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13516-27-3

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13516-27-3 Usage

Definition

ChEBI: A member of the class of guanidines that is dioctylamine in which a hydrogen from each of the terminal methyl groups is replaced by a guanidino group. Once used as a fungicidal seed dressing, it is no longer approved for use in the European Union.

Check Digit Verification of cas no

The CAS Registry Mumber 13516-27-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,1 and 6 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13516-27:
(7*1)+(6*3)+(5*5)+(4*1)+(3*6)+(2*2)+(1*7)=83
83 % 10 = 3
So 13516-27-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H41N7/c19-17(20)24-15-11-7-3-1-5-9-13-23-14-10-6-2-4-8-12-16-25-18(21)22/h23H,1-16H2,(H4,19,20,24)(H4,21,22,25)

13516-27-3SDS

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 iminoctadine

1.2 Other means of identification

Product number -
Other names 1,17-diguanidino-9-azaheptadedace

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:13516-27-3 SDS

13516-27-3Downstream Products

13516-27-3Related news

Subacute and delayed toxicity of IMINOCTADINE (cas 13516-27-3) liquid formulation, which contains IMINOCTADINE (cas 13516-27-3) triacetate as an antifungal component on a nontarget domesticated insect, the silkworm, Bombyx mori L. (Lepidoptera: Bombycidae)08/10/2019

We investigated insecticidal effects of iminoctadine liquid formulation, a fungicide containing iminoctadine triacetate, on the silkworm Bombyx mori that is an important domesticated insect. Iminoctadine liquid formulation was incorporated in an artificial diet and fed to silkworms for 24 h on t...detailed

A bioactivity and biochemical analysis of IMINOCTADINE (cas 13516-27-3) tris (albesilate) as a fungicide against Corynespora cassiicola08/09/2019

Iminoctadine tris (albesilate) is a bis-guazatine fungicide, and its specific modes of action and efficacy against C. cassiicola are not yet clear. In this study, baseline sensitivity data for mycelial growth showed that the frequency distribution curve of iminoctadine tris (albesilate) EC50 val...detailed

13516-27-3Relevant articles and documents

Diamine and Triamine Analogs and Derivatives as Inhibitors of Deoxyhypusine Synthase: Synthesis and Biological Activity

Lee, Young Bok,Park, Myung Hee,Folk, J. E.

, p. 3053 - 3061 (2007/10/03)

Deoxyhypusine synthase catalyzes the initial step in the posttranslational formation of the amino acid hypusine ε-(4-amino-2-hydroxybutyl)lysine> in eukaryotic initiation factor 5A (eIF-5A). eIF-5A and its hypusine modification are believed to be essential for cell growth.A number of compounds related to diamines and triamines were synthesized and tested as inhinitors of this enzyme.The findings indicate that the long chain triamines 2a and 2b and their guanyl derivatives 3a, 3b, 4a, and 4b exert inhibition by binding to enzyme through only a portion of their structures at any one time.The inhibition exhibited by N-ethyl-1,7-diaminoheptane 20 and its guanyl derivative 21 supports this notion and is evidence for participation of the secondary amino group in binding to enzyme.There is preliminary evidence that amidino and isothiuronium groups may also serve as basic centers for binding to enzyme.Few of the compounds tested here were comparable in inhibitory potency to 1-guanidino-7-aminoheptane (GC7) the most effective known inhibitor of deoxhypusine synthase, and none proved nearly as efficient as GC7 in inhibiting the enzyme in Chinese hamster ovary cells.Hence, unlike the antiproliferative effect of GC7, for which there is evidence of cause by interference with deoxhypusine synthase catalysis (Park, M.H.; Wolff, E.C.; Lee, Y.B.; Folk, J.E.J.Biol.Chem. 269, 1994, 27827-27832), the effective growth arrest exerted by several of the newly synthesized compounds cannot be attributed to inhibition of hypusine synthesis.

Agricultural and horticultural guanidine-type fungicide and process for production thereof

-

, (2008/06/13)

An agricultural and horticultural fungicide of low phytotoxicity comprising as an active ingredient an addition salt between a fungicidal guanidine compound and an acid having an oleophilic group with at least 9 carbon atoms in total. The acid addition salt is produced by reacting a fungicidal guanidine compound or its acid addition salt with an acid having an oleophilic group with at least 9 carbon atoms in total or its salt.

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