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Chiral Alcohols

Discover Reisch’s expertise in high-purity chiral alcohols for pharmaceuticals and chemicals. We offer custom synthesis, rigorous quality assurance, and secure handling of your projects, ensuring precision and reliability from R&D to large-scale production.

Products You May Be Interested In
(R)-(+)-1-Phenylethanol

CAS NO. 1517-69-7

Synonyms: (R)-(+)-sec-Phenethyl alcohol; (R)-(+)-alpha-Methylbenzyl alcohol
(S)-(-)-sec-Phenethyl alcohol

CAS No. 1445-91-6

Synonyms: (S)-(-)-alpha-Methylbenzyl alcohol
(S)-1-(2-Fluorophenyl)ethanol

CAS NO. 171032-87-4

Synonyms: (S)-1-(o-Fluorophenyl)ethanol; (S)-2'-Fluorophenylethan-1-ol
(S,S)-2,3-Butanediol

CAS NO. 19132-06-0

Synonyms: (2S,3S)-(+)-2,3-Butanediol; (S,S)-2,3-Butylene glycol; (S,S)-Butane-2,3-diol
(2R,5R)-hexane-2,5-diol

CAS NO. 17299-07-9

Boiling Point: 198.53 ºC, 213.4±8.0 ºC (760 mmHg)
(R,R)-2,4-Pentanediol

CAS NO. 42075-32-1

Synonyms (2R,4R)-(-)-Pentanediol; (2R,4R)-2,4-Pentanediol; (2R,4R)-Pentanediol
(2S,4S)-(+)-2,4-Pentanediol

CAS NO. 72345-23-4

Boiling Point: 178.10 ºC, 199.5±0.0 ºC (760 mmHg)
(R)-(-)-1,3-Butanediol

CAS NO. 6290-03-5

Boiling point: 107-110 ºC (23 mmHg)
(R)-1-(3-Nitrophenyl)ethanol

CAS NO. 76116-24-0

Boiling point: 218 ºC / Flash point: 124 ºC
(R)-4-Bromo-alpha-methylbenzyl alcohol

CAS NO. 76155-78-7

Synonyms: (R)-1-(4-Bromophenyl)ethanol
(2S,5S)-hexane-2,5-diol

CAS NO. 34338-96-0

Boiling Point: 198.53 ºC, 199.5±0.0 ºC (760 mmHg)
(R,R)-2,3-Butanediol

CAS NO. 24347-58-8

Synonyms: (2R,3R)-(-)-2,3-Butanediol; (2R,3R)-(-)-2,3-Butylene glycol; (R,R)-Butane-2,3-diol
(S)-(+)-1-Phenyl-1,2-ethanediol

CAS NO. 25779-13-9

Synonyms: (S)-(+)-alpha,beta-Dihydroxyethylbenzene; (S)-(+)-Styrene glycol
(S)-1-(2-Chlorophenyl)ethanol

CAS NO. 131864-71-6

Boiling point: 231 ºC / Flash point: 94 ºC
(S)-1-(3-Chlorophenyl)ethanol

CAS NO. 135145-34-5

Synonyms: (-)-1-(m-Chlorophenyl)ethanol; (S)-1-(m-Chlorophenyl)ethanol
(alphaS)-alpha-Methyl-3-pyridinemethanol

CAS NO. 5096-11-7

Synonyms: (S)-(-)-1-(3-Pyridyl)ethanol; (S)-1-(3-Pyridyl)ethanol
(S)-2-Chloro-1-(2,4-dichlorophenyl)ethanol

CAS NO. 126534-31-4

Synonyms: (S)-2,4-Dichloro-alpha-(chloromethyl)-benzenemethanol

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Chiral Alcohols: Essential Intermediates in Chemical Synthesis

Chiral alcohols play a crucial role in the realm of chemical synthesis, particularly in the pharmaceutical and fine chemical industries. These compounds, characterized by their unique three-dimensional structures, are indispensable intermediates in the production of a wide range of chiral molecules, which are often necessary for creating effective and safe drugs.

Table of Contents

Importance of Chiral Alcohols

Chirality is a property of asymmetry where a molecule has a non-superimposable mirror image. This characteristic is vital in the pharmaceutical industry because the two enantiomers (mirror images) of a chiral molecule can have drastically different effects in biological systems. One enantiomer might be therapeutically beneficial, while the other could be inactive or even harmful. Therefore, the production of enantiomerically pure compounds is essential for drug development and manufacturing.

Chiral alcohols are used as building blocks or intermediates in the synthesis of these enantiomerically pure compounds. Their ability to influence the stereochemistry of the molecules they help create makes them invaluable in the design and production of pharmaceuticals, agrochemicals, and fine chemicals.

Synthesis of Chiral Alcohols

The synthesis of chiral alcohols can be achieved through various methods, each chosen based on the desired end product’s complexity and requirements. Some of the common methods include:

Asymmetric Reduction:

Enzymatic or chemical reduction of ketones or aldehydes to produce chiral alcohols. This method often employs chiral catalysts to ensure high enantioselectivity.

Asymmetric Catalysis:

Using chiral ligands in transition metal-catalyzed reactions to introduce chirality into the alcohol.

Biocatalysis:

Utilizing enzymes such as lipases, esterases, or dehydrogenases to catalyze the formation of chiral alcohols with high specificity and under mild conditions.

Resolution of Racemates:

Separating racemic mixtures (equal parts of both enantiomers) into individual enantiomers through physical or chemical methods, such as crystallization or chromatography.

Applications in the Pharmaceutical Industry

The pharmaceutical industry relies heavily on chiral alcohols for the synthesis of active pharmaceutical ingredients (APIs). These intermediates are used to create complex molecules with precise three-dimensional structures necessary for drug efficacy and safety. For example, many antiviral, anticancer, and cardiovascular drugs are synthesized using chiral alcohol intermediates.

In addition to pharmaceuticals, chiral alcohols find applications in the production of agrochemicals, where the selective action of chiral pesticides and herbicides can be exploited to enhance effectiveness and reduce environmental impact.

Quality and Purity Considerations

The production of chiral alcohols demands high levels of purity and enantiomeric excess to ensure the desired pharmacological effects.

Advanced analytical techniques, such as nuclear magnetic resonance (NMR), high-performance liquid chromatography (HPLC), and gas chromatography (GC), are employed to characterize and verify the purity and stereochemistry of these compounds.

Reisch's Commitment to Excellence

At Reisch, we specialize in the custom synthesis of high-purity chiral alcohols tailored to meet the specific needs of our clients in the pharmaceutical and chemical industries. Our state-of-the-art facilities and expert team ensure that we deliver products of the highest quality, adhering to stringent regulatory standards.

Our services include:

Custom Synthesis

Tailored solutions for the production of specific chiral alcohols.

Quality Assurance

Rigorous testing and validation to ensure purity and enantiomeric excess.

Confidentiality

Secure handling of client information and intellectual property.

By leveraging advanced synthetic techniques and a deep understanding of stereochemistry, Reisch provides reliable and efficient solutions for the production of chiral alcohols. Whether for research and development or large-scale manufacturing, our commitment to quality and precision ensures that our clients receive the best possible products and services.

Contact Reisch today to learn more about how our expertise in chiral alcohol synthesis can support your pharmaceutical and chemical projects. Together, we can achieve your goals with precision and reliability.

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