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| Product | Description | |
|---|---|---|
| Ruthenium Red | Ruthenium Red acts as an inhibitor of mitochondrial ETC complexes I and III. Inhibitor of mitochondrial calcium uniporter. Group: Heterocyclic organic compound. Alternative Names: AK175476; degrees +/->> AENo>> iE; 11103-72-3; SR-01000076250-2; Ruthenium Red, for microscopy, 85.0-115.0% (calc. on dry basis, AT); MFCD00011479; Ruthenium Red, Technical grade; Ruthenium Red, for microscopy, >=85% (calc. on dry substance, AT). CAS No. 11103-72-3. Molecular formula: Cl6H46N14O2Ru3. Mole weight: 790.374g/mol. IUPACName: azane; ruthenium(2+); hexachloride; dihydrate. Canonical SMILES: N. N. N. N. N. N. N. N. N. N. N. N. N. N. O. O. [Cl-]. [Cl-]. [Cl-]. [Cl-]. [Cl-]. [Cl-]. [Ru+2]. [Ru+2]. [Ru+2]. Catalog: ACM11103723. |  |
| Ruthenium Red | Ruthenium Red. Group: Biochemicals. Alternative Names: Ammoniated Ruthenium Oxychloride; C.I. 77800; Ruthenium Oxychloride Ammoniated. Grades: Highly Purified. CAS No. 11103-72-3. Pack Sizes: 100mg. Molecular Formula: Cl6H42N14O2Ru3, Molecular Weight: 786.36. US Biological Life Sciences. |  Worldwide |
| Ruthenium Red tetrahydrate | Heterocyclic Organic Compound. Alternative Names: AMMONIATED RUTHENIUM OXYCHLORIDE;RR;RUTHENIUM TETRAMMINOHYDROXYCHLOROCHLORIDE; RUTHENIUM OXYCHLORIDE AMMONIATED TETRAHYDRATE;RUTHENIUM RED TETRAHYDRATE;RUTHENIUM SALT;RUTHENIUM (III) CHLORIDE OXIDE, AMMONIATED;RUTHENIUM CHLORIDE OXIDE, AMMONIATE. CAS No. 12790-48-6. Molecular formula: Cl6O2Ru3.4H2O.14H3N. Mole weight: 858.41. Catalog: ACM12790486. | |
| 1, 1'-Bis (dicyclohexylphosphino)ferrocene | Ligand for palladium-catalyzed synthesis of oxindoles by amide ?-arylation. Ligand for palladium-catalyzed alkoxycarbonylation of aryl chlorides. Ligand for ruthenium-catalyzed alcohol-allene C-C coupling reaction via hydrohydroxyalkylation of 1,1-disubstituted allenes employing alcohols. Ligand for nickel-catalyzed cross-coupling reaction of arylboronic acids with aryl carbonates. Ligand for palladium-catalyzed regiodivergent hydroesterification of aryl olefins with phenyl formate to form linear structured phenyl arylpropanoates. Ligand for palladium-catalyzed direct borylation of benzyl alcohol and its analogues in the absence of bases. Group: Organic phosphine compounds. Alternative Names: 1,1-Bis(dicyclohexylphosphino)ferrocene; 1,1-Bis(Dicyclohexylphosphino)Ferrocene; 1,1-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE. CAS No. 146960-90-9. Molecular formula: C34H52FeP2. Mole weight: 578.57. Appearance: Orange-red powder. Purity: 0.98. IUPACName: dicyclohexyl(cyclopentyl)phosphane; iron. Canonical SMILES: C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. [Fe]. Catalog: ACM146960909. | |
| [1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride M71-S1Pr | Enhanced activity ruthenium "boomerang" pre-catalyst used in the olefin metathesis, enyne metathesis, and cross metathesis reactions, that can be recycled, and leaves reduced ruthenium in the product after silica gel chromatography. Group: Ruthenium series catalysts. Alternative Names: 1212008-99-5; MFCD12545950; (1, 3-bis (2, 6-diisopropylphenyl) imidazolidin-2-yliden; e) (2-isopropoxy-5- (2, 2, 2-trifluoroacetamido) benzylidene) ruthenium (VI) chloride; [1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride; [1, 3-Bis (2, 6-di-i-propylphenyl) -4, 5-dihydroimidazol-2-ylidene]-[2-i-propoxy-5- (trifluoroacetamido) phenyl]methyleneruthenium (II) dichloride M71-S1Pr. CAS No. 1212008-99-5. Molecular formula: C39H50Cl2F3N3O2Ru. Mole weight: 821.813g/mol. IUPACName: [1, 3-bis[2, 6-di (propan-2-yl) phenyl]imidazolidin-2-ylidene]-dichloro-[[2-propan-2-yloxy-5-[ (2, 2, 2-trifluoroacetyl) amino]phenyl]methylidene]ruthenium. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2CCN (C2=[Ru] (=CC3=C (C=CC (=C3)NC (=O)C (F) (F)F)OC (C)C) (Cl)Cl)C4=C (C=CC=C4C (C)C)C (C)C. Catalog: ACM1212008995. | |
| 2-(2-Chlorophenyl)ethanol | 2-(2-Chlorophenyl)ethanol is used in the triethylborane-catalyzed reduction of carbonyl functions to alcohols. 2-(2-Chlorophenyl)ethanol is also used in the preparation of alcohols via ruthenium-catalyzed hydrogenation of carboxylic acids. Group: Biochemicals. Grades: Highly Purified. CAS No. 19819-95-5. Pack Sizes: 1g, 5g. Molecular Formula: C8H9ClO, Molecular Weight: 156.61. US Biological Life Sciences. | Worldwide |
| 2-Amino-5-nitroso-4,6-pyrimidinediol | 2-Amino-5-nitroso-4,6-pyrimidinediol is used as a reagent in the synthesis of 6-amino-2,3-dimethylpyrimido[4,5-e][1,2,4]triazine-8-one as an inhibitor of dihydropteridine reductase (DHPR). 2-Amino-5-nitroso-4,6-pyrimidinediol is also used in analytical studies for determination of ruthenium and transition metals. Group: Biochemicals. Grades: Highly Purified. CAS No. 55482-22-9. Pack Sizes: 1g, 10g. Molecular Formula: C4H4N4O3, Molecular Weight: 156.1. US Biological Life Sciences. | Worldwide |
| [Bis(pyrazol-1-yl)(acetimino)hydridoborato](p-cymene)ruthenium(II) trifluoromethanesulfonate | Dual site catalyst for the mild, selective nitrile reduction. Group: Ruthenium catalysts. Alternative Names: 3-Methyl-6-propan-2-ylcyclohexa-1,4-diene. CAS No. 1607436-49-6. Molecular formula: C19H26BF3N5O3RuS. Mole weight: 573.4. Appearance: Yellow powder. Purity: 0.98. IUPACName: di(pyrazol-1-yl)boron; ethanimine; 3-methyl-6-propan-2-ylcyclohexa-1, 4-diene; ruthenium(2+); trifluoromethanesulfonate. Canonical SMILES: [B](N1C=CC=N1)N2C=CC=N2. C[C]=N. CC1C=CC(C=C1)C(C)C. C(F)(F)(F)S(=O)(=O)[O-]. [Ru+2]. Catalog: ACM1607436496-1. | |
| BOLD-100 | BOLD-100 (NKP-1339; IT-139) is the first-in-class ruthenium-based anticancer agent in development against solid cancer with limited side effects. BOLD-100 induces G2/M cell cycle arrest, blockage of DNA synthesis , and induction of apoptosis via the mitochondrial pathway. BOLD-100 has a high tumor targeting potential, strongly binds to serum proteins such as albumin and transferrin and activates in the reductive tumor milieu [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: NKP-1339; IT-139; KP-1339. CAS No. 197723-00-5. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 50 mg; 100 mg. Product ID: HY-16350. |  |
| Borane Ammonia Complex | Borane Ammonia Complex is used as a reducing agent in the synthesis of nanotubes supported by ruthenium nanoparticles. Group: Biochemicals. Grades: Highly Purified. CAS No. 13774-81-7. Pack Sizes: 1g, 2.5g. Molecular Formula: NH3; (BH3), Molecular Weight: 17.03. US Biological Life Sciences. | Worldwide |
| CORM-3 | CORM-3 is a water-soluble carbon monoxide-releasing molecule with anti-inflammatory and cardioprotective activity. It attenuates NF-κB p65 nuclear translocation, reduces ROS generation and enhances intracellular glutathione and superoxide dismutase levels. Synonyms: Tricarbonylchloro (glycinato)ruthenium; (OC-6-44)-Tricarbonylchloro(glycinato-κN,κO)ruthenium; CORM3; CORM 3. Grades: >98%. CAS No. 475473-26-8. Molecular formula: C5H4ClNO5Ru. Mole weight: 294.61. |  |
| Dichlorobis (2- (diphenylphosphino) ethylamine) ruthenium (II) | Efficient catalyst for the dihydrogen reduction of carboxylic esters and amides to alcohols. Group: Ruthenium series catalysts. Alternative Names: Dichlororuthenium;2-diphenylphosphanylethanamine. CAS No. 506417-41-0. Molecular formula: C28H32Cl2N2P2Ru. Mole weight: 630.5. Appearance: Powder. Purity: 0.95. IUPACName: dichlororuthenium;2-diphenylphosphanylethanamine. Canonical SMILES: C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2. C1=CC=C(C=C1)P(CCN)C2=CC=CC=C2. Cl[Ru]Cl. Catalog: ACM506417410-1. | |
| Dichlorodi-μ-chlorobis[(1, 2, 3, 6, 7, 8-η-2, 7-dimethyl-2, 6-octadiene-1, 8-diyl]diruthenium(IV) | Versatile starting material for the preparation of cyclic and acyclic bis(η5 -dienyl)ruthenium (II) compounds. Group: Ruthenium series catalysts. Alternative Names: Tetrachlorobis(2,7-dimethyl-2,6-octadienylene)diruthenium. CAS No. 34801-97-3. Molecular formula: C20H32Cl4Ru2. Mole weight: 616.42. Appearance: red to purple powder. Purity: 0.98. Catalog: ACM34801973. | |
| Dichloro(p-cymene)ruthenium(II) dimer | Hydrosilylation Catalysts Umicore Precatalysts for Asymmetric and Cross-Coupling Catalysis Cyclometalated ruthenium complexes with arylimines and nitrogen-containing heterocycles via C-H bond activation. Group: Ruthenium series catalysts. Alternative Names: Bis(p-cymene)diruthenium(II) tetrachloride-di-mu-chlorobis[(p-cymene)chlororuthenium(II)]. CAS No. 52462-29-0. Molecular formula: C20H28Cl4Ru2. Mole weight: 612.39. Appearance: Orange red crystalline powder. Purity: 0.99. IUPACName: dichlororuthenium;1-methyl-4-propan-2-ylbenzene. Canonical SMILES: CC1=CC=C(C=C1)C(C)C. CC1=CC=C(C=C1)C(C)C. Cl[Ru]Cl. Cl[Ru]Cl. ECNumber: 435-530-5. Catalog: ACM52462290-1. | |
| Dichlorotris(1,10-phenanthroline)ruthenium(II) hydrate | The oxygen sensitivity and phototoxicity of [Ru(Phen)] in chicken embryo chorioallantoic membrane was investigated. Uses: Fluorescence quenching of dichloro(tris-1,10-phenanthroline) ruthenium (II) hydrate is is triggered by oxygen.1 (ru(phen)3cl2 may be used to imprint mesoporous molecular sieves (sba-15). Group: Organic & printed electronics. Alternative Names: Dichlorotris(1,10-phenanthroline)ruthenium(II) hydrate. CAS No. 207802-45-7. Molecular formula: C36H26Cl2N6ORu. Mole weight: 730.6. Appearance: Bright red powder. Purity: 0.99. IUPACName: Dichlororuthenium;1,10-phenanthroline;hydrate. Canonical SMILES: C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1. C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1. C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1. O. Cl[Ru]Cl. Catalog: ACM207802457-2. | |
| KP1019 | KP1019, also known as FFC14A, is just the second ruthenium-based anticancer agent after NAMI-A which was developed to the stage of clinical trials. Important steps in the mode of action of KP1019 are thought to be the binding to the serum protein transferrin and the transport into the cell via the transferrin pathway. Additionally, the selective activation by reduction in the tumor might contribute to the low side effects observed in in vivo studies. Apoptosis is induced at non-toxic levels via the mitochondrial pathway. These features distinguish it from the established platinum anticancer drugs and suggest that different types of cancer might be treatable with this drug. Indeed, promising activity against certain types of tumors, which are not successfully treatable with cisplatin, and only a very low incidence of acquired resistance has been observed in in vitro and in vivo studies. Recently, a clinical phase I trial was finished in which none of the treated patients experienced serious side effects, while disease stabilization in five of six evaluable patients was achieved. Synonyms: KP1019; KP 1019; KP-1019; FFC14A; indazolium trans-[tetrachlorobis(1H-indazole)ruthenate(III)]. CAS No. 124875-20-3. Molecular formula: C21H19Cl4N6Ru. Mole weight: 598.30. | |
| NAMI-A | NAMI-A is a ruthenium anticancer agent and a metastasis inhibitor. NAMI is an acronym for "New Anti-tumour Metastasis Inhibitor", while the -A suffix indicates that this is the first of a potential series. NAMI-A is a potent agent for the treatment of solid tumor metastases as well as when these tumor lesions are in an advanced stage of growth. NAMI-A is endowed with a mechanism of action unrelated to direct tumor cell cytotoxicity, and such mechanism of action is responsible for a reduced host toxicity. Synonyms: ImH[trans-RuCl4(DMSO)Im]; Na[trans-RuCl(4)(DMSO)Im; Imidazolium trans-imidazoledimethyl sulfoxide-tetrachlororuthenat; Imidazolium-bis (imidazole) di methyl sulfoxideimidazotetrachlororuthenate (III) ; Imidazolium-bis (imidazole) di methyl sulfoxideimidazotetrachlororuthenate (III). Grades: >98%. CAS No. 201653-76-1. Molecular formula: C8H15Cl4N4ORuS. Mole weight: 458.18. | |
| RuCl2[(S)-xylbinap][(S)-daipen] | Highly active catalyst for hydrogenation of simple ketones giving high enantioselectivity when sterically unsymmetrical ketones such as acetophenone, heteroaryl ketones, benzophenones, cyclopropyl ketones, and cyclohexyl ketones are substrates. Ee's are enhanced with XylBINAP relative to BINAP. The otherwise poorly bonded ketone is held in the transition state by hydrogen bonding to the protic bidentate amine. Carbonyl groups are selectively reduced even when olefins exist in the same molecule. In the presence of strong base, and catalyst, simple ketones, having substituents at the α-position, may be induced to undergo dynamic kinectic resolution during their hydrogenation to produce two chiral carbon centers in high yield. Group: Heterocyclic organic compound. Alternative Names: RuCl2[(S)-(DM-BINAP)][(S)-DAIPEN], 220114-01-2, Dichloro[(S)-(-)-2,2 inverted exclamation marka-bis[di(3,5-xylyl)phosphino]-1,1 inverted exclamation marka-binaphthyl][(2S)-(+)-1,1-bis(4-methoxyphenyl)-3-methyl-1,2-butanediamine]ruthenium(II). CAS No. 220114-01-2. Molecular formula: C71H74Cl2N2O2P2Ru. Mole weight: 1221.3. Purity: 0.96. IUPACName: [ (2S) -1-azanidyl-1, 1-bis (4-methoxyphenyl) -3-methylbutan-2-yl]azanide; [1-[2-bis (3, 5-dimethylphenyl) phosphaniumylnaphthalen-1-yl]naphthalen-2-yl]-bis (3, 5-dimethylphenyl) phosphanium; dichlororuthenium (2+). Catalog: ACM220114012. | |
| [RuCl(p-cymene)((S)-tolbinap)]Cl | 1. Useful ligand for palladium-catalyzed carbon-oxygen bond formation. 2. Ligand for palladium-catalyzed α-arylation of ketones. 3. Ligand for Cu-catalyzed asymmetric conjugate reduction. 4. Ligand for Cu-catalyzed asymmetric dienolate addition to aldehydes. 5. Enantioselective conjugate reduction of lactones and lactams. 6. Ligand used in the enantioselective cycloaddition of allenylsilanes with α-Imino esters. 7. Catalytic Aldol reaction to ketones. 8. Ligand with rhodium catalyses [2+2+2] cycloaddition reaction of alkenes and alkynes. 9. Ligand used in the iridium-catalyzed enantioselective C-H bond activation of 2-(alkylamino)-pyridine with alkenes. 10. Iridium-catalyzed regio-, diastereo-, and enantioselective tert-(hydroxyl)-prenylation of alcohols. 11. Rhodium-catalyzed cross cyclotrimerization. Group: Ruthenium series catalysts. Alternative Names: SC10123; (R)-RuCl[(p-cymene)(T-BINAP)]Cl; Chloro[(R)-(+)-2,2 -bis(di-p-tolylphosphino)-1; CHLORO[(S)-(-)-2,2'-BIS(DI-P-TOLYLPHOSPHINO)-1,1'-BINAPHTHYL](P-CYMENE)RUTHENIUM(II) CHLORIDE; MFCD09753014; (S)-RuCl[(p-cymene)(T-BINAP)]Cl; C58H54Cl2P2Ru. CAS No. 228120-95-4. Molecular formula: C58H54Cl2P2Ru. Mole weight: 984.988g/mol. IUPACName: [1-[2-bis(4-methylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(4-methylphenyl)phosphane; dichlororuthenium; 1-methyl-4-propan-2-ylbenzene. Canonical SMILES: CC1=CC=C (C=C1)C (C)C. CC1=CC=C (C=C1)P (C | |
| (R)-(+)-XylBINAP | Ligand used in copper-catalyzed asymmetric Mannich-type reactions of N-acylimino esters. Ligand used in the enantioselective fluorination of oxindoles. Ligand used in [2+2+2] cycloaddition of tetraynes and hexaynes. Ligand used in the asymmetric reduction of ketone via ruthenium-catalyzed transfer hydrogenation. Asymmetric hydroboration of unsaturated imines. Group: Heterocyclic organic compound. CAS No. 137219-86-4. Molecular formula: C52H48P2. Mole weight: 734.904g/mol. IUPACName: [1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane. Canonical SMILES: CC1=CC (=CC (=C1)P (C2=C (C3=CC=CC=C3C=C2)C4=C (C=CC5=CC=CC=C54)P (C6=CC (=CC (=C6)C)C)C7=CC (=CC (=C7)C)C)C8=CC (=CC (=C8)C)C)C. Catalog: ACM137219864. | |
| [(S)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl]ruthenium(II) Dichloride | Enantioselective catalyst for the asymmetric hydrogenation of α,β-unsaturated olefins. Efficient catalyst for the asymmetric reduction of carbonyl groups, such as β-ketoesters. Group: Ruthenium series catalysts. Alternative Names: (R)-[2,2 inverted exclamation marka-Bis(diphenylphosphino)-1,1 inverted exclamation marka-binaphthyl]dichlororuthenium; C44H34Cl2P2Ru; DICHLORO[(R)-(+)-2,2'-BIS(DIPHENYLPHOSPHINO)-; KS-00000HO2; Dichloro [(R)-(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphathyl] ruthenium(II); [R-(R*, R*)]-7-[2-(4-Fluorophenyl)-5-(1-methylethyl)-3-phenyl-4-(phenylaminocarbonyl)-1H-pyrrol-1-yl]-3,5-dihydroxy-heptanoic acid calcium salt; (R)-[1,1 inverted exclamation marka-Binaphthalene]-2,2 inverted exclamation marka-diylbis[diphenylphosphine]ruthenium complex; 134524-84-8; ST24030314; [(R)-[1,1 inverted exclamation marka-Binaphthalene]-2,2 inverted exclamation marka-diylbis [diphenylphosphine-|EP]]dichloro-ruthenium. CAS No. 134524-84-8. Molecular formula: C44H32Cl2P2Ru. Mole weight: 794.658g/mol. IUPACName: dichlororuthenium;[1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. Cl[Ru]Cl. Catalog: ACM134524848. | |
| (S)-(-)-XylBINAP | Ligand used in copper-catalyzed asymmetric Mannich-type reactions of N-acylimino esters. Ligand used in the enantioselective fluorination of oxindoles. Ligand used in [2+2+2] cycloaddition of tetraynes and hexaynes. Ligand used in the asymmetric reduction of ketone via ruthenium-catalyzed transfer hydrogenation. Asymmetric hydroboration of unsaturated imines. Group: Heterocyclic organic compound. CAS No. 135139-00-3. Molecular formula: C52H48P2. Mole weight: 734.904g/mol. IUPACName: [1-[2-bis(3,5-dimethylphenyl)phosphanylnaphthalen-1-yl]naphthalen-2-yl]-bis(3,5-dimethylphenyl)phosphane. Canonical SMILES: CC1=CC (=CC (=C1)P (C2=C (C3=CC=CC=C3C=C2)C4=C (C=CC5=CC=CC=C54)P (C6=CC (=CC (=C6)C)C)C7=CC (=CC (=C7)C)C)C8=CC (=CC (=C8)C)C)C. Catalog: ACM135139003. | |
| Tetrabutylphosphonium Bromide | Tetrabutylphosphonium bromide (TBPB) is a quaternary salt which can be used: As a medium to disperse ruthenium catalyst for the synthesis of ethylene glycol from synthesis gas via ruthenium melt catalysis. As a catalyst supported on silica or alumina for the halogen exchange reaction to synthesize alkyl bromide from alkyl chloride. To synthesize various ionic liquids on mixing with different proportions of 1,3-dimethylurea for capturing NO gas. 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 polymerization reagents. Alternative Names: Tetra-n-butylphosphonium bromide; Phosphonium, tetrabutyl-, bromide; Phosphonium, tetrabutyl-, bromide (1:1). CAS No. 3115-68-2. Product ID: tetrabutylphosphanium; bromide. Molecular formula: 339.34. Mole weight: C16H36BrP. CCCC[P+](CCCC)(CCCC)CCCC.[Br-]. 1S/C16H36P. 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. RKHXQBLJXBGEKF-UHFFFAOYSA-M. >99.0%(T). |  |
| Tetrabutylphosphonium Bromide | Tetrabutylphosphonium bromide (TBPB) is a quaternary salt which can be used: As a medium to disperse ruthenium catalyst for the synthesis of ethylene glycol from synthesis gas via ruthenium melt catalysis. As a catalyst supported on silica or alumina for the halogen exchange reaction to synthesize alkyl bromide from alkyl chloride. To synthesize various ionic liquids on mixing with different proportions of 1,3-dimethylurea for capturing NO gas. 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: Phosphonium ionic liquids. Alternative Names: Tetra-n-butylphosphonium bromide;Phosphonium, tetrabutyl-, bromide;Phosphonium, tetrabutyl-, bromide (1:1). CAS No. 3115-68-2. Molecular formula: C16H36BrP. Mole weight: 339.34. Appearance: White to Almost white powder to crystal. Purity: >99.0%(T). IUPACName: tetrabutylphosphanium;bromide. Canonical SMILES: CCCC[P+](CCCC)(CCCC)CCCC.[Br-]. ECNumber: 221-487-8. Catalog: ACM3115682. | |
| Triruthenium dodecacarbonyl | Atomic number of base material: 44 Ruthenium. Uses: Carbonyl cluster precursor and h-transfer catalyst. used in the reductive carbonylation of aromatic nitro compounds to carbamates. the phosphine-stabilized carbonyl cluster has been tethered to oxide supports. applied in improved catalysis of the allylic amination of unactivated olefins by nitroarenes.[5]. Group: Micro/nanoelectronics. Alternative Names: Ruthenium carbonyl, tri-Ruthenium dodecacarbonyl. CAS No. 15243-33-1. Molecular formula: Ru3(CO)12. Mole weight: 639.33. Appearance: orange crystals. Purity: Ru ≥25.7%. Canonical SMILES: [Ru]. [Ru]. [Ru]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. ECNumber: 239-287-4. Catalog: ACM15243331. | |
| Triruthenium dodecacarbonyl | Atomic number of base material: 44 Ruthenium. Uses: Carbonyl cluster precursor and h-transfer catalyst. used in the reductive carbonylation of aromatic nitro compounds to carbamates. the phosphine-stabilized carbonyl cluster has been tethered to oxide supports. applied in improved catalysis of the allylic amination of unactivated olefins by nitroarenes.[5]. Group: Vapor deposition precursors. Alternative Names: Ruthenium carbonyl, tri-Ruthenium dodecacarbonyl. CAS No. 15243-33-1. Pack Sizes: 1, 5, 50 g in glass bottle. Molecular formula: 639.33. Mole weight: Ru3(CO)12. [Ru]. [Ru]. [Ru]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. [C-]#[O+]. 1S/12CO.3Ru/c12*1-2;;;, NQZFAUXPNWSLBI-UHFFFAOYSA-N. NQZFAUXPNWSLBI-UHFFFAOYSA-N. Ru ≥25.7%. | |
| Tris(1,10-phenanthroline)ruthenium(II) Bis(hexafluorophosphate) | Alfa Chemistry offers Tris(1,10-phenanthroline)ruthenium(II) Bis(hexafluorophosphate) products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page. Uses: It can be used as a solar energy source. Group: Red dopants. CAS No. 60804-75-3. Molecular formula: C36H24F12N6P2Ru. Mole weight: 931.63. Appearance: Light yellow to Brown powder to crystal. Purity: >98.0%(HPLC). IUPACName: 1, 10-phenanthroline; ruthenium(2+); dihexafluorophosphate. Canonical SMILES: C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1. C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1. C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1. F[P-](F)(F)(F)(F)F. F[P-](F)(F)(F)(F)F. [Ru+2]. Catalog: ACM60804753-2. | |
| Bis[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(3-phenyl-1H-inden-1-ylidene)ruthenium(II) | Alkene Metathesis→Cross Metathesis; Alkene Metathesis→Ring Arrangement Metathesis ; Alkene Metathesis→Ring Closing Metathesis; Alkene Metathesis→Ring Opening Metathesis; Alkene Metathesis→Ring Opening Metathesis Polymerization. Group: Catalysts for pharmaceutical. CAS No. 1383684-54-5. Molecular formula: C57H62Cl2N4Ru. Mole weight: 975.1. Appearance: red to brown. Purity: Metal purity 99.95. Catalog: ACM1383684545. | |
| cis-[1, 3-Bis (2, 4, 6-trimethylphenyl)-2-imidazolidinylidene]dichloro (3-phenyl-1H-inden-1-ylidene) (triisopropylphosphite)ruthenium (II) | Alkene Metathesis→Cross Metathesis; Alkene Metathesis→Enyne Metathesis; Alkene Metathesis→Self Metathesis. Group: Catalysts for pharmaceuticalasymmetric reactions. CAS No. 1255536-61-8. Molecular formula: C45H57N2Cl2O3PRu. Mole weight: 876.91. Appearance: red brown. Purity: Metal purity 99.95. Catalog: ACM1255536618-1. | |
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