Are you a Purchasing Manager or Technical Director struggling with inconsistent API quality, high freight costs, and delayed shipments?
Get Free Quote in 24 h1. Sky‑rocketing prices – Many suppliers charge a 20‑30 % premium for “high‑purity” grades that still contain hidden impurities.
2. Unreliable quality control – Batch‑to‑batch variance can exceed 0.5 %, forcing you to re‑run assays and waste valuable time.
3. Slow delivery cycles – Traditional Asian supply chains often need 45‑60 days from order to gate, missing critical product launch windows.
4. Expensive freight and customs delays – Oversized pallets and lack of DDP (Delivered Duty Paid) options add up to $5,000‑$8,000 per shipment.
5. Limited customization – OEM/ODM capabilities are either non‑existent or hidden behind minimum orders of >10 kg, unsuitable for early‑stage development.
In a 2025 industry survey, 73 % of US‑based pharmaceutical R&D teams reported that API supply issues delayed at least one product launch in the past 12 months. Imagine the market share you could capture if you eliminated those bottlenecks.
Discover the solution that eliminates these pain points →Core Advantages
| Parameter | Value | Test Method |
|---|---|---|
| Chemical Name | 2 Amino 2 Methyl 1 Propanol | CAS 107‑15‑3 |
| Purity | ≥ 99.9 % | HPLC (USP USP < < >), GC‑MS |
| Appearance | Clear, colourless liquid | Visual inspection, Refractive Index |
| Water Content | <0.05 % | Karl Fischer Titration |
| Melting Point | – 24 °C (− 10 °F) | Differential Scanning Calorimetry |
| Stability | Shelf life ≥ 24 months at 25 °C | ICH‑Q1A(R2) |
1. Early‑stage drug discovery – A US‑based biotech used our 2 Amino 2 Methyl 1 Propanol (100 g) to synthesize a novel kinase inhibitor. The high purity reduced downstream purification steps by 45 %, cutting R&D costs by $120,000 in 3 months.
2. GMP‑compliant bulk manufacturing – A contract manufacturing organization (CMO) placed a 2‑ton order for continuous production. Our in‑house GMP line delivered the product within 14 days, enabling the CMO to meet a FDA‑approved launch timeline.
3. Custom API formulation – A specialty chemical firm required a crystalline form with a particle size of 10‑15 µm. Our R&D team provided an ODM solution, resulting in a 22 % increase in tablet dissolution rate.
See How Others Benefit →Standard DDP shipping from our Zhengzhou hub reaches any US port within 7 business days. Air‑freight options are available within 48 hours for urgent projects.
Yes. Every batch is accompanied by a full CoA, including HPLC, NMR, and Karl Fischer results, signed by our GMP‑qualified quality manager.
Absolutely. Our R&D team can tailor crystal form, particle size (5‑50 µm), and packaging (glass ampoules, HDPE drums, bulk totes) from 100 g up to 5 tonnes.

We offer L/C at sight, T/T (30 % deposit, 70 % before shipment), and Open Account for qualified US distributors.
All shipments are provided with DDP (Delivered Duty Paid) documentation, so you receive the product ready for use without hidden fees.
Our 24/7 technical hotline and dedicated account engineers are on standby to assist with formulation queries, stability studies, and regulatory documentation.
Act now—stock is limited to the first 50 US‑based buyers. Risk‑free trial with a money‑back guarantee if the product does not meet your specifications.
Phone: +86 199 4383 0844 | Full contact page
Emily R. – Senior Purchasing Officer, BioGenix
“The 2 Amino 2 Methyl 1 Propanol batch we received last month performed exactly as the CoA promised. We reduced our downstream chromatography steps by 40 % and saved $150k in reagents.”
Michael T. – Operations Manager, PharmaCore
“Fast 7‑day delivery allowed us to meet an FDA filing deadline that would have otherwise been missed. The DDP service removed all customs headaches.”
Sarah L. – Head of R&D, Orion Therapeutics
“Their OEM crystal‑size service gave us a 22 % increase in tablet dissolution—critical for our immediate‑release formulation.”
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Certificates & Compliance
- CE Marking (EU)
- FDA Registration (US)
- ISO 9001:2015
- GMP (cGMP‑compliant facilities)
- RoHS, REACH, FCC, GS, CB, VDE, SAA
- HACCP / GMP for pharmaceutical intermediates
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