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Tetracycline Hydrochloride CAS 64-75-5 Antibiotic Veterinary API
US$0.80-1.50
100 g
Product profile
Customization
AvailableCAS No.
64-75-5Formula
C22h25cln2o8Packaging Material
PaperStorage Method
NormalShelf Life
>12 MonthsNutrient Composition
MineralResource
NaturalThe content of active substances
0%~30%The Content Active Substances
0%~30%Einec
200-593-8Stock
AvailableDocuments
COA, MSDSOther Products
AvailableMOQ
10gTransport Package
Box/DrumSpecification
99%Trademark
VANZOrigin
ChinaHS Code
29225000Production Capacity
5000kg/MonthKey features
High Purity Active Ingredient: Pure L-Carnitine Powder with 99% purity and CAS 541-15-1.
Custom Synthesis Services: Tailored solutions for intermediates and APIs available.
GMP Compliant Manufacturing: Facilities comply with Good Manufacturing Practices for safety and efficacy.
Extensive R&D Capabilities: 1000 sqm center with 4 synthesis labs and experienced chemist team.
Large Scale Production: Manufacturing site features reactors from 100L to 5000L for various reactions.
Global Shipping Network: International shipping available with full regulatory compliance and documentation.
Flexible MOQ: Minimum Order Quantity starts from 10g for testing and small batches.
Comprehensive Documentation: COA and MSDS documents available upon request for all products.
Company profile
Business Type: Manufacturer/FactoryExport Year: 2013-01-01Nearest Port: shanghaiAverage Response Time: ≤7.73hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF, FAS, FCA
AI-Powered supplier vetting
SummaryThe supplier is identified as a factory in Jiayu County, Hubei, producing pharmaceutical intermediates with stated annual productivity of 40 tons. It reports ISO 9001 certification, documented service-assessment, corrective-action, and customer-complaint procedures, and export capability covering multiple regions. Its capabilities include sample-based customization, ODM, and OEM services, while it does not provide 3D software design, has no available SDK, and reported no new products in the past year. The company description states that it has completed R&D for more than 20 APIs and intermediates and operates several laboratories, although other records classify it as not being a professional technical supplier. Overseas warehouses, showrooms, agents or branches, and offline trade-show participation are not available. Customer-specific cases are not explicitly provided.
Supplier typeThe supplier is explicitly identified as a factory, with pharmaceutical intermediates as its stated product and annual productivity of 40 tons. It also holds self-operated import and export rights, indicating manufacturing and direct export capability.
CertificationsThe supplier reports ISO 9001 certification for its management system. This is explicit evidence of holding a recognized quality-management certification.
After-Sales capabilityThe supplier has written and followed procedures for service assessment, corrective and preventive actions, and customer complaints. However, it lacks overseas warehouses, showrooms, agents or branches, and has not participated in offline trade shows, so the evidence supports formal service processes but not broad overseas service coverage.
Production capacityThe supplier is a factory producing pharmaceutical intermediates with stated annual productivity of 40 tons, 6–10 quality-control staff, and stated order fulfillment within 15 working days in both peak and off-peak seasons. These records explicitly support production capability and operational capacity.
Customization capabilityThe supplier provides customization from samples and reports both ODM and OEM services, including services for popular brands. These explicit offerings demonstrate customization and outsourced design/manufacturing capability, although no 3D software design service or SDK is available.
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Hubei Vanz Pharm Co., Ltd.
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