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Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder

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Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder

Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder
Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder

Large Image :  Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder Get Best Price

Product Details:
Place of Origin: China
Brand Name: YW
Certification: GMP, ISO9001, USP, KOSHER
Model Number: 23076-35-9
Payment & Shipping Terms:
Minimum Order Quantity: 10g
Price: Negotiable
Packaging Details: Discreet disguised package or as required
Delivery Time: 3-7 working days
Payment Terms: Western Union, MoneyGram, Bank transfer
Supply Ability: 5000kg/week
Detailed Product Description
CAS No.: 1094-61-7 MF: C12H17ClN2S
MW: 256.79 Appearance: White Powder
Purity: 99% Usage: Anti-aging
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Analgesic Materials XYLAZINE HYDROCHLORIDE CAS 23076-35-9 White Powder
 
Basic information:
 
Chemical name: XYLAZINE HYDROCHLORIDE
MF: C12H17ClN2S
MW: 256.79
CAS: 23076-35-9
Appearance: white powder
Purity: over 99%
 
Description:
 
Xylazine is used as a sedative and analgesic in Cervidae and other species of wildlife when it is desirable to produce a reversible state of sedation accompanied by a short period of analgesia.
Xylazine hydrochloride is an alpha-two agonist with sedative, analgesic, and muscle relaxant properties. It was developed by the Bayer company in Germany in the 1960s and thus has a long history of use in veterinary medicine and wildlife.
It is an excellent sedative and muscle relaxant that can easily be delivered using small darts, resulting in more accurate dart delivery and reduced trauma to the animal. It is commonly used in conjunction with ketamine, etorphine and carfentanil in numerous species.
 
Pharmacology:
 
Xylazine HCl Injection (xylazine), a non-narcotic compound, is a sedative and analgesic as well as muscle relaxant. Its sedative and analgesic activity is related to central nervous system depression. Its muscle relaxant effect is based on inhibition of the intraneural transmission of impulses in the central nervous system. The principal pharmacological activities develop within 10 to 15 minutes after intramuscular injection in horses and Cervidae, and within 3 to 5 minutes following intravenous administration in horses.
 
A sleeplike state, the depth of which is dose-dependent, is usually maintained for 1 to 2 hours, while analgesia lasts from 15 to 30 minutes. The centrally-acting muscle relaxant effect causes relaxation of the skeletal musculature, complementing sedation and analgesia.
 
In horses and Cervidae under the influence of Xylazine HCl Injection (xylazine), the respiratory rate is reduced as in natural sleep. Following treatment with Xylazine HCl Injection (xylazine), the heart rate is decreased and a transient change in the conductivity of the cardiac muscle may occur, as evidenced by a partial atrioventricular block. This resembles the atrioventricular block often observed in normal horses.1,2,3,4 Partial A-V block may occasionally occur following intramuscular injection of Xylazine HCl Injection (xylazine). When given intravenously in horses, the incidence of partial A-V block is higher. Intravenous administration causes a transient rise in blood pressure in horses, followed by a slight decrease.
 
Xylazine HCl Injection (xylazine) has no effect on blood clotting time or other hematologic parameters.
 
Dosage:
 
Xylazine can be administered intravenously, intramuscularly, subcutaneously or orally. The commercial product contains 23.32 mg/ml xylazine hydrochloride in water based injectable solution. Xylazine can be obtained also as pure crystalline powder. There is a significant species dependent response to xylazine administration. Intramuscular dose of up to 0.3 mg/kg for cattle has been suggested by the manufacturer. The recommended doses for horses were 0.6 mg/kg and for sheep 1.0 mg/kg (Garcia-Villar et al., 1981). For dogs the dose was even higher.

 

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