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Merck
CN

792047

2-溴异丁酸N-羟基琥珀酰亚胺酯

98% (GC)

别名:

1-(2-溴-2-甲基-1-氧代丙氧基)-2,5-吡咯烷二酮, 2,5-二氧杂吡咯烷-1-基-2-溴-2-甲基丙酸酯, 2-溴-2-甲基丙酸2,5-二氧代-1-吡咯烷基酯, 2-溴异丁酰基(N-羟基琥珀酰亚胺), N-羟基琥珀酰亚胺基-2-溴-2-甲基丙酸酯, NHS ATRP引发剂, NHS-BiB, NHS保护的溴代异丁酸酯

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关于此项目

经验公式(希尔记法):
C8H10BrNO4
化学文摘社编号:
分子量:
264.07
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12162002
MDL number:
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产品名称

2-溴异丁酸N-羟基琥珀酰亚胺酯, 98% (GC)

InChI

1S/C8H10BrNO4/c1-8(2,9)7(13)14-10-5(11)3-4-6(10)12/h3-4H2,1-2H3

SMILES string

O=C1N(OC(C(C)(C)Br)=O)C(CC1)=O

InChI key

QBJWGGWPQPRVKW-UHFFFAOYSA-N

assay

98% (GC)

form

liquid

mp

135-140 °C

storage temp.

2-8°C

Quality Level

Application

具有 NHS 酯部分的原子转移自由基聚合(ATRP)引发剂,用于缀合化学,可用于生物连接。

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Bhalchandra S Lele et al.
Biomacromolecules, 6(6), 3380-3387 (2005-11-15)
We have developed a novel technique to synthesize near-uniform protein-polymer conjugates by initiating atom transfer radical polymerization of monomethoxy poly(ethylene glycol)-methacrylate from 2-bromoisobutyramide derivatives of chymotrypsin (a protein-initiator). Polymerization initiated from the monosubstituted protein-initiator resulted in the conjugate containing a
Bailey Risteen et al.
Small (Weinheim an der Bergstrasse, Germany), 14(46), e1802060-e1802060 (2018-09-11)
A thermally "switchable" liquid-crystalline (LC) phase is observed in aqueous suspensions of cellulose nanocrystals (CNCs) featuring patchy grafts of the thermoresponsive polymer poly(N-isopropylacrylamide) (PNIPAM). "Patchy" polymer decoration of the CNCs is achieved by preferential attachment of an atom transfer radical
Shuaidong Huo et al.
Nature chemistry, 13(2), 131-139 (2021-01-31)
Pharmaceutical drug therapy is often hindered by issues caused by poor drug selectivity, including unwanted side effects and drug resistance. Spatial and temporal control over drug activation in response to stimuli is a promising strategy to attenuate and circumvent these

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Over the past two decades, the rapid advance of controlled living polymerization (CLP) techniques.

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