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35418-52-1

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35418-52-1 Usage

Description

Schizokinen is a hydroxamic acid that is formed through the condensation of the primary amino group of N-(3-aminopropyl)-N-hydroxyacetamide with the carboxy groups at positions 1 and 3 of citric acid. It is a siderophore produced by Bacillus megaterium and Anabaena species, which are known for their ability to bind and transport iron.

Uses

Used in Pharmaceutical Industry:
Schizokinen is used as an iron-chelating agent for its ability to bind and transport iron, which can be beneficial in treating conditions related to iron imbalance or iron-related diseases.
Used in Microbiology Research:
In the field of microbiology, Schizokinen is used as a research tool to study the mechanisms of iron uptake and transport in bacteria, particularly in Bacillus megaterium and Anabaena species. This can help in understanding the role of siderophores in bacterial growth and survival.
Used in Environmental Science:
Schizokinen can be employed in environmental science applications to study the role of siderophores in the iron cycle in various ecosystems, as well as their potential use in bioremediation processes to remove excess iron from contaminated environments.
Used in Agricultural Applications:
In agriculture, Schizokinen may be used to improve plant growth and health by enhancing iron availability in the soil, particularly in iron-deficient soils where plant growth can be limited by low iron levels.
Used in Chemical Synthesis:
Schizokinen can be utilized in the synthesis of various chemical compounds, taking advantage of its unique structure and iron-binding properties to create new molecules with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 35418-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,4,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35418-52:
(7*3)+(6*5)+(5*4)+(4*1)+(3*8)+(2*5)+(1*2)=111
111 % 10 = 1
So 35418-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H28N4O9/c1-11(21)19(28)7-3-5-17-13(23)9-16(27,15(25)26)10-14(24)18-6-4-8-20(29)12(2)22/h27-29H,3-10H2,1-2H3,(H,17,23)(H,18,24)(H,25,26)

35418-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name schizokinen

1.2 Other means of identification

Product number -
Other names 4-[3-[acetyl(hydroxy)amino]propylamino]-2-[2-[3-[acetyl(hydroxy)amino]propylamino]-2-oxoethyl]-2-hydroxy-4-oxobutanoic 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:35418-52-1 SDS

35418-52-1Downstream Products

35418-52-1Relevant articles and documents

Synthesis and iron coordination properties of schizokinen and its imide derivative

Chuljerm, Hataichanok,Chen, Yu-Lin,Srichairatanakool, Somdet,Hider, Robert C.,Cilibrizzi, Agostino

, p. 17395 - 17401 (2019/12/02)

The iron(iii) affinity constants for schizokinen and its imide derivative are reported for the first time. Surprisingly, schizokinen possesses a higher affinity for iron(iii) than desferrioxamine B; log?KFeIII (FeL), 36.2 and 30.6, respectively. This incr

Synthesis of Schizokinen, Homoschizokinen, Its Imide and the Detection of Imide with 13C-N.M.R.-Spectroscopy

Milewska, Maria J.,Chimiak, Andrzej,Glowacki, Zdzislaw

, p. 447 - 456 (2007/10/02)

A new method for the synthesis of homoschizokinen 1 and schizokinen 2 is described. 2-tert-Butyl-1,3-di-N-hydroxysuccinimidyl citrate has been applied as the key substrate.The method excludes the possibility of imide formation.The imide of compound 1 has

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