Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid

Basic Information

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CAS Number

882847-34-9

Molecular Formula

C30H41NO10

Molecular Weight

575.66 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Ethers

Fine Chemicals Dyes and Pigments Organic Dyes

Fine Chemicals Surfactants Anionic Surfactants

Basic Physical Properties

Physical State

No data available

Melting Point

No data available

Boiling Point

734.8±60.0℃/760mmHg

Density

1.202±0.06 g/cm3 (20 ºC 760 Torr),

Flash Point

398.2±32.9 °C

SMILES

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C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCOCCOCCOCCOCCOCCOCCC(=O)O

InChI

InChI=1S/C30H41NO10/c32-29(33)9-11-35-13-15-37-17-19-39-21-22-40-20-18-38-16-14-36-12-10-31-30(34)41-23-28-26-7-3-1-5-24(26)25-6-2-4-8-27(25)28/h1-8,28H,9-23H2,(H,31,34)(H,32,33)

InChIKey

HEGZERUHBVYZPH-UHFFFAOYSA-N

LogP

3.0994000000000037

Topological Polar Surface Area

131.01000000000002 Å²

Hydrogen Bond Donor/Acceptor

2 / 11

Complexity

689

Safety Information

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Hazard Statement

H315 Causes skin irritation
Skin corrosion/irritation

H319 Causes serious eye irritation
Serious eye damage/eye irritation

Synonyms & References

English

5,8,11,14,17,20-Hexaoxa-2-azatricosanedioicacid, 1-(9H-fluoren-9-ylmethyl) ester
(Fmoc-amino)-PEG6-carboxylic Acid
Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid
Fmoc-PEG6-propionic acid
FMoc-21-aMino-4,7,10,13,16,19-hexaoxaheneicosanoic
Fmoc-amido-dPEG6 acid
FMoc-NH-PEG6-CH2CH2COOH
N-Fmoc-1-amino-3,6,9,12,15,18-hexaoxahenicosan-21-oic acid
N-Fmoc-amido-PEG6-acid
Carboxy-PEG6-(Fmoc-amine)
21-[(9H-Fluoren-9-ylmethoxy)carbonylamino]-4,7,10,13,16,19-hexaoxahenicosanoic Acid
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22-heptaoxa-4-azapentacosan-25-oic Acid
21-(Fmoc-amino)-4,7,10,13,16,19-hexaoxahenicosanoic Acid
Fmoc-N-amido-PEG6-acid
3-[2-[2-[2-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid
C30H41NO10
Fmoc-nh-dpeg(6)-cooh
SC
Fmoc-NH-PEG6-CH2CH2COOH
1-(9H-Fluoren-9-ylmethyl) 5,8,11,14,17,20-hexaoxa-2-azatricosanedioate (ACI)
1-{[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AMINO}-3,6,9,12,15,18-HEXAOXAHENICOSAN-21-OIC ACID
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22-heptaoxa-4-azapentacosan-25-oic acid
Fmoc-NH-PEG6-acid
BP-21630
HY-W040246
F1183
DTXSID101154275
5,8,11,14,17,20-Hexaoxa-2-azatricosanedioic acid 1-(9H-fluoren-9-ylmethyl) ester
(Fmoc-amino)-PEG6-carboxylic Acid (~90%)
AKOS025405482
MFCD06656474

MDL Number

MFCD06656474

FAQ

What are the physical and chemical properties of Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9)?

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9) is a crystalline compound with a molecular weight of approximately 721.47 g/mol. It is slightly soluble in water and organic solvents. It exhibits amide group reactivity typical of carboxylic acids, making it suitable for coupling reactions in organic synthesis. Its solubility and reactivity make it an important reagent in peptide chemistry.

How is Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9) typically synthesized?

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9) is synthesized through a multi-step process involving the condensation of 21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid with Fluorenylmethoxycarbonyl (Fmoc) group. The synthesis typically requires careful control of pH and temperature, and the use of appropriate catalysts to ensure high yield and selectivity. Common solvents like dichloromethane and triethylamine are employed in this process.

What industries use Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9)?

Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9) is primarily used in pharmaceutical and biotechnology industries for the synthesis of peptide-based drugs. It is also utilized in the development of sensor technologies and semiconductor materials due to its unique chemical properties. Its application in polymer chemistry for the modification of biomaterials is also significant.

What precautions should be taken when handling Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9)?

When handling Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid (CAS: 882847-34-9), it is essential to wear appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats. Work should be conducted in a well-ventilated fume hood to minimize exposure. Spills should be cleaned up immediately using appropriate solvents. Always refer to the Safety Data Sheet (SDS) for specific handling and disposal instructions to ensure laboratory safety.