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Supply High Purity Powder Naltrexone Hydrochloride CAS 16676-29-2
Negotiable
10 Gram
Sample price:US$100.00/gram.Request sample
Product profile
CAS No.
16676-29-2Formula
C20h24clno4EINECS
240-723-0Model NO.
CAS 16676-29-2Type
Synthesis Material IntermediatesAppearance
PowderQuality
RefinedColour
TransparentSample
Small Quantities AvailablePacking
PE Bag, Aluminium Foil BagTesting
HPLC, Gc, NmrColor
WhiteTransport Package
PE Bag, Foil Aluminum Bag, Cardboard DrumSpecification
10g, 20g, 50g, 100g, 500gTrademark
MTOrigin
ChinaHS Code
2937290090Production Capacity
500kgs /MonthKey features
High Purity Grade: 99% purity meeting Medical Standard for pharmaceutical applications.
Verified Specifications: CAS 16676-29-2, Formula C20H24ClNO4, MW 377.87, White Powder appearance.
Rigorous Testing: Quality controlled via HPLC, GC, and NMR testing methods.
Flexible Sampling: Small quantities of samples are available for evaluation.
Secure Packaging: Available in PE Bag or Aluminium Foil Bag for safe transport.
Fast Delivery: Lead time within 15 workdays for both peak and off-peak seasons.
Global Shipping: Export from Shanghai or Ningbo ports with FOB, EXW, CFR, CIF, DDP terms.
Diverse Payment: Accepts LC, T/T, PayPal, Western Union, Money Gram, and small-amount payments.
Company profile

Zhejiang Multinpharma Co., Ltd.Zhejiang, China
Business Type: Manufacturer/FactoryExport Year: 2008-11-05Nearest Port: Shanghai, NingboAverage Response Time: ≤3.12hTerms of Payment: LC, T/T, PayPal, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, DDP
AI-Powered supplier vetting
SummaryThe supplier is a science and technology company focused on pharmaceutical and chemical production technology services, CRO customization, continuous-flow microreaction technology, and microreaction equipment solutions. It reports broad customization, 3D software design, ODM, OEM for well-known brands, and SDK capabilities. Production information includes three production lines, stated pharmaceutical and chemical capacity, and documented finished-product inspection procedures. Management and service procedures are documented for supplier assessment, corrective actions, and complaint handling, although the approved-supplier list lacks approval signatures or dates. The supplier holds multiple stated management-system certifications. Evidence of overseas service infrastructure is absent, and no new products were reported during the past year. Customer-specific cases are not identified.
Supplier typeThe supplier is described as a science and technology company providing pharmaceutical and chemical production technology services, CRO customization, continuous-flow microreaction services, and overall microreaction equipment solutions. Its stated business scope also covers technology development, specialized chemical and pharmaceutical equipment, machinery, and related technical services, indicating a technology/service-oriented manufacturer and solution provider.
CertificationsThe supplier lists BSCI, TS 16949, ISO 14001, ISO 9001, ISO 20000, GMP, and QC 080000 certifications. The provided information explicitly confirms multiple certification holdings, although certificate validity, scope, and issuing bodies are not supplied.
After-Sales capabilityThe supplier has written procedures and records for service-capability assessment, corrective and preventive actions, and effective customer-complaint handling. However, it reports no overseas warehouse, showroom, overseas agent or branch, and no prior offline trade-show participation; therefore, documented service processes exist but overseas physical support is not demonstrated.
R&D capabilityThe supplier provides 3D software design, ODM services, an available SDK, and technology research and development related to pharmaceutical, chemical, biotechnology, and microreaction applications. Nevertheless, it explicitly reports no new products during the past year, so current technical capability is evident while recent product innovation is not demonstrated.
Production capacityThe supplier reports three production lines and annual pharmaceutical and chemical capacity entries of 100,000 tons, 200,000 tons, and 200,000 tons, supported by processing-line and stirrer facilities. It also states that finished products are inspected under written instructions that are uniformly followed, indicating documented production and quality-control practices.
Customization capabilityThe supplier explicitly offers customization from samples, customization from designs, minor customization, full customization, and flexible customization. Its stated CRO customization, 3D software design, ODM, and microreaction-equipment solution services further support broad customization capability.
Client casesThe supplier states that it provides OEM services for well-known brands, which is evidence of experience serving brand customers. However, no customer names, project descriptions, product details, or verifiable case records are provided, so the breadth and quality of customer cases cannot be independently assessed.
Product Q&A
Q:What is the purity level of Naltrexone Hydrochloride?
A:
The product has a purity of 99% and meets the Medical Standard grade.
Q:What testing methods are used for quality control?
A:
We utilize HPLC, GC, and NMR for comprehensive testing and verification.
Q:Is it possible to order samples?
A:
Yes, small quantities of samples are available for purchase.
Q:How long does it take to deliver the product?
A:
The average lead time is within 15 workdays, regardless of the season.
Q:What packaging options are available?
A:
We offer packaging in PE Bags or Aluminium Foil Bags.
Send Inquiry
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Zhejiang Multinpharma Co., Ltd.
Zhejiang Multinpharma Co., Ltd.*Content:
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