CAS 118-23-0
:Bromodiphenhydramine
Description:
Bromodiphenhydramine, with the CAS number 118-23-0, is an antihistamine that belongs to the diphenhydramine class of compounds. It is characterized by its chemical structure, which includes a bromine atom substituted on one of the phenyl rings of diphenhydramine. This modification enhances its pharmacological properties. Bromodiphenhydramine exhibits sedative effects and is commonly used to alleviate allergy symptoms, such as sneezing, runny nose, and itching, as well as to induce sleep due to its central nervous system depressant activity. The compound is typically administered orally and is known for its relatively rapid onset of action. In addition to its antihistaminic properties, bromodiphenhydramine may also possess anticholinergic effects, which can lead to side effects such as dry mouth, dizziness, and drowsiness. As with other antihistamines, caution is advised when using this substance, particularly in combination with alcohol or other CNS depressants. Overall, bromodiphenhydramine is a useful therapeutic agent in managing allergic reactions and sleep disorders.
Formula:C17H20BrNO
InChI:InChI=1S/C17H20BrNO/c1-19(2)12-13-20-17(14-6-4-3-5-7-14)15-8-10-16(18)11-9-15/h3-11,17H,12-13H2,1-2H3
InChI key:InChIKey=NUNIWXHYABYXKF-UHFFFAOYSA-N
SMILES:C(OCCN(C)C)(C1=CC=C(Br)C=C1)C2=CC=CC=C2
Synonyms:- 2-(p-Bromo-α-phenylbenzyloxy)-N,N-dimethylethylamine
- 2-[(4-Bromophenyl)phenylmethoxy]-N,N-dimethylethanamine
- 4-Bromodiphenhydramine
- Ambodryl
- Bromanautine
- Bromazin base
- Bromdiphenhydramine
- Bromo-Benadryl
- Bromo-Benadryl base
- Bromodiphenhydramine
- Deserol
- Deserol base
- Ethanamine, 2-[(4-bromophenyl)phenylmethoxy]-N,N-dimethyl-
- Ethylamine, 2-[(p-bromo-α-phenylbenzyl)oxy]-N,N-dimethyl-
- Histabromamine
- N-2-(4-bromobenzhydryloxy)ethyldimethylamine
- Neo-Benadryl
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Found 3 products.
Bromodiphenhydramine
CAS:<p>Ambodryl, an antihistamine effective against many bacteria, aids in skin allergy studies.</p>Formula:C17H20BrNOColor and Shape:SolidMolecular weight:334.25

