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Clonidin

CLONIDINE Struktur
4205-90-7
CAS-Nr.
4205-90-7
Bezeichnung:
Clonidin
Englisch Name:
CLONIDINE
Synonyma:
Kapvay;734571A;m-5041t;Arkamin;Clonidin;Nexiclon;ST-155-BS;Catapress;CLONIDINE;ClonidinHCl
CBNumber:
CB6505769
Summenformel:
C9H9Cl2N3
Molgewicht:
230.09
MOL-Datei:
4205-90-7.mol

Clonidin Eigenschaften

Schmelzpunkt:
141-142℃
Siedepunkt:
369.21°C (rough estimate)
Dichte
1.3946 (rough estimate)
Brechungsindex
1.6300 (estimate)
Flammpunkt:
9℃
storage temp. 
-20°C
L?slichkeit
DMSO:100.0(Max Conc. mg/mL);434.61(Max Conc. mM)
pka
8.10±0.50(Predicted)
Aggregatzustand
Solid
Farbe
White to Off-White
CAS Datenbank
4205-90-7(CAS DataBase Reference)
EPA chemische Informationen
1H-Imidazol-2-amine, N-(2,6-dichlorophenyl)-4,5-dihydro- (4205-90-7)
Sicherheit
  • Risiko- und Sicherheitserkl?rung
  • Gefahreninformationscode (GHS)
Kennzeichnung gef?hrlicher F,T
R-S?tze: 11-23/24/25-39/23/24/25
S-S?tze: 16-36/37-45
RIDADR  UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany  1
HS Code  2933290000
Giftige Stoffe Daten 4205-90-7(Hazardous Substances Data)
Toxizit?t LD50 oral in rat: 67300ug/kg
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H301 Giftig bei Verschlucken. Akute Toxizit?t oral Kategorie 3 Achtung GHS hazard pictogramssrc="/GHS06.jpg" width="20" height="20" /> P264, P270, P301+P310, P321, P330,P405, P501
Sicherheit

Clonidin Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Clonidine may be useful in the treatment of acute opioid withdrawal. Epidural clonidine 1–2μgkg –1 increases the duration and potency of analgesia provided by epidural opioid or local anaesthetic drugs.

Definition

ChEBI: A clonidine that is 4,5-dihydro-1H-imidazol-2-amine in which one of the amino hydrogens is replaced by a 2,6-dichlorophenyl group.

Pharmakokinetik

Clonidine is lipid soluble and rapidly absorbed after oral administration, with a peak plasma concentration occurring in 60–90min. O ral, intravenous and intramuscular routes may be used for sedation or analgesia. I n addition, epidural and intrathecal clonidine is used to augment regional anaesthesia, but perineural administration is of limited or no effect. The elimination halflife is 9–13h and is prolonged in renal failure. Fifty percent of an administered dose is excreted unchanged by the kidneys, and 50% is metabolised in the liver to inactive metabolites.

Stoffwechselwegen

Clonidine is well absorbed orally, with peak plasma concentrations after 60–90min. I t is highly lipid soluble, and approximately 50% is metabolised in the liver to inactive metabolites; the rest is excreted unchanged via the kidneys, with an elimination half-life of 9–12h.

Clonidin Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Clonidin Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 103)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-18192627656
1059@dideu.com China 3003 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29685 60
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28172 58
career henan chemical co
+86-0371-86658258 +8613203830695
factory@coreychem.com China 29809 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000
marketing@targetmol.com United States 32160 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763
sales@tnjchem.com China 34563 58
CR Corporation Limited
+8613062833949
fred.wen@crcorporation.cn China 8647 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923
1026@dideu.com China 8670 58
TargetMol Chemicals Inc.

support@targetmol.com United States 38631 58
GIHI CHEMICALS CO.,LIMITED
+8618058761490
info@gihichemicals.com China 49986 58

4205-90-7(Clonidin)Verwandte Suche:


  • CLONIDINE (200 MG)
  • clonidine (amino form)
  • clonidine (imino form)
  • 2-((2,6-dichlorophenyl)amino)-2-imidazoline
  • 2-(2,6-dichloroanilino)-1,3-diazacyclopentene-(2)
  • 2-(2,6-dichloroanilino)-2-imidazolin
  • 2-(2,6-dichloroanilino)-2-imidazoline
  • 2-(2,6-Dichlorophenylamino)-2-imidazoline
  • 2,6-dichloro-n-2-imidazolidinylidene-benzenamin
  • 2,6-dichloro-n-2-imidazolidinylidenebenzenamine
  • 2-[(2,6-Dichlorophenyl)imino]imidazolidine
  • 2-[(2,6-Dichlorophenyl)imino]imidazoline
  • 2-Imidazoline, 2-(2,6-dichloroanilino)-
  • 734571A
  • CLONIDINE BASE
  • Clonidine (base and/or unspecified salts)
  • Clonidine solution
  • 1H-Imidazol-2-amine, N-(2,6-dichlorophenyl)-4,5-dihydro-
  • Benzenamine, 2,6-dichloro-N-2-imidazolidinylidene-
  • Catapres-TTS
  • Clonidin
  • m-5041t
  • n-(2,6-dichlorophenyl)-4,5-dihydro-1h-imidazol-2-amin
  • N-(2,6-Dichlorophenyl)-4,5-dihydro-1H-imidazol-2-amine
  • ST-155-BS
  • 2,6-dichloro-N-(2-imidazolin-2-yl)aniline
  • ClonidinHCl
  • Clonidinhydrochlorid
  • ClonidineHCI-4,4,5,5(-imidazoline-D4)
  • CLONIDINE,1.0MG/MLINMETHANOL
  • ClonidineCI-4,4,5,5(-imidazoline-D4)
  • Arkamin
  • Catapress
  • Catapressan
  • CLONIDINE
  • Kapvay
  • Nexiclon
  • CLONIDINE USP/EP/BP
  • Clonidine (1140393)
  • Clonidine,α2-adrenergic,inhibit,Inhibitor,anesthesia,Adrenergic Receptor,Beta Receptor
  • Clonidine 2,6-Dichloro-N-(imidazolidin-2-ylidene)aniline
  • 4205-90-7
  • C9H9Cl2N3
  • C9H5D4N3Cl2HCl
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