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Boc-NH-PEG2-CH2COOH

CAS No.
108466-89-3
Chemical Name:
Boc-NH-PEG2-CH2COOH
Synonyms
Boc-AEEA-OH;2,2-DiMethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid;Boc-N-amido-PEG2-CH2CO2H;2-[2-[2-[(2-Methylpropan-2-yl)oxycarbonylaMino]ethoxy]ethoxy]acetic acid;Boc-O 2 Oc-OH;2-diMethyl-4-oxo-;BocNH-PEG2-CH2COOH;NHBoc-PEG2-CH2COOH;t-Boc-N-amido-PEG2-CH2CO2H;t-Boc-N-Amido-PEG2-CH2COOH
CBNumber:
CB02639228
Molecular Formula:
C11H21NO6
Molecular Weight:
263.29
MDL Number:
MFCD17019374
MOL File:
108466-89-3.mol
MSDS File:
SDS
Last updated:2026-05-27 17:37:32

Boc-NH-PEG2-CH2COOH Properties

Boiling point 425.7±30.0 °C(Predicted)
Density 1.145±0.06 g/cm3(Predicted)
storage temp. -20°C
pka 3.40±0.10(Predicted)
form liquid
color Yellow
InChI InChI=1S/C11H21NO6/c1-11(2,3)18-10(15)12-4-5-16-6-7-17-8-9(13)14/h4-8H2,1-3H3,(H,12,15)(H,13,14)
InChIKey OMBVJVWVXRNDSL-UHFFFAOYSA-N
SMILES C(O)(=O)COCCOCCNC(=O)OC(C)(C)C
UNSPSC Code 51171641
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
WGK Germany  WGK 3
HS Code  2918999090
Storage Class 10 - Combustible liquids

Boc-NH-PEG2-CH2COOH price More Price(64)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 901577 t-Boc-N-amido-PEG2-CH2CO2H ≥95% 108466-89-3 50MG $39.3 2026-04-30 Buy
Biosynth FN161445 N-(tert-Butyloxycarbonyl)-8-amino-3,6-dioxaoctanoic acid 108466-89-3 5g $900 2026-06-04 Buy
Biosynth FN161445 N-(tert-Butyloxycarbonyl)-8-amino-3,6-dioxaoctanoic acid 108466-89-3 50g $900 2026-06-04 Buy
Biosynth FN161445 N-(tert-Butyloxycarbonyl)-8-amino-3,6-dioxaoctanoic acid 108466-89-3 2g $900 2026-06-04 Buy
Biosynth FN161445 N-(tert-Butyloxycarbonyl)-8-amino-3,6-dioxaoctanoic acid 108466-89-3 25g $900 2026-06-04 Buy
Product number Packaging Price Buy
901577 50MG $39.3 Buy
FN161445 5g $900 Buy
FN161445 50g $900 Buy
FN161445 2g $900 Buy
FN161445 25g $900 Buy

Boc-NH-PEG2-CH2COOH Chemical Properties, Uses, Production

Description

t-Boc-N-amido-PEG2-CH2CO2H is a PEG linker containing a terminal carboxylic acid and Boc-protected amino group. The hydrophilic PEG spacer increases solubility in aqueous media. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond. The Boc group can be deprotected under mild acidic conditions to form the free amine.

Uses

t-Boc-N-amido-PEG2-CH2CO2H is a heterobifunctional, PEGylated crosslinker featuring a Boc-protected amine at one end and a carboxyl group at the other. The hydrophillic PEG linker facilitates solubility in biological applications. t-Boc-N-amido-PEG2-CH2CO2H can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC molecules) for targeted protein degradation.

reaction suitability

reagent type: linker

Synthesis

To a stirred solution of 2-(2-(2-Aminoethoxy)ethoxy)acetic acid (5.0 g, 30.6 mmol) in 1,4-Dioxane (50 mL), Sodium carbonate (8.12 g, 76.5 mmol, dissolved in 10 mL water) and (Boc)2O (9.98 mL, 45.7 mmol) were added and stirred at room temperature for 12 h. The progress of the reaction was monitored by TLC. The reaction mass was partitioned between diethyl ether and water. Then, the aqueous layer was made acidic (pH = 3) by 3N HC1 solution and was extracted with DCM (2 x 200 mL). The organic layer was washed with water, and brine, dried over Na2504 and evaporated under reduced pressure to yield 50 g of pure Boc-NH-PEG2-CH2COOH (Yield:62.1 per cent).

IC 50

PEGs; Alkyl/ether

References

[1] Organic and Biomolecular Chemistry, 2008, vol. 6, # 17, p. 3065 - 3078
[2] Patent: US2015/73042, 2015, A1. Location in patent: Paragraph 0150; 0151
[3] Patent: WO2015/33303, 2015, A1. Location in patent: Page/Page column 26; 27

24424-99-5
105-36-2
929-06-6
108466-89-3
Synthesis of Boc-NH-PEG2-CH2COOH from Di-tert-butyl dicarbonate and Ethyl bromoacetate and 2-(2-Aminoethoxy)ethanol
Global Suppliers ( 217)
Supplier Tel Email Country ProdList Advantage
Shaanxi Youbang Biomedical Technology Co., Ltd. 0913-7167565 13852786668 605375102@qq.com China 212 58
CAS Aldone(Dalian) Pharmaceutical Science and Technology Co, Ltd. 86-13062552990 13062552990 sales@casaldone.com China 279 58
CHENGDU YINGNUOLING PHARMACEUTICAL TECHNOLOGY CO.,LTD 17882285575 1276966012@qq.com China 399 58
Shanghai Yanfen Biochemical Technology Co.,LTD 13611955358 15002190549 yanfen2023@126.com China 2573 58
Hangzhou Xinjiayuan Biological Technology Co., LTD 18258867343; 15858275893 3275393843@qq.com China 25 58
Changzhou Huanling Chemical Co., Ltd. 89803005 18206112582 info@huanlingchem.com China 983 68
Jia Xing Isenchem Co.,Ltd 0573-85285100 18627885956 isenchem@163.com China 9389 66
Accela ChemBio Co.,Ltd. 021-50795510 4000665055 marketing@accelachem.com China 10972 64
Chembon Pharmaceutical Co., Ltd. 028-84252981 18583719936 sales@chembon.com.cn China 854 64
Beijing Isomersyn Technology CO;LTD 010-82954736 13391601435 sales@isomersyn.com China 3294 57

View Latest Price from Boc-NH-PEG2-CH2COOH manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
2,2-dimethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid pictures 2026-07-24 2,2-dimethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid
108466-89-3
1g 98% 1g/bottle, 10g/bottle, 100g/bottle XIAMEN SINOPEG BIOTECH CO., LTD.
Boc-NH-PEG2-CH2COOH pictures 2026-05-11 Boc-NH-PEG2-CH2COOH
108466-89-3
10g TargetMol Chemicals Inc.
BocNH-PEG2-CH2COOH pictures 2026-01-28 BocNH-PEG2-CH2COOH
108466-89-3
1g 98% 100kg LAURENT

Boc-NH-PEG2-CH2COOH Spectrum

t-boc-N-amido-PEG2-acetic acid 3,8,11-Trioxa-5-azatridecan-13-oic acid, 2,2-diMethyl-4-oxo- 8-tert-butyloxycarbonylaMino-3,6-dioxaoctanoic acid 2-[2-[2-[(2-Methylpropan-2-yl)oxycarbonylaMino]ethoxy]ethoxy]acetic acid t-Boc-N-amido-PEG2-CH2CO2H BocNH-PEG2-CH2COOH T-BOC-NH-AMIDO-PEG2-CH2CO2H 2-[2-[2-(Boc-amino)ethoxy]ethoxy]acetic Acid 2-[2-(2-{[(tert-butoxy)carbonyl]amino}ethoxy)ethoxy]acetic acid 3,6,11-Trioxa-9-azatridecanoic acid, 12,12-dimethyl-10-oxo- 3,8,11-Trioxa-5-azatridecan-13-oic acid, 2,2-diMethyl-4-oxo- USP/EP/BP 11-Trioxa-5-azatridecan-13-oic acid 2-diMethyl-4-oxo- NHBoc-PEG2-CH2COOH t-Boc-N-Amido-PEG2-CH2COOH N-Boc-8-amino-3,6-dioxaoctanoic acid Boc-O 2 Oc-OH 2-[2-(2-([(tert-butoxy)carbonylaminoJethoxy)ethoxylacetic acid 2,2-dimethyl-4,13-dioxo-3,8,11-trioxa-5-azatetradecan-14-oic acid Boc-NH-PEG2-CH2COOH/Boc-AEEA-OH t-Boc-N-amido-PEG2-CH2CO2H 2- [2- (tert butoxycarbonylamino) ethoxy] ethoxyacetic acid N-(tert-Butyloxycarbonyl)-8-amino-3,6-dioxaoctanoic acid 2,2-DiMethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid Boc-AEEA-OH Boc-N-amido-PEG2-CH2CO2H 108466-89-3 137978-97-5 peg