Schiffs Reagent

Schiff Reagent is used in the Periodic Acid Staining Procedure. Intended for use with blood, bone marrow, tissue touch preparations or routine tissue sections. FDA approved for in vitro diagnostic use.

Harmonized Tariff Code:  3822.00 Hazard Statements: H315-H319-H335 Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation. Precautionary Statements: P261-P280-P305+P351+P338-P304+P340-P405-P501a Avoid breathing dust/fume/gas/mist/vapours/spray. Wear…

Storage: 2-8°C

Synonyms: Fuchsin sulfurous acid UNSPSC Code: 12352300

pH: 1.5 (H2O, 20°C) Solubility: (20°C) soluble Density: 1.00 g/cm3 (20°C)

suitable for detection of glycoproteins Empirical Formula: C₂₀H₂₁N₃O₃S Formula Weight: 383.46 Linear Formula: C₂₀H₂₁N₃O₃S Storage: 2-8°C RIDADR: UN 1789 8 / PGIII

… Prepared from dyes certified by the Biological Stain Commission (BSC)For In-Vitro Diagnostic Use.For Professional Use.For P.A.S. Reaction. May be used as replacement for Schiff Reagent in the PAS Kit. Legal Information: HARLECO is a registered trademark of Merck KGaA, Darmstadt, Germany

…AFB Molecular Weight: 323.83 Melting Point: 268-270 C (decomposes) Density: 1.22 g/cm3 at 20 C Application: HARLECO(R) For staining acid-fast bacillus in the Periodic Acid Schiff method Legal Information: HARLECO is a registered trademark of Merck KGaA, Darmstadt, Germany

p-Dimethylaminobenzaldehyde is used as a reagent for the determination of amino acids and peptides, amines, indoles, hydrazines and hydrogen peroxides as it forms colored condensation products (Schiff bases) with pyrroles and primary amines; spray reagent for tryptophan; For the determination of…

Storage: 2-8°C

…• Synthesis of bacterial peptide deformylase (PDF) inhibitor fumimycin • Asymmetric amination of glycine Schiff bases Other Notes: Acid labile reagent for Mitsunobu reactions allowing facile isolation of products 8 ; Electrophilic amination and hydrazination of enolates and…

UN Number: UN3085

Glutaraldehyde is a bifunctional protein cross-linking reagent, reacting with NH2 groups to form Schiff's bases. Sporicidal agent. Glutaraldehyde reacts through cross-linking to impart water resistance to protein and polyhydroxy compounds. It is also a reducing agent for photochemicals. In…

… MFCD00011344 Purity: >=99.0% (RT) Melting Point: 122 C (lit.) Application: Periodic acid may be used in the synthesis of diiodine heptoxide (I2O7). It may be used in the Periodic acid Schiff staining procedures. Other Notes: for the histochemical detection of polysaccharides

Synonyms: Ehrlich's reagent Formula: (CH₃)₂NC₆H₄CHO Formula Weight: 149.19 CAS No.: 100-10-7 Purity: 99% Application: Forms colored condensation products (Schiff bases) with pyrroles 1 and primary amines. 2 Packaging: 25, 100, 250, 500…

…aldehydes, ketones and glyoxals, react with amines to form Schiff base intermediates that are in equilibrium with their free forms.The labile Schiff’s base interaction can be stabilized by chemical reduction. If the Schiff’s base is formed between an aldehyde and an amine then sodium…

…(lit.) Application: 3-tert-Butyl-2-hydroxybenzaldehyde may be used in the synthesis of: •5-bromo-3-tert-butyl-2-hydroxybenzaldehyde •3-tert-butyl-5-(chloro-methyl)-2- hydroxybenzaldehyde •chiral Schiff base-titanium alkoxide catalysts •2 -(3-tert-butyl -2-hydroxybenzyl)aminomethylpyridine

… Formula Weight: 223.23 CAS No.: 723-89-7 Purity: 97% Application: Reactant for preparation of: • Indolin-2,3-dione Schiff bases as potential antimycobacterial agents • Antipyretic agents • Antiproliferative agents • Selective Cannabinoid…

… 2,3-Dichlorobenzaldehyde has been used in preparation of:. 4-(2,3-dichlorobenzylideneamino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one, Schiff base. ethyl 4-(2,3-dichlorophenyl)-1,6-dimethyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate via Biginelli condensation. benzyl…

… Formula Weight: 234.33 CAS No.: 37942-07-7 Purity: 99% Packaging: Used in the preparation of a chiral Schiff base ligand for an enantioselective copper-catalyzed addition of phenylacetylene to imines. 1 Also used to prepare…

…Biochem Physiol Actions: Cyanoborohydride Coupling Buffer is a reagent suitable for reductive amination processes, that contributes to transformation of simple alcohols into more complex amines. It is used in the conversion of Schiff base, by reducing it, to form a secondary amine without affecting…

Incorporates the proven Schiff's reagent and method.

…• α-Nucleophiles for hydrolysis of organophosphorus nerve agents • Xanthine oxidase inhibitors • Non-complexes Schiff base hydrazones • Methylated (±)-epigallocatechin gallate library for anticancer activity studies Packaging: 5 g in glass…

…at 25 C(lit.) Refractive Index: n20/D 1.412(lit.) Beilstein Registry Number: 385668 EC Number: 221-921-6 UNSPSC Code: 12352100 Application: Widely used N-acylating agent for amines, Schiff bases, and pyrrolidinones as well as O-acylating agent for alcohols, lactones, and saccharides.

… CAS No.: 104548-30-3 UN Number: UN3263 Purity: ~1.6% active oxygen basis Application: Reagent for: • Oxidation of Hantzsch 1,4-Dihydropyridines catalyzed by manganese(III) Schiff Base complexes • Epoxidation of alkenes • Oxidation of sulfides and olefins…

… 12352100 General description: 1,2-Diaminopropane undergoes condensation with salicylaldehyde and its derivatives to form Schiff base. It reacts with formaldehyde and hydrogen peroxide in aqueous acidic solution to give cage peroxide, 1,6-diaza-3,4,8,9-tetraoxa-11-methylbicyclo[4.4.2]dodecane.…

…dioxygenationUsed for: . Cation-induced molecular motion of spring-like [2]catenanes. Complexation of tweezer molecule with barium ion. Preparation of Schiff base macrocyclic barium complexes and studies of antibacterial activityReactant for oxidation of bis(amine)

…with catecholamine to form an orange water-soluble dye during flow injection-spectrophotometric determination of catecholamine drugs. Application: p-Toluidine has been used in preparation of:. aromatic azo compounds. bidentate Schiff base ligands via condensation with salicylaldehyde

…Number: 207-988-4 UNSPSC Code: 12352100 General description: 2-Aminopyridine is a basic building block of several heterocyclic compounds and Schiff bases. Application: 2-Aminopyridine (2AP) is a derivatizing agent which can be used as a fluorescent label for oligosaccharide detection,…

…• Lead dicyanamide-bridged nitronyl nitroxide radical polymeric complex • Antiferromagnetically coupled hexanuclear copper(II) Schiff base complexes with dicyanamido bridges • CuII2L based polymeric ladders using dicyanamide bridges • Luminous…