Bromo-PEG5-bromide

 CAS No.: 67705-77-5  Cat No.: BP-500702  Purity: ≥95% 4.5  

Bromo-PEG5-bromide is a bifunctional polyethylene glycol linker bearing terminal bromides, providing a flexible, hydrophilic chain that can be used to connect PROTAC components through ether-forming or substitution-based conjugation strategies. Structurally, it comprises a short PEG spacer with brominated leaving groups at both ends, enabling controlled linkage to nucleophilic sites on ligands such as cereblon-recruiting motifs or target-binding warheads. In PROTAC design, PEG linkers are widely used to tune effective molarity, reduce steric clashes, and improve solubility, thereby facilitating productive ternary complex formation between the recruited E3 ligase and the target protein. This reagent is valuable for researchers seeking modular synthesis of degraders, allowing systematic variation of linker length and attachment chemistry to optimize degradation potency and selectivity while maintaining aqueous compatibility for biochemical and cell-based assays.

Bromo-PEG5-bromide

Structure of 67705-77-5

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
PROTAC Linker
Molecular Formula
C12H24Br2O5
Molecular Weight
408.12
Appearance
Colorless to Light Brown Oil to Thick Oily Matter

* For research and manufacturing use only. Not for human or clinical use.

SizePriceStockQuantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

  • Comprehensive PROTAC Platform
  • Scientific Expertise & Technical Support
  • Custom Synthesis & Design Service
  • Extensive Product Coverage
  • Cutting-Edge Innovation
  • Fast Delivery & Global Support
  • 24/7 customer service
  • 100% quality assurance
Popular Publications Citing BOC Sciences Products
Purity
≥95%
Solubility
Soluble in Methanol (Slightly), Water (Slightly)
Appearance
Colorless to Light Brown Oil to Thick Oily Matter
Application
A cross-linking reagent.
Storage
Store at 2-8°C under inert atmosphere
Shipping
Room temperature in continental US; may vary elsewhere.
IUPACName
1-[2-(2-bromoethoxy)ethoxy]-2-[2-[2-(2-bromoethoxy)ethoxy]ethoxy]ethane
Synonyms
Br-PEG5-Br; Br-PEG5-bromide; Br-PEG5-CH2CH2Br; 3,6,9,12,15-Pentaoxaheptadecane-1,17-diyl Bis-bromide; 1,17-Dibromo-3,6,9,12,15-pentaoxaheptadecane; Bis[2-[2-(2-bromoethoxy)ethoxy]ethyl] ether; 3,6,9,12,15-Pentaoxaheptadecane, 1,17-dibromo-
Boiling Point
175°C at 0.1 mmHg
Density
1.433±0.06 g/cm3 (Predicted)
InChI Key
LACSKPODWQXGSB-UHFFFAOYSA-N
InChI
InChI=1S/C12H24Br2O5/c13-1-3-15-5-7-17-9-11-19-12-10-18-8-6-16-4-2-14/h1-12H2
SMILES
C(COCCOCCBr)OCCOCCOCCBr

Bromo-PEG5-bromide is a PEG-based bifunctional linker designed for modular assembly of PROTACs, enabling efficient spatial separation and flexible conformational tuning between a ligand for the target protein and an E3 ligase recruiter. Its two terminal bromides support robust synthetic coupling strategies commonly used in targeted protein degradation workflows. The linker’s ether-rich scaffold enhances solubility and can reduce steric constraints, improving the practicality of iterative PROTAC synthesis. Detailed structural and reactivity considerations are provided below.

Structure: The molecule is a poly(ethylene glycol) chain bearing bromide leaving groups at both termini. It contains repeating ether linkages that confer flexibility, polarity, and hydrogen-bond-accepting character, while the C–Br bonds provide electrophilic handles for substitution. The overall architecture supports formation of stable carbon–heteroatom connectivity in PROTAC constructs.

Reactivity: Bromo-PEG5-bromide is typically used in nucleophilic substitution reactions where the terminal bromides are displaced by nucleophiles such as amines or other carbon- and heteroatom-based nucleophiles. Practical conditions often involve polar aprotic solvents, controlled base strength, and temperature optimization to balance substitution efficiency and minimize side reactions. The reaction proceeds via an SN-type substitution mechanism for alkyl bromides, with product formation driven by nucleophile strength and solvation effects.

Stock concentration: *
Desired final volume: *
Desired concentration: *

L

* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
g/mol
g

Related Product Recommendations

BOC Sciences Support

Please contact us with any specific requirements and we will get back to you as soon as possible.


  • Verification code
Inquiry Basket