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2439-10-3

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2439-10-3 Usage

Description

Dodine, also known as N-dodecylguanidine acetate, is a white crystalline solid that is primarily used as a fungicide in the agricultural industry. It is an acetate salt resulting from the reaction of equimolar amounts of 1-dodecylguanidine and acetic acid. Dodine exhibits strong antifungal properties, making it an effective agent for controlling various fungal diseases in crops.

Uses

Used in Agricultural Industry:
Dodine is used as an agricultural fungicide for controlling scab on apples, pears, and pecans. It is also effective against leaf spot diseases of cherries, olives, blackcurrants, celery, and other crops. Additionally, it is used to manage foliar diseases of strawberries and is applicable to other fruit, vegetable, nut, and ornamental crops, as well as shade trees.
Used in Horticultural Industry:
Dodine is employed as a fungicide to control black spot on apples, pears, and pecans. It is also used to manage brown rot and foliar diseases on peaches, nectarines, cherries, strawberries, black walnuts, and sycamore trees.
Used in Industrial Applications:
In the industrial sector, Dodine is utilized as a biocide and preservative. It may also be used to catalyze organic reactions, further expanding its range of applications.

Reactivity Profile

Acidic organic/inorganic salts, such as Dodine, are generally soluble in water. The resulting solutions contain moderate to high concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.

Trade name

AC 5223?; AMERICAN CYANAMID? 5223; APADODINE?; CARPENE?; CURITAN?; CYPREX?; CYPREX? 65W; CYTOX? 2160; DOQUADINE?; EFUZIN?; KARPEN?; MELPREX?; MELPREX? 65; MILPREX?; QUESTURAN?; Radspor L; SULGEN?; SYLLIT?; SYLLIT? 65; SYLLIT? 400SC, TEBULAN?; TSITREX?; VANDODINE?; VENTUROL?; VONDODINE?

Metabolic pathway

No information is available on the fate of dodine in soils but in plants it is converted into creatine by the action of a methyltransferase, and simultaneously the dodecyl moiety is oxidatively cleaved (PM).

Degradation

Dodine is stable in neutral and moderately alkaline or acidic media but the free base is liberated by concentrated alkali (PM).

Check Digit Verification of cas no

The CAS Registry Mumber 2439-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,3 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2439-10:
(6*2)+(5*4)+(4*3)+(3*9)+(2*1)+(1*0)=73
73 % 10 = 3
So 2439-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H29N3.C3H6O2/c1-2-3-4-5-6-7-8-9-10-11-12-16-13(14)15;1-2-3(4)5/h2-12H2,1H3,(H4,14,15,16);2H2,1H3,(H,4,5)

2439-10-3SDS

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 1-dodecylguanidine acetate

1.2 Other means of identification

Product number -
Other names DODENE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Fungicide
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:2439-10-3 SDS

2439-10-3Downstream Products

2439-10-3Relevant articles and documents

Compounding method for dozine

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Paragraph 0045; 0046; 0050; 0051; 0052, (2017/11/30)

The invention provides a compounding method for dozine. The method comprises the following steps: taking guanidine hydrochloride as an initial raw material to react with chlorododecane, thereby acquiring a midbody A; adding an alkali aqueous solution into the midbody A for reaction; adding glacial acetic acid for reaction; performing after-treatment, thereby acquiring a target product dozine. The compounding method is characterized by easily acquired raw materials, few reaction steps, mild reaction condition, simplicity in operation and higher yield and is an environment-friendly compounding method, so that the compounding method is suitable for large-scale industrial production and has wide application prospect and market potential.

Soluble polymer based matrix for chemically active water insoluble components

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, (2008/06/13)

This invention relates to a water soluble matrix composition comprising an anionic surfactant, a C6 to C18 alkyl pyrrolidone, urea and a water insoluble copolymer of vinyl pyrrolidone with not more than 50 wt. % of a comonomer selected from the group of an α-olefin, vinyl acetate, an acrylic or methacrylic acid ester and methacrylamide as a free flowing particulate solid which matrix is suitably mixed with a water insoluble, chemically active component, such as an agrochemical, to provide a clear sprayable film forming emulsion, such as a non-leachable film on a plant or other substrate surface. The invention also relates to the method of preparing the matrix and to the incorporation of an agrochemical concentrate and plant spray composition.

Preservative for aqueous products and systems

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, (2008/06/13)

An antimicrobial composition for preserving products or systems containing an aqueous phase comprising from 10 to 60% by weight or tert.-butyl hydroperoxide, from 3 to 50% by weight of a monophenylglycol ether of formulas I or II herein, and the remainder a diluent which is water, an organic solvent or a mixture of water and organic solvent; and a method of use of the antimicrobial composition. The antimicrobial composition may additionally include up to about 20% by weight of a biocide selected from certain non-halogenated phenols, certain heterocyclic compounds and guanidine, phthalimide and urea derivatives.

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