Salbutamol
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Salbutamol Eigenschaften
- Schmelzpunkt:
- 157-160℃
- Siedepunkt:
- 381.97°C (rough estimate)
- Dichte
- 1.0700 (rough estimate)
- Brechungsindex
- 1.4800 (estimate)
- storage temp.
- 2-8°C
- L?slichkeit
- Sparingly soluble in water, soluble in ethanol (96 per cent).
- pka
- pKa 9.07(H2O t = 25.0±0.05 I = 0.10) (Uncertain);10.37(H2O t = 25.0±0.05 I = 0.10) (Uncertain)
- Aggregatzustand
- Solid
- Farbe
- White
- Wasserl?slichkeit
- 17.95g/L(25 ºC)
- Merck
- 13,215
- BRN
- 6405698
- Henry's Law Constant
- 1.5×1010 mol/(m3Pa) at 25℃, HSDB (2015)
- BCS Class
- 3
- Stabilit?t:
- Stable, but light sensitive. Incompatible with strong oxidizing agents.
- Major Application
- clinical testing
- InChI
- 1S/C13H21NO3/c1-13(2,3)14-7-12(17)9-4-5-11(16)10(6-9)8-15/h4-6,12,14-17H,7-8H2,1-3H3
- InChIKey
- NDAUXUAQIAJITI-UHFFFAOYSA-N
- SMILES
- CC(C)(C)NCC(O)c1ccc(O)c(CO)c1
- LogP
- 0.64
- CAS Datenbank
- 18559-94-9(CAS DataBase Reference)
- EPA chemische Informationen
- 1,3-Benzenedimethanol, .alpha.1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy- (18559-94-9)
Sicherheit
- Risiko- und Sicherheitserkl?rung
- Gefahreninformationscode (GHS)
| Kennzeichnung gef?hrlicher | Xn,T,F | ||
|---|---|---|---|
| R-S?tze: | 22-39/23/24/25-23/24/25-11 | ||
| S-S?tze: | 36-45-36/37-16-7 | ||
| RIDADR | 3249 | ||
| WGK Germany | 3 | ||
| RTECS-Nr. | ZE4400000 | ||
| HazardClass | 6.1(b) | ||
| PackingGroup | III | ||
| HS Code | 2922504500 | ||
| Speicherklasse | 11 - Combustible Solids | ||
| Hazard Classifications | Acute Tox. 4 Oral Aquatic Chronic 3 Eye Irrit. 2 Skin Sens. 1B |
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| Giftige Stoffe Daten | 18559-94-9(Hazardous Substances Data) |
| Bildanzeige (GHS) |
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Salbutamol Chemische Eigenschaften,Einsatz,Produktion Methoden
R-S?tze Betriebsanweisung:
R22:Gesundheitssch?dlich beim Verschlucken.S-S?tze Betriebsanweisung:
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.Beschreibung
Albuterol is a β2-adrenergic sympathomimetic amine with pharmacological similarities to terbutaline. It has almost no effect on β1-adrenoreceptors of the heart. It has expressed broncholytic effects—prevention or relief of bronchi spasms, lowering respiratory tract resistance, and increasing the vital capacity of the lungs.Chemische Eigenschaften
solidHistory
In 1968, Salbutamol (Albuterol) will become the most prescribed bronchodilator in the world. Discovered by DAVID HARTLEY, DAVID JACK, LAWRENCE LUNTZ AND ALEXANDER RITCHIE of the British company Allen and Hanburys, former division of Glaxo-smith kline marketed under the name of Ventolin; who will stop the acute crisis and save the life of the asthmatic.In 2008, a study shows its action in cases of neuromuscular diseases.
In February 2020, the U.S. Food and Drug Administration (FDA) approved the first generic of an albuterol sulfate inhalation aerosol for the treatment or prevention of bronchospasm in people four years of age and older with reversible obstructive airway disease and the prevention of exercise-induced bronchospasm in people four years of age and older. The FDA granted approval of the generic albuterol sulfate inhalation aerosol to Perrigo Pharmaceutical.
Verwenden
immune suppressant, antineoplastic, antiviralDefinition
ChEBI: A member of the class of phenylethanolamines that is 4-(2-amino-1-hydroxyethyl)-2-(hydroxymethyl)phenol having a tert-butyl group attached to the nirogen atom. It acts as a beta-adrenergic agonist used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).Biologische Funktion
Levalbuterol is the R-(–)-isomer of albuterol and is available only in solution to be administered via nebulizer. Because it is the active isomer, the dose is fourfold less than that of albuterol. Pirbuterol is the pyridine isostere of albuterol. It has pharmacokinetics similar to albuterol but is half as potent at the β2-receptor. Pirbuterol is only available as an inhaler, whereas albuterol comes in tablet, syrup, solution, and aerosol formulations.Allgemeine Beschreibung
Standard for Supelco MIP SPE cartridges. For more information request Supelco Literature T407075, T706019, T706030, T706020. Salbutamol is classified under the β-agonist group of chemicals which are known to possess powerful pharmacological activities.Clinical Use
Albuterol has the N-t-butyl and a salicyl alcohol phenyl ring, which gives it optimal β2-selectivity. It is resistant to COMT and slowly metabolized by MAO, giving it good oral bioavailability. Its onset by inhalation is within 5 minutes, with a duration of action between 4 and 8 hours. It currently is the drug of choice for relief of the acute bronchospasm of an asthmatic attack.Nebenwirkungen
Adverse effects of pirbuterol are nervousness, tremor, and headache, which is less than the profile for albuterol, which adds nausea, vomiting, dizziness, hypertension, insomnia, tachycardia, and palpitations.Environmental Fate
Tachycardia occurs as a reflex to the drop in mean arterial pressure (MAP) or as a result of b-1 stimulus. b-Adrenergic receptors in the locus coeruleus also regulate norepinephrineinduced inhibitory effects, resulting in agitation, restlessness, and hand tremor. Stimulation of nonpulmonary b2 receptors may lead to an increase in heart rate, QTc interval prolongation, nonspecific T-wave changes, skeletal muscle tremor, and slight increases in blood glucose and nonesterified fatty acids. Hypokalemia is more pronounced in patients receiving intravenous albuterol. Hypotension is also known to occur mostly in overdose. The buildup of cyclic AMP in the liver stimulates glycogenolysis and an increase in serum glucose.In skeletal muscle, this process results in increased lactate production. Direct stimulus of sodium/potassium ATPase in skeletal muscle produces a shift of potassium from the extracellular space to the intracellular space. Relaxation of smooth muscle produces a dilation of the vasculature supplying skeletal muscle, which results in a drop in diastolic and MAP.Myocardial ischemia and infarction have been associated with excessive tachycardia in elderly patients. The skin may be warm and pink with evidence of diaphoresis.
Salbutamol Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte
Salbutamol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.
Global( 276)Lieferanten
| Firmenname | Telefon | Land | Produktkatalog | Edge Rate | |
|---|---|---|---|---|---|
| ARCTIC EXPORTS INC | +1-3026880818 |
ARCTICEXPORTSINC@GMAIL.COM | Canada | 72 | 58 |
| Shenzhen Aoxi Technology Co., Ltd. | +852-46424790 |
frank88rawpowder@outlook.com | China | 162 | 58 |
| Ningbo Qingteng Plastic Cost.,Ltd. | +86-15028138352 +86-19322619905 |
admin@nbqingteng.com | China | 342 | 58 |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 |
info@tianfuchem.com | China | 21585 | 55 |
| Nanjing ChemLin Chemical Industry Co., Ltd. | 025-83697070 |
product@chemlin.com.cn | CHINA | 3009 | 60 |
| Shanghai Safer Pharmaceutical Technology Co., Ltd. | 021-31761238 |
sales@saferph.com | CHINA | 897 | 58 |
| TargetMol Chemicals Inc. | +1-781-999-5354; +1-00000000000 |
marketing@targetmol.com | United States | 32468 | 58 |
| Hubei Ipure Biology Co., Ltd | +8618062405514 |
ada@ipurechemical.com | China | 10236 | 58 |
| Hefei TNJ Chemical Industry Co.,Ltd. | +86-0551-65418671 +86-189 4982 3763 |
sales@tnjchem.com | China | 34563 | 58 |
| HONG KONG IPURE BIOLOGY CO.,LIMITED | 86 18062405514 18062405514 |
ada@ipurechemical.com | CHINA | 3461 | 58 |
18559-94-9(Salbutamol)Verwandte Suche:
Thiophanat-methyl
Diphenylsilandiol
2-Aminoethanol
5-tert-Butyl-2,4,6-trinitro-m-xylol
3,6-Bis[(4-chlor-2-phosphonophenyl)azo]-4,5-dihydroxynaphthalin-2,7-disulfonsure
m-Xylol
Xylol, Isomerengemisch
Kresoxim-methyl
Methyl
Brommethan
Bis[(tert-butyl)(β,3,4-trihydroxyphenethyl)ammonium]sulfat
2-(Diethylamino)ethanol
2-Dimethylaminoethanol
4-(Benzyloxy)-α-[[tert-butylamino]methyl]-m-xylol-α,α'-diol
Salbutamol
- sultanol
- Albuterol, α-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,αμ-diol
- 4-Hydroxy-3-hydroxymethyl-α-[(tert-butylamino)methyl]benzyl alcohol
- rac-(R*)-4-Hydroxy-3-(hydroxymethyl)-α-[[(tert-butyl)amino]methyl]benzyl alcohol
- (S)-1-(4-Hydroxy-3-hydroxymethylphenyl)-2-(1,1-dimethylethylamino)ethanol
- (S)-1-(4-Hydroxy-3-hydroxymethylphenyl)-2-tert-butylaminoethanol
- (S)-4-Hydroxy-3-(hydroxymethyl)-α-[[(tert-butyl)amino]methyl]benzyl alcohol
- 2-(Hydroxymethyl)-4-[(S)-1-hydroxy-2-[(1,1-dimethylethyl)amino]ethyl]phenol
- Salbuamol
- alpha-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-alpha,alpha-diol
- Salbutamol
- SAGEROOTEXTRACT
- Albuterol-D3 (3-hydroxymethyl-D2 α-D1)
- Salbutamol,α-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α′-diol, Albuterol
- Albuterol (200 mg)
- Albuterol-d9
- 4-[2-(tert-butylamino)-1-hydroxy-ethyl]-2-methylol-phenol
- Salbutamol (Albuterol) & Salbutamol Sulfate
- R,S-Albuterol USP
- SalbutaMol Solution
- rac Albuterol
- 1,3-BenzenediMethanol, a1-[[(1,1-diMethylethyl)aMino]Methyl]-4-hydroxy-
- Albuterol Solution, 100ppm
- Albuterol solution
- 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol, Albuterol
- α-[(tert-Butylamino)methyl]-4-hydroxy-m-xylene-α,α′-diol Albuterol
- 2-(tert-butylamino)-1-(4-hydroxy-3-hydroxymethylphenyl)ethanol
- 4-hydroxy-3-hydroxymethyl-alpha-((tert-butylamino)methyl)benzylalcohol
- ah3365
- alpha’-diol,alpha’-((tert-butylamino)methyl)-4-hydroxy-m-xylene-alph
- alpha-1-(((1,1-dimethylethyl)amino)methyl)-4-hydroxy-3-benzenedimethanol
- alpha-diol,alpha-1-((tert-butylamino)methyl)-4-hydroxy-m-xylene-alph
- SALBUTAMOL VETRANAL, 100 MG
- SALBUTAMOL, IMPURITY G2-[BENZYL(1,1-DIMETHYLETHYL)AMINO]-1-[4-HYDROXY-3-(HYDROXYMETHYL)PHENYL]ETHANONE EP STANDARD
- SALBUTAMOL, IMPURITY B(1RS)-2-[(1,1-DIMETHYLETHYL)AMINO]-1-(4-HYDROXYPHENYL)ETHANOL EP STANDARD
- SALBUTAMOL, KETONE IMPURITY BP STANDARD
- SALBUTAMOL, IMPURITY D(1RS)-2-[(1,1-DIMETHYLETHYL)AMINO]-1-HYDROXYETHYL]-2-HYDROXYBENZALDEHYDE EP STANDARD
- SALBUTAMOL, IMPURITY I(1RS)-2-[(1,1-DIMETHYLETHYL)AMINO]-1-[3-(HYDROXYMETHYL)-4-BENZYLOXYPHENYL]ETHANOL EP STANDARD
- SALBUTAMOL, BP STANDARD
- SALBUTAMOL, ALDEHYDE IMPURITY BP STANDARD
- SALBUTAMOL, EP STANDARD
- SALBUTAMOL, IMPURITY F1,1'[OXYBIS[METHYLENE(4-HYDROXY-1,3-PHENYLENE)]]BIS[2-[(1,1-DIMETHYLETHYL)AMINO]ETHANOL] EP STANDARD
- Albuterol USP/BP Base
- Alpha1-((Tert-Butylamino)Methyl)-4-Hydroxy-M-Xylene-Alpha,Alpha-Diol
- SALBUTANOL
- 1,3-Benzenedimethanol, .alpha.1-(1,1-dimethylethyl)aminomethyl-4-hydroxy-
- α-[(tert-butylamino)methyl]-4-hydroxy-m-xylene-α,α'-diol
- ALBUTEROL BASE USP/BP
- ALBUTEROL,USP
- 1-(tert-Butylaminomethyl)-4-hydroxy-m-xylene-a1,a3-diol
- 1,3-Benzenedimethanol, a1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy- (9CI)
- a1-tert-Butylaminomethyl-4-hydroxy-m-xylene-a1,a3-diol
- Airomir
- DL-N-tert-Butyl-2(4-hydroxy-3-hydroxymethylphenyl)2-hydroxyethylamine
- Eolene
- m-Xylene a,a'-diol, a-[(tert-butylamino)methyl]-4-hydroxy-
- m-Xylene-a,a'-diol, a1-[(tert-butylamino)methyl]-4-hydroxy- (8CI)
- Proventil Inhaler




