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Amino/Bromide PEG reagent, N-Boc-PEG4-bromide, Purity 98%
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-YW0271

Amino/Bromide PEG reagent, N-Boc-PEG4-bromide, Purity 98%

Synonym: 1392499-32-9; N-Boc-PEG4-bromide; N-Boc-PEG5-bromide; BocNH-PEG4-CH2CH2Br

  • MDL: MFCD31536756
  • CAS Number: 1392499-32-9
  • PubChem CID: 88853548
Size
100 mg; 250 mg; 500 mg
Price
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Datasheet
Datasheet
MSDS
MSDS
Properties
Description
N-Boc-PEG4-bromide is a PEG linker compound featuring a tert-butoxycarbonyl (Boc)-protected amino group and a bromide group. The incorporation of the Boc protecting group shields the amino functionality, providing stability during synthetic processes. Under mild acidic conditions, the Boc group can be selectively removed, yielding the free amine for further chemical reactions. The presence of the bromide (Br) moiety imparts reactivity to the molecule, serving as an excellent leaving group for nucleophilic substitution reactions. Moreover, the hydrophilic nature of the PEG spacer enhances the solubility of N-Boc-PEG4-bromide in aqueous environments, facilitating its use in aqueous-based reactions and biological applications.
Molecular Weight
400.3
Molecular Formula
C15H30BrNO6
Functional Group 1
Amino
Functional Group 2
Bromide
Functional Group 3
None
Form
Liquid
Purity
98%
Solubility
DCM
Identity
Confirmed by NMR.
Applications
N-Boc-PEG4-bromide can be used as a versatile building block in organic synthesis and chemical conjugation strategies. The Boc protecting group ensures the controlled deprotection of the amino functionality, enabling precise manipulation of the PEG linker. Upon deprotection, the resulting free amine can undergo various conjugation reactions or participate in bioconjugation processes. The bromide group enhances the synthetic flexibility of N-Boc-PEG4-bromide, allowing for the introduction of diverse functional groups or biomolecules onto the PEG backbone via- nucleophilic substitution reactions.
Storage
Store at -20°C
For Research Use Only. Not For Clinical Use.
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