Skip to Content
Merck
All Photos(1)

Key Documents

62453

Sigma-Aldrich

Atto 540 Q maleimide

BioReagent, suitable for fluorescence

Sign Into View Organizational & Contract Pricing


About This Item

MDL number:
UNSPSC Code:
12352108
NACRES:
NA.32

product line

BioReagent

Assay

≥90% (HPLC)
≥90% (degree of coupling)

form

solid

manufacturer/tradename

ATTO-TEC GmbH

technique(s)

UV/Vis spectroscopy: suitable

λ

in ethanol (with 0.1% trifluoroacetic acid)

UV absorption

λ: 542-548 nm Amax

suitability

corresponds for UV test
suitable for fluorescence

storage temp.

−20°C

Legal Information

This product is for Research use only. In case of intended commercialization, please contact the IP-holder (ATTO-TEC GmbH, Germany) for licensing.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Thiol reactive probes and chemosensors.
Peng H, Chen W, Cheng Y, et al.
Sensors, 12, 15907-15946 (2012)
Limin Ma et al.
The Analyst, 137(21), 5046-5050 (2012-09-13)
4-Nitro-1,8-naphthalic anhydride (NNA) was used to distinguish cysteine from homocysteine and other potentially interfering thiols through a novel sequential substitution mechanism. The discrimination involves a blue-fluorescent thioether formation via nucleophilic aromatic substitution of the nitro group by thiol, followed by
Hyo Sung Jung et al.
Biomaterials, 33(33), 8495-8502 (2012-08-22)
We have synthesized a series of coumarins (1-3) that can emit fluorescence in a turn-on manner through a Michael-type reaction with thiol-containing compounds. The only difference among the coumarins is the position of a carboxyl group on its benzene ring

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service