Dodine CAS 2439-10-3
Introduction：Basic information about Dodine CAS 2439-10-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Dodine Basic information
| Product Name: | Dodine |
| Synonyms: | Dodine65%WP;americancyanamid5,223;americancyanamid5223;apadodine;carpen;Carpene;CL 7521;Curitan |
| CAS: | 2439-10-3 |
| MF: | C15H33N3O2 |
| MW: | 287.44 |
| EINECS: | 219-459-5 |
| Product Categories: | Agricultural fungicide;Aliphatics;Amines;INSECTICIDE;Aliphatics containing nitrogenAlphabetic;D;DJ - DZ;Fungicides;Pesticides |
| Mol File: | 2439-10-3.mol |
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) |
| Fp | >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 |
| Major Application | agriculture environmental |
| InChI | 1S/C13H29N3.C2H4O2/c1-2-3-4-5-6-7-8-9-10-11-12-16-13(14)15;1-2(3)4/h2-12H2,1H3,(H4,14,15,16);1H3,(H,3,4) |
| InChIKey | YIKWKLYQRFRGPM-UHFFFAOYSA-N |
| SMILES | CC(O)=O.CCCCCCCCCCCCNC(N)=N |
| 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 |
| TSCA | TSCA listed |
| HS Code | 29252900 |
| Storage Class | 11 - Combustible Solids |
| Hazard Classifications | Acute Tox. 4 Oral Aquatic Acute 1 Aquatic Chronic 1 Eye Irrit. 2 Skin Irrit. 2 |
| Hazardous Substances Data | 2439-10-3(Hazardous Substances Data) |
| Toxicity | LC50 in harlequin fish: 0.6 mg/l (Hourdakis) |
| Chemical Properties | White Solid |
| Uses | Dodine is used to control scab on apples, pears and pecans, leafspot diseases of cherries, olives, blackcurrants, celery and other crops, andfoliar diseases of strawberries. It is also used on other fruit, vegetable, nutand 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 sycamoretrees. In industry, used as a biocide and preservative. Mayalso 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®; RadsporL; 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 isconverted into creatine by the action of a methyltransferase, and simultaneouslythe dodecyl moiety is oxidatively cleaved (PM). |
| Degradation | Dodine is stable in neutral and moderately alkaline or acidic media butthe free base is liberated by concentrated alkali (PM). |
Dodine Preparation Products And Raw materials
| Raw materials | Cyanamide-->Dodecylamine-->Acetic acid |
