Reagents and tools for chemical synthesis, including catalysts, ligands, building blocks, solvents, and specialized reagents. Locate materials by reaction need and review key specifications such as purity, grade, and storage guidance.
Chemical Synthesis
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Browse chiral auxiliaries for stereocontrolled synthesis and route development. Use these tools to guide selectivity in asymmetric transformations and intermediate preparation.
Explore flavor and fragrance ingredients, intermediates, and related compounds for formulation, screening, and synthesis work. This category helps support aroma and sensory chemistry workflows.
Find organometallic reagents for bond formation, functionalization, and synthetic method development. Compare reactive systems used in route design and laboratory synthesis.
Browse boronic acids and derivatives for Suzuki coupling, medicinal chemistry, and building block sourcing. This page helps you identify versatile partners for C–C bond formation.
Explore Grignard reagents for nucleophilic addition, bond construction, and route development. Review practical organomagnesium options for synthesis workflows.
Find organosilicon reagents for protection, coupling, materials chemistry, and synthesis. Compare silicon-based tools used across method development and functional group manipulation.
Browse ionic liquids for green chemistry, separations, catalysis, and specialty processing workflows. This category helps you source alternative media and functional ionic systems.
Source reagents used in C–C bond formation and core scaffold construction. Use this page to compare synthetic tools for building complex molecules more efficiently.
Explore coupling reagents for amide bond formation, peptide chemistry, and general synthesis. Review options suited to activation, efficiency, and reaction optimization.
Find halogenation reagents for selective functionalization and synthetic route development. Compare practical tools for installing or modifying halogenated motifs.
Browse oxidation reagents for functional group interconversion, route development, and laboratory synthesis. Choose oxidants that fit selectivity, substrate scope, and workflow needs.
Explore protection and deprotection reagents for multistep synthesis and functional-group management. This page helps you source tools for cleaner sequence planning and execution.
Find reducing agents for functional group conversion, hydrogen transfer, and general synthetic workflows. Compare reagents used for selective reduction and reaction optimization.
Popular Products
- (+)-(S)-N,N-Dimethyl-1-[(R)-1′,2-bis(diphenylphosphino)ferroCAS: 55650-59-4 Formula: C38H37FeNP2 Molecular Weight: 625.5In Stock Item #: S115631View ProductPricing & Pack Sizes
Technical Identifiers
- Synonyms
- (S)-(R)-BPPFA
- (+)-Dibenzoyl-D-tartaric AcidCAS: 17026-42-5 Formula: C18H14O8 Molecular Weight: 358.3In Stock Item #: D154781View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- (2S,3S)-2,3-dibenzoyloxybutanedioic acid
- SMILES
- C1=CC=C(C=C1)C(=O)OC(C(C(=O)O)OC(=O)C2=CC=CC=C2)C(=O)O
- InChIKey
- YONLFQNRGZXBBF-KBPBESRZSA-N
- InChI
- 1S/C18H14O8/c19-15(20)13(25-17(23)11-7-3-1-4-8-11)14(16(21)22)26-18(24)12-9-5-2-6-10-12/h1-10,13-14H,(H,19,20)(H,21,22)/t13-,14-/m0/s1
- Synonyms
- D-(+)-Di-O,O-benzoyltartaric acid | D3826 | (2S,3S)-2,3-dibenzoyloxybutanedioic acid | Dibenzoyltartaric acid, (+)-D-...
- 1,3-CyclohexanedioneIn Stock Item #: C106972View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- cyclohexane-1,3-dione
- SMILES
- C1CC(=O)CC(=O)C1
- InChIKey
- HJSLFCCWAKVHIW-UHFFFAOYSA-N
- InChI
- 1S/C6H8O2/c7-5-2-1-3-6(8)4-5/h1-4H2
- Synonyms
- F0001-1313 | Hydroresorcinol | NSC57477 | NSC-57477 | EC 207-980-0 | 6UK3D2BXJT | STL145900 | UNII-6UK3D2BXJT | BDBM2...
- 1,3-CyclopentanedioneIn Stock Item #: C138777View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- cyclopentane-1,3-dione
- SMILES
- C1CC(=O)CC1=O
- InChIKey
- LOGSONSNCYTHPS-UHFFFAOYSA-N
- InChI
- 1S/C5H6O2/c6-4-1-2-5(7)3-4/h1-3H2
- Synonyms
- p-Chlorophenylhydrazine | cyclopentane-1,3-quinone | FT-0606601 | BBL011146 | NSC364015 | NSC-364015 | AKOS000278923 ...
- (1R,2R)-(-)-1-Amino-2-indanolCAS: 163061-73-2 Formula: C9H11NO Molecular Weight: 149.19In Stock Item #: R160940View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- (1R,2R)-1-amino-2,3-dihydro-1H-inden-2-ol
- SMILES
- C1C(C(C2=CC=CC=C21)N)O
- InChIKey
- LOPKSXMQWBYUOI-RKDXNWHRSA-N
- InChI
- 1S/C9H11NO/c10-9-7-4-2-1-3-6(7)5-8(9)11/h1-4,8-9,11H,5,10H2/t8-,9-/m1/s1
- Synonyms
- (1R,2R)-1-amino-2,3-dihydro-1H-inden-2-ol | C44ZZ4E55A | 1H-Inden-2-ol, 1-amino-2,3-dihydro-, (1R,2R)-rel- | D86558 |...
- (S)-(-)-1,1,2-Triphenyl-1,2-ethanediolCAS: 108998-83-0 Formula: C20H18O2 Molecular Weight: 290.36In Stock Item #: I165871View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- (2S)-1,1,2-triphenylethane-1,2-diol
- SMILES
- C1=CC=C(C=C1)C(C(C2=CC=CC=C2)(C3=CC=CC=C3)O)O
- InChIKey
- GWVWUZJOQHWMFB-IBGZPJMESA-N
- InChI
- 1S/C20H18O2/c21-19(16-10-4-1-5-11-16)20(22,17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15,19,21-22H/t19-/m0/s1
- Synonyms
- AC-8872 | (S)-2,2,1-Triphenyl-ethane-1,2-diol | MFCD00075492 | (S)-1,1,2-Triphenyl-1,2-ethanediol | DTXSID501294087 |...
- (S)-(-)-1-(1-Naphthyl)ethylamineCAS: 10420-89-0 Formula: C12H13N Molecular Weight: 171.24In Stock Item #: N122375View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- (1S)-1-naphthalen-1-ylethanamine
- SMILES
- CC(C1=CC=CC2=CC=CC=C21)N
- InChIKey
- RTCUCQWIICFPOD-VIFPVBQESA-N
- InChI
- 1S/C12H13N/c1-9(13)11-8-4-6-10-5-2-3-7-12(10)11/h2-9H,13H2,1H3/t9-/m0/s1
- Synonyms
- AI3-26858 | (1S)-1-naphthalen-1-ylethanamine | 1-Naphthalenemethanamine, alpha-methyl-, (.alpha.S)- | (1S)-(-)-1-(Nap...
- (S)-(-)-1-Boc-2-pyrrolidinecarbonitrileCAS: 228244-04-0 Formula: C10H16N2O2 Molecular Weight: 196.25In Stock Item #: B119264View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- tert-butyl (2S)-2-cyanopyrrolidine-1-carboxylate
- SMILES
- CC(C)(C)OC(=O)N1CCCC1C#N
- InChIKey
- MDMSZBHMBCNYNO-QMMMGPOBSA-N
- InChI
- 1S/C10H16N2O2/c1-10(2,3)14-9(13)12-6-4-5-8(12)7-11/h8H,4-6H2,1-3H3/t8-/m0/s1
- Synonyms
- (S)-1-Boc-2-pyrrolidinecarbonitrile | Ald3-H_000013 | (R)-N-BOC-2-pyrrolidinonitrile | tert-butyl(2S)-2-cyano-1-pyrro...
- 1-ThioglycerolIn Stock Item #: T109440View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- 3-sulfanylpropane-1,2-diol
- SMILES
- C(C(CS)O)O
- InChIKey
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N
- InChI
- 1S/C3H8O2S/c4-1-3(5)2-6/h3-6H,1-2H2
- Synonyms
- NCGC00260427-01 | 1,2-Propanediol, 3-mercapto- | HSDB 2184 | D92320 | 2,3-Dihydroxypropanethiol | 3-Mercapto-1,2-prop...
- 1-TriacontanolIn Stock Item #: T113181View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- triacontan-1-ol
- SMILES
- CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO
- InChIKey
- REZQBEBOWJAQKS-UHFFFAOYSA-N
- InChI
- 1S/C30H62O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-31/h31H,2-30H2,1H3
- Synonyms
- 1-?Triacontanol | Melissyl alcohol | Myricyl alcohol | FT-0608318 | NSC402492 | NSC-402492 | Q4860821 | Well-Bloom | ...
- 1-Trifluoromethyl-1,2-benziodoxol-3-(1H)-oneIn Stock Item #: T189226View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- 1-(trifluoromethyl)-1λ3,2-benziodoxol-3-one
- SMILES
- C1=CC=C2C(=C1)C(=O)OI2C(F)(F)F
- InChIKey
- XHEOXSQMBWJOKP-UHFFFAOYSA-N
- InChI
- 1S/C8H4F3IO2/c9-8(10,11)12-6-4-2-1-3-5(6)7(13)14-12/h1-4H
- Synonyms
- DHY074A7WG | Togni's reagents carbonyl compound [MI] | FT-0603356 | FT-0685225 | EN300-136055 | MFCD18800706 | 1-Trif...
- 1-Trifluoromethylcyclopropane-1-carboxylicAcidIn Stock Item #: T137562View ProductPricing & Pack Sizes
Technical Identifiers
- IUPAC Name
- 1-(trifluoromethyl)cyclopropane-1-carboxylic acid
- SMILES
- C1CC1(C(=O)O)C(F)(F)F
- InChIKey
- SKCBKBCACWDALV-UHFFFAOYSA-N
- InChI
- 1S/C5H5F3O2/c6-5(7,8)4(1-2-4)3(9)10/h1-2H2,(H,9,10)
- Synonyms
- FT-0608323 | 1-(Trifluoromethyl)cyclopropane-1-carboxylic acid | CYCLOPROPANECARBOXYLIC ACID, 1-(TRIFLUOROMETHYL)- | ...
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Frequently Asked Questions
How do I choose between coupling reagents for my reaction?
For peptide synthesis, compare HATU, HBTU, and TBTU efficiency and racemization. For Suzuki coupling, boronic acids vs. esters depend on stability. Match reagent to substrate, solvent, and required temperature.
Which subcategory covers organometallic reagents?
Browse Organometallic Reagents for general organolithium, organozinc, and organotin compounds. Use Grignard Reagents for organomagnesium chemistry, or Boronic Acids and Derivatives for Suzuki and Chan-Lam couplings.
What specifications matter for synthesis reagents?
Purity and titer are critical for stoichiometric reagents. Watch for moisture content in organometallics, peroxide content in ethers, and water sensitivity overall. Solvent and concentration matter for solution-form reagents.
Are flavor and fragrance compounds also available here?
Yes. Flavors & Fragrances products are listed within Chemical Synthesis since many serve as building blocks or final intermediates in synthesis workflows.