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P6902

Pheniramine maleate salt

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5 g
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CLP 134,000

About This Item

Empirical Formula (Hill Notation):
C16H20N2 · C4H4O4
CAS Number:
Molecular Weight:
356.42
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352116
EC Number:
205-051-4
MDL number:
Form:
powder
Quality level:

CLP 134,000


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form

powder

Quality Level

SMILES string

OC(=O)\C=C/C(O)=O.CN(C)CCC(c1ccccc1)c2ccccn2

InChI

1S/C16H20N2.C4H4O4/c1-18(2)13-11-15(14-8-4-3-5-9-14)16-10-6-7-12-17-16;5-3(6)1-2-4(7)8/h3-10,12,15H,11,13H2,1-2H3;1-2H,(H,5,6)(H,7,8)/b;2-1-

InChI key

SSOXZAQUVINQSA-BTJKTKAUSA-N

Gene Information

human ... HRH1(3269)

Biochem/physiol Actions

Pheniramine maleate is a H1 histamine receptor antagonist.[1] It is an alkylamine derivative.[2] Structurally, pheniramine contains a chiral carbon atom with a hydrogen atom. Other substituents include the pyridyl, alkylamine and phenyl groups.[3] It is used as an antiallergic drug for treating the common cold, respiratory allergies,[4] urticaria, and systematic allergic reactions.[2]

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P5514C3025P9233
form

powder

form

powder

form

powder

form

powder

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

Gene Information

human ... HRH1(3269)

Gene Information

human ... HRH1(3269)

Gene Information

human ... HRH1(3269)

Gene Information

human ... DRD3(1814)


pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3



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Kerem Karaman et al.
American journal of surgery, 205(2), 213-219 (2012-09-05)
Laparoscopic cholecystectomy (LC) still leads to significant postoperative nausea and vomiting (PONV) and pain. Our aim was to evaluate the efficacy of dexamethasone or pheniramine hydrogen maleate, either alone or combined, in reducing the stress response and symptoms after LC.
M R Louhaichi et al.
Talanta, 78(3), 991-997 (2009-03-10)
A new simple, rapid and sensitive liquid chromatographic method has been developed and validated for the simultaneous determination of pseudoephdrine, pheniramine, guaifenisin, pyrilamine, chlorpheniramine and dextromethorphan in cough and cold pharmaceuticals. The separation of these compounds was achieved within 13
Wenhua Gao et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 904, 121-127 (2012-08-21)
A rapid and efficient dual preconcentration method of on-line single drop liquid-liquid-liquid microextraction (SD-LLLME) coupled to sweeping micellar electrokinetic chromatography (MEKC) was developed for trace analysis of three antihistamines (mizolastine, chlorpheniramine and pheniramine) in human urine. Three analytes were firstly



Global Trade Item Number

SKUGTIN
P6902-5G04061834394136

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