Vara: 6-klór-3-metýlúrasíl
CAS NR.: 4318-56-3
EINECS NR.: 610-113-2
Sameindaformúla: C5H5ClN2O2
Mólþungi: 160.55
Hreinleiki:98%
Application of 6-Chloro-3-methyluracil :Alógliptin millistig
Pökkun of 6-Chloro-3-methyluracil:25 kg/poki
Annað nafn 6-klór-3-metýlúrasíls:
| 6-klór-3-metýlpýrimídín-2,4(1H,3H)-díón |
| T6MVNVJ C1 FG |
| 6-klór-3-metýl-1H-pýrimídín-2,4-díón |
| 6-klór-3-metýúrasíl |
| 6-klór-3-metýl-2,4(1H,3H)-pýrimídíndíón |
| MFCD01074837 |
| 6-klór-3-metýlúrasíl |
| 511456 |
| 2,4(1H,3H)-pýrimídíndíón, 6-klór-3-metýl- |
| 6-klór-3-dímetýlúrasíl |
Q1:Hver er styrkur fyrirtækisins þíns?
A1: Við höfum meira en 20 margra ára reynslu í efnaiðnaði. Með góðri samvinnu verksmiðjum og við höfum strangt gæðaeftirlitskerfi.
Sp.: Hvernig meðhöndlar þú gæðakvörtun?
A: Við höfum verklagsreglur til að meðhöndla kvartanir viðskiptavina, sem hér segir:
1.1The sales department is responsible for the collection of customer complaint information and the handling of customer complaints due to non-intrinsic quality of the product; The collected complaint information shall be transmitted to the quality control department in a timely manner. The quality management department is responsible for the handling of product quality complaints. The handlers should have rich professional knowledge and work experience and be able to objectively evaluate customers’ opinions.
1.2 Allar athugasemdir viðskiptavina skulu sendar tafarlaust til kvörtunaraðilans og enginn annar skal meðhöndla þær án heimildar.
1.3Við móttöku kvörtunar viðskiptavinar skal umsjónarmaður tafarlaust finna orsök kvörtunarinnar, meta hana, ákvarða eðli og tegund vandans og gera tímanlega ráðstafanir til að bregðast við því.
1.4Þegar svarað er viðskiptavinum ættu vinnsluskoðanir að vera skýrar, tungumálið eða tónninn ætti að vera hóflegur, þannig að viðskiptavinir skilji og auðvelt sé að samþykkja þær sem meginreglu.
2Skráðu kvörtunarskýrslur viðskiptavina
2.1 Allar kvartanir viðskiptavina skulu skráðar á skriflegu formi, þar á meðal vöruheiti, lotunúmer, dagsetningu kvörtunar, kvörtunaraðferð, ástæðu kvörtunar, meðferðarúrræði, meðferðarniðurstöður o.s.frv.
2.2 Viðhalda þróunargreiningu á kvörtunum viðskiptavina. Ef það er einhver óhagstæð þróun, greina rót orsakir og grípa til viðeigandi úrbóta.
2.3 Skrár yfir kvartanir viðskiptavina og aðrar viðeigandi upplýsingar skulu geymdar og varðveittar.
1 3 dimethylurea
96 31 1
cas 96 31 1
cas no 96 31 1
Lestu nýjustu fréttir okkar
Apr.16，2026
Strategic Growth and Quality Guide for api pharma business
The global pharmaceutical landscape is evolving rapidly, placing a heightened emphasis on the quality and reliability of Active Pharmaceutical Ingredients (APIs). Navigating the api pharma business requires a deep understanding of regulatory compliance, chemical synthesis innovation, and supply chain resilience. For companies aiming to scale, the ability to source high-purity intermediates and maintain stringent quality control is the cornerstone of success. In this guide, we will explore the critical components of managing a successful API enterprise, from regulatory hurdles to the integration of green chemistry, ensuring your business remains competitive in an increasingly demanding market.
Lestu meira
Apr.09，2026
Importance and Quality Standards of api of pharmaceutical
In the complex world of drug manufacturing, the api of pharmaceutical, or Active Pharmaceutical Ingredient, serves as the biological heart of any medication. While a pill may contain various fillers, binders, and coatings, the API is the specific component responsible for producing the desired therapeutic effect in the patient. Ensuring the purity, stability, and efficacy of these ingredients is not just a technical requirement but a critical safety mandate for global healthcare. From simple pain relievers to complex oncology treatments, the quality of the API dictates the success of the final medical product.
Lestu meira
Apr.07，2026
Comprehensive Guide to API of Drugs Global Sourcing and Quality Control
In the complex world of pharmaceutical ingredient sourcing, understanding the API of drugs – Active Pharmaceutical Ingredients – is paramount. These are the biologically active components that produce the intended effects in medications. This article will provide a detailed overview of APIs, their sourcing, quality control, and the role of trusted suppliers like KXD Chem in navigating the global market. Effective API sourcing is crucial for pharmaceutical companies aiming for cost-efficiency, quality, and regulatory compliance.
Lestu meira