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Hubei Moxin Biotechnology Co., Ltd

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Hubei Moxin Biotechnology Co., Ltd

Country: China (Mainland)

Business Type:Lab/Research institutions

Ms.Du

Tel: +86-173-20513646

Mobile: 17320513646

Tel: +86-173-20513646

Fax:

URL: http://www.molcoo.com

Province/state: Hu Bei

City: Wuhan

Street: Company address: Room 005, 15th Floor, Building D2, Phase III, Software New Town, No. 8 Huacheng Avenue, East Lake High-tech Development Zone, Wuhan, Hubei Province, China

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Pharmaceutical Grade CAS 240407-05-0 with competitive price

CAS NO.240407-05-0

  • FOB Price: USD: 10.00-10.00 /Metric Ton Get Latest Price
  • Min.Order: 10 Milligram
  • Payment Terms: T/T,Other
  • Available Specifications:

    1(10--1)Metric Ton

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Product Details

Keywords

  • Benzoic acid, 4-(1-methyl-3-oxopropyl)-, methyl ester (9CI)
  • methyl 4-(4-oxobutan-2-yl)benzoate
  • Pemetrexed Impurity

Quick Details

  • ProName: Benzoic acid, 4-(1-methyl-3-oxopropyl)...
  • CasNo: 240407-05-0
  • Molecular Formula: C12H14O3
  • Appearance: white or almost white crystalline powd...
  • Application: Pharmaceutical research
  • DeliveryTime: prompt delivery
  • PackAge: food packages,foil bags
  • Port: shenzhen/hongkong
  • ProductionCapacity: 500 Gram/Year
  • Purity: 95%+
  • Storage: cool and dry
  • Transportation: DHL,FedEx,UPS,EMS,TNT;
  • LimitNum: 10 Milligram
  • Moisture Content: 0.1%
  • Impurity: 0.1%

Superiority

We supply over 20000 types of spot impurity reference materials, with sufficient supply and same day delivery to meet customers' urgent needs for replenishment at any time. The company has its own research and development center and laboratory, and the team members have over ten years of experience in developing drug impurity reference standards. Our website www.molcoo.com covers over 98% of cutting-edge generic drug projects, with complete structural formulas that greatly save customers time in impurity structure analysis and inference. All products undergo strict quality control testing and provide relevant information such as COA, H-NMR, C-NMR, MS/GC-MS, HPLC/GC purity, QNMR quantification, TGA thermogravimetric analysis, IR infrared, UV ultraviolet, two-dimensional (COSY, NOESY, HMBC, HMQC), etc. These structural confirmation spectra ensure quality and reliability. Our products have a wide range of categories, fast delivery time, good quality, and low prices, which can quickly solve various customer needs such as replenishment and consistency evaluation.

Details

 

Our products are mainly drug impurity reference products, drug standards, analytical chemistry, standard substances, organic chemical synthesis, chemical custom synthesis. For impurity localization, quantification, and quality control in drug development processes. Our laboratory area is more than 5000 square meters, we have more than 20 analytical instruments such as HPLC and MS/LC-MS/GC-MS, we also have TGA, IR and other testing instruments. We have the most advanced SFC preparation separation equipment.

Pemetrexed Impurity Reference Standard

Product Name: Pemetrexed Impurity Reference Standard

Description:

Pemetrexed impurity reference standards are high-purity reference materials used in drug development, quality control, and pharmaceutical analysis. These impurity reference standards help identify and quantify various impurities that may be present in drugs, thereby ensuring their safety and effectiveness.

Main Components:

This product primarily contains specific impurities of pemetrexed, which are isolated from pemetrexed active pharmaceutical ingredients (APIs) or related formulations using advanced separation and purification techniques.

Product Characteristics:

  1. High Purity: Rigorous purification processes ensure that the impurities meet analytical purity requirements.
  2. Good Stability: Under appropriate storage conditions, the impurity reference standards remain stable and are not susceptible to degradation.
  3. Easy to Use: The impurity reference standards are typically provided in solid form, facilitating weighing and dissolution.

Applications:

  1. Drug Development: Used to identify and quantify potential impurities during drug synthesis and formulation development.
  2. Quality Control: Monitored and controlled the impurity content during drug production to ensure compliance with quality standards.
  3. Pharmaceutical Analysis: Served as reference materials for calibrating instruments and analytical methods in drug testing and inspection processes.

Storage Conditions:

Store according to the instructions on the packaging, typically in a dry, light-protected, and appropriately tempered environment.