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m-PEG7-Azide, a click chemistry reagent, is a versatile molecule that features a polyethylene glycol (PEG) chain with seven repeating units and an azide (N3) group. The azide group can readily react with alkyne, BCN, and DBCO through click chemistry, resulting in the formation of a stable triazole linkage. This unique property makes m-PEG7-Azide a valuable tool in various applications across different industries.

208987-04-6

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208987-04-6 Usage

Uses

1. Used in Bioconjugation:
m-PEG7-Azide is used as a bioconjugation agent for the covalent attachment of biomolecules, such as proteins, peptides, and nucleic acids, to other molecules or surfaces. The stable triazole linkage formed through click chemistry ensures the robustness and reliability of the conjugation process.
2. Used in Drug Delivery:
m-PEG7-Azide is used as a component in the design and synthesis of drug delivery systems. The PEG chain provides solubility and stability, while the azide group allows for the attachment of drug molecules or targeting ligands through click chemistry, enhancing the specificity and efficiency of drug delivery.
3. Used in PEG Hydrogels:
m-PEG7-Azide is used as a crosslinking agent in the formation of PEG hydrogels. The hydrogels can be tailored for various applications, such as tissue engineering, wound healing, and controlled drug release, by adjusting the crosslinking density and the molecular weight of the PEG chains.
4. Used as a Crosslinker:
m-PEG7-Azide is used as a crosslinker in the synthesis of various materials, including polymers, dendrimers, and nanoparticles. The azide group enables the formation of stable triazole linkages, which can improve the mechanical properties, stability, and functionality of the resulting materials.
5. Used in Surface Functionalization:
m-PEG7-Azide is used for the functionalization of surfaces, such as in the modification of sensors, implants, and lab-on-a-chip devices. The azide group allows for the covalent attachment of functional molecules or biomolecules to surfaces through click chemistry, enabling the creation of tailored surface properties for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 208987-04-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,9,8 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 208987-04:
(8*2)+(7*0)+(6*8)+(5*9)+(4*8)+(3*7)+(2*0)+(1*4)=166
166 % 10 = 6
So 208987-04-6 is a valid CAS Registry Number.

208987-04-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-azido-2-[2-[2-[2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethane

1.2 Other means of identification

Product number -
Other names azidoheptaethylene glycol methyl ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:208987-04-6 SDS

208987-04-6Relevant articles and documents

NIR-emitting squaraine J-aggregate nanosheets

Shen, Chia-An,Würthner, Frank

, p. 9878 - 9881 (2020)

Click chemistry and Yamamoto coupling afforded an S-shaped π-scaffold composed of two directly connected dicyanomethylene-substituted squaraine dyes. This bis(squaraine) self-assembles into nanosheets in a cooperative self-assembly process, affording an absorption maximum at 886 nm and a fluorescence peak at 904 nm due to strong J-type exciton coupling.

Synthesis and transport properties of new dendritic core-shell architectures based on hyperbranched polyglycerol with biphenyl-PEG shells

Kurniasih, Indah N.,Liang, Hua,Moeschwitzer, Vicki D.,Quadir, Mohiuddin A.,Radowski, Michal,Rabe, Juergen P.,Haag, Rainer

, p. 371 - 379 (2012)

A new core-shell type of nano-architectures based on hyperbranched polyglycerol (hPG) has been designed by attaching a mono(methoxy)polyethylene glycol (mPEG) shell either directly or through a hydrophobic biphenyl spacer to the hPG scaffold. Alternativel

Well-defined poly(lactic acid)s containing poly(ethylene glycol) side chains

Castillo, Jose A.,Borchmann, Dorothee E.,Cheng, Amy Y.,Wang, Yufeng,Hu, Chunhua,Garcia, Andres J.,Weck, Marcus

, p. 62 - 69 (2012)

Poly(ethylene glycol) (PEG) side-chain functionalized lactide analogues have been synthesized in four steps from commercially available l-lactide. The key step in the synthesis is the 1,3-dipolar cycloaddition between PEG-azides and a highly strained spir

Photophysics of Perylene Diimide Dianions and Their Application in Photoredox Catalysis

Li, Han,Wenger, Oliver S.

supporting information, (2021/12/23)

The two-electron reduced forms of perylene diimides (PDIs) are luminescent closed-shell species whose photochemical properties seem underexplored. Our proof-of-concept study demonstrates that straightforward (single) excitation of PDI dianions with green

Monitoring Fluorinated Dendrimer-Based Self-Assembled Drug-Delivery Systems with 19F Magnetic Resonance

Liu, Xin,Yuan, Yaping,Bo, Shaowei,Li, Yu,Yang, Zhigang,Zhou, Xin,Chen, Shizhen,Jiang, Zhong-Xing

, p. 4461 - 4468 (2017/08/23)

Monitoring a drug-delivery system with an imaging modality is of great importance for detailed understanding of drug-delivery processes and for achieving optimal therapeutic effects. Here, novel fluorinated self-assembled dendrimers with a single 19

Supramolecular graft copolymers in moderately polar media based on hydrogen-bonded aromatic oligoamide units

Pan, Xusong,Chen, Chao,Peng, Jiang,Yang, Yongan,Wang, Yinghan,Feng, Wen,Deng, Pengchi,Yuan, Lihua

, p. 9510 - 9512 (2012/11/06)

By exploiting hetero-complementary aromatic oligoamide units containing hextuple hydrogen bonds, supramolecular graft copolymers were successfully constructed in moderately polar media.

Esters Of Glucuronide Prodrugs Of Anthracyclines And Method Of Preparation And Use In Tumor-Selective Chemotherapy

-

Page/Page column 14, (2009/09/25)

The invention relates to novel esters and in particular to some novel esters of glucuronide prodrugs of anthracyclines having tunable water-solubility, their synthesis and use in tumor-selective chemotherapy. It appeared that in the final step in the synt

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