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Salbutamol

Salbutamol Struktur
34391-04-3
CAS-Nr.
34391-04-3
Englisch Name:
Salbutamol
Synonyma:
Salbutamol;r-albuterol;LEVALBUTEROL;Levalbutreol;(L)-ALBUTEROL;Levosalbutamol;R-SALBUTAMOL HCL;LEVALBUTEROL HCL;LEVOSALBUTEROLHCL;Levosalbutamol (Levalbuterol)
CBNumber:
CB0275903
Summenformel:
C13H21NO3
Molgewicht:
239.31
MOL-Datei:
34391-04-3.mol

Salbutamol Eigenschaften

Siedepunkt:
433.5±40.0 °C(Predicted)
Dichte
1.152±0.06 g/cm3(Predicted)
pka
9.99±0.31(Predicted)
InChI
InChI=1/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/t12-/s3
InChIKey
NDAUXUAQIAJITI-PLAQIDKDNA-N
SMILES
C1(=CC=C(O)C(CO)=C1)[C@@H](O)CNC(C)(C)C |&1:9,r|
CAS Datenbank
34391-04-3(CAS DataBase Reference)

Sicherheit

Kennzeichnung gef?hrlicher Xn
R-S?tze: 22
S-S?tze: 36

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

Levalbuterol was launched in the US for the treatment or prevention of bronchospasm in patients with reversible obstructive airway disease. It is the single R-enantiomer version of racemic albuterol (salbutamol) marketed for more than 30 years as a mainstay in the treatment of asthma. The R-isomer can be obtained with an excellent optical purity by enantiomeric purification based on the separation of diastereomeric tartrates. This isomer retains solely the desired bronchodilating effect of the racemic mixture due to a potent agonistic effect on β2-adrenoceptors, with a lower incidence of β- mediated side effects such as pulse rate increase, tremor and decrease in blood glucose and potassium levels. A pivotal clinical trial with two doses of levalbuterol and racemic albuterol, given by nebulization, demonstrated a greater improvement in lung function for the pure enantiomer levalbuterol.

Verwenden

(R)-Salbutamol is used in composition and methods to reduce beta-agonist-mediated tachyphylaxis.

Salbutamol Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Salbutamol Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 73)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
hebei hongtan Biotechnology Co., Ltd
+86-86-1913198-3935 +8617331935328
sales03@chemcn.cn China 970 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21634 55
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873
sales@chemdad.com China 39894 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763
sales@tnjchem.com China 34563 58
AFINE CHEMICALS LIMITED
+86-0571-85134551
sales@afinechem.com China 15352 58
Baoji Guokang Healthchem co.,ltd
+8615604608665 15604608665
dominicguo@gk-bio.com CHINA 9414 58
sgtlifesciences pvt ltd
+8617013299288
dj@sgtlifesciences.com China 12373 58
Wuhan Cell Pharmaceutical Co., Ltd
+86-13129979210 +86-13129979210
sales@cellwh.com China 376 58
Suzhou ARTK Medchem Co., Ltd.
+86-512-68323658 +86-18168183658
sales1@artkmedchem.com China 39004 58
XIAMEN AMITY INDUSTRY AND TRADE CO., LTD.
+8618950047208
ellena@amitychem.com China 43416 58

34391-04-3()Verwandte Suche:


  • LEVALBUTEROL
  • LEVALBUTEROL HCL
  • (L)-ALBUTEROL
  • R-SALBUTAMOL HCL
  • (-)-alpha(sup1)-(((1,1-dimethylethyl)amino)methyl)-4-hydroxy-1,3-benzenedime
  • 1,3-benzenedimethanol,alpha(sup1)-(((1,1-dimethylethyl)amino)methyl)-4-hydrox
  • alpha’-diol,alpha(sup1)-((tert-butylamino)methyl)-4-hydroxy-m-xylene-alph
  • r-albuterol
  • 2-(hydroxymethyl)-4-[1-hydroxy-2-(tert-butylamino)ethyl]phenol
  • LEVOSALBUTEROLHCL
  • 1,3-Benzenedimethanol, a1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-, (a1R)- (9CI)
  • 1,3-Benzenedimethanol, a1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-, (R)-
  • Levosalbutamol
  • m-Xylene-a,a'-diol, a1-[(tert-butylamino)methyl]-4-hydroxy-, (R)-(-)- (8CI)
  • 2-(hydroxymethyl)-4-[(1R)-1-hydroxy-2-(tert-butylamino)ethyl]phenol
  • 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
  • Levalbutreol
  • Salbutamol
  • (R)-1-(4-Hydroxy-3-hydroxymethylphenyl)-2-(1,1-dimethylethylamino)ethanol
  • (R)-1-(4-Hydroxy-3-hydroxymethylphenyl)-2-tert-butylaminoethanol
  • (R)-4-Hydroxy-3-(hydroxymethyl)-α-[[(tert-butyl)amino]methyl]benzyl alcohol
  • (αR)-α-[(tert-Butylamino)methyl]-4-hydroxy-1,3-benzenedimethanol
  • 4-[(1R)-2-(tert-butylamino)-1-hydroxy-ethyl]-2-(hydroxymethyl)phenol
  • 4-[(1R)-2-(tert-butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
  • 4-[(1R)-2-(tert-butylamino)-1-hydroxy-ethyl]-2-methylol-phenol
  • Levosalbutamol (Levalbuterol)
  • 2-(Hydroxymethyl)-4-{(1R)-1-hydroxy-2-[(2-methyl-2-propanyl)amino]ethyl}phenol
  • 1,3-Benzenedimethanol, α1-[[(1,1-dimethylethyl)amino]methyl]-4-hydroxy-, (α1R)-
  • (+/-) - Albuterol (Levalbuterol)
  • 34391-04-3
  • 51022-72-9
  • C13H21NO3
  • API
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