• Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
  • Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
  • Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
  • Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
  • Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
  • Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone

Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone

Powder: Yes
Customized: Customized
Certification: GMP, HSE, ISO 9001, USP, BP
Suitable for: Elderly, Adult
State: Powder
Purity: >99%
Samples:
US$ 30/g 1 g(Min.Order)
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Customization:
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  • Overview
  • Product Description
  • Product Details
  • Application&Function
  • Specification
Overview

Basic Info.

Model NO.
D-sung Naltrexone
Product Name
Naltrexone
Name
Naltrexone Powder
Appearance
White Powder
Color
White
Grade
Pharmaceutical Grade
Assay
HPLC 99%
Application
Pharmaceutical
Specific
COA
Test Method
HPLC
Shelf Life
2 Years
CAS No.
16590-41-3
Mf
C20h23no4
Boiling Point
558.1
Melting Point
168-170
Density
1.47
Transport Package
Negotiable
Specification
99%
Trademark
D-sung
Origin
Shaanxi Xi′an
Production Capacity
1000kg/Month

Product Description

Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Product Description
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride NaltrexonePharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Product Details
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Product Name Naltrexone
CAS 16590-41-3
Appearance White crystalline powder
MF C20H23NO4
MW 341.407
Purity 99%
Shelf Life 2 Years

Naltrexone is a medication primarily used to manage alcohol or opioid dependence. An opioid-dependent person should not receive naltrexone before detoxification. It is taken by mouth or by injection into a muscle. Effects begin within 30 minutes. A decreased desire for opioids, though, may take a few weeks.

 
Application&Function
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone

Naloxone hydrochloride occurs as a white to slightly off-white powder, and is soluble in water, in dilute acids, and in strong alkali; slightly soluble in alcohol; practically insoluble in ether.
Naloxone hydrochloride injection is available as a sterile solution for intravenous, intramuscular, and subcutaneous administration. Each mL contains 0.4 mg of Naloxone hydrochloride. Each mL contains 8.9 mg of sodium chloride. The pH is adjusted between 3.0 to 6.5. The air in the cartridges has been displaced by nitrogen gas.
The most common side effects reported with naltrexone are gastrointestinal complaints such as diarrhea and abdominal cramping.

These adverse effects are analogous to the symptoms of withdrawal, as the mu receptor blockade will increase GI motility.

 

Specification
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride NaltrexonePharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride NaltrexonePharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride NaltrexonePharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
Pharmaceutical CAS 16590-41-3 Naltrexone Powder Naltrexone Hydrochloride Naltrexone
 

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Management System Certification
ISO 9001, ISO 14001, GMP, HACCP