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7-AMINO-4-METHYL-3-COUMARINYLACETIC ACID (AMCA) is a blue fluorescent dye characterized by its relatively large Stoke's shift and resistance to photobleaching. It is a versatile compound used in various applications due to its desirable properties, such as its ability to form photostable amide links with lysine residues upon activation with UV light.

106562-32-7

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106562-32-7 Usage

Uses

Used in Fluorescent Labeling:
AMCA is used as a fluorescent protein labeling agent for various applications, including multiplex immunophenotyping. Its N-hydroxysuccinimide ester reacts with lysine residues to form stable amide links, and upon activation with UV light, it displays emission maxima of 400-460 nm.
Used in Contrasting Probes:
In the field of microscopy and imaging, 7-AMINO-4-METHYL-3-COUMARINYLACETIC ACID is used as contrasting probes for double and triple labeling in immunofluorescence assays. Its blue fluorescence allows for clear differentiation between multiple markers, enhancing the accuracy and efficiency of these assays.
Used in Non-Activated, Amine-Reactive Fluorescent Probes:
AMCA is also utilized as a non-activated, amine-reactive fluorescent probe in various research and diagnostic applications. Its ability to form stable amide links with lysine residues makes it a valuable tool for detecting and analyzing proteins and other biomolecules.

Check Digit Verification of cas no

The CAS Registry Mumber 106562-32-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,5,6 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 106562-32:
(8*1)+(7*0)+(6*6)+(5*5)+(4*6)+(3*2)+(2*3)+(1*2)=107
107 % 10 = 7
So 106562-32-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H11NO4/c1-6-8-3-2-7(13)4-10(8)17-12(16)9(6)5-11(14)15/h2-4H,5,13H2,1H3,(H,14,15)

106562-32-7 Well-known Company Product Price

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  • Sigma

  • (08445)  7-Amino-4-methyl-3-coumarinylacetic acid  BioReagent, suitable for fluorescence, ~90% (HPLC)

  • 106562-32-7

  • 08445-100MG

  • 730.08CNY

  • Detail
  • Sigma

  • (08445)  7-Amino-4-methyl-3-coumarinylacetic acid  BioReagent, suitable for fluorescence, ~90% (HPLC)

  • 106562-32-7

  • 08445-500MG

  • 2,511.99CNY

  • Detail

106562-32-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(7-amino-4-methyl-2-oxochromen-3-yl)acetic acid

1.2 Other means of identification

Product number -
Other names 2-(7-Amino-4-methyl-2-oxo-2H-chromen-3-yl)acetic 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:106562-32-7 SDS

106562-32-7Relevant academic research and scientific papers

Gasotransmitter Regulation of Phosphatase Activity in Live Cells Studied by Three-Channel Imaging Correlation

Ou, Pan,Zhang, Ruilong,Liu, Zhengjie,Tian, Xiaohe,Han, Guangmei,Liu, Bianhua,Hu, Zhangjun,Zhang, Zhongping

, p. 2261 - 2265 (2019)

Enzyme activity in live cells is dynamically regulated by small-molecule transmitters for maintaining normal physiological functions. A few probes have been devised to measure intracellular enzyme activities by fluorescent imaging, but the study of the re

A labeled guanidine ligand for studying sweet taste

Feng, Yangbo,Burgess, Kevin,Pledger, David,Cairns, Nick,Linthicum, D. Scott

, p. 881 - 884 (2007/10/03)

A synthesis of a biotinylated-, coumarin-substituted-N,N'-diarylguanidin 1 is reported. This ligand has structural features conducive to studying sweet taste including a fluorescent tag to facilitate spectroscopic studies of binding to protein-receptors f

7-amino-4-methyl-coumarin-3-carboxyalkyl derivates and fluorescent conjugates thereof

-

, (2008/06/13)

A novel compound having the formula (I): STR1 or a reactive derivative or functional equivalent thereof, wherein m is an integer from 1 to 4, and R1 and R2 are same or different and selected from hydrogen and 1-4C alkyl; a fluorescent conjugate having the formula (III): STR2 wherein m R1 and R2 have the meaning given in claim 1, and R4 is a substituent attached to the keto group of formula (III) by a covalen bond. The new compounds and conjugates are usefual as fluorescent labelling agents.

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