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| Product | Description | |
|---|---|---|
| 1, 1, 2, 2-Tetra hydroperfluorodecanol | 1, 1, 2, 2-Tetra hydroperfluorodecanol is applied to the formation of a barrier and self-healing coating on zinc metal materials. This compound has also been seen to induce cell death and formation of oxidative or reactive oxygen species in cerebellar granule cells. Group: Biochemicals. Alternative Names: 3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 9, 9, 10, 10, 10-Heptadecafluoro-1-decanol; (Perfluorooctyl) ethanol; 1, 1, 2, 2-Tetra hydroheptadecafluoro decanol; 1, 1, 2, 2-Tetra hydroperfluorodecan-1-ol; 1, 1, 2, 2-Tetra hydroperfluorodecanol; 1, 1, 2, 2-Tetra hydroperfluorodecyl Alcohol; 1H,1H,2H,2H-Perfluorodecan-1-ol; 1H,1H,2H,2H-Perfluorodecanol; 2- (Heptadecafluorooctyl) ethanol; 2- (Perfluorooctyl) ethanol; 2-(Perfluorooctyl)ethyl Alcohol; 3, 3, 4, 4, 5, 5, 6, 6, 7, 7, 8, 8, 9, 9, 10, 10, 10-Heptadecafluoro-1-decanol; 8-2 Fluorotelomer alc.; 8-2 Fluorotelomer alcohol; 8-2 Telomer B alcohol; 8:2 FTOH; A 1820; C 1820; Daikin A 1820; Fluowet EA 800; PFA 8; β - (Heptadecafluorooctyl) ethanol. Grades: Highly Purified. CAS No. 678-39-7. Pack Sizes: 10g. US Biological Life Sciences. |  Worldwide |
| 6beta-Chloro-17-Acetoxy progesterone | 6beta-Chloro-17-Acetoxy progesterone. Uses: For analytical and research use. Group: Impurity standards. Alternative Names: 6beta-Chloro-17-Acetoxy Progesterone; [(6R,8R,9S,10R,13S,14S,17R)-17-Acetyl-6-Chloro-10,13-Dimethyl-3-Oxo-2,6,7,8,9,11,12,14,15,16-Decahydro-1H-Cyclopenta[A]Phenanthren-17-Yl] Acetate; ZINC5434441; 6; A-Chloro-17-Acetoxy Progesterone. CAS No. 2658-74-4. Pack Sizes: 10MG. IUPAC Name: [(6S,8R,9S,10R,13S,14S,17R)-17-acetyl-6-chloro-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] acetate. Molecular Formula: C23H31ClO4. Mole Weight: 406.94. Catalog: APS2658744. SMILES: CC (=O)O[C@@]1 (CC[C@H]2[C@@H]3C[C@H] (Cl)C4=CC (=O)CC[C@]4 (C)[C@H]3CC[C@]12C)C (=O)C. Format: Neat. |  |
| Bacitracin, Zinc | Bacitracin is a heterogeneous mixture of cyclic polypeptides which inhibit formation of bacterial cell walls. Group: Biochemicals. Grades: USP. CAS No. 1405-89-6S. Pack Sizes: 100KU, 500KU, 1MU. US Biological Life Sciences. | Worldwide |
| BMS 299897 | BMS 299897, under the IUPAC name 4-[2-[(1R)-1-(N-(4-chlorophenyl)sulfonyl-2,5-difluoroanilino)ethyl]-5-fluorophenyl]butanoic acid, synthesized by the radiosynthesis group at Bristol-Myers Squibb, is a β-secretase inhibitor that has the potential for treatment of Alzheimer's diseases (IC50 = 12 nM; gamma-secretase express: EC50 = 7 nM (CHO cells)). BMS 299897 blocks the formation of Aβ40 (IC50 = 7.9 nM) and Aβ42 (IC50 = 7.9 nM) in the brain, and reduces Aβ in the brain, plasma and cerebrospinal fluid in vivo. Synonyms: 4-[2-[(1R)-1-(N-(4-chlorophenyl)sulfonyl-2,5-difluoroanilino)ethyl]-5-fluorophenyl]butanoic acid; 4-(2-((1R)-1-(((4-chlorophenyl)sulfonyl)-2,5-difluoroanilino)ethyl)-5-fluorophenyl)butanoic acid; BMS299897; BMS 299897; BMS-299897; 290315-45-6; 2-[(1R)-1-[[(4-Chlorophenyl)sulfonyl](2,5-difluorophenyl)amino]ethyl]-5-fluoro-benzenebutanoic acid; C24H21ClF3NO4S; CHEMBL247471; SCHEMBL6394108; DTXSID50460039; 3496AH; ZINC28883606; AKOS024457319; CCG-222540; CS-1339; NCGC00346875-01; HY-50883; KB-75603; DB-017854; W-5550; BRD-K02950022-001-01-1; 2-[(1R)-1-[[(4-chlorophenyl)sulfonyl](2,5-difluorophenyl)amino]ethyl]-5-fluoroBenzenebutanoic acid; BMS 299897|2-[(1R)-1-[[(4-Chlorophenyl)sulfonyl](2,5-difluorophenyl)amino]ethyl-5-fluorobenzenebutanoic acid. CAS No. 290315-45-6. Molecular formula: C24H21ClF3NO4S. Mole weight: 511.94. |  |
| BrettPhos | Ligand for palladium-catalyzed cross-coupling reactions using aryl mesylates with electron-deficient anilines. Ligand for palladium-catalyzed cross-coupling of primary arylamines at low catalyst loading. Ligand for palladium-catalyzed cross-coupling of aryl iodides and primary amines. Ligand for the Suziki-Miyaura coupling of tosylates and mesylates. Ligand for the palladium-catalyzed trifluoromethylation of aryl chlorides. Ligand for the palladium-catalyzed formation of aryl-SCF3 compounds from aryl bromides. Ligand for the nickel-catalyzed cross-coupling of styrenyl epoxides with boronic acids. Ligand for the palladium-catalyzed intramolecular CH difluoroalkylation. Group: Organic phosphine compounds. Alternative Names: C35H53O2P; dicyclohexyl-(2',4',6'-triisopropyl-3,6-dimethoxy-biphenyl-2-yl)-phosphane; BrettPhos; 2-(Dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl; ZINC43220891; ST24046493; 2-DICYCLOHEXYLPHOSPHINO-2',4',6'-TRIISOPROPYL-3,6-DIMETHOXYBIPHENYL; AS-19342; 2-(Dicyclohexylphosphino)3,6-dimethoxy-2 inverted exclamation marka,4 inverted exclamation marka,6 inverted exclamation. CAS No. 1070663-78-3. Molecular formula: C35H53O2P. Mole weight: 536.781g/mol. IUPACName: dicyclohexyl-[3,6-dimethoxy-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=C (C=CC (=C2P (C3CCCCC3)C4CCCCC4)OC)OC)C (C)C. Catalog: ACM1070663783. |  |
| CGP 52411 | CGP 52411, also called DAPH, inhibits and reverses the formation of Aβ42 fibers (β-sheet content of aggregated β-amyloid (1-42): IC50 = 4.5 μM) in neurons associated with Alzheimer's disease. And it is also a selective inhibitor of the epidermal growth factor receptor (EGFR) (IC50 = 0.3 μM in vitro). Uses: Anti-alzheimer agents; amyloid-β inhibitor. Synonyms: CGP 52411; CGP52411; CGP-52411; 5,6-dianilinoisoindole-1,3-dione; 406-050-3; Z13D008FZ2; 4,5-dianilinophthalimide; DAPH; Cgp 52411; 5,6-Bis(phenylamino)-1H-isoindole-1,3(2H)-dione; 145915-58-8; Cgp-52411; UNII-Z13D008FZ2; CHEMBL268868; 5,6-dianilino-1h-isoindole-1,3(2h)-dione; CHEBI:53110; Z13D008FZ2; AC1Q6JME; DAPH-1; SCHEMBL11017; 4,5-Bis(anilino)phthalimide; D3943_SIGMA; 4,5-bis-(anilino)phthalimide; AC1L1C19; ZINC6094; DTXSID4040393; CTK8D4606; AAALVYBICLMAMA-UHFFFAOYSA-N; BCPP000288; HMS3260P13; 5,6-dianilinoisoindole-1,3-dione; Tox21_500236; ABP000886; AR-1G6110; BDBM50040929; MFCD00236442; AKOS024457581; BCP9000511; CCG-221540; LP00236; CGP 52411/CGP52411; NCGC00093700-01; NCGC00093700-02; NCGC00093700-03; NCGC00093700-04; NCGC00093700-05; NCGC00260921-01; AK393267; HE062397; HE312151; 5,6-Bis-phenylamino-isoindole-1,3-dione; 5,6-Bis(phenylamino)isoindoline-1,3-dione; J587.895K; 1H-Isoindole-1,3(2H)-dione, 5,6-bis(phenylamino)-; BRD-K13087974-001-01-7; CGP 52411|DAPH|5,6-Bis(phenylamino)-1H-isoindole-1,3(2H)-dione. CAS No. 145915-58-8. Molecular formula: C20H15N3O2. Mole weight: 329.35. | |
| Chromium(III) chloride | Chromium(III) chloride at elevated termperatures decomposes to chromium( II) chloride and chlorine: 2CrCl3→2CrCl2 + Cl2 Heating with excess chlorine produces vapors of chromium(IV) chloride, CrCl4. The tetrahedral tetrachloride is unstable, and occurs only in vapor phase. When heated with hydrogen, it is reduced to chromium(II) chloride with the formation of hydrogen chloride: 2CrCl3 + H2→2CrCl2 + 2HCl Chromium(III) chloride has very low solubility in pure water. However, it readily dissolves in the presence of Cr2+ ion. Reducing agents such as SnCl2 can "solubilize" CrCl3 in water. It forms adducts with many donor ligands. For example, with tetrahydrofuran (THF) in the presence of zinc, it forms the violet crystals of the complex CrCl3 3THF. Group: Metal & ceramic materials. Alternative Names: Chromium(III) trichloride. CAS No. 10025-73-7. Molecular formula: CrCl3. Mole weight: 158.35. Appearance: Violet flakes. Purity: 99%+. IUPACName: Trichlorochromium. Canonical SMILES: Cl[Cr](Cl)Cl. Density: 2.87 g/mL at 25 °C (lit.). ECNumber: 256-852-0. Catalog: ACM10025737. | |
| Chromium(III) chloride | Chromium(III) chloride. Uses: Chromium(iII) chloride at elevated termperatures decomposes to chromium( II) chloride and chlorine: 2crcl3→2crcl2 + cl2 heating with excess chlorine produces vapors of chromium(iv) chloride, crcl4. the tetrahedral tetrachloride is unstable, and occurs only in vapor phase. when heated with hydrogen, it is reduced to chromium(II) chloride with the formation of hydrogen chloride: 2crcl3 + h2→2crcl2 + 2hcl chromium(iII) chloride has very low solubility in pure water. however, it readily dissolves in the presence of cr2+ ion. reducing agents such as sncl2 can "solubilize" crcl3 in water. it forms adducts with many donor ligands. for example, with tetrahydrofuran (thf) in the presence of zinc, it forms the violet crystals of the complex crcl3 3thf. Group: Electrolytes. Alternative Names: Chromium(III) trichloride. CAS No. 10025-73-7. Product ID: Trichlorochromium. Molecular formula: 158.35. Mole weight: CrCl3. Cl[Cr](Cl)Cl. InChI=1S/3ClH.Cr/h3*1H;/q;+3/p-3. QSWDMMVNRMROPK-UHFFFAOYSA-K. 99%+. |  |
| Coproporphyrin III dihydrochloride | Coproporphyrin III dihydrochloride is a bioactive molecule excreted by nostril- and skin-associated Propionibacterium species that induces aggregation of Staphylococcus aureus (conditions: during early stationary phase growth, low pH: 4-6). Coproporphyrin III dihydrochloride also induces plasma-independent biofilm formation on abiotic surfaces by Staphylococcus aureus. Coproporphyrin III dihydrochloride may be an important mediator of S. aureus accumulation and/or biofilm formation in the nostrils or other sites where Propionibacterium and S. aureus inhabit [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Zincphyrin dihydrochloride. CAS No. 68938-73-8. Pack Sizes: 10 mM * 1 mL; 1 mg; 5 mg; 10 mg. Product ID: HY-W412175. |  |
| Diethylenetriaminepentaacetic acid, 99% | Diethylenetriaminepentaacetic Acid is a component of manganese and zinc fertilizers.Pentetic acid is mainly used as a chelating agent in the preparation of imaging and contrast agents for radionuclide and magnetic resonance imaging.It is also used as a carrier excipient for neutron-capture isotopes in, for example, radiotherapy.Pentetic acid-isotope complexes have also been considered as model active substances in scintigraphic imaging studies.Pentetic acid has been used to chelate metal ions to reduce formation of reactive oxygen species during lyophilization. Group: Heterocyclic organic compound. Alternative Names: FT-0083201; Pentetic acid, United States Pharmacopeia (USP) Reference Standard; Detarex; Hamp-Ex Acid; NSC-759314; NCGC00261116-01; Diethylenetriaminepentaacetic acid. (Note-The sodium salts are named as follows: pentetate monosodium (1 Na ion); NSC759314; NSC7340; AN-DTPA. CAS No. 67-43-6. Molecular formula: C14H23N3O10. Mole weight: 393.349g/mol. IUPACName: 2-[bis[2-[bis (carboxymethyl) amino]ethyl]amino]acetic acid. Canonical SMILES: C (CN (CC (=O)O)CC (=O)O)N (CCN (CC (=O)O)CC (=O)O)CC (=O)O. ECNumber: 200-652-8. Catalog: ACM67436. | |
| Native Bacillus thermoproteolyticus Thermolysin | Thermolysin is a thermostable neutral metalloproteinase enzyme produced by the Gram-positive bacteria Bacillus thermoproteolyticus. It requires one zinc ion for enzyme activity and four calcium ions for structural stability. Thermolysin specifically catalyzes the hydrolysis of peptide bonds containing hydrophobic amino acids. However thermolysin is also widely used for peptide bond formation through the reverse reaction of hydrolysis. Thermolysin is the most stable member of a family of metalloproteinases produced by various Bacillus species. These enzymes are also termed 'neutral' proteinases or thermolysin-like proteinases (TLPs). Group: Enzymes. Synonyms: thermolysin; Bacillus thermoproteolyticus neutral proteinase; thermoase; thermoase Y10; TLN; EC 3.4.24.27. Enzyme Commission Number: EC 3.4.24.27. CAS No. 9073-78-3. TLN. Mole weight: 36.2kDa. Activity: Reverse-phase HPLC analysis shows <30% of undigested insulin after 10 minutes of incubation with Thermolysin at 75°C using a 1:20 thermolysin:insulin ratio. Form: Lyophilized. Source: Bacillus thermoproteolyticus. thermolysin; Bacillus thermoproteolyticus neutral proteinase; thermoase; thermoase Y10; TLN; EC 3.4.24.27. Cat No: NATE-0705. |  |
| Native Geobacillus stearothermophilus Thermolysin | Thermolysin is a thermostable neutral metalloproteinase enzyme produced by the Gram-positive bacteria Bacillus thermoproteolyticus. It requires one zinc ion for enzyme activity and four calcium ions for structural stability. Thermolysin specifically catalyzes the hydrolysis of peptide bonds containing hydrophobic amino acids. However thermolysin is also widely used for peptide bond formation through the reverse reaction of hydrolysis. Thermolysin is the most stable member of a family of metalloproteinases produced by various Bacillus species. These enzymes are also termed 'neutral' proteinases or thermolysin-like proteinases (TLPs). Suitable for cell culture. Applica... of n-terminal to phe which is preferred over the others. often used to do limited proteolysis for peptide mapping and studies of protein structure and conformational changes. Group: Enzymes. Synonyms: thermolysin; Bacillus thermoproteolyticus neutral proteinase; thermoase; thermoase Y10; TLN; EC 3.4.24.27. Enzyme Commission Number: EC 3.4.24.27. CAS No. 9073-78-3. TLN. Activity: 30-175 units/mg protein (E1%/280). Storage: -20°C. Form: lyophilized powder containing calcium and sodium acetate buffer salts. Source: Geobacillus stearothermophilus. thermolysin; Bacillus thermoproteolyticus neutral proteinase; thermoase; thermoase Y10; TLN; EC 3.4.24.27. Cat No: NATE-0704. | |
| Nitroxoline | Nitroxoline (8-Hydroxy-5-nitroquinoline), an antibiotic , is an orally active antibiofilm agent. Nitroxoline reduces the formation and induces the dispersal of Pseudomonas aeruginosa biofilms by chelation of iron and zinc. Nitroxoline can be used for the urinary tract infections and cancer research [1] [2] [3]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 8-Hydroxy-5-nitroquinoline; 5-Nitro-8-quinolinol. CAS No. 4008-48-4. Pack Sizes: 10 mM * 1 mL; 500 mg; 1 g. Product ID: HY-B1159. | |
| NQTrp | NQTrp, also called 1,4-Naphthoquinon-2-yl-L-tryptophan, inhibits amyloid β (Aβ) oligomerization and fibrillization (IC50 = 50 nM for formation of fibrils from Aβ1-42) to treat Alzheimer's disease. Uses: Anti-alzheimer agents; amyloid-β inhibitor. Synonyms: NQTrp; NQ-Trp; NQ Trp; (2S)-2-[(1,4-dioxonaphthalen-2-yl)amino]-3-(1H-indol-3-yl)propanoic acid; 185351-19-3; nqtrp; TRY001; DTXSID30717912; ZINC100222454; KB-274843; N-(1,4-Dioxo-1,4-dihydronaphthalen-2-yl)-L-tryptophan; L-Tryptophan, N-(1,4-dihydro-1,4-dioxo-2-naphthalenyl)-; NQTrp|N-(1,4-Dihydro-1,4-dioxo-2-naphthalenyl)-L-tryptophan. CAS No. 185351-19-3. Molecular formula: C21H16N2O4. Mole weight: 360.36. | |
| peptidyl-dipeptidase A | A Cl--dependent, zinc glycoprotein that is generally membrane-bound. A potent inhibitor is captopril. Important in elevation of blood pressure, through formation of angiotensin II (vasoconstrictor) and destruction of bradykinin (vasodilator). Two molecular forms exist in mammalian tissues, a widely-distributed somatic form of 150- to 180-kDa that contains two non-identical catalytic sites, and a testicular form of 90- to 100-kDa that contains only a single catalytic site. Type example of peptidase family M2. Group: Enzymes. Synonyms: dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase (ambiguous); peptidyl dipeptidase; angiotensin converting enzym. Enzyme Commission Number: EC 3.4.15.1. CAS No. 9015-82-1. Angiotensin Converting Enzyme. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4053; peptidyl-dipeptidase A; EC 3.4.15.1; 9015-82-1; dipeptidyl carboxypeptidase I; peptidase P; dipeptide hydrolase (ambiguous); peptidyl dipeptidase; angiotensin converting enzyme; kininase II; angiotensin I-converting enzyme; carboxycathepsin; dipeptidyl carboxypeptidase; peptidyl dipeptidase I; peptidyl-dipeptide hydrolase; peptidyldipeptide hydrolase; endothelial cell peptidyl dipeptidase; ACE; peptidyl dipeptidase-4; PDH; peptidyl dipeptide hydrolase; DCP. Cat No: EXWM-4053. | |
| protein farnesyltransferase | This enzyme, along with protein geranylgeranyltransferase types I (EC 2.5.1.59) and II (EC 2.5.1.60), constitutes the protein prenyltransferase family of enzymes. Catalyses the formation of a thioether linkage between the C-1 of an isoprenyl group and a cysteine residue fourth from the C-terminus of the protein. These protein acceptors have the C-terminal sequence CA1A2X, where the terminal residue, X, is preferably serine, methionine, alanine or glutamine; leucine makes the protein a substrate for EC 2.5.1.59. The enzymes are relaxed in specificity for A1, but cannot act if A2 is aromatic. Substrates of the prenyltransferases include Ras, Rho, Rab, other Ras-related small GTP-binding proteins, γ-subunits of heterotrimeric G-proteins, nuclear lamins, centromeric proteins and many proteins involved in visual signal transduction. A zinc metalloenzyme that requires Mg2+ for activity. Group: Enzymes. Synonyms: FTase. Enzyme Commission Number: EC 2.5.1.58. CAS No. 131384-38-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2795; protein farnesyltransferase; EC 2.5.1.58; 131384-38-8; FTase. Cat No: EXWM-2795. | |
| protein geranylgeranyltransferase type I | This enzyme, along with protein farnesyltransferase (EC 2.5.1.58) and protein geranylgeranyltransferase type II (EC 2.5.1.60), constitutes the protein prenyltransferase family of enzymes. Catalyses the formation of a thioether linkage between the C-1 atom of the geranylgeranyl group and a cysteine residue fourth from the C-terminus of the protein. These protein acceptors have the C-terminal sequence CA1A2X, where the terminal residue, X, is preferably leucine; serine, methionine, alanine or glutamine makes the protein a substrate for EC 2.5.1.58. The enzymes are relaxed in specificity for A1, but cannot act if A2 is aromatic. Known targets of this enzyme include most γ-subunits of heterotrimeric G proteins and Ras-related GTPases such as members of the Ras and Rac/Rho families. A zinc metalloenzyme. The Zn2+ is required for peptide, but not for isoprenoid, substrate binding. Group: Enzymes. Synonyms: GGTase-I; GGTaseI. Enzyme Commission Number: EC 2.5.1.59. CAS No. 135371-29-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2796; protein geranylgeranyltransferase type I; EC 2.5.1.59; 135371-29-8; GGTase-I; GGTaseI. Cat No: EXWM-2796. | |
| (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine | Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. Asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. Nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: Stereospecific formation of diarylalkanes and triarylmethanes. Enantioselective reduction of prochiral ketones with NaBH4/Me2SO4/(S)-Me-CBS. Group: Other. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Molecular formula: C18H20BNO. Mole weight: 277.174g/mol. IUPACName: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Canonical SMILES: B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. Catalog: ACM112022818. | |
| (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine | (S)-5,5-Diphenyl-2-methyl-3,4-propano-1,3,2-oxazaborolidine. Uses: Convenient catalyst for the enantioselective borane reduction of ketones at ambient temperatures. asymmetric synthesis of α-chiral hydroxyalkylphosphines via a catalytic, enantioselective reduction of acylphosphines. nickel-catalyzed cross-couplings of benzylic pivalates with arylboroxines: stereospecific formation of diarylalkanes and triarylmethanes. enantioselective reduction of prochiral ketones with nabh4/me2so4/(s)-me-cbs. Group: other electronic materials. Alternative Names: AKOS015840981; (S)-1-methyl-3,3-diphenyltetrahydro-1H,3H-pyrrolo[1,2-c][1,3,2]oxazaborole; MFCD00078439; (S)- Methyl-CBS-oxazaborolidine; ZINC169743318; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3 H-pyrrolo[1,2-c][1,3,2] oxazaborole; (S)-1-methyl-3,3-diphenylhexahydropyrrolo-[1,2-c][1,3,2]oxazaborole; (S)-tetrahydro-1-methyl-3,3-diphenyl-1 H,3H-pyrrolo[1,2-c]-[1,3,2]oxazaborole; (S)-Me-CBS; Corey catalyst. CAS No. 112022-81-8. Product ID: (3aS)-1-methyl-3,3-diphenyl-3a,4,5,6-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole. Molecular formula: 277.174g/mol. Mole weight: C18H20BNO. B1 (N2CCCC2C (O1) (C3=CC=CC=C3)C4=CC=CC=C4)C. InChI=1S / C18H20BNO / c1-19-20-14-8-13-17 (20) 18 (21-19, 15-9-4-2-5-10-15) 16-11-6-3-7-12-16 / h2-7, 9-12, 17H, 8, 13-14H2, 1H3 / t17- / m0 / s1. VMKAFJQFKBASMU-KRWDZBQOSA-N. | |
| S-(hydroxymethyl)glutathione dehydrogenase | The substrate, S-(hydroxymethyl)glutathione, forms spontaneously from glutathione and formaldehyde; its rate of formation is increased in some bacteria by the presence of EC 4.4.1.22, S-(hydroxymethyl)glutathione synthase. This enzyme forms part of the pathway that detoxifies formaldehyde, since the product is hydrolysed by EC 3.1.2.12, S-formylglutathione hydrolase. The human enzyme belongs to the family of zinc-dependent alcohol dehydrogenases. Also specifically reduces S-nitrosylglutathione. Group: Enzymes. Synonyms: NAD-linked formaldehyde dehydrogenase (incorrect); formaldehyde dehydrogenase (incorrect); formic dehydrogenase (incorrect); class III . Enzyme Commission Number: EC 1.1.1.284. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0192; S-(hydroxymethyl)glutathione dehydrogenase; EC 1.1.1.284; NAD-linked formaldehyde dehydrogenase (incorrect); formaldehyde dehydrogenase (incorrect); formic dehydrogenase (incorrect); class III alcohol dehydrogenase; ADH3; χ-ADH; FDH (incorrect); formaldehyde dehydrogenase (glutathione) (incorrect); GS-FDH (incorrect); glutathione-dependent formaldehyde dehydrogenase (incorrect); NAD-dependent formaldehyde dehydrogenase; GD-FALDH; NAD- and glutathione-dependent formaldehyde dehydrogenase. Cat No: EXWM-0192. | |
| Zinc phthalocyanine | Zinc (II) phthalocyanine (ZnPc) complexes show photosensitizing properties. Phthalocyanines show significant Π-Π interactions and easy formation of H aggregates. Uses: Zinc phthalocyanine finds general applications in industry (catalysts, photoconductors etc) and biomedical (photodynamic therapy, pdt). znpc may be used to photooxidise cyclohexane. a study reports functionalization of polymer membrane with znpc. Group: Organic photovoltaic (opv). Alternative Names: [29H, 31H-Phthalocyaninato(2-)-N29, N30, N31, N32]zinc. CAS No. 14320-04-8. Molecular formula: C32H16N8Zn. Mole weight: 577.9. Appearance: Powder. Purity: 0.99. IUPACName: Zinc;2, 11, 20, 29, 37, 39-hexaza-38, 40-diazanidanonacyclo[28.6.1.13, 10.112, 19.121, 28.04, 9.013, 18.022, 27.031, 36]tetraconta-1, 3, 5, 7, 9, 11, 13, 15, 17, 19(39), 20, 22, 24, 26, 28, 30(37), 31, 33, 35-nonadecaene. Canonical SMILES: C1=CC=C2C (=C1)C3=NC4=NC (=NC5=C6C=CC=CC6=C ([N-]5)N=C7C8=CC=CC=C8C (=N7)N=C2[N-]3)C9=CC=CC=C94. [Zn+2]. ECNumber: 238-262-5. Catalog: ACM14320048-4. | |
| Zinc phthalocyanine | Zinc (II) phthalocyanine (ZnPc) complexes show photosensitizing properties. Phthalocyanines show significant Π-Π interactions and easy formation of H aggregates. Uses: Zinc phthalocyanine finds general applications in industry (catalysts, photoconductors etc) and biomedical (photodynamic therapy, pdt). znpc may be used to photooxidise cyclohexane. a study reports functionalization of polymer membrane with znpc. Group: Phthalonitriles & naphthalonitrilesdye-sensitized solar cell (dssc) materials electronic materials molecular conductorsorganic field effect transistor (ofet) materials organic solar cell (opv) materials perovskite solar cell (psc) materials other materials phthalocyanine dyes, porphyrin dyes. Alternative Names: [29H, 31H-Phthalocyaninato(2-)-N29, N30, N31, N32]zinc. CAS No. 14320-04-8. Pack Sizes: 5, 25 g in glass bottle. Product ID: Zinc; 2, 11, 20, 29, 37, 39-hexaza-38, 40-diazanidanonacyclo[28.6.1.13, 10.112, 19.121, 28.04, 9.013, 18.022, 27.031, 36]tetraconta-1, 3, 5, 7, 9, 11, 13, 15, 17, 19(39), 20, 22, 24, 26, 28, 30(37), 31, 33, 35-nonadecaene. Molecular formula: 577.9. Mole weight: C32H16N8Zn. C1=CC=C2C (=C1)C3=NC4=NC (=NC5=C6C=CC=CC6=C ([N-]5)N=C7C8=CC=CC=C8C (=N7)N=C2[N-]3)C9=CC=CC=C94. [Zn+2]. InChI=1S/C32H16N8. Zn/c1-2-10-18-17 (9-1)25-33-26 (18)38-28-21-13-5-6-14-22 (21)30 (35-28)40-32-24-16-8-7-15-23 (24)31 (36-32)39-29-20-12-4-3-11-19 (20)27 (34-29)37-25; /h1-16H; /q-2; +2. PODBBOVV | |
| 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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