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Amine/Boc protecting PEG reagent, t-Boc-N-amido-PEG23-amine, Purity 95%
Products
Hots Products

Amino PEG
Amino-PEG10-acid (Cat#: X24-03-YW0001) N-(Mal-PEG6)-N-bis(PEG3-amine) (Cat#: X24-03-YW0002) Amino-PEG23-amine (Cat#: X24-03-YW0056) Amino-PEG20-t-butyl ester (Cat#: X24-03-YW0057) Amino-PEG1-amine (Cat#: X24-03-YW0058) Gly-PEG3-amine TFA salt (Cat#: X24-03-YW0064) Amino-PEG9-amine (Cat#: X24-03-YW0068) Amino-PEG8-amine (Cat#: X24-03-YW0072) Amino-PEG8-t-butyl ester (Cat#: X24-03-YW0087)
Biotin PEG
Biotin-PEG2-azide (Cat#: X24-03-YW0091) Biotin-PEG5-azide (Cat#: X24-03-YW0113) Biotin-PEG6-t-butyl ester (Cat#: X24-03-YW0114) Dde biotin azide plus (Cat#: X24-03-YW0115) Biotin-PEG2-NH-Boc (Cat#: X24-03-YW0116) Biotin-PEG11-amine (Cat#: X24-03-YW0117) Biotin-PEG4-amide (Cat#: X24-03-YW0118) Biotin-PEG4-azide (Cat#: X24-03-YW0119) Biotin-PEG12-NHS ester (Cat#: X24-03-YW0124)
DBCO PEG
DBCO-PEG5-TFP ester (Cat#: X24-03-YW0294) DBCO-C3-alcohol (Cat#: X24-03-YW0306) Hydroxy-PEG7-DBCO (Cat#: X24-03-YW0307) DBCO-C5-acid (Cat#: X24-03-YW0308) DBCO-PEG2-amine (Cat#: X24-03-YW0310) DBCO STP ester (Cat#: X24-03-YW0311) DBCO-PEG6-DBCO (Cat#: X24-03-YW0312)
Poly PEG
m-PEG-succinic acid (Cat#: X24-10-WXX03) Lipoamide-PEG-Mal (Cat#: X24-10-WXX05) m-PEG-SPDP (Cat#: X24-10-WXX06) Lipoamide-PEG-biotin (Cat#: X24-10-WXX07) Rhodamine-PEG-Mal (Cat#: X24-10-WXX08) Cholesterol-PEG-methoxy (Cat#: X24-10-WXX10) DSPE-PEG-Ald (Cat#: X24-10-WXX12) 4-Arm PEG-OH (Cat#: X24-10-WXX13)
PEG Acid
m-PEG4-(CH2)3-acid (Cat#: X24-09-YYX001) m-PEG9-acid (Cat#: X24-09-YYX005) m-PEG1-acid (Cat#: X24-09-YYX008) Biotin-PEG2-acid (Cat#: X24-09-YYX011) Acid-PEG4-t-butyl ester (Cat#: X24-09-YYX015) Amino-PEG3-acid (Cat#: X24-09-YYX018) m-PEG11-CH2CO2H (Cat#: X24-09-YYX020) Amino-PEG4-CH2CO2H (Cat#: X24-09-YYX022)
PEG Azide
t-boc-N-amido-PEG5-azide (Cat#: X24-09-YYX148) Aminooxy-PEG4-azide (Cat#: X24-09-YYX246) AZD-PEG2-azide (Cat#: X24-09-YYX248) Azido-PEG12-azide (Cat#: X24-09-YYX249) Trityl-PEG10-azide (Cat#: X24-09-YYX250) Bromoacetamido-PEG2-azide (Cat#: X24-09-YYX251) Azido-PEG24-alcohol (Cat#: X24-09-YYX255) m-PEG6-azide (Cat#: X24-09-YYX257)
Bromo PEG
Bromo-PEG2-methyl ester (Cat#: X24-03-YW0205) Bromoacetamido-PEG8-acid (Cat#: X24-03-YW0209) Bromoacetamido-PEG3-acid (Cat#: X24-03-YW0213) Amino-PEG8-Bromo (Cat#: X24-03-YW0215) Bis-bromoacetamido-PEG11 (Cat#: X24-03-YW0216) Bromoacetamido-PEG8-t-butyl ester (Cat#: X24-03-YW0218) Bromo-PEG1-CH2CO2-t-Bu (Cat#: X24-03-YW0220)


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Cat. No.: X24-03-YW0278

Amine/Boc protecting PEG reagent, t-Boc-N-amido-PEG23-amine, Purity 95%

Synonym: Boc-NH-PEG23-NH2; BocNH-PEG23-CH2CH2NH2; SCHEMBL25835350

  • MDL: MFCD28385468
  • PubChem CID: 91757820
Size
100 mg; 250 mg; 500 mg
Price
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Datasheet
Datasheet
MSDS
MSDS
Properties
Description
t-Boc-N-amido-PEG23-amine is a monodisperse polyethylene glycol (PEG) linker featuring an amino group and a tert-butoxycarbonyl (Boc)-protected amino group, connected by a twenty-three-unit PEG spacer. The hydrophilic nature of the PEG chain enhances the solubility of the linker in aqueous environments, facilitating its use in aqueous-based reactions and formulations. The Boc protection of one amino group provides stability during synthesis and allows for selective deprotection under mild acidic conditions, enabling the generation of free amino groups for subsequent chemical modifications.
Molecular Weight
1,173.5
Molecular Formula
C53H108N2O25
Functional Group 1
Amine
Functional Group 2
Boc protecting
Functional Group 3
None
Reactive Group 1
Carboxylic acid
Reactive Group 2
NHS
Form
Solid
Purity
95%
Identity
Confirmed by NMR.
Applications
t-Boc-N-amido-PEG23-amine can be used in various bioconjugation, drug delivery, and materials science applications. Its monodisperse nature ensures uniformity and reproducibility in conjugation reactions, making it suitable for the synthesis of precise PEGylated compounds. The hydrophilic PEG spacer enhances the water solubility of the linker, making it ideal for aqueous-based bioconjugation reactions with biomolecules or nanoparticles. Upon deprotection of the Boc group under mild acidic conditions, the free amino groups become available for further functionalization, such as coupling with activated esters, carboxylic acids, or aldehydes, enabling the synthesis of diverse bioconjugates tailored for specific applications in biotechnology.
Storage
Store at -20°C
For Research Use Only. Not For Clinical Use.
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