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S5013

Salbutamol hemisulfate salt

≥98%

Synonym(e):

α-([t-Butylamino]methyl)-4-hydroxy-m-xylene-α,α′-diol, Albuterol

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Größe/SKUVerfügbarkeitPreis
25 mg
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€ 71,70
50 mg
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€ 118,00
100 mg
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€ 199,00
250 mg
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€ 311,00

Über diesen Artikel

Lineare Formel:
C13H21NO3 · 1/2H2SO4
CAS-Nummer:
Molekulargewicht:
288.35
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
256-916-8
MDL number:
Assay:
≥98%

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Quality Segment

assay

≥98%

solubility

1 M NaOH: 50 mg/ml, clear to slightly hazy, yellow-green

originator

GlaxoSmithKline

SMILES string

OS(O)(=O)=O.CC(C)(C)NCC(O)c1ccc(O)c(CO)c1.CC(C)(C)NCC(O)c2ccc(O)c(CO)c2

InChI

1S/2C13H21NO3.H2O4S/c2*1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15;1-5(2,3)4/h2*4-6,12,14-17H,7-8H2,1-3H3;(H2,1,2,3,4)

InChI key

BNPSSFBOAGDEEL-UHFFFAOYSA-N

Gene Information

human ... ADRB2(154)

Application

Salbutamol hemisulfate salt was used as standard in analysis of fortified meat for LABA content using ELISA kits.3 It was used to study the response of prostaglandin 2α to various β-adrenergic agonists in cultured bovine endometrial cells.4
Salbutamol hemisulfate salt has been used as reference standards of drugs for the validation of β-agonist residue.

Biochem/physiol Actions

β2-Adrenergic receptor agonist.
Salbutamol is a β2 adrenoceptor agonist with short acting bronchodilation and anti-inflammatory effects. It relaxes the airway smooth muscles and inhibits bronchoconstriction induced by adenosine-5′ -monophosphate (AMP).1 Salbutamol is particularly effective in treatment of asthma as it provides immediate relief.2
Salbutamol is a β2 adrenoceptor agonist with short acting bronchodilation and anti-inflammatory effects. It relaxes the airway smooth muscles and inhibits bronchoconstriction induced by adenosine-5′ -monophosphate (AMP). Salbutamol is particularly effective in treatment of asthma as it provides immediate relief. Salbutamol is one of the most popular short-acting BA (SABA). It is useful in treating the symptoms of EIB (exercise induced bronchospasm).

Features and Benefits

This compound is featured on the β-Adrenoceptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

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Dieser Artikel
S0150000BP3021012633
description

≥98%

description

European Pharmacopoeia (EP) Reference Standard

description

British Pharmacopoeia (BP) Reference Standard

description

United States Pharmacopeia (USP) Reference Standard

assay

≥98%

assay

-

assay

-

assay

-

Quality Level

200

Quality Level

-

Quality Level

-

Quality Level

-

solubility

1 M NaOH: 50 mg/ml, clear to slightly hazy, yellow-green

solubility

-

solubility

-

solubility

-

originator

GlaxoSmithKline

originator

-

originator

-

originator

-

Gene Information

human ... ADRB2(154)

Gene Information

human ... ADRB2(154)

Gene Information

human ... ADRB2(154)

Gene Information

human ... ADRB2(154)


Piktogramme

Health hazardExclamation mark

Signalwort

Warning

Gefahrencodes

Hazard Classifications

Carc. 2 - Repr. 2 - Skin Sens. 1

Lagerklasse

11 - Combustible Solids

Was ist los?

WGK 2

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

PSA (Persönliche Schutzausrüstung)

Eyeshields, Gloves, type N95 (US)



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Questions

  1. is salbutamol an anticholinergic?

    1 answer
    1. Salbutamol hemisulfate is not an anticholinergic. This compound is a β2-Adrenergic receptor agonist.

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