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88997

Sigma-Aldrich

6-Carboxy-tetramethylrhodamine N-succinimidyl ester

BioReagent, suitable for fluorescence

Synonym(s):

"5-Carboxytetramethylrhodamine N-succinimidyl ester"

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About This Item

Empirical Formula (Hill Notation):
C29H25N3O7
CAS Number:
Molecular Weight:
527.52
MDL number:
UNSPSC Code:
12352202
NACRES:
NA.21

product line

BioReagent

form

powder

solubility

DMF: 2 mg/mL, clear
acetonitrile: soluble

fluorescence

λex 543 nm; λem 575 nm in 0.1 M phosphate pH 7.0

suitability

suitable for fluorescence

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

−20°C

InChI

1S/C29H25N3O7/c1-30(2)17-6-9-20-23(14-17)38-24-15-18(31(3)4)7-10-21(24)27(20)22-13-16(5-8-19(22)28(35)36)29(37)39-32-25(33)11-12-26(32)34/h5-10,13-15H,11-12H2,1-4H3

InChI key

PAOQTZWNYMMSEE-UHFFFAOYSA-N

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Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Fluorescent labeling of peptides after chemical modification; Fluorescent labeling of aminoglycoside antibiotics

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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P Hoogerhout et al.
The journal of peptide research : official journal of the American Peptide Society, 54(5), 436-443 (1999-11-24)
The mechanism which enables lipopeptides to induce cytotoxicity is not known. By preparing fluorescent-labeled lipopeptides one might unravel the mechanism of their entry into the cell and their intracellular pathway. A method of preparing double-fluorescent-labeled peptides by solid-phase chemistry is
S.J. Bark et al.
Journal of the American Chemical Society, 122, 3567-3567 (2000)
Y Wang et al.
Biochemistry, 35(38), 12338-12346 (1996-09-24)
RNA aptamers had previously been selected which were able to bind to the aminoglycoside antibiotic tobramycin with high affinity (Wang & Rando, 1995). Consensus sequences are found in a variety of constructs, and these sequences were mapped to stem-loop regions

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