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3729 results for "3-Phenyl-3-(trifluoromethyl)-3H-diazepine"

3729 Results for: "3-Phenyl-3-(trifluoromethyl)-3H-diazepine"

HALO® ES-C18, BIOCLASS, HPLC Columns, Advanced Materials Technology

HALO® ES-C18, BIOCLASS, HPLC Columns, Advanced Materials Technology

Supplier: Advanced Materials Technology

HALO® BIOCLASS ES-C18 Peptide columns made with innovative Fused-Core® particle technology are ideal for both ultrafast- and ultrahigh-resolution separations of peptides and polypeptides up to 20 kDa. HALO® peptide columns offer comparable peak capacity to sub-2 μm non-core columns at 40 to 50% back pressure (2.7 μm), and 20% higher peak capacity than sub-2 μm non-core columns at comparable back pressure (2 μm). HALO 160 Å peptide columns are optimized for high performance in HPLC, UHPLC and LCMS peptide applications.

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SDA (NHS-Diazirine) (succinimidyl 4,4′-azipentanoate), Pierce™

SDA (NHS-Diazirine) (succinimidyl 4,4′-azipentanoate), Pierce™

Supplier: Thermo Scientific

Thermo Scientific Pierce SDA (NHS-Diazirine) combines proven NHS-ester and diazirine-based photoreaction chemistries with conjugate amine-containing molecules with nearly any other functional group via long-wave UV-light activation. A 3.9Å spacer arm separates the two photoreactive groups.

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GsBP®-35MS Mid-Polar GC Columns, GS-Tek

GsBP®-35MS Mid-Polar GC Columns, GS-Tek

Supplier: General Separation Technologies, Inc.

Typical application: Amytriptyline and Nortriptyline, Anilines, Barbiturates (Acid-neutral drugs), Basic drugs (Underivatized), Benzodiazepines, Chlordane, CLP Pesticides, Cold medication (Basic drugs - Underivatized), Endocrine disruptos: Butyl tins (hexyl derivatives), EPA Method 552.2, EPA Method 615-Chlorophenoxyacid herbicides, Ethanolamines, Fentanyl, Organo Tins, Organochlorine pesticides I EPA Method 8081A, Organochlorine pesticides IV, Organophosphorus pesticides II EPA 8141A, PCBs by EPA Method 8082, Pesticides, EPA 508.1, Phenols, Phenoxy acid herbicides - Methyl Derivative, EPA 8151A, Primary amines, Sympathomimetic amines (Basic drugs - Underivatized), Toxaphene.

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LC-SDA (NHS-LC-Diazirine) (succinimidyl 6-(4,4′-azipentanamido)hexanoate), Pierce™

LC-SDA (NHS-LC-Diazirine) (succinimidyl 6-(4,4′-azipentanamido)hexanoate), Pierce™

Supplier: Thermo Scientific

Thermo Scientific Pierce LC-SDA (NHS-LC-Diazirine) combines proven NHS-ester and diazirine-based photoreaction chemistries with conjugate amine-containing molecules with nearly any other functional group via long-wave UV-light activation. A 12.5Å spacer arm separates the two photoreactive groups.

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Sulfo-SDAD (Sulfo-NHS-SS-Diazirine) (sulfosuccinimidyl 2-[(4,4′-azipentanamido)ethyl]-1,3′-dithiopropionate], Pierce™

Sulfo-SDAD (Sulfo-NHS-SS-Diazirine) (sulfosuccinimidyl 2-[(4,4′-azipentanamido)ethyl]-1,3′-dithiopropionate], Pierce™

Supplier: Thermo Scientific

Thermo Scientific Pierce Sulfo-SDA (Sulfo-NHS-Diazirine) combines proven NHS-ester and diazirine-based photoreaction chemistries with conjugate amine-containing molecules with nearly any other functional group via long-wave UV-light activation. A 3.9Å spacer arm separates the two photoreactive groups.

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HALO® ES-CN, BIOCLASS, HPLC Columns, Advanced Materials Technology

HALO® ES-CN, BIOCLASS, HPLC Columns, Advanced Materials Technology

Supplier: Advanced Materials Technology

HALO® BIOCLASS ES-CN Peptide columns made with innovative Fused-Core® particle technology are ideal for both ultrafast- and ultrahigh-resolution separations of peptides and polypeptides up to 20 kDa. HALO® peptide columns offer comparable peak capacity to sub-2 μm non-core columns at 40 to 50% back pressure (2.7 μm). HALO® 160 Å peptide columns are optimized for high performance in HPLC, UHPLC and LCMS peptide applications.

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SDAD (NHS-SS-Diazirine) (succinimidyl 2-((4,4'-azipentanamido)ethyl)-1,3'-dithiopropionate), Pierce™

SDAD (NHS-SS-Diazirine) (succinimidyl 2-((4,4'-azipentanamido)ethyl)-1,3'-dithiopropionate), Pierce™

Supplier: Thermo Scientific

Thermo Scientific Pierce SDAD (NHS-SS-Diazirine) combines proven NHS-ester and diazirine-based photoreaction chemistries with conjugate amine-containing molecules with nearly any other functional group via long-wave UV-light activation. A 13.5Å spacer arm containing a cleavable disulfide bond separates the two photoreactive groups.

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Sulfo-SDAD (Sulfo-NHS-SS-Diazirine) (sulfosuccinimidyl 2-[(4,4′-azipentanamido)ethyl]-1,3′-dithiopropionate], Pierce™

Sulfo-SDAD (Sulfo-NHS-SS-Diazirine) (sulfosuccinimidyl 2-[(4,4′-azipentanamido)ethyl]-1,3′-dithiopropionate], Pierce™

Supplier: Thermo Scientific

Thermo Scientific Pierce Sulfo-SDAD (Sulfo-NHS-SS-Diazirine) combines proven NHS-ester and diazirine-based photoreaction chemistries with conjugate amine-containing molecules with nearly any other functional group via long-wave UV-light activation. A 13.5Å spacer arm containing a cleavable disulfide bond separates the two photoreactive groups.

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Sulfo-LC-SDA (Sulfo-NHS-LC-Diazirine) (sulfosuccinimidyl 6-(4,4′-azipentanamido)hexanoate), Pierce™

Sulfo-LC-SDA (Sulfo-NHS-LC-Diazirine) (sulfosuccinimidyl 6-(4,4′-azipentanamido)hexanoate), Pierce™

Supplier: Thermo Scientific

Thermo Scientific Pierce Sulfo-LC-SDA (Sulfo-NHS-LC-Diazirine) combines proven NHS-ester and diazirine-based photoreaction chemistries with conjugate amine-containing molecules with nearly any other functional group via long-wave UV-light activation. A 12.5Å spacer arm separates the two photoreactive groups.

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