Catalysts

Catalysts for organic and inorganic synthesis, including transition-metal catalysts and supporting systems (where available). Browse by catalyst class and application, and compare composition and handling requirements to optimize reactions.

Browse by type, application, or key specifications such as purity, grade, packaging, and handling requirements.

3,867 products

Browse chiral catalysts for asymmetric synthesis and stereoselective reaction development. Use this page to compare catalyst systems that support enantioselective transformations and method optimization.

Explore organocatalysts for metal-free reaction design, asymmetric catalysis, and practical synthetic workflows. Compare catalyst classes suited to activation, selectivity control, and screening.

Find photocatalysts for visible-light chemistry, redox activation, and modern synthetic method development. This category supports reaction discovery and optimization in photochemical workflows.

Browse transition metal catalysts for coupling, hydrogenation, oxidation, and general synthesis. Compare catalyst systems used in reaction screening, optimization, and scale-up.

Source cross-coupling catalysts for C–C and C–heteroatom bond formation. Use this page to compare catalyst options for Suzuki, Buchwald–Hartwig, Sonogashira, and related transformations.

Explore hydrogenation catalysts for reduction workflows, saturation chemistry, and process development. Review catalyst systems suitable for selective hydrogenation and reaction optimization.

Browse olefin metathesis catalysts for ring-closing, cross-metathesis, and related alkene transformations. This page supports catalyst comparison for method development and synthesis planning.

Find Buchwald catalyst systems for amination and cross-coupling workflows. Compare catalyst options built for efficient C–N and related bond-forming reactions.

Explore inorganic catalysts used in synthesis, process chemistry, and materials-related reactions. This category helps you compare practical catalyst options across varied reaction classes.

Browse C–H activation catalysts for direct functionalization and streamlined synthetic route design. Use this page to compare catalyst systems for modern bond-forming chemistry.

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  1. Diphenyl(methyl)sulfonium Tetrafluoroborate
    CAS: 10504-60-6 PubChem CID: 2758717 Formula: C13H13S·BF4 Molecular Weight: 288.11
    In Stock Item #: D155602
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    Technical Identifiers
    IUPAC Name
    methyl(diphenyl)sulfanium;tetrafluoroborate
    SMILES
    [B-](F)(F)(F)F.C[S+](C1=CC=CC=C1)C2=CC=CC=C2
    InChIKey
    LHAMVDBAOJCBDW-UHFFFAOYSA-N
    InChI
    1S/C13H13S.BF4/c1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13;2-1(3,4)5/h2-11H,1H3;/q+1;-1
    Synonyms
    SY108932 | Methyldiphenylsulphonium tetrafluoroborate(1-) | LHAMVDBAOJCBDW-UHFFFAOYSA-N | SCHEMBL283734 | EINECS 234-...
  2. Lithium Tetrakis(pentafluorophenyl)borate - Ethyl Ether Complex
    CAS: 155543-02-5 PubChem CID: 23701484 Formula: C24BF20Li·nC4H10O
    In Stock Item #: L157763
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    Technical Identifiers
    IUPAC Name
    lithium;ethoxyethane;tetrakis(2,3,4,5,6-pentafluorophenyl)boranuide
    SMILES
    [Li+].[B-](C1=C(C(=C(C(=C1F)F)F)F)F)(C2=C(C(=C(C(=C2F)F)F)F)F)(C3=C(C(=C(C(=C3F)F)F)F)F)C4=C(C(=C(C(=C4F)F)F)F)F.CCOCC
    InChIKey
    KPLZKJQZPFREPG-UHFFFAOYSA-N
    InChI
    1S/C24BF20.C4H10O.Li/c26-5-1(6(27)14(35)21(42)13(5)34)25(2-7(28)15(36)22(43)16(37)8(2)29,3-9(30)17(38)23(44)18(39)10(3)31)4-11(32)19(40)24(45)20(41)12show more
    Synonyms
    Lithium(1+), [1,1'-oxybis[ethane]]-, tetrakis(2,3,4,5,6-pentafluorophenyl)borate(1-) (1:1) | Tetrakis(pentafluorophen...
  3. Bis[tetrakis(hydroxymethyl)phosphonium] sulfate solution
    CAS: 55566-30-8 EC Number: 259-709-0 Formula: C8H24O12P2S Molecular Weight: 406.28
    Liquid 75% in water
    In Stock Item #: B101527
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    Technical Identifiers
    IUPAC Name
    tetrakis(hydroxymethyl)phosphanium;sulfate
    SMILES
    C(O)[P+](CO)(CO)CO.C(O)[P+](CO)(CO)CO.[O-]S(=O)(=O)[O-]
    InChIKey
    YIEDHPBKGZGLIK-UHFFFAOYSA-L
    InChI
    1S/2C4H12O4P.H2O4S/c2*5-1-9(2-6,3-7)4-8;1-5(2,3)4/h2*5-8H,1-4H2;(H2,1,2,3,4)/q2*+1;/p-2
    Synonyms
    Bis(tetrakis(hydroxymethyl)phosphonium)sulfate (salt) | TETRAKIS(HYDROXYMETHYL)PHOSPHONIUM SULFATE | 5I8RSL9E6S | Oct...
  4. Bismuth iodide
    CAS: 7787-64-6 EC Number: 232-127-4 PubChem CID: 111042 Formula: BiI3 Molecular Weight: 589.69
    Solid ≥98%
    In Stock Item #: B104975
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    Technical Identifiers
    IUPAC Name
    triiodobismuthane
    SMILES
    I[Bi](I)I
    InChIKey
    KOECRLKKXSXCPB-UHFFFAOYSA-K
    InChI
    1S/Bi.3HI/h;3*1H/q+3;;;/p-3
    Synonyms
    BiI3 | Bismuthine, triiodo- | NSC 103681 | DTXSID3064853 | Bismuth iodide, BiI3 | AKOS015902622 | UNII-BGX9X3FOLL | B...
  5. Zinc Phthalocyanine
    CAS: 14320-04-8 EC Number: 238-262-5 PubChem CID: 2735172 Formula: C32H16N8Zn Molecular Weight: 577.92
    In Stock Item #: Z163005
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    Technical Identifiers
    IUPAC Name
    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,show more
    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]
    InChIKey
    PODBBOVVOGJETB-UHFFFAOYSA-N
    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-show more
    Synonyms
    ZnPc | SR-01000883715-1 | Zinc phthalocyanine | MFCD00041955 | Zinc Phthalocyanine (purified by sublimation) | Phthal...
  6. Benzyldodecyldimethylammonium Bromide
    CAS: 7281-04-1 EC Number: 230-698-4 Formula: C21H38BrN Molecular Weight: 384.45
    Solid ≥97%(T)
    In Stock Item #: B152300
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    Technical Identifiers
    IUPAC Name
    benzyl-dodecyl-dimethylazanium;bromide
    SMILES
    CCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1.[Br-]
    InChIKey
    KHSLHYAUZSPBIU-UHFFFAOYSA-M
    InChI
    1S/C21H38N.BrH/c1-4-5-6-7-8-9-10-11-12-16-19-22(2,3)20-21-17-14-13-15-18-21;/h13-15,17-18H,4-12,16,19-20H2,1-3H3;1H/q+1;/p-1
    Synonyms
    BENZODODECINIUM BROMIDE (MART.) | FT-0733931 | BENZODODECINIUM BROMIDE (II) | Benzododecinium bromure | Benzalkonium ...
  7. Calcium(II) Bis(trifluoromethanesulfonyl)imide
    CAS: 165324-09-4 PubChem CID: 46242197 Formula: C4CaF12N2O8S4 Molecular Weight: 600.35
    In Stock Item #: C153286
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    Technical Identifiers
    IUPAC Name
    calcium;bis(trifluoromethylsulfonyl)azanide
    SMILES
    C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.C(F)(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(F)(F)F.[Ca+2]
    InChIKey
    WFABOCFDABTAPE-UHFFFAOYSA-N
    InChI
    1S/2C2F6NO4S2.Ca/c2*3-1(4,5)14(10,11)9-15(12,13)2(6,7)8;/q2*-1;+2
    Synonyms
    EN300-20787115 | Calcium(II) Bis(trifluoromethanesulfonyl)imide | Calcium(II) Triflimide | Bis(trifluoromethanesulfon...
  8. Benzoin methyl ether
    CAS: 3524-62-7 EC Number: 222-538-7 Formula: C15H14O2 Molecular Weight: 226.27
    In Stock Item #: B104003
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    Technical Identifiers
    IUPAC Name
    2-methoxy-1,2-diphenylethanone
    SMILES
    COC(C1=CC=CC=C1)C(=O)C2=CC=CC=C2
    InChIKey
    BQZJOQXSCSZQPS-UHFFFAOYSA-N
    InChI
    1S/C15H14O2/c1-17-15(13-10-6-3-7-11-13)14(16)12-8-4-2-5-9-12/h2-11,15H,1H3
    Synonyms
    alpha-Methoxybenzyl phenyl ketone | (+/-)-METHYL BENZOIN | 1H-PYRAZOL-3-AMINE, 5-ETHYL- | Benzoin methyl ester | Benz...
  9. Benzoin Isobutyl Ether
    CAS: 22499-12-3 Formula: C18H20O2 Molecular Weight: 268.36
    In Stock Item #: B152114
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    Technical Identifiers
    IUPAC Name
    2-(2-methylpropoxy)-1,2-diphenylethanone
    SMILES
    CC(C)COC(C1=CC=CC=C1)C(=O)C2=CC=CC=C2
    InChIKey
    JMVZGKVGQDHWOI-UHFFFAOYSA-N
    InChI
    1S/C18H20O2/c1-14(2)13-20-18(16-11-7-4-8-12-16)17(19)15-9-5-3-6-10-15/h3-12,14,18H,13H2,1-2H3
    Synonyms
    2-(2-methylpropoxy)-1,2-di(phenyl)ethanone | DTXSID6051485 | Q27237309 | 2-Isobutoxy-2-phenylacetophenone | MFCD00008...
  10. Lithium Bis(pentafluoroethanesulfonyl)imide(LiBETI)
    CAS: 132843-44-8 Formula: C4F10LiNO4S2 Molecular Weight: 387.09
    Out of Stock Item #: L157765
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    Technical Identifiers
    IUPAC Name
    lithium;bis(1,1,2,2,2-pentafluoroethylsulfonyl)azanide
    SMILES
    [Li+].C(C(F)(F)S(=O)(=O)[N-]S(=O)(=O)C(C(F)(F)F)(F)F)(F)(F)F
    InChIKey
    ACFSQHQYDZIPRL-UHFFFAOYSA-N
    InChI
    1S/C4F10NO4S2.Li/c5-1(6,7)3(11,12)20(16,17)15-21(18,19)4(13,14)2(8,9)10;/q-1;+1
    Synonyms
    Bis(pentafluoroethanesulfonyl)imide Lithium Salt | BS-26591 | L0267 | Ethanesulfonamide, 1,1,2,2,2-pentafluoro-N-((pe...
  11. Tetra-n-octylphosphonium Bromide
    CAS: 23906-97-0 PubChem CID: 3015167 Formula: C32H68BrP Molecular Weight: 563.77
    In Stock Item #: T162754
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    Technical Identifiers
    IUPAC Name
    tetraoctylphosphanium;bromide
    SMILES
    CCCCCCCC[P+](CCCCCCCC)(CCCCCCCC)CCCCCCCC.[Br-]
    InChIKey
    QVBRLOSUBRKEJW-UHFFFAOYSA-M
    InChI
    1S/C32H68P.BrH/c1-5-9-13-17-21-25-29-33(30-26-22-18-14-10-6-2,31-27-23-19-15-11-7-3)32-28-24-20-16-12-8-4;/h5-32H2,1-4H3;1H/q+1;/p-1
    Synonyms
    Tetraoctylphosphonium bromide
  12. Cyclopropyldiphenylsulfonium Tetrafluoroborate
    CAS: 33462-81-6 Formula: C15H15BF4S Molecular Weight: 314.15
    Out of Stock Item #: C153418
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    Technical Identifiers
    IUPAC Name
    cyclopropyl(diphenyl)sulfanium;tetrafluoroborate
    SMILES
    [B-](F)(F)(F)F.C1CC1[S+](C2=CC=CC=C2)C3=CC=CC=C3
    InChIKey
    DWEYKSWKFYZEGZ-UHFFFAOYSA-N
    InChI
    1S/C15H15S.BF4/c1-3-7-13(8-4-1)16(15-11-12-15)14-9-5-2-6-10-14;2-1(3,4)5/h1-10,15H,11-12H2;/q+1;-1
    Synonyms
    J-520194 | cyclopropyl(diphenyl)sulfanium;tetrafluoroborate | CYCLOPROPYLDIPHENYLSULFONIUMTETRAFLUOROBORATE | Cyclopr...
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Frequently Asked Questions

Which catalyst subcategory should I start with?
Start with the reaction type: chiral catalysts for asymmetric synthesis, organocatalysts for metal-free reactions, photocatalysts for light-driven workflows, transition metal catalysts for broad synthetic applications, or specialized families like Buchwald, olefin metathesis, and C–H activation catalysts.
How do I choose between organocatalysts and metal catalysts?
Organocatalysts offer metal-free selectivity, simpler workup, and lower toxicity. Metal catalysts provide broader substrate scope and often higher reactivity. Consider substrate, desired selectivity, and downstream purification needs.
What specifications matter most when comparing catalysts?
Focus on catalyst family, metal center, purity or grade, ligand compatibility, moisture or air sensitivity, and package size. Storage conditions and special handling requirements are critical for sensitive systems.
Are pre-formed metal-ligand complexes available?
Yes. Browse Buchwald Catalysts, Cross-Coupling Catalysts, and Hydrogenation Catalysts for pre-formed complexes ready to use, eliminating the need to combine metal and ligand in situ.

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