Antihistamines or H1 blockers

DIPHENHYDRAMINE N-OXIDE HYDROCHLORIDE

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including MSDS and any product information leaflets have been developed and issued under the Authority of the

A stable-labeled internal standard for diphenhydramine testing or isotope dilution methods by GC/MS or LC/MS for clinical toxicology, urine drug testing, or forensic analysis. Diphenhydramine is an antihistamine sold over the counter under the

The diphenyl derivatives, having potency for inhibiting InhA (an essential enoyl acyl carrier protein reductase involved in mycolic acid biosynthesis), were studied.Diphenyl ether may be used to synthesize dibenzofuran via intramolecular cyclization

The diphenyl derivatives, having potency for inhibiting InhA (an essential enoyl acyl carrier protein reductase involved in mycolic acid biosynthesis), were studied.Diphenyl ether may be used to synthesize dibenzofuran via intramolecular cyclization

Diphenyl-1，2，4-triazin-3-amine.

Diphenyl-1，2，4-triazin-3-amine.

Diphenyl-1，2，4-triazin-3-amine.

Diphenylamine, a secondary aromatic amine, is an N -substituted derivative of aniline. Application Diphenylamine may be used in the preparation of diphenylamine reagent, which is employed for the quantitative estimation of nucleic acid (DNA) from

Diphenylamine, a secondary aromatic amine, is an N -substituted derivative of aniline. Application Diphenylamine may be used in the preparation of diphenylamine reagent, which is employed for the quantitative estimation of nucleic acid (DNA) from

Application Diphenylamine can undergo palladium-catalyzed intramolecular cyclization to form carbazole. It may also be used as a starting material in the synthesis of triphenylamine.