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Chemical synthesis reagents are essential to transform building blocks into target molecules quickly, safely, and cleanly. The Thermo Scientific
portfolio includes over 5,000 organic synthesis reagents spanning a wide range of R&D applications. The compounds include reducing and
oxidizing reagents, organometallics, commonly used functional reagents, and specialty reagents for specific reactions.
Our organic synthesis products are available in a range of purity grades, concentrations, and pack sizes. Packaging options include our industry-leading AcroSeal packaging for safe handling of air- or moisture-sensitive, pyrophoric, or hazardous reagents. Our Custom and Bulk Chemical Services group can take you beyond the catalog to provide customized solutions for your unique organic synthesis needs.
We offer a broad range of reagents and product subsets for organic synthesis, including relatively simple molecules like acetic anhydride, complex molecules like EDTA, and reagents that facilitate a wide variety of transformations.
Phenols are organic aromatic compounds made of a phenyl functional group (C6H5) bonded to a hydroxyl functional group (OH).
Halogen inorganic salts are inorganic compounds made of metals and halogen elements, including fluorine, chlorine, bromine, iodine, and astatine.
Ethylenediaminetetraacetic acid (EDTA) is an aminopolycarbcoxylic acid that readily binds to iron and calcium ions to form water-soluble complexes, even at neutral pH.
Acetic anhydrides are common electrophiles, as the leaving group is carboxylate.
Commonly requested reagents | Available in pre-made solutions reagents | High purity reagents |
Tetrabutylammonium hydroxide | Glutaraldehyde (25% and 50% in water) | Sodium borohydride |
Trifluoroacetic anhydride | Sodium biphenyl (in diethylene glycol diethyl ether) | N-bromosuccinimide |
Oxalyl chloride | Sodium methoxide (in methanol) | |
Polypropylene glycol | Borane-tetrahydrofuran complex (in THF) |
Organometallics and organometalloids are widely used in organic chemistry due to their diversity and versatility. Organometallic compounds contain at least one bond between the carbon atom of an organic compound and a metal atom, while organometalloids have at least one bond between a carbon and a semimetal.
Due to the electropositive nature of their metals, these compounds are highly reactive. Organometallics function in organic synthesis as strong bases, as nucleophiles, as reducing agents, and in metal exchange reactions.
Grignard reagents are highly reactive organomagnesium halides that react with most organic compounds as well as H2O, CO2, and O2. They are often used in reaction with aldehydes and ketones to form alcohols.
Organolithium compounds possess direct bonds between carbon and lithium atoms. Organolithium reagents are strongly basic, highly reactive nucleophiles used to transfer organic groups or lithium atoms to substrates during organic synthesis reactions.
Organozinc compounds are pyrophoric organometallics with direct bonds between carbon and zinc atoms. Available in various chemical compositions, they are less reactive than analogous organometallic reagents and often appear as intermediates in reactions.
Organotin compounds are based on tin with hydrocarbon substituents and commonly have an oxidation state of Sn(IV). Available in various chemical compositions, these compounds have multiple industrial and research applications.
Reagent |
Diisobutylaluminium hydride |
Titanium(IV) n-butoxide |
Octacarbonyldicobalt |
Sodium 1-heptanesulfonate monohydrate |
Organosilanes are used in organic chemistry research for protecting groups to act as intermediates in organic synthesis.
Type | Usage |
Silyls | Protecting and derivatization reagents |
Organosilanes | Reducing agents |
Silanes | Cross-coupling chemistry |
Allylsilanes | Stabilization of a-carbanions and b-carbocations |
Reagent |
Tetramethylsilane |
Tert-butyldimethylchlorosilane |
Triisopropylsilane |
3-glycidoxypropyltrimethoxysilane |
N,O-bis(trimethylsilyl)trifluoroacetamide |
Named chemical reactions—such as the Grignard reaction, Claisen rearrangement, and Clemmensen reduction, named after their discoverers一play a crucial role in organic synthesis and the creation of more complex and diverse chemical molecules.
The table lists major categories of named reactions used in organic synthesis along with key reactions in each category. For more information on their history, applications, and mechanisms, videos of key named reactions, and tables of building blocks for individual reactions, follow the links in the table toour Organic Chemistry Resources center.
Category | Selected reactions |
Electrophilic aromatic substitution reactions
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Nucleophilic substitution reactions
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Transition metal-catalyzed couplings
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Electrophilic addition reactions
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AcroSeal is our industry-leading packaging solution for safe handling of air- and moisture-sensitive solvents, as well as pyrophoric and hazardous reagents.The AcroSeal sealing system was recently redesigned to make it both easier and safer to remove the whole system and place it back on the bottle securely without need of a special tool. This facilitates access to larger volumes of product and packaging recycling after use.
Thermo Fisher Scientfic resources for organic synthesis include an eBook and online resources center detailing widely used named reactions such as the Grignard, Claisen, and Clemmensen reactions. Other organic synthesis resources include our interactive periodic table of elements search tool, our chemical structure search tool, and other Chemicals Resources.
For Research Use Only. Not for use in diagnostic procedures.