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  • 135198-04-8 , 癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside
  • 135198-04-8 , 癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside
135198-04-8 , 癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside135198-04-8 , 癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside

135198-04-8 , 癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside

135198-04-8 ,癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,
Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside,
Cas:135198-04-8
C24H41NO9 / 487.58
MFCD08704066

Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside

癸基-2,3,4,6-四-氧-乙酰基-b-D-吡喃氨基葡萄糖苷,

Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-b-D-glucopyranoside is a coordination compound that is used as an indicator for the determination of heavy metal ions in water. It has been shown to be stable and to provide consistent results. Decyl 2-acetamido-3,4,6-tri-O-acetyl-2,6-dideoxyglucopyranoside can be used to measure the concentration of heavy metal ions in aqueous solutions. The optimal conditions of use are pH 6 and a temperature range of 20°C - 25°C. The indicator is sensitive to light and should not be exposed to UV radiation.

Decyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-B-D-glucopyranoside, also known as DATG, is a synthetic glycoside compound that belongs to the octyl and decyl series of nonionic surfactants. It is synthesized from a glucose derivative and decylamine, and is commonly used in various fields of research and industry.

Synthesis and Characterization:

The synthesis of DATG involves the reaction of decylamine with a glucose derivative in the presence of acetic anhydride as a catalyst. The product is then characterized using various analytical techniques such as nuclear magnetic resonance (NMR), mass spectrometry (MS), and high-performance liquid chromatography (HPLC).

Analytical Methods:

Various analytical methods are used to detect the presence of DATG in samples, including HPLC, MS, and gas chromatography-mass spectrometry (GC-MS). These methods are highly sensitive and can detect low concentrations of DATG in samples.

Biological Properties:

DATG has various biological properties, including antimicrobial, antiviral, and anti-tumor activities. It has been shown to inhibit the growth of various bacterial strains, including Staphylococcus aureus and Escherichia coli. In addition, DATG has been shown to inhibit the replication of the hepatitis B virus and the growth of cancer cells.

Toxicity and Safety in Scientific Experiments:

DATG has low toxicity and is generally considered safe for use in scientific experiments. However, it is important to use proper safety precautions, including protective clothing and equipment, when handling DATG.

Applications in Scientific Experiments:

DATG has a wide range of applications in scientific experiments, including as a surfactant in membrane proteins, as a biomaterial for cosmetic products, and as a drug delivery system.

Current State of Research:

Research on DATG is ongoing, and new applications and uses for this compound are continually being discovered. Research is also being conducted on the safety and toxicity of DATG in various applications.

Potential Implications in Various Fields of Research and Industry:

DATG has the potential to have significant implications in various fields of research and industry, including drug delivery systems, cosmetics, and biotechnology. Its unique properties make it a promising compound for use in these fields.

Limitations and Future Directions:

One limitation of DATG is its stability in solution, which may limit its use in certain applications. Future directions for research on DATG include improving the stability of the compound in solution, and identifying new applications and uses for this versatile compound.

- Developing new formulations of DATG for use as a drug delivery system.

- Investigating the use of DATG as a biosurfactant in microbial enhanced oil recovery.

- Researching the potential use of DATG as a biosurfactant in bioremediation.

- Conducting further studies on the antimicrobial properties of DATG against other strains of bacteria.

- Investigating the use of DATG in the development of novel biomaterials for tissue engineering.

- Investigating the use of DATG in the development of new cosmetic products.

- Developing new methods for the synthesis of DATG that are more sustainable and environmentally friendly.

- Conducting further studies on the toxicity and safety of DATG in various applications.

- Exploring the use of DATG in the development of new materials for use in the food industry.

- Investigating the potential use of DATG in the development of new agricultural products.

CAS Number135198-04-8
Product NameDecyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-B-D-glucopyranoside
IUPAC Name[(2R,3S,4R,5R,6R)-5-acetamido-3,4-diacetyloxy-6-decoxyoxan-2-yl]methyl acetate
Molecular FormulaC24H41NO9
Molecular Weight487.58 g/mol
InChIInChI=1S/C24H41NO9/c1-6-7-8-9-10-11-12-13-14-30-24-21(25-16(2)26)23(33-19(5)29)22(32-18(4)28)20(34-24)15-31-17(3)27/h20-24H,6-15H2,1-5H3,(H,25,26)/t20-,21-,22-,23-,24-/m1/s1
InChI KeyRVOHFQLIULTWCK-MRKXFKPJSA-N
SMILESCCCCCCCCCCOC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C
Canonical SMILESCCCCCCCCCCOC1C(C(C(C(O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C
Isomeric SMILESCCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)COC(=O)C)OC(=O)C)OC(=O)C)NC(=O)C


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