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DABSYL-L-PROLINE is a chemical compound that serves as a derivatization reagent for amino acids, particularly in high performance liquid chromatography (HPLC) analysis. It is a derivative of the amino acid proline, featuring a dabsyl group attached to its amino group. This modification enhances the separation and detection capabilities of amino acids within complex mixtures, making DABSYL-L-PROLINE a valuable tool in analytical chemistry and biochemistry.
Used in Analytical Chemistry:
DABSYL-L-PROLINE is used as a derivatization reagent for improving the separation and detection of amino acids in HPLC analysis. Its application allows for better sensitivity and resolution, which is crucial for accurate characterization and analysis of amino acids and related compounds.
Used in Biochemistry:
In the field of biochemistry, DABSYL-L-PROLINE is utilized for the analysis of peptides and proteins. Its use in this context aids researchers in studying enzyme kinetics and peptide synthesis, contributing to a deeper understanding of biological processes and the development of related applications.
Used in Pharmaceutical Research:
DABSYL-L-PROLINE can be employed in pharmaceutical research as a tool for analyzing drug candidates and their interactions with biological molecules. Its ability to enhance the detection and separation of amino acids can be instrumental in the development of new drugs and therapies.
Overall, DABSYL-L-PROLINE plays a significant role across various scientific disciplines, offering a reliable and effective means for the analysis and study of amino acids, peptides, and proteins.

89131-09-9

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89131-09-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89131-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,3 and 1 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89131-09:
(7*8)+(6*9)+(5*1)+(4*3)+(3*1)+(2*0)+(1*9)=139
139 % 10 = 9
So 89131-09-9 is a valid CAS Registry Number.
InChI:InChI=1/C19H22N4O4S/c1-22(2)16-9-5-14(6-10-16)20-21-15-7-11-17(12-8-15)28(26,27)23-13-3-4-18(23)19(24)25/h5-12,18H,3-4,13H2,1-2H3,(H,24,25)/b21-20+/t18-/m0/s1

89131-09-9 Well-known Company Product Price

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  • TCI America

  • (D1458)  Dabsyl-L-proline  >98.0%(HPLC)

  • 89131-09-9

  • 100mg

  • 1,730.00CNY

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89131-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-1-[4-[[4-(dimethylamino)phenyl]diazenyl]phenyl]sulfonylpyrrolidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names Dabsylproline

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:89131-09-9 SDS

89131-09-9Downstream Products

89131-09-9Relevant articles and documents

Trichoderins, novel aminolipopeptides from a marine sponge-derived Trichoderma sp., are active against dormant mycobacteria

Pruksakorn, Patamaporn,Arai, Masayoshi,Kotoku, Naoyuki,Vilchze, Catherine,Baughn, Anthony D.,Moodley, Prashini,Jacobs Jr., William R.,Kobayashi, Motomasa

experimental part, p. 3658 - 3663 (2010/09/17)

Three new aminolipopeptides, designated trichoderins A (1), A1 (2), and B (3), were isolated from a culture of marine sponge-derived fungus of Trichoderma sp. as anti-mycobacterial substances with activity against active and dormant bacilli. The chemical structures of trichoderins were determined on the basis of spectroscopic study. Trichoderins showed potent anti-mycobacterial activity against Mycobacterium smegmatis, Mycobacterium bovis BCG, and Mycobacterium tuberculosis H37Rv under standard aerobic growth conditions as well as dormancy-inducing hypoxic conditions, with MIC values in the range of 0.02-2.0 μg/mL.

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