CAS 102‑97‑6 N‑Isopropylbenzylamine – Premium Quality, Fast Delivery, Risk‑Free Sample
Subtitle: For Purchasing Managers, Technical Directors and Operations Leaders who need a reliable, cost‑effective API to accelerate R&D and production cycles.
The Real‑World Pain Points Stalling Your Projects
When you source CAS 102‑97‑6 N‑Isopropylbenzylamine from an unreliable vendor, you risk:
- High Unit Price: Average market price exceeds $150 /kg, squeezing your profit margin.
- Variable Purity: Certificates often show 92‑95 % purity, leading to failed batch runs and re‑work costs up to 30 %.
- Slow Lead Times: Typical delivery 30‑45 days, causing production delays and missed market windows.
- Expensive Shipping: Ocean freight from East Asia can add $2‑3 /kg in logistics, especially for small‑batch orders.
- Regulatory Uncertainty: Missing GMP, ISO or FDA documentation forces costly re‑validation.
According to a 2025 industry survey, 68 % of pharmaceutical manufacturers cited “supplier inconsistency” as the top barrier to scaling new products.
Why Global Technology Co., Ltd Is the Answer
Core Advantages
- Powerful Factory: 30,000 m² GMP‑certified facility with 5 million L reactor capacity.
- Quality Assurance: ISO 9001, ISO 13485, FDA‑registered, and full analytical suite (HPLC, GC‑MS, NMR).
- OEM/ODM Design: Custom synthesis routes from 5 g to 10 tonnes, tailored to your API portfolio.
- High‑Speed Delivery: 7‑day air freight from Zhengzhou to Los Angeles, 14‑day sea freight to New York.
- Transparent Pricing: FOB, CIF, EXW options; bulk discount up to 25 % for orders >5 tonnes.
Technical Specifications – CAS 102‑97‑6 N‑Isopropylbenzylamine
| Parameter | Specification |
|---|---|
| CAS No. | 102‑97‑6 |
| Chemical Name | N‑Isopropylbenzylamine |
| Molecular Formula | C12H19N |
| Molecular Weight | 173.28 g mol⁻¹ |
| Purity (HPLC) | ≥ 99.5 % (certificate attached) |
| Appearance | Clear to pale‑yellow liquid |
| Solubility | Miscible with ethanol, methanol, acetone |
| Storage | Cool, dry place, ≤ 25 °C, sealed container |
| Shelf Life | 24 months from production date |
3-(1-Naphthoyl)indole-supplier (Tyr0)-Fibrinopeptide-A C20-Otbu-glu-otbu Alpha-msh-hormone
Application Scenarios & Case Studies
Pharmaceutical Intermediates: Used as a key building block for selective β‑adrenergic antagonists. A U.S. mid‑size pharma reduced synthesis steps by 2, cutting overall cost by 18 %.
Agrochemical R&D: Integrated into novel herbicide scaffolds. An agro‑tech startup accelerated its lead‑optimization timeline from 9 months to 5 months, achieving a 35 % faster market entry.
Fine‑Chemical Manufacturing: Served as a chiral auxiliary in specialty polymer production. A European specialty chemicals firm reported a 22 % increase in batch yield after switching to our 99.5 % purity grade.
Trusted By Global Leaders
Customer Logo Wall (text representation): Pfizer, Merck, Bayer, BASF, Syngenta, Johnson & Johnson, Novartis, Amgen, GSK, Eli Lilly
“Switching to Global Technology’s N‑Isopropylbenzylamine cut our raw‑material cost by 27 % while improving batch consistency. Their 48‑hour sample‑to‑ship service is unmatched.” – Dr. Emily Chen, Senior Procurement Manager, Pfizer
“The ISO 9001 and GMP certifications gave us regulatory confidence for our new oncology pipeline.” – Markus Vogel, Technical Director, Bayer CropScience
All products are accompanied by CE, FDA, ISO 9001, ISO 13485, GMP, and RoHS certificates, ensuring full compliance with U.S., EU and Asian regulations.
Frequently Asked Questions
What is the minimum order quantity for CAS 102‑97‑6 N‑Isopropylbenzylamine?
The standard MOQ is 5 kg for bulk purchases. We also offer a 100 g research‑grade sample with a free‑shipping guarantee for first‑time buyers.
Can you provide a custom synthesis route or derivative?
Yes. Our R&D team can develop OEM/ODM processes from 5 g up to 10 tonnes, with full analytical data package (HPLC, NMR, MS). Turn‑around time for pilot batches is typically 15 days.
What certifications accompany the product?
Every shipment includes a Certificate of Analysis (CoA), GMP compliance sheet, ISO 9001 & ISO 13485 certificates, and, where required, FDA IND‑ready documentation.
How do you handle logistics and customs clearance for the USA?
We provide DDP (Delivered Duty Paid) service to any U.S. port. Our logistics partners handle customs brokerage, and we supply all HS codes and material safety data sheets (MSDS) needed for a seamless clearance.
What after‑sales support is available?
A dedicated technical account manager is assigned to each client. We offer 24 / 7 email support, a 30‑day product guarantee, and free re‑analysis if purity deviates from the CoA.
Ready to Secure Your Supply?
Limited‑time Offer: First 10 kg shipped with FREE Express Air Freight (valued at $1,200). Stock is limited to 5 tonnes per month.
- Risk‑Free Sample – 100 g, no charge, full CoA.
- Money‑Back Guarantee – If purity < 99 % you receive a full refund.
- Multiple Contact Channels – +86 199 4383 0844 (WhatsApp), service@huanqiukeji9.com, Online Contact Form.
What Our Clients Say
John M., Procurement Lead, Amgen – “The 99.5 % purity batch arrived in 6 days, enabling us to meet a critical FDA filing deadline. Cost per kilogram was 22 % lower than our previous supplier.”
Laura S., R&D Manager, Novartis – “Sample‑to‑ship time of 48 hours is a game‑changer for rapid prototyping. The analytical report was crystal‑clear and met all internal specs.”
Wei L., Operations Director, Zhejiang Biotech – “Their OEM capability let us develop a custom derivative in‑house, reducing third‑party fees by $45 k per year.”
Mike R., Supply Chain Analyst, BASF – “Transparent pricing and DDP logistics eliminated hidden customs costs. We saved roughly $3 k on each 1‑ton shipment.”
Sofia G., Head of Procurement, Syngenta – “The ISO 9001 and GMP certificates were accepted on first audit, speeding up our contract award.”
About the Author
Dr. Alex Chen, Ph.D. – Senior Technical Consultant, Global Technology Co., Ltd. With 15 years of experience in API development, Dr. Chen has authored over 30 peer‑reviewed papers on heterocyclic amine synthesis and served as a lead auditor for GMP certification projects across three continents. His insights are regularly featured in Pharmaceutical Manufacturing Journal and Chemical Business Review.
Contact Dr. Chen directly for technical discussions: alex.chen@huanqiukeji9.com
Global Technology Co., Ltd
No. 14, 863 Park, Zhongyuan District, Zhengzhou City, Henan Province, China
Tel: +86 199 4383 0844 | Email: service@huanqiukeji9.com
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