2514 Results for: "Isochinolin-5-amin Hydrochlorid&amp"

Supplier: Honeywell Chemicals

High quality inorganic and organic reference materials produced according to ISO 9001.

Supplier: Thermo Fisher Scientific

6-Benzyladenine hydrochloride 98%

Supplier: Molekula

3-Chloropropyldimethylammonium chloride

Supplier: Thermo Fisher Scientific

Imipramine hydrochloride

Supplier: Spectrum Chemical

Cyclohexylamine Hydrochloride is an organic compound that is an aliphatic amine. The compound is a high-melting solid. Cyclohexylamine hydrochloride is used as an intermediate in the synthesis of other organic compounds.

Supplier: MP Biomedicals

Xylazine hydrochloride is an alpha agonist with sedative, analgesic and muscle relaxant properties.

Supplier: Merck

2-Amino-4,5-dimethylthiazole hydrochloride, Sigma-Aldrich®

Supplier: COMBI-BLOCKS

3-Phenylaniline hydrochloride

Supplier: Thermo Fisher Scientific

Benzydamine hydrochloride

Supplier: Merck

9-Aminoacridine hydrochloride monohydrate, Sigma-Aldrich®

Supplier: Merck

Bis(2-chloroethyl)ammonium chloride, Sigma-Aldrich®

Supplier: Merck

2-Chloropropyldimethylammonium chloride, Sigma-Aldrich®

Supplier: Merck

3-Chloropropyldimethylammonium chloride, Sigma-Aldrich®

Supplier: Molekula

9-Aminoacridine hydrochloride monohydrate

Supplier: Thermo Fisher Scientific

Atomoxetine hydrochloride

Supplier: Molekula

Bis(2-chloroethyl)ammonium chloride

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

Supplier: Spectrum Chemical

Amantadine hydrochloride USP

Supplier: Thermo Fisher Scientific

Tizanidine hydrochloride 98%

Supplier: LGC Standards PROMOCHEM

Amantadine hydrochloride

Supplier: Merck

2-Adamantylamine hydrochloride, Sigma-Aldrich®

Supplier: Thermo Scientific

2-Adamantylamine hydrochloride

Supplier: Merck

Amantadine hydrochloride, Sigma-Aldrich®

Supplier: LGC Standards PROMOCHEM

Amantadine hydrochloride

Supplier: Molekula

Amantadine hydrochloride

Supplier: Merck

Cystamine dihydrochloride, Sigma-Aldrich®

Supplier: Molekula

Cystamine dihydrochloride

Supplier: Merck

Cystamine dihydrochloride, Sigma-Aldrich®

Supplier: Merck

Cystamine dihydrochloride, Sigma-Aldrich®