1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31-decaoxa-4-azatetratriacontan-34-oic acid
97%
- Product Code: 39535
CAS:
1191064-81-9
Molecular Weight: | 707.80 g./mol | Molecular Formula: | C₃₆H₅₃NO₁₃ |
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EC Number: | MDL Number: | MFCD28385470 | |
Melting Point: | Boiling Point: | 803.9±65.0°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of bioconjugation and material science due to its unique structure, which combines a fluorenyl group with a polyether chain and a carboxylic acid terminus. The fluorenyl group provides UV absorbance and fluorescence properties, making it useful for tracking and detection in various applications. The polyether chain enhances solubility in aqueous and organic solvents, facilitating its use in creating biocompatible surfaces or coatings. The carboxylic acid group allows for covalent attachment to other molecules, such as proteins, peptides, or polymers, enabling its role in the development of drug delivery systems, biosensors, and functionalized nanomaterials. Its versatility makes it valuable in research and industrial settings for designing advanced materials and bioactive compounds.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless liquid or white solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,980.00 |
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0.250 | 10-20 days | ฿12,900.00 |
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1.000 | 10-20 days | ฿46,890.00 |
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1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31-decaoxa-4-azatetratriacontan-34-oic acid
This chemical is primarily utilized in the field of bioconjugation and material science due to its unique structure, which combines a fluorenyl group with a polyether chain and a carboxylic acid terminus. The fluorenyl group provides UV absorbance and fluorescence properties, making it useful for tracking and detection in various applications. The polyether chain enhances solubility in aqueous and organic solvents, facilitating its use in creating biocompatible surfaces or coatings. The carboxylic acid group allows for covalent attachment to other molecules, such as proteins, peptides, or polymers, enabling its role in the development of drug delivery systems, biosensors, and functionalized nanomaterials. Its versatility makes it valuable in research and industrial settings for designing advanced materials and bioactive compounds.
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