Sustained Release, Implants
Hydroxyl(-OH) PEG
- *
| Catalog No. | Name | Structure | M.W. | Purity | Buy |
|---|---|---|---|---|---|
| BPG-4330 | t-butyl-ester-PEG4-(CH2)3OH |
|
336.4 | 0.98 | |
| BPG-4329 | Amino-PEG8-C3-alcohol |
|
427.5 | 0.95 | |
|
BPG-4328
CAS: 2100306-78-1
|
t-Butyl 3-(hydroxypropoxyl)-propanoate |
|
204.3 | 0.98 | |
| BPG-4327 | C11-PEG13-alcohol |
|
701 | 0.95 | |
|
BPG-4326
CAS: 35056-97-4
|
C11-PEG9-alcohol |
|
524.7 | 0.95 | |
|
BPG-4325
CAS: 92691-26-4
|
C11-PEG6-alcohol |
|
392.6 | 0.95 | |
|
BPG-4324
CAS: 88299-47-2
|
C11-PEG4-alcohol |
|
304.5 | 0.95 | |
|
BPG-4323
CAS: 306771-83-5
|
Amino-PEG4-C3-alcohol |
|
251.3 | 0.98 | |
|
BPG-4318
CAS: 42749-28-0
|
PEG7-Tos |
|
436.5 | 0.98 | |
| BPG-4316 | N-(Hydroxy-PEG3)-N-Boc-PEG4-t-butyl ester |
|
597.8 | 0.98 | |
|
BPG-4315
CAS: 2279944-66-8
|
N,N-diethanol amine-PEG4-tert-butyl ester |
|
409.5 | N/A | |
| BPG-4314 | N-(t-butyl-PEG2)-N-bis(PEG3-alcohol) |
|
613.7 | 0.98 | |
| BPG-4313 | N-(alcohol-PEG2)-N-bis(PEG2-propargyl) |
|
357.5 | N/A | |
| BPG-4312 | Dimethylanaline-PEG35-alcohol |
|
1778.2 | N/A | |
|
BPG-4311
CAS: 1807512-41-9
|
1,1,1-Trifluoroethyl-PEG5-alcohol |
|
276.3 | 0.98 | |
|
BPG-4310
CAS: 2351-42-0
|
Hydroxy-PEG3-2-methylacrylate |
|
218.3 | 0.98 | |
|
BPG-4309
CAS: 2052305-98-1
|
1,4-Di(3-Hydroxypropoxy)butane |
|
206.3 | N/A | |
|
BPG-4308
CAS: 4669-05-0
|
PEG17 |
|
722.9 | >97% | |
|
BPG-4306
CAS: 92417-25-9
|
THP-PEG12 |
|
586.7 | 0.98 | |
| BPG-4304 | t-Boc-Aminooxy-PEG11-alcohol |
|
617.7 | 0.98 |
Background
Hydroxyl PEG (OH PEG) is a polyethylene glycol compound with hydroxyl functional groups. Hydroxyl PEG is reactive and can be chemically reacted with other compounds or biomolecules for modification and functionalization of PEG. Hydroxy PEG can be used to construct biomaterials such as hydrogels, polymer microspheres and scaffold materials. By adjusting the molecular weight and concentration of hydroxy PEG, the physical properties, biocompatibility and degradation properties of the materials can be modulated to meet specific tissue engineering and biomedical application requirements.
Fig. 1. Stabilization of nanoparticles with hydroxyl-PEG-phosphonic acid (Langmuir. 2019, 35(29): 9474-9482).
Examples of Hydroxyl PEG
Amine PEG Hydroxyl
Amine PEG Hydroxyl is a heterobifunctional PEG. Heterobifunctional hydroxy PEG amine products are commonly used as crosslinking agents or as spacer groups between two different chemical entities. The PEG portion of the heterobifunctional PEG derivative provides water solubility, biocompatibility and flexibility.
OPSS-PEG-OH
OPSS-PEG-OH has an OPSS and a hydroxyl group at each end of the molecular chain and is a linear heterofunctional PEG reagent. It is a useful cross-linking reagent for PEG spacers. OPSS stands for o-pyridyl disulfide or o-pyridyl disulfide, which reacts with thiols and sulfhydryl groups to form S-S bonds. Through the pyridyl disulfide bond, OPSS-PEG-OH can selectively react with sulfhydryl groups to form a stable disulfide bond while releasing the thiol pyridyl group. Through this reaction, it can modify biomolecules or other materials.
C18-PEG-OH
C18-PEG-OH is a PEG derivative modifier with a C18 hydrocarbon chain on one end and a hydroxyethyl group on the other. The simultaneous presence of polar and non-polar groups makes it a useful amphiphilic surfactant. As a PEG modifier, C18-PEG-OH helps to improve the solubility and stability of modified biomolecules while reducing the immunogenicity of peptides and proteins and inhibiting the non-specific binding of charged molecules on the modified surface.
How Hydroxyl PEG Derivatives are Prepared?
Step 1: Carboxyl Group Introduction
Carboxyl group introduction requires choosing a suitable polyethylene glycol as the starting material and mixing this starting material with hydroxyl reagent to react. After hydroxylation reaction, the crude product is purified to obtain the target product.
Step 2: Post-hydroxylation Modification
After obtaining the hydroxylated polyethylene glycol, the hydroxylated PEG is modified by reacting it with the groups to be modified (amino group, carbon chain, etc.).
Advantages of Hydroxyl PEG
Hydroxyl PEG has the following advantages as a PEG derivative, in addition to biocompatibility, ease of modification, high stability, and structural modification.
Multifunctional Splice Sites
The hydroxyl group of OH-PEG provides multiple sites for the affixation of various functional groups, which can be modified by chemical reactions such as esterification, amidation or etherification. The modified PEG derivatives can then be attached to targeted ligands, drug molecules, and other substances to enhance the development of targeted drug delivery systems or biomaterials.
Invisible Properties
Hydroxy PEG is hydrophilic and can reduce interactions with proteins and cells by forming a hydrated layer, thereby reducing immune recognition and clearance by the body's defense mechanisms.
BOC Sciences has strong manufacturing capabilities for hydroxyl PEG and related products. We offer a variety of hydroxyl PEG derivatives with different PEG chain lengths and linkage groups to meet specific customer needs. Our manufacturing process is conducted under strict quality control standards to ensure the highest quality and purity of our products. We also provide technical support and expertise to help customers with hydroxyl PEG applications.
Reference
- Lu, C. et al. Hydroxyl-PEG-phosphonic acid-stabilized superparamagnetic manganese oxide-doped iron oxide nanoparticles with synergistic effects for dual-mode MR imaging. Langmuir. 2019, 35(29): 9474-9482.
Planning to purchase or looking for custom solutions?
Get in touch with our experts today! We'll respond within 24 hours to discuss your project needs and provide a customized quote.
You May Also Be Interested In
From custom PEG synthesis to PEGylation support, explore tailored services designed to meet the specific needs of your research.
Gain Deeper Insights
Browse related content to gain a deeper understanding of PEG synthesis and manufacturing.
PEG and PEG Derivatives
-

-

Crosslinking, Surface Coating
-

Branched Polymers, Multifunctionality
-

Polymer Synthesis, Manufacturing
-

Targeting, Cancer Therapy
-

Polymerization, Functionalization
-

Biodegradable Carriers, Delivery
-

Copper-Free Click Chemistry
-

Lipid Delivery, Membrane Targeting
-

Liposome, Drug Delivery
Online Inquiry