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900238

Sigma-Aldrich

CdSe/ZnS core-shell type quantum dots

amine functionalized, fluorescence λem 600 nm, 4 μM in 10 mM PBS

Synonym(s):

Fluorescent nanocrystals, QDs

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About This Item

Linear Formula:
CdSe/ZnS
UNSPSC Code:
26111700
NACRES:
NA.23
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Quality Level

form

dispersion

λmax

585 nm

fluorescence

λem 600 nm
λem 600 nm±10 nm, quantum yield >50%

functional group

amine

storage temp.

2-8°C

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1 of 4

This Item
900235900214900218
functional group

amine

functional group

amine

functional group

-

functional group

-

fluorescence

λem 600 nm, λem 600 nm±10 nm, quantum yield >50%

fluorescence

λem 540 nm, λem 540 nm±10 nm, quantum yield >50%

fluorescence

λem 520 nm, λem 520 nm±10 nm, quantum yield >50%

fluorescence

λem 600 nm, λem 600 nm±10 nm, quantum yield >50%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

dispersion

form

dispersion

form

dispersion

form

dispersion

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

-

storage temp.

-

λmax

585 nm

λmax

525 nm

λmax

505 nm

λmax

585

General description

Reactive group: Amine.

Application

The amine functionalized CdS/ZnS or CdSe/ZnS quantum dots (QDs) find applications in bioimaging and biosensing. The three main conjugation approaches reported in literature are conjugation using glutaraldehyde as a linker, conjugations with carboxylic acid containing molecules by using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC) coupling, and direct conjugation with isothiocyanates bearing molecules.[1][2][3][4]

Legal Information

Product of Ocean Nanotech, LLC.

Pictograms

Environment

Hazard Statements

Precautionary Statements

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Nathaniel H Park et al.
Angewandte Chemie (International ed. in English), 54(28), 8259-8262 (2015-06-03)
In Pd-catalyzed C-N cross-coupling reactions, α-branched secondary amines are difficult coupling partners and the desired products are often produced in low yields. In order to provide a robust method for accessing N-aryl α-branched tertiary amines, new catalysts have been designed

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