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ChemicalBook--->CAS DataBase List--->882847-34-9

882847-34-9

882847-34-9 Structure

882847-34-9 Structure
IdentificationBack Directory
[Name]

FMOC-21-AMINO-4,7,10,13,16,19-HEXAOXAHENEICOSANOIC ACID
[CAS]

882847-34-9
[Synonyms]

Fmoc-NH-PEG6-COOH
FmocNH-PEG6-C2-COOH
FMoc-PEG6-CH2CH2COOH
Fmoc-N-amido-PEG6-acid
Fmoc-N-amido-PEG7-acid
FMoc-NH-PEG6-CH2CH2COOH
Fmoc-PEG6-propionic acid
Carboxy-PEG6-(Fmoc-amine)
FMOC-AMINO-PEG6-PROPANOIC ACID
(Fmoc-amino)-PEG6-carboxylic Acid
(Fmoc-amino)-PEG6-carboxylic Acid (~90%)
FMoc-21-aMino-4,7,10,13,16,19-hexaoxaheneicosanoic
FMOC-21-AMINO-4,7,10,13,16,19-HEXAOXAHENEICOSANOIC ACID
21-(Fmoc-amino)-4,7,10,13,16,19-hexaoxahenicosanoic Acid
Fmoc-NH-(PEG)6-CH2CH2COOH
Fmoc-PEG6-OH Fmoc-21-amino-4,7,10,13,16,19-hexaoxaheneicosanoic acid
FMOC-21-AMINO-4,7,10,13,16,19-HEXAOXAHENEICOSANOIC ACID ISO 9001:2015 REACH
5,8,11,14,17,20-Hexaoxa-2-azatricosanedioic acid 1-(9H-fluoren-9-ylmethyl) ester
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22-heptaoxa-4-azapentacosan-25-oic Acid
21-[(9H-Fluoren-9-ylmethoxy)carbonylamino]-4,7,10,13,16,19-hexaoxahenicosanoic Acid
Name:1-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3,6,9,12,15,18-hexaoxahenicosan-21-oic acid
Fmoc-NH-PEG6-CH2CH2COOH/5,8,11,14,17,20-Hexaoxa-2-azatricosanedioic acid, 1-(9H-fluoren-9-ylmethyl) ester
[Molecular Formula]

C30H41NO10
[MDL Number]

MFCD06656474
[MOL File]

882847-34-9.mol
[Molecular Weight]

575.65
Chemical PropertiesBack Directory
[Boiling point ]

734.8±60.0 °C(Predicted)
[density ]

1.202±0.06 g/cm3 (20 ºC 760 Torr)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMSO (Slightly), Methanol (Slightly)
[form ]

Oil
[pka]

4.28±0.10(Predicted)
[color ]

Colourless
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

29225090
Hazard InformationBack Directory
[Description]

Fmoc-N-amido-PEG6-acid is a PEG linker containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
[Chemical Properties]

Yellowish oil
[Uses]

(Fmoc-amino)-PEG6-carboxylic acid (CAS# 882847-34-9) is a useful building block used in the preparation of cyclic megamolecules, and in L- and D-oligopeptides with circularly polarized luminescence.
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