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
Löslichkeit
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 Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher F,T
R-Sätze: 11-23/24/25-39/23/24/25
S-Sätze: 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)
Toxizität 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 Toxizität 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 Händler.

Global( 96)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
sales@capotchem.com China 29797 60
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
career henan chemical co
+86-0371-86658258 15093356674;
factory@coreychem.com China 29826 58
Hefei TNJ Chemical Industry Co.,Ltd.
0551-65418671
sales@tnjchem.com China 34572 58
Hebei Lingding Biotechnology Co., Ltd.
+86-18031140164 +86-19933155420
erin@hbldbiotech.com China 878 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250
1026@dideu.com China 29220 58
CR Corporation Lomited

fred.wen@crcorporation.cn CHINA 12069 58
Alfa Chemistry
+1-5166625404
Info@alfa-chemistry.com United States 21317 58
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923
1026@dideu.com China 9116 58
TargetMol Chemicals Inc.
+1-781-999-5354
support@targetmol.com United States 19973 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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