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Bis[2-(2-bromoisobutyryloxy)undecyl] disulfide

Name: Bis[2-(2-bromoisobutyryloxy)undecyl] disulfide
Brand: ALDRICH

97%

Synonym(s):

11,11′-Dithiobis[1-(2-bromo-2-methylpropionyloxy)undecane], DTBU

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About This Item

Empirical Formula (Hill Notation):

C₃₀H₅₆Br₂O₄S₂

CAS Number:

402828-41-5

Molecular Weight:

704.70

UNSPSC Code:

12162002

PubChem Substance ID:

329764807

NACRES:

NA.23

Quality Level

100

Assay

97%

form

solid

solubility

1.500 at 20 °C

density

1.177 g/mL at 25 °C

SMILES string

CC(C)(Br)C(=O)OCCCCCCCCCCCSSCCCCCCCCCCCOC(=O)C(C)(C)Br

InChI

1S/C30H56Br2O4S2/c1-29(2,31)27(33)35-23-19-15-11-7-5-9-13-17-21-25-37-38-26-22-18-14-10-6-8-12-16-20-24-36-28(34)30(3,4)32/h5-26H2,1-4H3

InChI key

IEGYEGYUHSQEAZ-UHFFFAOYSA-N

Related Categories

Polymerization Tools

Application

Atom transfer Radical Polymerisation (ATRP) initiator commonly used to functionalize noble metal surfaces, and in the preparation of polymer brushes and biodegradable hydrogels. Also may be used to introduce a temperature and light sensitive cleavable region into the polymer.

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Fabrication of an SPR sensor surface with antifouling properties for highly sensitive detection of 2,4,6-trinitrotoluene using surface-initiated atom transfer polymerization.

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Sensors (Basel, Switzerland), 13(7), 9294-9304 (2013-07-24)

In this study, we modified a surface plasmon resonance immunosensor chip with a polymer using surface-initiated atom transfer polymerization (SI-ATRP) for the highly sensitive detection of 2,4,6-trinitrotoluene (TNT). To immobilize a TNT analogue on the polymer, mono-2-(methacryloyloxy)ethylsuccinate (MES), which has

Kinetic and high-throughput profiling of epigenetic interactions by 3D-carbene chip-based surface plasmon resonance imaging technology.

Shuai Zhao et al.

Proceedings of the National Academy of Sciences of the United States of America, 114(35), E7245-E7254 (2017-08-16)

Chemical modifications on histones and DNA/RNA constitute a fundamental mechanism for epigenetic regulation. These modifications often function as docking marks to recruit or stabilize cognate "reader" proteins. So far, a platform for quantitative and high-throughput profiling of the epigenetic interactome

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