6-Carboxy-tetramethylrhodamine N-succinimidyl ester

Name: 6-Carboxy-tetramethylrhodamine <I>N</I>-succinimidyl ester
Brand: SIGMA

BioReagent, suitable for fluorescence

Synonym(s):

"5-Carboxytetramethylrhodamine N-succinimidyl ester"

Slide 1 of 1

Select a Size

Pricing and availability is not currently available.

About This Item

Empirical Formula (Hill Notation):

C₂₉H₂₅N₃O₇

CAS Number:

150810-69-8

Molecular Weight:

527.52

MDL number:

MFCD03453266

UNSPSC Code:

12352202

NACRES:

NA.21

Key Documents

View All Documentation

product line

BioReagent

form

powder

solubility

DMF: 2 mg/mL, clear
acetonitrile: soluble

fluorescence

λ_ex 543 nm; λ_em 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

SMILES string

[N+](=[c]1cc2[o]c3c(c(c2cc1)c4c(ccc(c4)C(=O)ON5C(=O)CCC5=O)C(=O)[O-])ccc(c3)N(C)C)(C)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

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item	21953	94506	46935
Sigma-Aldrich 88997 6-Carboxy-tetramethylrhodamine N-succinimidyl ester	Sigma-Aldrich 21953 5(6)-Carboxytetramethylrhodamine	Sigma-Aldrich 94506 Tetramethylrhodamine-5-maleimide	Sigma-Aldrich 46935 6-[Fluorescein-5(6)-carboxamido]hexanoic acid
suitability suitable for fluorescence	suitability suitable for fluorescence	suitability suitable for fluorescence	suitability suitable for fluorescence
fluorescence λ_ex 543 nm; λ_em 575 nm in 0.1 M phosphate pH 7.0	fluorescence λ_ex 543 nm; λ_em 572 nm in methanol	fluorescence λ_ex 543 nm; λ_em 575 nm in 0.1 M phosphate pH 7.0	fluorescence λ_ex 491 nm; λ_em 515 nm in 0.1 M Tris pH 9.0
form powder	form solid	form powder	form solid
application(s) diagnostic assay manufacturing hematology histology	application(s) -	application(s) -	application(s) -
solubility DMF: 2 mg/mL, clear, acetonitrile: soluble	solubility DMF: soluble, DMSO: soluble	solubility DMSO: soluble, methanol: soluble	solubility DMF: soluble, DMSO: soluble
Quality Level 200	Quality Level 100	Quality Level 100	Quality Level 200

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Fluorescent labeling of peptides after chemical modification[1][2]; Fluorescent labeling of aminoglycoside antibiotics[3]

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

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

S.J. Bark et al.

Journal of the American Chemical Society, 122, 3567-3567 (2000)

RNA molecules that specifically and stoichiometrically bind aminoglycoside antibiotics with high affinities.

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

Solid-phase synthesis and application of double-fluorescent-labeled lipopeptides, containing a CTL-epitope from the measles fusion protein.

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

Questions

Reviews

No rating value

Active Filters

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