695 Results for: "Chiral"

Supplier: Merck

Chiral derivatizing agent employed in the assay of the enantiomeric purity of amino acids with OPA

Supplier: Merck

Chiral derivatizing agent for alcohols; some methyl substituted primary alcohols which are difficult to separate otherwise, can also be separated.

Supplier: Merck

(R)-(-)-a-Methoxy-a-(trifluoromethyl)phenylacetyl chloride (Mosher’s acid chloride) is generally used as a chiral derivatizing agent.

Supplier: Merck

(R)-(-)-a-Methoxy-a-(trifluoromethyl)phenylacetyl chloride (Mosher’s acid chloride) is generally used as a chiral derivatizing agent.

Supplier: Merck

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl isothiocyanate is a chiral derivatization reagent which reacts mainly with enantiomeric amino acids.

Supplier: Merck

Nα-(2,4-Dinitro-5-fluorophenyl)-L-valinamide [L-FDVA] is a derivatizing chiral agent.

Supplier: Merck

Nα-(2,4-Dinitro-5-fluorophenyl)-L-alaninamide (FDAA) is a chiral derivatizing agent (CDA), has high enantioselectivity but low sensitivity as compared to other CDAs. It is generally used to assign the stereochemistry of amino acids in trace amounts.

Supplier: Merck

(+)-1-(9-Fluorenyl)ethyl chloroformate [(+)-FLEC] is a chiral derivatizing reagent. It helps in separating enantiomers of α-amino acids, as well as helps in determining its optical purity using HPLC method.

Supplier: MACHEREY-NAGEL

Silica based phases for HPLC enantiomer separation in which CHIRAL-1 seperation is based on ligand exchange and CHIRAL-2 or CHIRAL-3 on charge-transfer and further interactions as well as on steric effects.

Supplier: DR MAISCH

HPLC column - ReproSil-Pur Chiral-NR.

Supplier: Merck

D-FDVA may be used as derivatizing agent for nullifying the possibility of minor compounds to be diastereomer of xenortide A, during HPLC-MS screening.

Supplier: DR MAISCH

USP L51 column: amylose tris-3,5-dimethylphenylcarbamate coated to porous silica particles.

Supplier: DR MAISCH

USP L51 column: amylose tris-3,5-dimethylphenylcarbamate coated on porous silica particles.

Supplier: DR MAISCH

USP L40 column: cellulose tris-3,5-dimethylphenylcarbamate coated to porous silica particles.

Supplier: DR MAISCH

USP L40 column: cellulose tris-3,5-dimethylphenylcarbamate coated on porous silica particles.

Supplier: Merck

ChiraDex® is a versatile HPLC column characterised by broad enantioselectivity and can be used for the separation of enantiomers of numerous different classes of substances. ChiraDex® is based on beta-cyclodextrin covalently linked to spherical particles of silica, and is ideal for chiral separation of hydrocarbons, steroids, phenol esters and derivatives, aromatic amines, heterocycles with five- to seven-membered ring. Simply composed RP-eluents can be used in most separations.

Supplier: USP

USP Reference Standards are specified for use in conducting official USP–NF tests and assays. USP also provides Reference Standards specified in the Food Chemicals Codex as well as authentic substances—high-quality chemical samples—as a service to analytical, clinical, pharmaceutical and research laboratories. To confirm accuracy and reproducibility, USP Reference Standards are rigorously tested and evaluated by multiple independent laboratories including USP, commercial, regulatory, and academic labs. USP also provide publicly available, official documentary standards for pharmaceutical ingredients in the USP–NF that link directly with our primary reference standards.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Resonac

CDBS-453: Separates optical isomers by using their conformational compatibility differences. Versatile column for chiral separations.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: Avantor

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.

Supplier: MACHEREY-NAGEL

These columns contain a silica-based protein phase for HPLC enantiomer separation. The base material is NUCLEOSIL® silica, the chiral selector bovine serum albumin (BSA).

Supplier: DR MAISCH

One of the most versatile chiral column available for normal phase HPLC. Use on compounds with aromatic, amide, carbamate, ester groups, alkyl amines, and compounds with multiple stereogenic sites.