | We offer the products in four grades: ISA; Fill Solution; 0.1 M Standard; 1000ppm Standard. Group: Ion selective electrode solutions. Alternative Names: Ammonium ion electrode solution. | |
| Ammonium ion solution for ISE | 0.1 M NH4+, analytical standard (for ion-selective electrodes). Group: Ion standard solutions for ise. | |
| BENZYLTRIMETHYLAMMONIUM CHLORIDE, 60%AQUEOUS SOLUTION | BENZYLTRIMETHYLAMMONIUM CHLORIDE, 60%AQUEOUS SOLUTION. Uses: Solvent for cellulose, gelling inhibitor in polyester resins, intermediate. Additional or Alternative Names: CAS-56-93-9; F8880-1007; ACMC-209lv0; Tmbac; BCP24461; EC 200-300-3; ST51046799; benzyltrimethyl-ammonium chloride; AN-23571; Tox21_303260. Product Category: Ammonium Ionic Liquids. CAS No. 56-93-9. Molecular formula: C10H16ClN. Mole weight: 185.695g/mol. IUPACName: benzyl(trimethyl)azanium;chloride. Canonical SMILES: C[N+](C)(C)CC1=CC=CC=C1.[Cl-]. Density: 1.07 at 68 ° F (USCG, 1999);1.07 @ 20 deg C/20 deg C. ECNumber: 200-300-3. Product ID: ACM56939. Alfa Chemistry ISO 9001:2015 Certified. |  |
| Photochromic Ion Channel Blocker, QAQ (2, 2- ( (diazene-1, 2-diylbis (4, 1-phenylene))bis (azanediyl))bis (N, N, N-triethyl-2-oxoethanaminium) formate, Quaternary Ammonium-Azobenzene-Quaternary Ammonium) | A membrane-impermeant Na+, K+, and Ca2+ channel blocker that is structurally composed of two azo-linked QX-314 type quaternary amines. Both QX-314 and QAQ are shown to selectively target excitability of nociceptor neurons via TRPV1-dependent cellular uptake. Unlike QX-314, the channel blocking activity of QAQ can be quickly switched on and off via optical cis-to-trans (500nM) and trans-to-cis (320nM) isomerization. Its efficacy as a pain-selective, photochromic anesthetic has been demonstrated in rats in vivo. QAQ cellular uptake can also be achieved by ATP-activated P2X7 receptor. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. |  Worldwide |
| Tetrabutylammonium (fluoride) (solution),1M in THF | Tetrabutylammonium fluoride is an organic compound containing both ammonium and fluorine functional groups. It is commonly used as a reagent in various chemical synthesis applications, especially as a source of fluoride ions for nucleophilic reactions. Tetrabutylammonium fluoride has several properties that make it suitable for these applications, including its high solubility in polar solvents and its ability to selectively activate certain chemical bonds. In addition, it can be used as a catalyst for organic reactions and as an electrolyte for batteries. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: TBAF. CAS No. 429-41-4. Pack Sizes: 500 mL. Product ID: HY-Y0971. |  |
| TETRAMETHYLAMMONIUM HYDROXIDE, SOLUTION1.0 Mol/L in WATER, REAGENT (ACS) | TETRAMETHYLAMMONIUM HYDROXIDE, SOLUTION1.0 Mol/L in WATER, REAGENT (ACS). Uses: Industry application role/benefit organic silicon production of dimethyl silicone oil, organic silicon resin, silicon rubber, etc. catalyst/removed easily; no pollution to the products chemical analysis polarography experiment polarographic reagent thermochemolysis to study fungal degradation of wood analytical reagent chemical purification removal of metal elements as. Additional or Alternative Names: Tetramethylammonium hydroxide solution, ~25% in H2O; tetra methyl ammonium hydroxide; 75-59-2; Tetrametiloamonio hydroxido; Tetramethylammonium hydroxide solution, 25 wt. % in methanol; Tetrametanoamonio hydroxido; A838458; DB-050413; tetramethylammoniumhydroxide; AC1Q29QX. Product Category: Ammonium Ionic Liquids. CAS No. 75-59-2. Molecular formula: C4H13NO. Mole weight: 91.154g/mol. IUPACName: tetramethylazanium;hydroxide. Canonical SMILES: C[N+](C)(C)C.[OH-]. Density: Specific gravity of solution approximately 1.00 at 24 deg C/4 deg C. ECNumber: 200-882-9. Product ID: ACM75592. Alfa Chemistry ISO 9001:2015 Certified. | |
| TETRAPROPYLAMMONIUM HYDROXIDE, 1 MAQUEOUS SOLUTION | TETRAPROPYLAMMONIUM HYDROXIDE, 1 MAQUEOUS SOLUTION. Uses: Designed for use in research and industrial production. Additional or Alternative Names: UNII-T686LUY7NK; EINECS 224-800-6; T1565; DB-050401; FT-0635328; Tetrapropyl ammonium hydroxide solution in Methanol; N,N,N-TRIPROPYL-1-PROPANAMINIUMHYDROXIDE; Tetra-n-propylammonium hydroxide, 40% w/w aqueous solution; N,N,N-Tripropyl-1-propanaminium hydroxide; AK106159. Product Category: Ammonium Ionic Liquids. CAS No. 4499-86-9. Molecular formula: C12H29NO. Mole weight: 203.37g/mol. IUPACName: tetrapropylazanium;hydroxide. Canonical SMILES: CCC[N+](CCC)(CCC)CCC.[OH-]. ECNumber: 224-800-6. Product ID: ACM4499869. Alfa Chemistry ISO 9001:2015 Certified. | |
| Type Y molecular sieve, ammonium ion, powder | DryPowder; DryPowder, PelletsLargeCrystals; OtherSolid. Group: Molecular sieve. CAS No. 1318-02-1. Product ID: dioxosilane; oxo(oxoalumanyloxy)alumane. Molecular formula: 162.05g/mol. Mole weight: Al2O5Si. O=[Al]O[Al]=O.O=[Si]=O. InChI=1S/2Al.O2Si.3O/c;;1-3-2;; : HNPSIPDUKPIQMN-UHFFFAOYSA-N. | |
| 1,3-Diethoxyimidazolium hexafluorophosphate | 1,3-Diethoxyimidazolium hexafluorophosphate can be prepared by reacting 1-hydroxyimidazole-3-oxide with diethyl sulfate and subsequently with ammonium hexafluorophosphate. It may be used in the preparation of 1,3-diethoxyimidazolium bis(trifluoromethanesulfonyl)imide via ion metathesis with lithium bis(trifluoromethanesulfonyl)imide. Group: Electrolytes. Alternative Names: (OEt)2Im-PF6. CAS No. 951020-87-4. Product ID: 1,3-diethoxyimidazol-1-ium; hexafluorophosphate. Molecular formula: 302.14999999999998. Mole weight: C7H13F6N2O2P. CCON1C=C[N+](=C1)OCC. F[P-](F)(F)(F)(F)F. 1S/C7H13N2O2. F6P/c1-3-10-8-5-6-9(7-8)11-4-2; 1-7(2, 3, 4, 5)6/h5-7H, 3-4H2, 1-2H3; /q+1; -1. OCMLXXOSZWGVIL-UHFFFAOYSA-N. ≥97%(H-NMR). | |
| 1,4-Dihydro-1-(5-methoxy-1H-benzimidazol-2-yl)-3,5-dimethyl-4-oxo-2-pyridinecarboxylic Acid Ammonium Salt | 1,4-Dihydro-1-(5-methoxy-1H-benzimidazol-2-yl)-3,5-dimethyl-4-oxo-2-pyridinecarboxylic Acid Ammonium Salt is an impurity of Omeprazole. Omeprazole is a proton pump inhibitor used in the treatment of dyspepsia. It binds to the proton pump hydrogen-potassium adenosine triphosphatase (H+/K+ ATPase) and inhibits its activity and the parietal cell secretion of H+ ions into the gastric lumen. Synonyms: OMP-A Ammonium Salt. CAS No. 2227107-89-1. Molecular formula: C16H18N4O4. Mole weight: 330.34. |  |
| 1-Allyl-1-methylpyrrolidinium Bis (trifluoromethane sulfonyl) imide | 1-Allyl-1-methylpyrrolidinium Bis (trifluoromethane sulfonyl) imide is used in the electrochemical characterizations of cyclic ammonium based ionic liquids with allyl substituents. Group: Biochemicals. Grades: Highly Purified. CAS No. 1059624-23-5. Pack Sizes: 250mg, 500mg. Molecular Formula: C8H16N; (C2F6NO4S2), Molecular Weight: 126.2228015. US Biological Life Sciences. | Worldwide |
| 1-Allyl-1-methylpyrrolidinium Bis(trifluoromethanesulfonyl)imide | 1-Allyl-1-methylpyrrolidinium Bis(trifluoromethanesulfonyl)imide. Uses: 1-allyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide is used in the electrochemical characterizations of cyclic ammonium-based ionic liquids with allyl substituents. Group: Battery materials. CAS No. 1059624-23-5. Product ID: bis(trifluoromethylsulfonyl)azanide; 1-methyl-1-prop-2-enylpyrrolidin-1-ium. Molecular formula: 406.36. Mole weight: C10H16F6N2O4S2. C[N+]1 (CCCC1)CC=C. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. InChI=1S/C8H16N. C2F6NO4S2/c1-3-6-9(2)7-4-5-8-9; 3-1(4, 5)14(10, 11)9-15(12, 13)2(6, 7)8/h3H, 1, 4-8H2, 2H3; /q+1; -1. RXYDHDCXRMFQBC-UHFFFAOYSA-N. >98.0%(T). | |
| Alanine Dehydrogenase from Bacillus cereus, Recombinant | L-Alanine dehydrogenase is an A-stereospecific dehydrogenase that catalyzes the reversible deamination of L-alanine to pyruvate and ammonium. It is important for the geneRation of pyruvate during sporulation. L-Alanine dehydrogenase from Bacillus subtilis has a predominately ordered kinetic mechanism in which NAD binds before L-alanine. Subsequently, ammonia, pyruvate, and NADH are released in that specific order. Optimal pH for the amination reaction is 8.8-9.0, whereas it is 10-10.5 for the deamination reaction. The enzyme is inactivated by divalent metal ions and p-chloromercuribenzoate, mercuric ion being most effective. The inactivation may be reversed by L-or D-cysteine. Group: Enzymes. Synonyms: L-Alanine Dehydrogenase; Alanine dehydrogenase; EC 1.4.1.1; 9029-06-5; AlaDH; NAD+-linked alanine dehydrogenase; alpha-alanine dehydrogenase; NAD+-dependent alanine dehydrogenase; alanine oxidoreductase; NADH-dependent alan. Enzyme Commission Number: EC 1.4.1.1. CAS No. 9029-6-5. AlaDH. Activity: > 350 units/ml. Storage: -20°C. Source: E. coli. Species: Bacillus cereus. L-Alanine Dehydrogenase; Alanine dehydrogenase; EC 1.4.1.1; 9029-06-5; AlaDH; NAD+-linked alanine dehydrogenase; alpha-alanine dehydrogenase; NAD+-dependent alanine dehydrogenase; alanine oxidoreductase; NADH-dependent alanine dehydrogenase. Cat No: NATE-0044. |  |
| ALC-0315 | ALC-0315 is a synthetic cationic lipid (or ionizable lipid). It is a colorless oily material, It has attracted attention as a component of the SARS-CoV-2 vaccine, BNT162b2, from BioNTech and Pfizer. Specifically, it is one of four components that form lipid nanoparticles (LNPs), which encapsulate and protect the otherwise fragile mRNA that is the active ingredient in these drugs. These nanoparticles promote the uptake of therapeutically effective nucleic acids such as oligonucleotides or mRNA both in vitro and in vivo. At physiological pH, ALC-0315 becomes protonated at the nitrogen atom, yielding an ammonium cation that is attracted to the messenger RNA (mRNA), which is anionic. (https://en.wikipedia.org/wiki/ALC-0315). Uses: Designed for use in research and industrial production. Additional or Alternative Names: ALC-0315; ALC 0315; ALC0315. Product Category: Others. Appearance: Colorless to light yellow oily liquid. CAS No. 2036272-55-4. Molecular formula: C48H95NO5. Mole weight: 766.29. Purity: >98%. IUPACName: [(4-Hydroxybutyl)azanediyl]di(hexane-6,1-diyl) bis(2-hexyldecanoate). Canonical SMILES: OCCCCN(CCCCCCOC(C(CCCCCC)CCCCCCCC)=O)CCCCCCOC(C(CCCCCC)CCCCCCCC)=O. Product ID: ACM2036272554-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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 |
| Azone | Azone. CAS No. 59227-89-3. Product ID: PE-0623. Molecular formula: C18H35NO. Mole weight: 281.48. Category: Surfactant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0623; Azone; Surfactant; C18H35NO; 59227-89-3. UNII: NA. Chemical Name: 1-dodecyl azocyclic heptanone 2-ketone. Grade: Pharmceutical Excipients. Administration route: Administration by injection, oral administration, percutaneous administration, vaginal administration. Dosage Form: injection, oral, percutaneous , vaginal preparations. Stability and Storage Conditions: It is stable to heat, but not to acid and base. Other functional components in the formula may separate oil from water. Source and Preparation: It is prepared by the reaction of bromododecane with caprolactam in the presence of strong bases such as metallic sodium and sodium hydroxide, or in the condition of phase transfer catalysis of quaternary ammonium salts. Applications: Azone, as an efficient skin penetration enhancer and a new type of non-ionic surfactant, has been widely applied in the fields of medicine, daily chemical, pesticide, printing and dyeing, chemical fiber, leather and so on. Safety: When the concentration is less than 50%, it has no irritation to the skin. It is a non-toxic, safe and efficient transdermal absorption promoter. |  |
| Benzyltriethylammonium chloride | Benzyltriethylammonium chloride. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Additional or Alternative Names: BTEAC. Product Category: Ammonium Ionic Liquids. CAS No. 56-37-1. Molecular formula: C13H22ClN. Mole weight: 227.77. Purity: 0.99. IUPACName: benzyl(triethyl)azanium;chloride. Canonical SMILES: CC[N+](CC)(CC)CC1=CC=CC=C1.[Cl-]. ECNumber: 200-270-1. Product ID: ACM56371-4. Alfa Chemistry ISO 9001:2015 Certified. | |
| Bephenium hydroxynaphthoate | analytical standard. Group: Additional drugsapi standardspharmaceutical toxicologypharmacopoeial standards. Alternative Names: Debefenium, Alcopar, Naphtamon, Ammonium, benzyldimethyl(2-phenoxyethyl)-, salt with 3-hydroxy-2-naphthoic acid (1:1) (8CI), Bephenium 3-hydroxy-2-naphthoate, Fedal-Uncin, Naphtamone, Benzenemethanaminium, N,N-dimethyl-N-(2-phenoxyethyl)-, salt with 3-hydroxy-2-naphthalenecarboxylic acid (1:1) (9CI), Befeniol, 2-Naphthalenecarboxylic acid, 3-hydroxy-, ion(1-), N,N-dimethyl-N-(2-phenoxyethyl)benzenemethanaminium (9CI), Lecibis, Naftamon, Benzyldimethyl(2-phenoxyethyl)ammonium 3-hydroxy-2-naphthoate (6CI,7CI), Frantin, Alcopara, Befen,Benzenemethanaminium, N,N-dimethyl-N-(2-phenoxyethyl)-, 3-hydroxy-2-naphthalenecarboxylate (1:1), Bephenium hydroxynaphthoate, 2-Naphthoic acid, 3-hydroxy-, ion(1-), benzyldimethyl(2-phenoxyethyl)ammonium (8CI), Nemex, Befenium, Bephenamine hydroxynaphthoate. | |
| Bisoctyl Dimethyl Ammonium Chloride | Bisoctyl Dimethyl Ammonium Chloride is used in the precipitation of silver ions and may be applied to the novel formation if nanoprecipitations using single reverse micellar system. Group: Biochemicals. Alternative Names: AQ 208; Bardac LF; Bardac LF 18; Bardac LF 80; Dioctyldimethyl Ammonium chloride; Dodigen 2617; HOE-S 2617; LF 80; Pentonium DO 50; Querton 28CL; Querton 28CL50; RC 5626; Swanol CA 3080; Dimethyldioctyl Ammonium Chloride; N,N-dimethyl-N-octyl-1-octanaminium Chloride. Grades: Highly Purified. CAS No. 5538-94-3. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Cetrimide | Cetrimide is a white to creamy white, free-flowing powder, with a faint but characteristic odor and a bitter, soapy taste. Synonyms: Bromat; Cetab; Cetavlon; Cetraol; cetrimidum; Lissolamine V; Micol; Morpan CHSA; Morphans; Quammonium; Sucticide. CAS No. 8044-71-1. Product ID: PE-0630. Molecular formula: C17H38BrN. Mole weight: 336.4. Category: Antimicrobial Preservative; Cationic Surfactant; Disinfectant. Product Keywords: Excipients for Liquid Dosage Form; Surfactant Excipients; PE-0630; Cetrimide; Antimicrobial Preservative; Cationic Surfactant; Disinfectant; C17H38BrN; 8044-71-1. UNII: NA. Chemical Name: Cetrimide. Grade: Pharmceutical Excipients. Stability and Storage Conditions: Cetrimide is chemically stable in the dry state, and also in aqueous solution at ambient temperatures. Aqueous solutions may be sterilized by autoclaving. Water containing metal ions and organic matter may reduce the antimicrobial activity of cetrimide. The bulk material should be stored in a well-closed container in a cool, dry place. Source and Preparation: Cetrimide is prepared by the condensation of suitable alkyl bromides and trimethylamine. Applications: Cetrimide is a quaternary ammonium compound that is used in cosmetics and pharmaceutical formulations as an antimicrobial preservative; see Section 10. It may also be used as a cationic surfactant. In eye-drops, it is used as a preservative at a concentration of 0.005% w/v. Therapeuti | |
| Diethylmethyl(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)imide | Diethylmethyl(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)imide is a room temperature ionic liquid (RTIL), which shows high CO2 solubility. It can be used to develop a polymeric gel electrolyte system that shows magnesium ion (Mg2+) mobility. Group: Electrolytes. Alternative Names: N, N-Diethyl-N-methyl-N- (2-methoxyethyl)ammoniumbis (trifluoromethanesulfonyl)imide. CAS No. 464927-84-2. Product ID: bis(trifluoromethylsulfonyl)azanide; diethyl-(2-methoxyethyl)-methylazanium. Molecular formula: 426.4. Mole weight: C10H20F6N2O5S2. CC[N+] (C) (CC)CCOC. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. 1S/C8H20NO.C2F6NO4S2/c1-5-9(3, 6-2)7-8-10-4;3-1(4, 5)14(10, 11)9-15(12, 13)2(6, 7)8/h5-8H2, 1-4H3;/q+1;-1. WUFQNPMBKMKEHN-UHFFFAOYSA-N. ≥98.5%(qNMR). | |
| Dinactin | A member of the macrotetrolide complex produced by a range of streptomyces species; a monovalent cation ionophore with high selectivity for ammonium and potassium; inhibits T-cell proliferation induced by IL-2 and cytokine production at nanomolar levels for IL-2, IL-4, IL-5 and interferon-&gamma. It is also resistant to gram-positive bacteria and mycobacteria. Synonyms: GNF-Pf-90; Antibiotic 170t; NSC63925; 4, 13, 22, 31, 37, 38, 39, 40-Octaoxapentacyclo(32.2.1.17, 10.116, 19.125, 28)tetracontane-3, 12, 21, 30-tetrone, 5,23-diethyl-2,11,14,20,29,32-hexamethyl-(VAN) (8CI). Grades: >95% by HPLC. CAS No. 20261-85-2. Molecular formula: C42H68O12. Mole weight: 764.98. | |
| Dinactin (Antibiotic AKD 1C, Antibiotic S 3466A) | Dinactin is a member of the macrotetrolide complex produced by a range of Streptomyces species. It is a monovalent cation ionophore with high selectivity for ammonium and potassium. Dinactin inhibited T-cell proliferation induced by IL-2 and cytokine production at nanomolar levels for IL-2, IL-4, IL-5 and interferon-g. Dinactin has not previously been available for intensive investigation. Group: Biochemicals. Alternative Names: Antibiotic AKD 1C, Antibiotic S 3466A. Grades: Highly Purified. CAS No. 20261-85-2. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Docosyltrimethylammonium methyl sulphate | This product is white flakes, soluble in water and ethanol, has good compatibility with cationic and non-ionic surfactants, and is stable below 100 °C. Good chemical stability, heat resistance, light resistance, pressure resistance, strong Acid and Alkali resistance. It has excellent thickening, emulsifying and softening properties. This product is used in hair care and shampoo products: conditioners, ointments, shampoos and other hair products softeners. Uses: Designed for use in research and industrial production. Additional or Alternative Names: Docosyltrimethylammonium methyl sulphate;1-Docosanaminium, N,N,N-trimethyl-, methyl sulfate;docosyl-triMethyl-azaniuM;Behenyl trimethyl ammonium methyl sulfate. Product Category: Heterocyclic Organic Compound. CAS No. 81646-13-1. Molecular formula: C26H57NO4S. Mole weight: 479.80008. Purity: 0.96. IUPACName: docosyl(trimethyl)azanium; methyl sulfate. Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C.COS(=O)(=O)[O-]. ECNumber: 279-791-1. Product ID: ACM81646131. Alfa Chemistry ISO 9001:2015 Certified. Categories: Behentrimonium methosulfate. | |
| Dodecyltrimethylammonium bromide | Dodecyltrimethylammonium bromide. Uses: Dodecyltrimethylammonium bromide is a quaternary ammonium salt useful as paint strippers, foaming stabilizers, and bactericidal lotions. Additional or Alternative Names: n-Dodecyl trimethylammonium bromide; N,N,N-trimethyl-1-dodecanaminium bromide. Product Category: Ammonium Ionic Liquids. Appearance: White crystal powder. CAS No. 1119-94-4. Molecular formula: C15H34BrN. Mole weight: 308.34. Purity: 0.99. IUPACName: dodecyl(trimethyl)azanium;bromide. Canonical SMILES: CCCCCCCCCCCC[N+](C)(C)C.[Br-]. ECNumber: 214-290-3. Product ID: ACM1119944. Alfa Chemistry ISO 9001:2015 Certified. | |
| Dodecyltrimethylammonium chloride | Dodecyltrimethylammonium chloride. Uses: Dodecyltrimethylammonium chloride belongs to quaternary ammonium salts,it is useful as paint strippers, foaming stabilizers, and bactericidal lotions. Additional or Alternative Names: Laurtrimonium chloride; Lauryl trimethy. Product Category: Ammonium Ionic Liquids. Appearance: White solid. CAS No. 112-00-5. Molecular formula: C15H34ClN. Mole weight: 263.89. Purity: 0.99. IUPACName: dodecyl(trimethyl)azanium;chloride. Canonical SMILES: CCCCCCCCCCCC[N+](C)(C)C.[Cl-]. ECNumber: 203-927-0. Product ID: ACM112005. Alfa Chemistry ISO 9001:2015 Certified. | |
| 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. | |
| Human Factor XIII | Factor XIII is the zymogenic form of the glutaminyl-peptide g-glutamyl transferase factor XIIIa (fibrinoligase, plasma transglutaminase, fibrin stabilizing factor, E.C. 2.3.2.13). Factor XIII is unique among transamidases in that it is a zymogen in vivo. Factor XIII is found both extracellularly in plasma and intracellularly in platelets, megakaryocytes, monocytes, placenta, uterus, liver and prostrate tissues. Plasma factor XIII is synthesized in the liver and circulates as a tetramer (Mr=320,000), composed of 2 pairs of nonidentical subunits (A2B2). The intra-cellular forms are synthesized in the tissues where they reside as dimers (Mr=146,000) of 2 identical A chains (A2). The A ...nly after the Ca2+ (Kd=10-3M) and fibrin(ogen) (Kd=10-8M) dependent dissociation of the B subunit dimer from the A2' dimer.In the coagulation cascade, factor XIIIa functions to stabilize the fibrin clot by crosslinking the a and g-chains of fibrin. Other proteins known to be substrates for Factor XIIIa which may be hemostatically important include fibronectin, α2-antiplasmin, collagen, factor V, von Willebrand Factor and thrombospondin.Factor XIII is purified from fresh frozen human plasma by a modification of the procedures described by Folke and Lorand involving barium citrate, ammonium sulfate and glycine precipitations, ion exchange chromatography and gel filtration. Factor | |
| Maduramicin Ammonium | Maduramcin ammonium is prepared from maduramicin by taking advantage of the acidic carboxylic acid which ionises and readily forms the salt in ammonium hydroxide solutions. The ammonium salt is the preferred formulation in animals to prevent coccidiosis. It is a polyether antibiotic chemically related to the Lonomycins. Uses: Anti-bacterial agents. Synonyms: Cygro; Maduramicin α, Monoammonium Salt; Prinicin Ammonium; CL 259971; Lonomycin A, 23,27-didemethoxy-2,6,22-tridemethyl-11-O-demethyl-22-((2,6-dideoxy-3,4-di-O-methyl-beta-L-arabino-hexopyranosyl)oxy)-6-methoxy-, monoammonium salt, (3R,4S,5S,6R,7S,22S)-. Grades: >95%. CAS No. 84878-61-5. Molecular formula: C47H83O17N. Mole weight: 934.16. | |
| Methyltri-n-octylammonium Chloride | Methyltri-n-octylammonium Chloride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 102055-EP2275469A1; Aliquat 336; UNII-07Q8S2MJ6A; N-Methyl-N,N-dioctyl-1-octanaminium chloride; EINECS 225-896-2; methyl(trioctyl)azanium chloride; 93810-EP2305625A1; methyl trioctylammonium chloride; XKBGEWXEAPTVCK-UHFFFAOYSA-M; NSC 61369. Product Category: Ammonium Ionic Liquids. CAS No. 5137-55-3. Molecular formula: C25H54ClN. Mole weight: 404.164g/mol. IUPACName: methyl(trioctyl)azanium;chloride. Canonical SMILES: CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC.[Cl-]. ECNumber: 225-896-2. Product ID: ACM5137553. Alfa Chemistry ISO 9001:2015 Certified. Categories: Methyltrioctylammonium chloride. | |
| MOLECULAR SIEVE | MOLECULAR SIEVE. Synonyms: SODIUM ALUMINIUM SILICATE;SODIUM ALUMINOSILICATE;SODIUM ALUMINUM SILICATE;P 820 A;MOLECULAR SIEVE, TYPE Y, AMMONIUM ION;MOLECULAR SIEVE, TYPE 5A, 8-12 MESH BEADS;MOLECULAR SIEVE, TYPE 5A;aluminosilicicacid,sodiumsalt. CAS No. 1344-00-9. Product ID: CDF4-0007. Molecular formula: AlNaO6Si2. Category: Anticaking Agents. Product Keywords: Food Ingredients; Anticaking Agents; MOLECULAR SIEVE; CDF4-0007; 1344-00-9; AlNaO6Si2; 215-684-8; 1344-00-9. Purity: 0.99. EC Number: 215-684-8. Physical State: Powder. Density: 2.05[at 20°C]. Product Description: Fine white powder. Many ordinary rocks (feldspars) are aluminosilicates. Aluminosilicates with more open three-dimensional structures than the feldspars are called zeolites. The openings in zeolites appear as polyhedral cavities connected by tunnels. Zeolites act as catalysts by absorbing small molecules in their interior cavities and holding them in proximity so that reaction among them occurs sooner. | |
| Monactin | A member of the macrotetrolide complex produced by a range of streptomyces species; a monovalent cation ionophore with high selectivity for ammonium and potassium; inhibits T-cell proliferation induced by IL-2 and cytokine production at nanomolar levels for IL-2, IL-4, IL-5 and IFN-&gamma. It is also resistant to gram-positive bacteria and mycobacteria. Synonyms: 4, 13, 22, 31, 37, 38, 39, 40-Octaoxapentacyclo[32.2.1.17, 10.116, 19.125, 28]tetracontane-3, 12, 21, 30-tetrone, 5-ethyl-2, 11, 14, 20, 23, 29, 32-heptamethyl-, (1R, 2R, 5R, 7R, 10S, 11S, 14S, 16S, 19R, 20R, 23R, 25R, 28S, 29S, 32S, 34S)-; Akd-1B. Grades: >95% by HPLC. CAS No. 7182-54-9. Molecular formula: C41H66O12. Mole weight: 750.95. | |
| Monactin (5-demethyl-5-ethylnonactin, Antibiotic AKD 1B) | Monactin is a member of the macrotetrolide complex produced by a range of Streptomyces species. Unlike nonactin, monactin has not previously been available for intensive investigation. Early literature reported that the related dinactin is a monovalent cation ionophore with high selectivity for ammonium and potassium. Monactin inhibits T-cell proliferation induced by IL-2 and cytokine production at nanomolar levels for IL-2, IL-4, IL-5 and interferon-gamma. Group: Biochemicals. Alternative Names: 5-demethyl-5-ethylnonactin, Antibiotic AKD 1B. Grades: Highly Purified. CAS No. 7182-54-9. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Native Bacillus subtilis L-Alanine Dehydrogenase | L-Alanine dehydrogenase is an A-stereospecific dehydrogenase that catalyzes the reversible deamination of L-alanine to pyruvate and ammonium. It is important for the geneRation of pyruvate during sporulation. L-Alanine dehydrogenase from Bacillus subtilis has a predominately ordered kinetic mechanism in which NAD binds before L-alanine. Subsequently, ammonia, pyruvate, and NADH are released in that specific order. Optimal pH for the amination reaction is 8.8-9.0, whereas it is 10-10.5 for the deamination reaction. The enzyme is inactivated by divalent metal ions and p-chloromercuribenzoate, mercuric ion being most effective. The inactivation may be reversed by L-or D-...genase. Enzyme Commission Number: EC 1.4.1.1. CAS No. 9029-6-5. AlaDH. Activity: Type I, ~30 units/mg protein (Lowry); Type II, > 20 units/mg protein (Lowry). Storage: -20°C. Form: Type I, buffered aqueous glycerol solution, Solution in 50% glycerol containing 10 mM potassium phosphate buffer, pH 7.7; Type II, ammonium sulfate suspension, Suspension in 2.4 M (NH4)2SO4 solution, pH 7.0. Source: Bacillus subtilis. L-Alanine Dehydrogenase; Alanine dehydrogenase; EC 1.4.1.1; 9029-06-5; AlaDH; NAD+-linked alanine dehydrogenase; alpha-alanine dehydrogenase; NAD+-dependent alanine dehydrogenase; alanine oxidoreductase; NADH-dependent alanine dehydrogenase. Cat No: NATE-0043. | |
| Nitrate(6CI,7CI,8CI,9CI) | Nitrate(6CI,7CI,8CI,9CI). Uses: Designed for use in research and industrial production. Additional or Alternative Names: NO3;NITROGEN STANDARD;NITRATE SINGLE COMPONENT STANDARD;NITRATE STANDARD;NITRATE;NITRATE, CERTIFIED ANION STANDARD;NITRATE IC STANDARD;NITRATE ION. Product Category: Heterocyclic Organic Compound. Appearance: Crystalline solids. Salts of nitrate, such as ammonium nitrate, potassium nitrate, and sodium nitrate. CAS No. 14797-55-8. Molecular formula: NO3. Mole weight: 62. Density: g/cm³. Product ID: ACM14797558. Alfa Chemistry ISO 9001:2015 Certified. | |
| Nonactin | Nonactin is a macrotetrolide antibiotic and mitochondrial uncoupler with antibacterial, insecticidal, and acaricidal activities. Nonactin acts as an ionophore for monovalent cations, including K + , and NH 4 + , and it can also inhibit the surface expression of endogenous HSP60. In addition, Nonactin can induce apoptosis in β-catenin mutant tumor cells and has anti-tumor activity [1] [2] [3] [4]. Uses: Scientific research. Group: Natural products. Alternative Names: Ammonium ionophore I. CAS No. 6833-84-7. Pack Sizes: 5 mg. Product ID: HY-N6790. | |
| Nonactin | Nonactin is the smallest member of the macrotetrolide complex produced by a range of Streptomyces species. Originally the name, nonactin, reflected the lack of biological activity. The literature is somewhat confusing in this respect, as virtually all sources of nonactin are contaminated with small amounts of the much more active monactin. The BioAustralis nonactin has been purifed to remove traces of other biologically-active macrotetrolides. Like the other macrotetrolides, nonactin is a monovalent cation ionophore with high selectivity for ammonium and potassium. Group: Biochemicals. Grades: Highly Purified. CAS No. 6833-84-7. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Nonactin | The smallest member of the macrotetrolide complex produced by a range of streptomyces species; a monovalent cation ionophore with high selectivity for ammonium and potassium. It is resistant to gram-positive bacteria, mycobacteria and fungi, and it also inhibits L cells. Synonyms: Werramycin-A; NSC 52141; BRN 0076434; 4, 13, 22, 31, 37, 38, 39, 40-Octaoxapentacyclo(32.2.1.17, 10.116, 19.125, 28)tetracontane-3, 12, 21, 30-tetrone, 2,5,11,14,20,23,29,32-octamethyl-(8CI). Grades: >99% by HPLC. CAS No. 6833-84-7. Molecular formula: C40H64O12. Mole weight: 736.93. | |
| Octadearyl dimethyl ammonium chloride | Octadearyl dimethyl ammonium chloride. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Product Category: Ammonium Ionic Liquids. CAS No. 112-03-8. Molecular formula: C21H46N.Cl. Mole weight: 348.05. Purity: 98% min. ECNumber: 203-929-1. Product ID: ACM112038. Alfa Chemistry ISO 9001:2015 Certified. Categories: Trimethylstearylammonium chloride. | |
| Pectin | D-Galacturonic acid is the main component of pectin, but some neutral sugars are also prevalent in pectin. The D-galacturonic acid units are linked together by α(1-4) glycosidic linkages. The polygalacturonic acid is partially esterified with methyl, and the free acid group can be partially or completely neutralized with sodium, potassium or ammonium ions. | |
| Phosphatase from Escherichia coli, Recombinant | A phosphatase is an enzyme that removes a phosphate group from its substrate by hydrolysing phosphoric acid monoesters into a phosphate ion and a molecule with a free hydroxyl group (see dephosphorylation). This action is directly opposite to that of phosphorylases and kinases, which attach phosphate groups to their substrates by using energetic molecules like ATP. A common phosphatase in many organisms is alkaline phosphatase. Another large group of proteins present in archaea, bacteria, and eukaryote exhibits deoxyribonucleotide and ribonucleotide phosphatase or pyrophosphatase activities that catalyse the decomposition of dNTP/NTP into dNDP/NDP and a free phosphate ... phosphatase is collectively called as protein phosphatase, which removes a phosphate group from the phosphorylated amino acid residue of the substrate protein. Protein phosphorylation is a common posttranslational modification of protein catalyzed by protein kinases, and protein phosphatases reverse the effect. Group: Enzymes. Synonyms: HAD2. Enzyme Commission Number: EC 3.1.3.-. Purity: >95 % as judged by SDS-PAGE. Phosphatase. Mole weight: 26827.7 Da. Activity: 1.905 U/mg. Storage: Store at 4°C (shipped at room temperature). Form: Supplied in 3.2 M ammonium sulphate. Source: Escherichia coli str. K-12 substr. MG1655. Phosphatase; HAD2; EC 3.1.3.-. Cat No: NATE-1226. | |
| Phosphomannose Isomerase from Escherichia coli, Recombinant | Phosphomannose Isomerase (PMI) catalyses the interconversion of mannose 6-phosphate (Man-6-P) and fructose 6-phosphate (Fru-6-P), which provides a link between glucose metabolism and mannosylation. Applications: Pmi is used to study cell wall synthesis and energy production. pmi has been used to study how edta and metal ions, such as zn++, co++, fe++, mn++ and cu++., can affect recovery and thermal stability. it may be used to study pmi?s effect on various alginate biosynthetic enzymes such as phosphomannomutase (pmm), gdp-mannose pyrophosphorylase (gmp), and gdp-mannose dehydrogenase (gmd). Group: Enzymes. Synonyms: phosphomannose isomerase; phosphohexomutase; phosphohexoisomerase; mannose phosphate isomerase; phosphomannoisomerase; D-mannose-6-phosphate ketol-isomerase; EC 5.3.1.8; mannos. Enzyme Commission Number: EC 5.3.1.8. CAS No. 9023-88-5. PMI. Activity: > 50 units/mg protein. Storage: 2-8°C. Form: ammonium sulfate suspension; Supplied as a suspension in 3.2 M ammonium sulfate. Source: E. coli. Species: Escherichia coli. phosphomannose isomerase; phosphohexomutase; phosphohexoisomerase; mannose phosphate isomerase; phosphomannoisomerase; D-mannose-6-phosphate ketol-isomerase; EC 5.3.1.8; mannose-6-phosphate isomerase; PMI. Pack: Bottomless glass bottle. Contents are inside inserted fused cone. Cat No: NATE-0599. | |
| Polypyrrole | Polypyrrole (PPy) is a conductive and highly stable polymer, doped with proprietary organic acids. It may be prepared by standard electrochemical technique. PPy may also be prepared by reacting β-napthalene sulfonic acid (NSA) and ammonium peroxo-disulphate in aqueous medium. The charges on the surfaces can be easily modified by doping the polymer during its synthesis.Solubility and conductivity measurements of PPy doped with camphor sulfonic and dodecyl benzene sulfonic acid has been reported. Polypyrrole(PPy) is a π-conjugated conductive polymer that can be electrochemically synthesized and deposited on a variety of surfaces. The deposited PPy can be used in a wide range of sensor based applications due to the following properties: Ion exchange capacity. Electrochromic effects. Redox activity. Corrosion resistant. Catalytic activity. Uses: Conducting polymers may be used in electronics, chemical sensors. ppy can be used in the development of devices including: conductive sensors for quality monitoring blended with nanotubes for supercapacitors nanowire actuators biosensors for drug delivery co2 absorption materials. Group: Bioelectronic materials. Alternative Names: PPy. Pack Sizes: 100 mL in poly bottle. Product ID: 1H-pyrrole. Molecular formula: 67.09g/mol. Mole weight: C4H5N. C1=CNC=C1. InChI=1S/C4H5N/c1-2-4-5-3-1/h1-5H. KAESVJOAVNADME-UHFFFAOYSA-N. | |
| Polypyrrole | Polypyrrole (PPy) is a conductive and highly stable polymer. It may be prepared by a standard electrochemical technique.PPy may also be prepared by reacting ß-napthalene sulfonic acid (NSA) and ammonium peroxo-disulphate in aqueous medium. The charges on the surfaces can be easily modified by doping the polymer during its synthesis. Solubility and conductivity measurements of PPy doped with camphor sulfonic and dodecyl benzene sulfonic acid has been reported.Electrosensitivity and lower oxidation potential of PPy make it potentially useful for drug delivery, chemical sensors, batteries, ion selective electrodes, biosensor and biochemistry research. Uses: Ppy may be used to prepare cobalt based electrocatalyst for anion exchange membrane fuel cells. Group: 3d printing materials bioelectronic materials. Alternative Names: PPy. CAS No. 30604-81-0. Pack Sizes: 10 g in glass bottle. Product ID: 1H-pyrrole. Molecular formula: 67.09g/mol. Mole weight: C4H5N. C1=CNC=C1. 1S/C4H5N/c1-2-4-5-3-1/h1-5H. KAESVJOAVNADME-UHFFFAOYSA-N. | |
| Sodium tetraphenylborate | Sodium tetraphenylborate. Uses: As reagent for determination of potassium, ammonium, rubidium and cesium ions: barnard, buechl, chemist-analyst 48, 44, 49 (1959); montequi, serrano, an. r. acad. farm. 26, 107 (1960). Additional or Alternative Names: Sodium tetraphenylboron; tetraphenyl-borate(1-sodiumsalt; Sodium tetraphenylborate(1-); FC0734; CS-0064837; Jsp002564; ST2419873; NSC5360; sodiumtetraphenylboride(1-); 143-66-8. Product Category: Borate. CAS No. 143-66-8. Molecular formula: C24H20BNa. Mole weight: 342.224g/mol. IUPACName: sodium;tetraphenylboranuide. Canonical SMILES: [B-](C1=CC=CC=C1)(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Na+]. ECNumber: 205-605-5. Product ID: ACM143668. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetrabutylammonium bromide | Tetrabutylammonium bromide is an organic ammonium compound, which is often used in catalytic reactions and separation and purification processes. It has a significant catalytic effect in some organic synthesis reactions, and can be used as a surfactant, stabilizer and antibacterial agent, etc. In addition, in some laboratory studies, this compound has also been used as an ion exchanger, solvent extractant, etc. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: AP 6G; Actiron 43-65; Aliquat 100. CAS No. 1643-19-2. Pack Sizes: 25 g; 50 g; 100 g. Product ID: HY-D0172. | |
| Tetrabutylammonium bromide | Tetrabutylammonium bromide (TBAB) is a quaternary ammonium compound. It is the most widely used phase transfer catalyst. Its interfacial properties have been studied in case of hydroxide initiated reactions. This may be applied in understanding the mechanism of phase transfer reactions. TBAB is reported to decrease retention time and remove peak tailing by acting as an ion pair reagent during the chromatographic analysis of quaternary ammonium compounds. In the molten state TBAB behaves like an ionic liquid which is a promising green alternative to organic solvents in organic synthesis. Its molar heat capacity, entropy and free energy function have been determined. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Group: Battery materials. Alternative Names: TBAB. CAS No. 1643-19-2. Pack Sizes: 25 kg/DRUMS. Product ID: tetrabutylazanium; bromide. Molecular formula: 322.37. Mole weight: C16H36BrN. CCCC[N+](CCCC)(CCCC)CCCC.[Br-]. InChI=1S/C16H36N. BrH/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; /h5-16H2, 1-4H3; 1H/q+1; /p-1. JRMUNVKIHCOMHV-UHFFFAOYSA-M. 99%. | |
| Tetrabutylammonium fluoride | Tetrabutylammonium fluoride. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-Butanaminium, N,N,N-tributyl-, fluoride (1:1). Product Category: Ammonium Ionic Liquids. CAS No. 429-41-4. Molecular formula: C16H36FN. Mole weight: 261.46. Purity: ≥98%. Product ID: ACM429414. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetrabutylammonium heptadecafluorooctanesulfonate | Description Application Tetrabutylammonium heptadecafluorooctanesulfonate [NBu4][(PFOc)SO3] can be used as: A model ionic liquid for the possible replacement of perfluorocarbons, which are used in oxygen therapeutics. A supporting electrolyte in the electropolymerization of 3,4-ethylenedioxythiophene (EDOT) derivatives to obtain superhydrophobic surfaces. Packaging 5 mL in glass bottle Other Notes Ionic liquid. Uses: Tetrabutylammonium heptadecafluorooctanesulfonate is an ionic liquid. Group: Electrolytes. Alternative Names: Heptadecafluorooctane sulfonicacidtetrabutyl Ammonium salt, Perfluorooctane sulfonicacidtetrabutyl Ammonium salt, Tetrabutyl Ammonium perfluorooctane sulfonate. CAS No. 111873-33-7. Product ID: 1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-heptadecafluorooctane-1-sulfonate; tetrabutylazanium. Molecular formula: 741.59. Mole weight: Linear Formula (CH3CH2CH2CH2)4N[CF3(CF2)7SO3]. CCCC[N+] (CCCC) (CCCC)CCCC. C (C (C (C (C (F) (F)S (=O) (=O)[O-]) (F)F) (F)F) (F)F) (C (C (C (F) (F)F) (F)F) (F)F) (F)F. 1S/C16H36N. C8HF17O3S/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; 9-1(10, 3(13, 14)5(17, 18)7(21, 22)23)2(11, 12)4(15, 16)6(19, 20)8(24, 25)29(26, 27)28/h5-16H2, 1-4H3; (H, 26, 27, 28)/q+1; /p-1. MUOQTHSUZGSHGW-UHFFFAOYSA-M. ≥95.0%(H-NMR). | |
| Tetrabutylammonium (hydrogen difluoride) | Tetrabutylammonium (hydrogen difluoride) is a quaternary ammonium salt containing fluoride ions. It is a highly active and effective reagent, often used in organic synthesis reactions, especially for the modification of organic molecules with fluorine atoms. Tetrabutylammonium (hydrogen difluoride) is also used as a catalyst for various chemical reactions such as esterification and transesterification. Additionally, it is used in the production of specialty chemicals such as surfactants and detergents. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 23868-34-0. Pack Sizes: 500 mg; 1 g. Product ID: HY-W036734. | |
| Tetrabutylammonium hydrogensulfate | Tetrabutylammonium hydrosulfate is a quaternary ammonium salt that is commonly used as a phase transfer catalyst, acid catalyst and reagent in various chemical reactions, especially in organic synthesis. Tetrabutylammonium hydrosulfate has unique chemical properties that allow it to facilitate the transfer of ions or molecules from one phase to another, making it an important ingredient in a variety of industrial processes. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: TBAHS-MB. CAS No. 32503-27-8. Pack Sizes: 5 g; 25 g. Product ID: HY-Y1045. | |
| Tetrabutylammonium Hydrogensulfate | Displays antibacterial properties due to the presence of the quaternary amine and the counter ion. Group: Biochemicals. Alternative Names: N,N,N-Tributyl-1-butanaminium Sulfate; Tetrabutyl-ammonium Sulfate; Tetrabutylammonium Hydrogen Sulfate; TBAHS-MB; Tetra-n-butylammonium Hydrogen Sulfate; Tetrabutylammonium Bisulfate; Tetrabutylammonium Hydrosulfate. Grades: Highly Purified. CAS No. 32503-27-8. Pack Sizes: 5g. US Biological Life Sciences. | Worldwide |
| TETRABUTYLAMMONIUM HYDROXIDE0.4 M AQUEOUS, ELECTROMETRIC GRADE | TETRABUTYLAMMONIUM HYDROXIDE0.4 M AQUEOUS, ELECTROMETRIC GRADE. Uses: Designed for use in research and industrial production. Additional or Alternative Names: SCHEMBL21980; Tetra-n-butylammonium hydroxide, 55% w/w aqueous solution; 1-Butanaminium, N,N,N-tributyl-, hydroxide (1:1); EINECS 265-614-5; tetra(n-butyl)ammonium hydroxide; Tetrabutylammonium hydroxide, 0.1N sol. in toluene/methanol for non-aq.titr.; AC1MC3CX; Tetrabutylammonium hydroxide, 1M solution in methanol, AcroSeal(R); Tetrabutylammonium hydroxide, 40 wt.% (1.5M) solution in water; tetra-n-butyl ammonium hydroxide. Product Category: Ammonium Ionic Liquids. CAS No. 2052-49-5. Molecular formula: C16H37NO. Mole weight: 259.478g/mol. IUPACName: tetrabutylazanium;hydroxide. Canonical SMILES: CCCC[N+](CCCC)(CCCC)CCCC.[OH-]. ECNumber: 218-147-6. Product ID: ACM2052495. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetrabutylammonium iodide | Tetrabutylammonium iodide is a quaternary ammonium salt commonly used as a phase transfer catalyst, surfactant, and stabilizer in various chemical reactions, especially in organic synthesis. Tetrabutylammonium iodide has unique chemical properties that facilitate the transfer of ions or molecules from one phase to another, making it an important ingredient in a variety of industrial processes. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Tetra-n-butylammonium iodide; TBAI. CAS No. 311-28-4. Pack Sizes: 10 mM * 1 mL; 25 g; 50 g. Product ID: HY-Y0791. | |
| Tetrabutylammonium methanesulfonate | Tetrabutylammonium methanesulfonate. Uses: Tetrabutylammonium methanesulfonate is a useful ionic liquid. Group: Electrolytes. Alternative Names: Methanesulfonicacidtetrabutyl Ammonium salt. CAS No. 65411-49-6. Product ID: methanesulfonate; tetrabutylazanium. Molecular formula: 337.56. Mole weight: Linear Formula [CH3CH2CH2CH2]4N(CH3SO3). CCCC[N+](CCCC)(CCCC)CCCC. CS(=O)(=O)[O-]. 1S/C16H36N. CH4O3S/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; 1-5(2, 3)4/h5-16H2, 1-4H3; 1H3, (H, 2, 3, 4)/q+1; /p-1. XHYYGJAYKIYARQ-UHFFFAOYSA-M. ≥97.0%(T). | |
| Tetrabutylammonium nitrate | Tetrabutylammonium nitrate. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N,N,N-tributyl-1-butanaminiunitrate. Product Category: Ammonium Ionic Liquids. CAS No. 1941-27-1. Molecular formula: C16H36N2O3. Mole weight: 304.47. Purity: 0.98. IUPACName: tetrabutylazanium;nitrate. Canonical SMILES: CCCC[N+](CCCC)(CCCC)CCCC.[N+](=O)([O-])[O-]. ECNumber: 217-726-0. Product ID: ACM1941271. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetrabutylammonium nonafluorobutanesulfonate | Tetrabutylammonium nonafluorobutanesulfonate is a fluorinated ionic liquid (FIL). Its solid-fluid transition and nanoscale structuring have been studied using differential scanning calorimetry (DSC), rheology techniques and molecular dynamic simulations. Packaging 5 g in poly bottle Other Notes Ionic liquid. Uses: Tetrabutylammonium nonafluorobutanesulfonate is an ammonium based ionic liquid. Group: Electrolytes. Alternative Names: Perfluorobutane sulfonicacidtetrabutyl Ammonium salt, Tetrabutyl Ammonium perfluorobutane sulfonate. CAS No. 108427-52-7. Product ID: 1,1,2,2,3,3,4,4,4-nonafluorobutane-1-sulfonate; tetrabutylazanium. Molecular formula: 541.55999999999995. Mole weight: Linear Formula (CH3CH2CH2CH2)4N(CF3CF2CF2CF2SO3). CCCC[N+] (CCCC) (CCCC)CCCC. C (C (C (F) (F)S (=O) (=O)[O-]) (F)F) (C (F) (F)F) (F)F. 1S/C16H36N. C4HF9O3S/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; 5-1(6, 3(9, 10)11)2(7, 8)4(12, 13)17(14, 15)16/h5-16H2, 1-4H3; (H, 14, 15, 16)/q+1; /p-1. VECGWISURDHBJL-UHFFFAOYSA-M. ≥98.0%. | |
| Tetrabutylammonium perchlorate | Tetrabutylammonium perchlorate is an organic compound containing ammonium ions and perchlorate ions. It is commonly used as an electrolyte in electrochemistry and as a source of perchlorate anion in analytical chemistry. Tetrabutylammonium perchlorate has a variety of applications in the production of batteries, fuel cells and electronic components due to its high ionic conductivity and stability under extreme conditions. In addition, it can be used as a reference standard in analytical methods such as ion chromatography. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Tetra-n-butylammonium perchlorate. CAS No. 1923-70-2. Pack Sizes: 5 g; 25 g. Product ID: HY-W127680. | |
| Tetrabutylphosphonium methanesulfonate | Ionic liquid at ambient temperature; more stable than the corresponding ammonium salt; Stationary phase for GC having unique selectivities. Uses: Cas: 98342-59-7, mf: c16h36p ch3so3, mw: 354.53. Group: Electrolytes. Alternative Names: Methane sulfonicacidtetrabutylphosphonium salt. CAS No. 98342-59-7. Product ID: methanesulfonate; tetrabutylphosphanium. Molecular formula: 354.53. Mole weight: Linear Formula (CH3CH2CH2CH2)4P(CH3SO3). CCCC[P+](CCCC)(CCCC)CCCC. CS(=O)(=O)[O-]. 1S/C16H36P. CH4O3S/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; 1-5(2, 3)4/h5-16H2, 1-4H3; 1H3, (H, 2, 3, 4)/q+1; /p-1. DSQCNXSPLHDLED-UHFFFAOYSA-M. ≥98.0%(NT). | |
| Tetraethylammonium bromide | Tetraethylammonium bromide is a quaternary ammonium salt consisting of a positively charged tetraethylammonium cation and a negatively charged bromide anion. This compound is commonly used as a phase transfer catalyst in organic chemical reactions, facilitating the transfer of reactants between immiscible phases. It can also be used as a reagent for the synthesis of various organic compounds, an electrolyte in electrochemical experiments, and a source of tetraethylammonium ions in biochemical and pharmacological research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: TEA bromide. CAS No. 71-91-0. Pack Sizes: 25 g. Product ID: HY-W014408. | |
| Tetraethylammonium bromide | Tetraethylammonium bromide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: N,N,N-Triethylethanaminium bromide. Product Category: Ammonium Ionic Liquids. CAS No. 71-91-0. Molecular formula: C8H20BrN. Mole weight: 210.16. Purity: 0.99. IUPACName: tetraethylazanium;bromide. Canonical SMILES: CC[N+](CC)(CC)CC.[Br-]. ECNumber: 200-769-4. Product ID: ACM71910-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetraethylammonium chloride | Tetraethylammonium chloride. Uses: Quarternary ammonium salts;ammonium chlorides (quaternary);ammonium-based ionic liquids compounds;ion channels;ammonium-based ionic liquids salt. Additional or Alternative Names: N,N,N,N-Tetraethylammoniumchloride. Product Category: Ammonium Ionic Liquids. Appearance: Colorless liquid. CAS No. 56-34-8. Molecular formula: C8H20ClN. Mole weight: 165.7. Purity: 0.99. IUPACName: tetraethylazanium;chloride. Canonical SMILES: CC[N+](CC)(CC)CC.[Cl-]. ECNumber: 200-267-5. Product ID: ACM56348-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetraethylammonium hexafluorophosphate | Tetraethylammonium hexafluorophosphate. Uses: Maintenance of fluoride atmospheres; preparation of bactericides and fungicides. Additional or Alternative Names: Tetraethylammoniumhexafluorophosphate; n,n,n-triethylethanaminium hexafluorophosphate; AC1L1U1K; ACM429072; Tetraethylammonium hexafluorophosphate, for electrochemical analysis, >=99.0%; AI3-16950; 429-07-2; Tetraethylammonium Hexafluorophosphate(V); Ethanaminium,N,N-triethyl-, hexafluorophosphate(1-); Ethanaminium, N,N,N-triethyl-, hexafluorophosphate(1-) (9CI). Product Category: Ammonium Ionic Liquids. CAS No. 429-07-2. Molecular formula: C8H20F6NP. Mole weight: 275.22. Purity: ≥98%. IUPACName: tetraethylazanium;hexafluorophosphate. Canonical SMILES: CC[N+](CC)(CC)CC.F[P-](F)(F)(F)(F)F. ECNumber: 207-056-7. Product ID: ACM429072. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetraethylammonium hydrogensulfate | Tetraethylammonium hydrogensulfate. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Additional or Alternative Names: N-[4-(9-fluorenylidenemethyl)phenyl]-N-methylnitrous amide. Product Category: Ammonium Ionic Liquids. CAS No. 16873-13-5. Molecular formula: C8H21NO4S. Mole weight: 227.32. Purity: ≥98%. ECNumber: 240-899-9. Product ID: ACM16873135. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetraethylammonium nitrate | Tetraethylammonium nitrate. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Additional or Alternative Names: Ethanaminium, N,N,N-triethyl-, nitrate. Product Category: Ammonium Ionic Liquids. CAS No. 1941-26-0. Molecular formula: C8H20N2O3. Mole weight: 192.26. Purity: ≥98%. IUPACName: tetraethylazanium;nitrate. Canonical SMILES: CC[N+](CC)(CC)CC.[N+](=O)([O-])[O-]. ECNumber: 217-725-5. Product ID: ACM1941260-1. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tetraethylammonium perchlorate | Tetraethylammonium perchlorate is an organic compound containing ammonium ions and perchlorate ions. It is commonly used as an electrolyte in electrochemistry and as a source of perchlorate anion in analytical chemistry. Due to its high ionic conductivity and stability under extreme conditions, tetraethylammonium perchlorate has a variety of applications in the production of batteries, fuel cells and electronic components. In addition, it can be used as a reference standard in analytical methods such as ion chromatography. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: N,N,N-Triethylethanaminium perchlorate. CAS No. 2567-83-1. Pack Sizes: 1 g. Product ID: HY-W127676. | |
| Tetraethylammonium tetrafluoroborate | Tetraethylammonium tetrafluoroborate is a quaternary ammonium salt consisting of a positively charged tetraethylammonium cation and a negatively charged tetrafluoroborate anion. This compound is commonly used as a phase transfer catalyst in organic chemical reactions, facilitating the transfer of reactants between immiscible phases. It can also be used as a reagent for the synthesis of various organic compounds, an electrolyte in electrochemical experiments, and a source of tetraethylammonium ions in biochemical and pharmacological research. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: N,N,N-Triethylethanaminium tetrafluoroborate. CAS No. 429-06-1. Pack Sizes: 5 g; 10 g. Product ID: HY-W014106. | |
| Tetraethylammonium trifluoroacetate | Tetraethylammonium trifluoroacetate. Uses: Designed for use in research and industrial production. Product Category: Ammonium Ionic Liquids. CAS No. 30093-29-9. Molecular formula: C10H20F3NO2. Mole weight: 243.27. Purity: ≥98%. Product ID: ACM30093299. Alfa Chemistry ISO 9001:2015 Certified. | |
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