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SML3994

Sigma-Aldrich

BODIPY TR-X NHS Ester

≥95% (HPLC)

Synonym(s):

(T-4)-[N-[6-[(2,5-Dioxo-1-pyrrolidinyl)oxy]-6-oxohexyl]-2-[4-[5-[[5-(2-thienyl)-2H-pyrrol-2-ylidene-κN]methyl]-1H-pyrrol-2-yl-κN]phenoxy]acetamidato]difluoroboron, 6-(((4-(4,4-Difluoro-5-(2-thienyl)-4-bora-3a,4a-diaza-s-indacene-3-yl)phenoxy)acetyl)amino)hexanoic acid succinimidyl ester, BODIPY TR-X, BODIPY TR-X NHS, BODIPY TR-X, SE

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5 L
₩270,092
6 X 1 L
₩330,900
25 KG
₩364,081
4 X 2.5 L
₩441,500

₩270,092


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5 L
₩270,092
6 X 1 L
₩330,900
25 KG
₩364,081
4 X 2.5 L
₩441,500

About This Item

Empirical Formula (Hill Notation):
C31H29BF2N4O6S
CAS Number:
Molecular Weight:
634.46
UNSPSC Code:
12352200

₩270,092


Please contact Customer Service for Availability

Request a Bulk Order
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Quality Level

Assay

≥95% (HPLC)

form

powder

color

, Red To very dark purple

solubility

DMSO: 2 mg/mL, clear

storage temp.

-10 to -25°C

SMILES string

O=C(CCCCCNC(COC1=CC=C(C2=CC=C3C=C4C=CC(C5=CC=CS5)=[N]4[B+3]([F-])([N-]32)[F-])C=C1)=O)ON6C(CCC6=O)=O

Biochem/physiol Actions

Amine reactive, red luminous fluorescent labeling reagent that can be used to tag antibodies, proteins, peptides, and nucleic acids.

BODIPY TR-X NHS Ester is a versatile, amine-sensitive red fluorescent labeling reagent useful to tag antibodies, proteins, peptides, and nucleic acids. BODIPY TR dyes, also called boron-dipyrromethene tetramethylrhodamine, are known for their exceptional photophysical properties, including high fluorescence quality and photostability, with wide spectral tuning. BODIPY TR has a narrow absorption range (~ 500-550 nm) and a broader emission range (~ 580-640 nm) for multi-color cell labeling. BODIPY TR-X offers an extended excited-state lifetime for fluorescence polarization assays and significant two-photon excitation capability. BODIPY TR-X NHS Ester is a valuable tool for fluorescence microscopy, flow cytometry, and IHC applications.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Lanthanide triflates as water-tolerant Lewis acids. Activation of commercial formaldehyde solution and use in the aldol reaction of silyl enol ethers with aldehydes in aqueous media.
Kobayashi S and Hachiya I.
The Journal of Organic Chemistry, 59(13), 3590-3596 (1994)
Lanthanide Trifluoromethanesulfonates as Stable Lewis Acids in Aqueous Media. Yb (OTf)3 Catalyzed Hydroxymethylation Reaction of Silyl Enol Ethers with Commercial Formaldehyde Solution.
Kobayashi S.
Chemistry Letters (Jpn), 12, 2187-2190 (1991)
Microwave synthesis of nanocrystalline metal sulfides in formaldehyde solution.
Liao X-H, et al.
Materials Science and Engineering, B, 85(1), 85-89 (2001)
Opas Bunkoed et al.
Analytica chimica acta, 659(1-2), 251-257 (2010-01-28)
We report the development of transparent sol-gels with entrapped sensitive and selective reagents for the detection of formaldehyde. The sampling method is based on the adsorption of formaldehyde from the air and reaction with beta-diketones (for example acetylacetone) in a
James Larkin et al.
The New England journal of medicine, 373(1), 23-34 (2015-06-02)
Nivolumab (a programmed death 1 [PD-1] checkpoint inhibitor) and ipilimumab (a cytotoxic T-lymphocyte-associated antigen 4 [CTLA-4] checkpoint inhibitor) have been shown to have complementary activity in metastatic melanoma. In this randomized, double-blind, phase 3 study, nivolumab alone or nivolumab plus

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