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715 Results for: "Chiral"

Avantor® Hichrom HI-DEX B-SE, GC Columns

Avantor® Hichrom HI-DEX B-SE, GC Columns

Supplier: VWR International

Unique selectivity for the separation of enantiomers. Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX G-01, GC Columns

Avantor® Hichrom HI-DEX G-01, GC Columns

Supplier: VWR International

Unique selectivity for the separation of enantiomers. Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX DAC Gamma, GC Columns

Avantor® Hichrom HI-DEX DAC Gamma, GC Columns

Supplier: VWR International

Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX DET Gamma, GC Columns

Avantor® Hichrom HI-DEX DET Gamma, GC Columns

Supplier: VWR International

Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX B-03, GC Columns

Avantor® Hichrom HI-DEX B-03, GC Columns

Supplier: VWR International

Unique selectivity for the separation of enantiomers. Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX DMT Beta, GC Columns

Avantor® Hichrom HI-DEX DMT Beta, GC Columns

Supplier: VWR International

Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX G-03, GC Columns

Avantor® Hichrom HI-DEX G-03, GC Columns

Supplier: VWR International

Unique selectivity for the separation of enantiomers. Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom, Chiral Columns

Avantor® Hichrom, Chiral Columns

Supplier: Avantor

Chiral columns are designed for the analysis of a wide range of enantiomers of pharmaceutical and agrochemical origin. This column contains a chiral dinitrophenyltartramide moiety is bonded to the silica surface through a propyl spacer group.

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Avantor® Hichrom HI-DEX DAC Beta, GC Columns

Avantor® Hichrom HI-DEX DAC Beta, GC Columns

Supplier: VWR International

Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX DET Beta, GC Columns

Avantor® Hichrom HI-DEX DET Beta, GC Columns

Supplier: VWR International

Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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Avantor® Hichrom HI-DEX DMP Beta, GC Columns

Avantor® Hichrom HI-DEX DMP Beta, GC Columns

Supplier: VWR International

Useful for the analysis of chiral compounds in fragrances, pesticides and pharmaceuticals in which the determination of the ratio of enantiomers in a sample is necessary.

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J.T.Baker® BAKERBOND®, Wide-Pore DEAM Chiral HPLC Columns

J.T.Baker® BAKERBOND®, Wide-Pore DEAM Chiral HPLC Columns

Supplier: AVANTOR PERFORMANCE MATERIAL LLC

J.T.Baker® BAKERBOND®, Wide-Pore DEAM Chiral HPLC Columns

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Hypersil™ Chiral-IFT HPLC Column

Supplier: Thermo Scientific

Separate a wide range of enantiomers with Thermo Scientific™ Hypersil™ Chiral HPLC columns, designed for normal-phase separations of neutral, acidic, and basic racemates.

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TLC Plates, Special Layers, Glass Backing, Chiral Plate, Macherey-Nagel

TLC Plates, Special Layers, Glass Backing, Chiral Plate, Macherey-Nagel

Supplier: Macherey-Nagel

These glass plates with a special layer are used for TLC enantiomer separations (e.g. amino acids, thiazolidine derivatives, dipeptides, lactones, α-hydroxycarboxylic acids).

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Hypersil™ Chiral-IZT HPLC Column

Supplier: Thermo Scientific

Separate a wide range of enantiomers with Thermo Scientific™ Hypersil™ Chiral HPLC columns, designed for normal-phase separations of neutral, acidic, and basic racemates.

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H-Pro-Pro-Asp-NH₂ Trifluoroacetate

Supplier: Bachem Americas

Absorbed to modified silica gel, PPD-amide is a highly efficient recyclable chiral catalyst for aldol reactions.

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Chiral Column Test Mix (9 Components), Restek

Supplier: Restek

The mix consists of (C10:0) Methyl decanoate (210 μg/ml), (C11:0) methyl undecanoate (210 μg/ml), (C12) n-dodecane 150 μg/ml, (C12:0) methyl dodecanoate (210 μg/ml), 2,3-butanediol (+/-) (500 μg/ml), 1-heptanol (180 μg/ml), 3-methylphenol (m-cresol) (160 μg/ml), 1-phenylethanol (+/-) (500 μg/ml) and α-pinene (+/-) (500 μg/ml).

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Poroshell 120 Chiral, Agilent Technologies

Poroshell 120 Chiral, Agilent Technologies

Supplier: AGILENT TECHNOLOGIES, INC (CSD) CA

Chiral selectors on superficially porous particles for fast chiral separations in NP, RP, and SFC.

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SGE GC Column, CYDEX-B, Trajan Scientific and Medical

SGE GC Column, CYDEX-B, Trajan Scientific and Medical

Supplier: Trajan Scientific and Medical

These chiral columns are designed for the separation of enantiomeric compounds found in natural products.

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CrossLab CycloSil-B Columns, Agilent Technologies

CrossLab CycloSil-B Columns, Agilent Technologies

Supplier: AGILENT TECHNOLOGIES, INC (CSD) CA

Delivers improved resolution of many chiral separations and is ideal for a number of chiral γ-lactones and terpenes.

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Rt®-βDEXcst Columns (Fused Silica), Restek

Rt®-βDEXcst Columns (Fused Silica), Restek

Supplier: Restek

By adding β or γ cyclodextrin to Restek's bonded Rtx®-1701 stationary phase, we greatly enhance overall utility and column lifetime for Restek's chiral columns, compared to columns that have pure cyclodextrin stationary phases.

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N-Benzylcinchonidinium chloride ≥98.0% (by HPLC, titration analysis)

Supplier: TCI America

[Chiral Phase-Transfer Catalyst]
CAS Number: 69257-04-1
MDL Number: MFCD00082422
Molecular Formula: C26H29ClN2O
Molecular Weight: 420.98
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Specific rotation [a]20/D: -184 deg (C=1, H2O)

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J&W HP-Chiral β Columns, Agilent Technologies

J&W HP-Chiral β Columns, Agilent Technologies

Supplier: AGILENT TECHNOLOGIES, INC (CSD) CA

Permethylated ß-cyclodextrin chiral stationary phase that resolves volatile optical isomers.

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Rt®-βDEXse Columns (fused silica), Restek

Rt®-βDEXse Columns (fused silica), Restek

Supplier: Restek

By adding β or γ cyclodextrin to Restek's bonded Rtx®-1701 stationary phase, we greatly enhance overall utility and column lifetime for Restek's chiral columns, compared to columns that have pure cyclodextrin stationary phases.

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Rt®-βDEXsa Columns (fused silica), Restek

Rt®-βDEXsa Columns (fused silica), Restek

Supplier: Restek

By adding β or γ cyclodextrin to Restek's bonded Rtx®-1701 stationary phase, we greatly enhance overall utility and column lifetime for Restek's chiral columns, compared to columns that have pure cyclodextrin stationary phases.

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Cyclo(-D-Ala-Val)

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

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Cyclo(-Ala-Glu)

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

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Cyclo(-Ser-Ser)

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

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N-Benzylquinidinium chloride ≥98.0% (by titrimetric analysis)

Supplier: TCI America

[Chiral Phase-Transfer Catalyst]
CAS Number: 77481-82-4
MDL Number: MFCD00198106
Molecular Formula: C27H31ClN2O2
Molecular Weight: 451.01
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Specific rotation [a]20/D: 215 deg (C=0.64, H2O)

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Cyclo(-Gly-Pro)

Supplier: Bachem Americas

Also known as dioxopiperazines, piperazine-2,5-diones or DKPs. Diketopiperazines may occur as by-products during peptide synthesis or during the degradation of peptides. These cyclic dipeptides have been detected as taste-modulating compounds in food, they often show biological activity. DKPs are valuable chiral synthons, employed e.g. in Schöllkopf's versatile bislactim ether approach. They also have found use as catalysts for enantioselective synthesis, e.g. in the asymmetric Strecker reaction. See also the TRH metabolite cyclo(-His-Pro), G-1745, and cyclo(-Asp-Phe), G-1695, the major degradation product of aspartame.

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