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4272-77-9

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4272-77-9 Usage

Description

5-(Dimethylamino)-1-naphthalenesulfonic acid is a fluorescent molecule characterized by its white to off-white or beige-greyish powder appearance. It is known for its distinctive chemical properties that make it suitable for various applications in different industries.

Uses

Used in Protein Analysis:
5-(Dimethylamino)-1-naphthalenesulfonic acid is used as a fluorescent probe for protein analysis, allowing researchers to study protein structures, interactions, and dynamics with enhanced visualization and detection capabilities.
Used in FRET Detection:
In the field of molecular biology, 5-(Dimethylamino)-1-naphthalenesulfonic acid is utilized as a donor molecule in F?rster Resonance Energy Transfer (FRET) detection. This technique is essential for monitoring molecular interactions and conformational changes in biological systems, providing valuable insights into cellular processes and mechanisms.
Used in Pharmaceutical Research:
5-(Dimethylamino)-1-naphthalenesulfonic acid's fluorescent properties also make it a valuable tool in the development of new drugs and therapies. It can be employed in high-throughput screening assays to identify potential drug candidates and study their interactions with target proteins.
Used in Analytical Chemistry:
This molecule is also used in analytical chemistry for the detection and quantification of various substances, taking advantage of its fluorescence properties to improve the sensitivity and accuracy of analytical methods.
Used in Material Science:
In the field of material science, 5-(Dimethylamino)-1-naphthalenesulfonic acid can be used to develop novel materials with enhanced optical properties, such as fluorescent sensors or imaging agents, by incorporating its fluorescent characteristics into the material's structure.

Check Digit Verification of cas no

The CAS Registry Mumber 4272-77-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,7 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4272-77:
(6*4)+(5*2)+(4*7)+(3*2)+(2*7)+(1*7)=89
89 % 10 = 9
So 4272-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO3S/c1-13(2)11-7-3-6-10-9(11)5-4-8-12(10)17(14,15)16/h3-8H,1-2H3,(H,14,15,16)/p-1

4272-77-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(dimethylamino)naphthalene-1-sulfonic acid

1.2 Other means of identification

Product number -
Other names 5-(Dimethylamino)-1-naphthalenesulfonic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4272-77-9 SDS

4272-77-9Relevant articles and documents

Photolysis of the sulfonamide bond of metal complexes of N-dansyl-1,4,7,10-tetraazacyclododecane in aqueous solution: A mechanistic study and application to the photorepair of cis,syn-cyclobutane thymine photodimer

Aoki, Shin,Tomiyama, Yumiko,Kageyama, Yoshiyuki,Yamada, Yasuyuki,Shiro, Motoo,Kimura, Eiichi

, p. 561 - 573 (2009)

Sulfonamide constitutes a ubiquitous functional group that is frequently used in organic chemistry, analytical chemistry, and medicinal chemistry. We report herein on the photolysis of a dansylamide moiety of 1-dansyl-1,4,7,10- tetraazzacyclododecane (Nda

Synthetic method of dansyl chloride for preparing fluorescent probe (by machine translation)

-

Paragraph 0029-0035, (2020/07/14)

The preparation method comprises the following steps: dissolving rhodamine sulfonic acid in an organic solvent to obtain an emulsion; sequentially dropwise adding thionyl chloride and phosphorus pentachloride into the suspension; controlling the temperature of the system to 40 - 45 °C; reacting 4 - 6h; adjusting pH to 5 - 6; and collecting the product to obtain the folic acid chloride. The invention further discloses a fluorescent probe prepared from the dansyl chloride. In the synthesis process of the target fluorescent compound, by adding the phosphorus pentachloride catalyst, the use amount of thionyl chloride is reduced, the reaction condition is mild, and the method can be carried out at a lower temperature. (by machine translation)

Dual signaling of thallium(III) ions via oxidative cleavage of a sulfonhydrazide linkage

Ahn, Sangdoo,Chang, Suk-Kyu,Choi, Myung Gil,Lee, Yu Jeong,Park, Tae Jung,Yoo, Jae Hoon

, (2020/03/17)

The thallium is widely used in various research and industrial applications but is very toxic. In this work, we developed a novel reaction-based dual signaling probe for the selective and sensitive determination of Tl3+ via the oxidative cleavage of a rhodamine–dansylhydrazide conjugate. The designed probe showed pronounced colorimetric and fluorescence signaling behavior toward Tl3+ with a detection limit of 1.3 × 10–7 M (0.027 ppm), as well as selectivity over other common metal ions, anions, and oxidants. The Tl3+ signaling process required less than 2 min and was not influenced by the solution pH within the range of 4.0–5.5; however, the signal diminished significantly above pH 6.0. To demonstrate the practical applicability of the designed probe, a simple and convenient colorimetric assay for the determination of Tl3+ in commercial reagents was established using an office scanner as a readily available signal capturing device.

A trifluoroacetic acid-labile sulfonate protecting group and its use in the synthesis of a near-IR fluorophore

Pauff, Steven M.,Miller, Stephen C.

supporting information, p. 711 - 716 (2013/02/25)

Sulfonated molecules exhibit high water solubility, a property that is valuable for many biological applications but often complicates their synthesis and purification. Here we report a sulfonate protecting group that is resistant to nucleophilic attack but readily removed with trifluoroacetic acid (TFA). The use of this protecting group improved the synthesis of a sulfonated near-IR fluorophore and the mild deprotection conditions allowed isolation of the product without requiring chromatography.

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