Cart
sales@molnova.com
Hydroxyzine free base
CAS No. 68-88-2
Hydroxyzine free base ( —— )
Catalog No. M22598 CAS No. 68-88-2
Hydroxyzine is an antagonist of histamine H1-receptor. Hydroxyzine is an antihistaminic with sedative properties used in the control of anxiety and emesis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 272 | In Stock |
|
| 10MG | 408 | In Stock |
|
| 25MG | 672 | In Stock |
|
| 50MG | 945 | In Stock |
|
| 100MG | 1278 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameHydroxyzine free base
-
NoteResearch use only, not for human use.
-
Brief DescriptionHydroxyzine is an antagonist of histamine H1-receptor. Hydroxyzine is an antihistaminic with sedative properties used in the control of anxiety and emesis.
-
DescriptionHydroxyzine is an antagonist of histamine H1-receptor. Hydroxyzine is an antihistaminic with sedative properties used in the control of anxiety and emesis.
-
Synonyms——
-
PathwayGPCR/G Protein
-
TargetHistamine Receptor
-
RecptorH1 receptor
-
Research Areanervous system
-
IndicationAgitation on Recovery From Sedation
Chemical Information
-
CAS Number68-88-2
-
Formula Weight374.9
-
Molecular FormulaC21H27ClN2O2?
-
Purity>98% (HPLC)
-
Solubility——
-
SMILESOCCOCCN1CCN(CC1)C(c1ccccc1)c1ccc(Cl)cc1
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1. Mcintyre I M , Mallett P , Trochta A , et al. Hydroxyzine distribution in postmortem cases and potential for redistribution[J]. Forensic ence International, 2013, 231(1-3):28-33.
molnova catalog
related products
-
Betahistine mesylate
Betahistine is an antivertigo drug first used for treating vertigo assosicated with Ménière’s disease.
-
Decloxizine dihydroc...
Decloxizine dihydrochloride is a histamine 1 receptor antagonist.
-
Ciproxifan maleate
Ciproxifan maleate(FUB-359 maleate) is a highly potent and selective histamin H3-receptor antagonist with IC50 of 9.2 nM, with low apparent affinity at other receptor subtypes.
