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Naltrexone hydrochloride

CAS No.
16676-29-2
Chemical Name:
Naltrexone hydrochloride
Synonyms
ReVia;Depade;nih8503;en1639a;Nalorex;Antaxone;4-D-butyl;Ccris 1168;NSC 409767;Nalmefene-3
CBNumber:
CB7121465
Molecular Formula:
C20H24ClNO4
Molecular Weight:
377.87
MDL Number:
MFCD00069324
MOL File:
16676-29-2.mol
MSDS File:
SDS
Last updated:2023-09-21 14:52:42

Naltrexone hydrochloride Properties

Melting point 274-2760C
storage temp. 2-8°C
solubility H2O: 50 mg/mL, clear, colorless
color White to Off-White
Water Solubility Soluble in water at 50mg/ml.
Sensitive Light Sensitive
Merck 13,6389
BRN 3580333
CAS DataBase Reference 16676-29-2(CAS DataBase Reference)
EWG's Food Scores 1
NCI Dictionary of Cancer Terms naltrexone hydrochloride; ReVia
FDA UNII Z6375YW9SF
NCI Drug Dictionary Depade

Pharmacokinetic data

Protein binding 21%
Excreted unchanged in urine <2%
Volume of distribution 1350 Litres (IV)
Biological half-life 4 (13 for active metabolite)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xn
Risk Statements  22
Safety Statements  22-36
WGK Germany  3
RTECS  QD2160000
8-10
HS Code  2932.99.7000
Toxicity guinea pig,LD50,oral,1490mg/kg (1490mg/kg),Medicamentos de Actualidad. Vol. 21, Pg. 264, 1985.
NFPA 704
0
1 0

Naltrexone hydrochloride price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich N3136 Naltrexone hydrochloride 16676-29-2 100mg $105 2024-03-01 Buy
Sigma-Aldrich N3136 Naltrexone hydrochloride 16676-29-2 1g $633 2024-03-01 Buy
TCI Chemical N1176 Naltrexone Hydrochloride 16676-29-2 250MG $145 2024-03-01 Buy
TCI Chemical N1176 Naltrexone Hydrochloride 16676-29-2 1G $433 2024-03-01 Buy
Alfa Aesar J60590 Naltrexone hydrochloride 16676-29-2 250mg $155 2023-06-20 Buy
Product number Packaging Price Buy
N3136 100mg $105 Buy
N3136 1g $633 Buy
N1176 250MG $145 Buy
N1176 1G $433 Buy
J60590 250mg $155 Buy

Naltrexone hydrochloride Chemical Properties,Uses,Production

Description

Naltrexone hydrochloride is a potent, long-acting, orally-effective narcotic antagonist useful in the management of narcotic addiction.

Chemical Properties

White Crystalline Powder

Originator

Endo (USA)

Uses

Narcotic antagonist, In treatment of?alcoholism

Uses

sulfonamide, carbonic anhydrase inhibitor, anti-glaucoma agent

Uses

Nonselective opioid receptor antagonist; congener of naloxone

Uses

Naltrexone hydrochloride has been used:
as an opioid antagonist, to analyse its effect on ethanol preference using Caenorhabditis elegans as a model.
to determine its effectiveness in reducing the preference for substance of abuse (SOA) like nicotine and cocaine using Caenorhabditis elegans as a model.
in the preparation of combinatorial drug, PXT3003 for treating Charcot-Marie-Tooth disease 1A (CMT1A) transgenic rat model Pmp22.

Definition

ChEBI: Naltrexone hydrochloride is a hydrochloride obtained by reaction of oxycodone with one molar equivalent of hydrochloric acid. it is a mu-opioid receptor antagonist that is used to treat alcohol dependence. It has a role as a mu-opioid receptor antagonist, an antidote to opioid poisoning and a central nervous system depressant. It contains a naltrexone(1+).

brand name

TREXAN

Biological Activity

Opioid antagonist.

Biochem/physiol Actions

Competitive antagonist for μ, κ, δ, and σ-opioid receptors; has greater oral efficacy and longer duration of action than naloxone.

Clinical Use

Opioid antagonist:
Adjunctive prophylactic treatment in patient’s previously opioid dependant
Treatment of alcohol dependence

Drug interactions

Potentially hazardous interactions with other drugs
Opioids: Avoid concomitant use.

Metabolism

Naltrexone is well absorbed from the gastrointestinal tract but is subject to considerable first-pass metabolism and may undergo enterohepatic recycling. It is extensively metabolised in the liver and the major metabolite, 6-β-naltrexol, may also possess weak opioid antagonist activity. It is excreted mainly in the urine, <5% is excreted in the faeces. The renal clearance for naltrexone ranges from 30-127 mL/min and suggests that renal elimination is primarily by glomerular filtration

storage

Room temperature

Purification Methods

This narcotic antagonist has been purified by recrystallisation from MeOH and dried in air. The free base has m 168-170o after recrystallisation from Me2CO. [Cone et al. J Pharm Sci 64 618 1975, Gold et al. Med Res Rev 2 211 1982.]

33522-95-1
1489-69-6
16676-29-2
Synthesis of Naltrexone hydrochloride from 7,8-Dihydro-14-hydroxy- normorphinone and Cyclopropanecarboxaldehyde

Naltrexone hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 295)Suppliers
Supplier Tel Email Country ProdList Advantage
Wuhan Nutra Biotechnology Co.,Ltd
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Beijing Yibai Biotechnology Co., Ltd
0086-182-6772-3597 sales04@yibaibiotech.com CHINA 419 58

View Lastest Price from Naltrexone hydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Naltrexone hydrochloride pictures 2024-11-01 Naltrexone hydrochloride
16676-29-2
US $50.00-0.00 / g 1g 98%+ 100kgs Wuhan Nutra Biotechnology Co.,Ltd
Naltrexone hydrochloride pictures 2024-04-17 Naltrexone hydrochloride
16676-29-2
US $1.10 / g 1g 99.0% min 100 tons min Shaanxi Dideu Medichem Co. Ltd
Naltrexone hydrochloride pictures 2023-07-22 Naltrexone hydrochloride
16676-29-2
US $30.00 / kg 1kg 99% 1000tons Henan Bao Enluo International TradeCo.,LTD

Naltrexone hydrochloride Spectrum

N-CYCLOPROPYLMETHYL-14-HYDROXYDI-HYDROMORPHINONE HYDROCHLORIDE NALTREXONE HYDROCHLORIDE (5alpha)-17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxymorphinan-6-one hydrochloride (5A)-17-(CYCLOPROPYLMETHYL)-4,5-EPOXY-3,14-DIHYDROMORPHINAN-6-ONE HYDROCHLORIDE 17-(cyclopropylmethyl)-4,5-alpha-epoxy-3,14-dihydroxy-morphinan-6-onehydroch 17-(cyclopropylmethyl)-4,5-alpha-epoxy-3,14-dihydroxy-morphinan-6-onhydr 17-(cyclopropylmethyl)-4,5-alpha-oxy-3,14-dihydoxy-morphinan-6-onhydrochlo 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-morphinan-6-onhydrochlor en1639a n-cyclopropylmethyl-noroxymorphonehydrochloride nih8503 Antaxone, Celupan Nalorex NALTREXONEHYDROCHLORIDE,USP 17-(Cyclopropylmethyl)-4,5-alpha-epoxy-3,14-dihydroxy-morphinan-6-one hydrochloride Ccris 1168 Depade Einecs 240-723-0 Morphinan-6-one, 17-(cyclopropylmethyl)-4,5-alpha-epoxy-3,14-dihydroxy-, hydrochloride Morphinan-6-one, 17-(cyclopropylmethyl)-4,5-alpha-oxy-3,14-dihydoxy-, hydrochloride Morphinan-6-one, 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-, hydrochloride, (5-alpha)- (5α)-17-(Cyclopropylmethyl)-4,5-epoxy-3,14-dihydromorphinan-6-onehydrochloride (5α)-17-(Cyclopropyl-Methyl-d3)-4,5-epoxy-3,14-dihydroxyMorphinan-6-one Hydrochloride Antaxone Morphinan-6-one,17-(cyclopropylMethyl)-4,5-epoxy-3,14-dihydroxy-, hydrochloride (1:1), (5a)- (5α)-17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-morphinan-6-one, hydrochloride (1:1) Naltrexone hydrochloride (5alpha)-17-(Cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxymorphinan-6-one hydrochloride Naltrexone HCl USP/EP (4R,4aS,7aR,12bS)-3-(cyclopropylmethyl)-4a,9-dihydroxy-2,3,4,4a,5,6-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7(7aH)-one hydrochloride (5-alpha)-id HIC-A90670115 Nalmefene-3 Nalmefene Hydrochloride Impurit Ⅰ:Naltrexone hydrochloride Morphinan-6-one, 17-(cyclopropylmethyl)-4,5α-epoxy-3,14-dihydroxy-, hydrochloride Nalmefene Impurity C Naltrexone HCl,Naltrexone Hydrochloride Sodium Pentosan Naltrexone (hydrochloride) (CRM) LTREXONE HYDROCHLORIDE Nalbuphine Impurity 5 Naltrexone hydrochloride CRS Morphinan-6-one, 17-(cyclopropylmethyl)-4,5-epoxy-3,14-dihydroxy-, hydrochloride (1:1), (5α)- Naltrexone hydrochloride USP/EP/BP (5α)-17-(CyclopropylMethyl)-4,5-epoxy-3,14-dihydroMorphinan-6-onehydrochloride Nalmefene Hydrochloride Impurit Ⅰ:Naltrexone hydrochloride 4-D-butyl Lironox 326 NSC 409767 ReVia Nalbuphine Impurity 5(Naltrexone hydrochloride、Nalfuranfine Impurity 8) Naltrexone hydrochloride in methanol 16676-29-2 16676-29-3 C20H23NO4HCl C20H23NO4ClH C20H23NO4HClH2O Biochemicals and Reagents BioChemical