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Postion:Product Catalog >3,6-Dichlorotrimellitic anhydride
3,6-Dichlorotrimellitic anhydride
  • 3,6-Dichlorotrimellitic anhydride

3,6-Dichlorotrimellitic anhydride NEW

Price $32 $54 $87
Package 5mg 10mg 25mg
Min. Order:
Supply Ability: 10g
Update Time: 2025-06-22

Product Details

Product Name: 3,6-Dichlorotrimellitic anhydride CAS No.: 81742-10-1
Purity: 98.68% Supply Ability: 10g
Release date: 2025/06/22

Product Introduction

Bioactivity

Name3,6-Dichlorotrimellitic anhydride
Description3,6-Dichlorotrimellitic anhydride serves as the essential precursor in the synthesis of various dichlorinated fluoresceins and rhodamines.
Cell ResearchInstructions I. Solution preparation 1. Stock solution: Dissolve 3,6-Dichlorotrimellitic anhydride in an appropriate solvent, such as anhydrous DMSO or DMF, to prepare a stock solution with a concentration of 1–10 mM. 2. Working solution: Dilute to an appropriate working concentration, usually 1–10 μM, using an experimental buffer (such as PBS, pH 7.4) according to experimental requirements. II. Experimental steps 1. Synthesis of chlorinated fluorescein or rhodamine derivatives 1) React 3,6-Dichlorotrimellitic anhydride with an appropriate aminofluorescein or rhodamine molecule, usually in an anhydrous solvent. 2) Reaction conditions: The reaction is usually carried out at 50–70°C for 2–6 hours. 3) After the reaction, purify using an appropriate solvent (such as methanol or water) to remove unreacted raw materials and by-products. 2. Labeling oligonucleotides or DNA 1) Label the target oligonucleotide or DNA with synthetic dichlorofluorescein or rhodamine derivatives. 2) Labeling is usually performed by covalent bonding, using chlorofluorescein or rhodamine to react with the amino or carbamate groups of nucleic acids. 3) Reaction time: Incubate at 4°C for 1–2 hours. After the reaction is completed, purify the labeled DNA or oligonucleotide using gel electrophoresis or liquid chromatography (HPLC). 3. Calibration and control 1) Control group: Use unreacted fluorescent dye or labeled DNA as a control to ensure the specificity of the labeling reaction. 2) Standard curve: Use a known concentration of labeled DNA sample to establish a standard curve between the fluorescence signal and the concentration. Notes 1) Photosensitivity: Synthetic chlorofluorescein and rhodamine derivatives are usually highly photosensitized. Avoid strong light exposure during the experiment to prevent the fluorescence signal from attenuating. 2) Storage conditions: 3,6-Dichlorotrimellitic anhydride and synthetic fluorescent markers should be stored at -20°C, away from light. 3) Solubility: 3,6-Dichlorotrimellitic anhydride may release chlorine gas when dissolved, and the experiment should be performed in a well-ventilated area. "
Storagekeep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice./Shipping at ambient temperature.
Solubility InformationDMSO : 55 mg/mL (210.71 mM), Sonication is recommended.
KeywordsInhibitor | inhibit | 3,6-Dichlorotrimellitic anhydride | 3,6Dichlorotrimellitic anhydride | 3,6 Dichlorotrimellitic anhydride

Company Profile Introduction

Target Molecule Corp. (TargetMol) is a global high-tech enterprise, headquartered in Boston, MA, specializing in chemical and biological research product and service to meet the research needs of global customers. TargetMol has evolved into one of the biggest global compound library and small molecule suppliers and a customer based on 40+ countries. TargetMol offers over 80 types of compound libraries and a wide range of high-quality research chemicals including inhibitors, activator, natural compounds, peptides, inhibitory antibodies, and novel life-science kits, for laboratory and scientific use. Besides, virtual screening service is also available for customers who would like to conduct the computer-aided drug discovery.

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