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Vanz Supply Pregnenolone Powder CAS 145-13-1 Purity 99%
Negotiable
10 gram

Product profile

Customization

Available

Packaging Material

Plastic

Storage Method

Normal

Model NO.

pregnenolone

Nutrient Composition

Vitamin

Resource

Chemosynthesis

Stock

Available

Documents

COA, MSDS

Other Products

Available

Transport Package

Box/Drum

Specification

99%

Trademark

VANZ

Origin

China

HS Code

29225000

Production Capacity

5000kg/Month

Key features

High Purity Product: Pregnenolone powder with 99% purity, tested via HPLC method.
Custom Synthesis Service: We provide tailored custom synthesis services for pharmaceutical intermediates and APIs.
GMP Compliant Manufacturing: Facilities comply with Good Manufacturing Practices to ensure product safety and efficacy.
Advanced R&D Center: 1000 sqm center with 4 synthesis labs, staffed by chemists with Master's degrees or higher.
Large Scale Production: Manufacturing site features reactors from 100L to 5000L for various reaction types.
Global Shipping Capability: We offer international shipping with experience in exporting worldwide and regulatory compliance.
Competitive Pricing: We provide cost-effective solutions for high-quality pharmaceutical products.
Responsive Support: Dedicated team available for inquiries, orders, and technical support via phone or email.

Company profile

Hubei Vanz Pharm Co., Ltd.
High Repeat Buyers ChoiceYears of Export ExperienceExperienced TeamFast Delivery
Business Type: Manufacturer/FactoryExport Year: 2013-01-01Nearest Port: shanghaiAverage Response Time: ≤6.80hTerms 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.

Product Q&A

Q:What is the purity and test method for Pregnenolone Powder?
A:
The product has a purity of 99% and is tested using the HPLC method.
Q:Does the company offer custom synthesis services?
A:
Yes, we provide custom synthesis services for pharmaceutical intermediates and APIs based on specific client requirements.
Q:What quality standards does the manufacturing facility follow?
A:
Our facilities are compliant with Good Manufacturing Practices (GMP) to ensure rigorous quality control and product safety.
Q:What payment methods are accepted?
A:
We accept various payment methods including bank transfers, credit cards, LC, T/T, D/P, Western Union, and Money Gram.
Q:What is the average lead time for orders?
A:
The average lead time is within 15 workdays for both peak and off-season periods.

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