Dodine Chemical Properties

Melting point:

136°C

Boiling point:

429.73°C (rough estimate)

Density 

0.9636 (rough estimate)

vapor pressure 

5 x 10^-6 Pa (20 °C, est.)

refractive index 

1.6500 (estimate)

Flash point:

>100 °C

storage temp. 

0-6°C

solubility 

DMSO (Slightly, Heated), Methanol (Slightly)

pka

>13 (strong base)

Water Solubility 

630 mg l^-1(25 °C)

Merck 

13,3442

BRN 

6546960

LogP

1.150

CAS DataBase Reference

2439-10-3(CAS DataBase Reference)

NIST Chemistry Reference

1-dodecylguanidinium acetate(2439-10-3)

EPA Substance Registry System

Dodine (2439-10-3)

Safety Information

Hazard Codes 

Xn;N,N,Xn

Risk Statements 

22-36/38-50/53

Safety Statements 

26-60-61

RIDADR 

UN 3077

WGK Germany 

3

RTECS 

MF1750000

HS Code 

29252900

Hazardous Substances Data

2439-10-3(Hazardous Substances Data)

Toxicity

LC50 in harlequin fish: 0.6 mg/l (Hourdakis)

MSDS

• Language:English Provider:Dodecylguanidine monoacetate

Dodine Usage And Synthesis

Chemical Properties

White Solid

Uses

Dodine is used to control scab on apples, pears and pecans, leaf spot diseases of cherries, olives, blackcurrants, celery and other crops, and foliar diseases of strawberries. It is also used on other fruit, vegetable, nut and ornamental crops and shade trees.

Uses

Used as agricultural fungicide.

Definition

ChEBI: An acetate salt resulting from the reaction of equimolar amounts of 1-dodecylguanidine and acetic acid. It is used as a fungicide to control black spot and foliar diseases on apples, pears, peaches, nectarines and strawberries.

General Description

White crystalline solid. Used as a fungicide.

Air & Water Reactions

Soluble in hot water.

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.

Agricultural Uses

Fungicide, Microbiocide: Used to control black spot on apples, pears and pecans; brown rot and foliar diseases on peaches and nectarines, cherries, strawberries, black walnuts and sycamore trees. In industry, used as a biocide and preservative. May also be used to 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).

Dodine(2439-10-3)Related Product Information

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• Ethylicin
• DITHIANON
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• Dodine
• DODINE [GUANIDINE-14C]
• DODINE SOLUTION 100UG/ML IN METHANOL 1ML