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Dodine

HCID 17110
NotesReactions
Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
2439-10-3
Standard SMILES
CC(=O)O.CCCCCCCCCCCCN=C(N)N
InChIKey
YIKWKLYQRFRGPM-UHFFFAOYSA-N
Molecular formula
C15H33N3O2
Average molar mass
287.44 g/mol
Monoisotopic mass
287.2572773

Overview

Dodine is a white crystalline solid. Used as a fungicide.

Names & identifiers

Preferred name
Dodine
IUPAC
acetic acid;2-dodecylguanidine
English name
Dodine
Molecular formula
C13H29N3.C2H4O2
Molecular weight
287.44

Names & synonyms

Dodine2439-10-3Dodecylguanidine acetateCarpeneMelprexRadsporMelprex Liquid DodineMelprex 65WDTXSID3020548American cyanamid 5223DTXCID70548259C423Y98
Show more names
LAURYLGUANIDINEDODEXSyllitcarpenAdodinKarpenac5223DODENE
AC-5223RefChem:135550219-459-5RNB1NU2RGGDodin1-Dodecylguanidine acetaten-Dodecylguanidine acetateLaurylguanidine acetate

Database identifiers

CAS
2439-10-3
PubChem CID
17110
DTXSID
DTXSID3020548
ChEMBL
CHEMBL450348、CHEMBL74474
ChEBI
CHEBI:74889
UNII
259C423Y98
EC Number
219-459-5

Properties

Computed structural properties

Topological polar surface area
102 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
3
Rotatable bonds
11
Heavy atoms
20
Formal charge
0
Complexity
194

Experimental & physicochemical properties

Pesticides · 6 items

Pesticide -> EPA IRIS

Agrochemicals -> Pesticide active substances

Active substance -> EU Pesticides database: Approved

Pesticides -> Fungicides

Fungicides

Pesticide (Dodine) -> USDA PDB

Color/Form · 2 items

Slightly waxy solid

Colorless crystals

Solubility · 5 items

Sol in alcohol, hot water; slightly sol in other solvents.

Insol in most org solvents. Readily sol in mineral acids.

IN LOW MOL WT ALCOHOLS RANGES FROM ABOUT 7% TO 23% @ ROOM TEMP; SOL IN ACIDS; 0.063% BY WT IN WATER @ 25 °C.

In distilled water 0.07%. Soluble in methanol, ethanol. Practically insoluble in most organic solvents.

In water, 630 mg/l @ 25 °C

CorrosivityNoncorrosive
DecompositionWhen heated to decomposition it emits very toxic fumes of /nitrogen oxides/.
Melting Point136 °C
Vapor Pressure · 2 items

0.00000015 [mmHg]

1.5X10-7 mm Hg @ 25 °C

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Warning

H302: Harmful if swallowed [Warning Acute toxicity, oral]

P264, P264+P265, P270, P273, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P264+P265, P270, P273, P280, P301+P317, P302+P352, P305+P351+P338, P321, P330, P332+P317, P337+P317, P362+P364, P391, and P501 (click each P-code to see the statement)

Hazard information

Regulatory Information · 4 items

Regulation (EC) No 396/2005 (amended)

Dodine is listed in the dataset of EPA Human Health Benchmarks for Pesticides under the Safe Drinking Water Act (40 eCFR 141)

2011/9/EU, Reg. (EU) 2020/2007, Reg. (EU) 2026/372 , Reg. (Eu) 2024/1206, Reg.(EU) 2018/1266, Reg.(EU) No 540/2011

Dodine: HSNO Approval: HSR003128 Approved with controls

Other Safety InformationIMAP assessments - Guanidine, dodecyl-, monoacetate: Environment tier I assessment
DOT LabelClass 9
Fire HazardsExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
Health HazardsExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
Hazards Summary · 1 item

A strong skin and eye irritant (concentrations >50%); [Hawley] Dodine and DGH (Dodecylguanidine hydrochloride) are toxicologically equivalent; No evidence of carcinogenicity; No evidence of reproductive or neurological toxicity; [EPA REDs] A skin, eye, and GI tract irritant; [HSDB] A skin and eye irritant; [eChemPortal: ESIS] See Dodecylguanidine hydrochloride.

Chemistry & industry

Pharmacology

Mechanism of Action... DODECYLGUANIDINE INHIBITS OXIDATION OF GLUCOSE BY CELLS OF FUNGUS (SACCHAROMYCES PASTORIANUS). OTHER STUDIES ATTRIBUTE TOXICITY OF DODINE TO BLOCKING OF VITAL ANIONIC SITES @ CELL SURFACE & INACTIVATION OF ENZYMES.
Metabolism/Metabolites · 2 items

... DEGRADATION OF (14)C DODINE OCCURRED AFTER APPLICATION TO APPLE TREES. ... ONE OF 4 CMPD DETECTED APPEARED TO BE GUANIDINE OR GUANIDINE MONOSUBSTITUTED WITH SMALL GROUP. NO METABOLITES HAVE BEEN DEMONSTRATED /IN FUNGI/.

IN PLANTS, DODINE IS CONVERTED TO CREATINE VIA THE ACTION OF A METHYLTRANSFERASEAND SIMULTANEOUS OXIDATIVE CLEAVAGE OF THE DODECYL MOIETY.

Absorption, Distribution and Excretion · 3 items

NO TRANSLOCATION FROM FOLIAGE TO FRUIT & DEGRADATION PRODUCTS TRANSLOCATED ONLY VERY SLIGHTLY.

TRACES OF RADIOTAGGED CARBON APPEARED IN FRUIT. ... MOST OF RADIOACTIVITY SETTLED IN PROTEIN OR PEPTIDE PORTION OF FRUIT /AFTER APPLICATION TO APPLE TREES/.

It is absorbed across the skin ... .

Uses & manufacturing

Uses · 5 items

Used as agricultural fungicide; [Merck Index] Used primarily on fruits and nuts; A similar product, dodecylguanidine hydrochloride (DGH) is used as a biocide against algae, fungi, and slime-forming bacteria; [EPA REDs]

Farming (Pesticides) [Category: Industry]

For Cyprex (USEPA/OPP Pesticide Code: 044301) ACTIVE products with label matches. /SRP: Registered for use in the U.S. but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses./

Dodecylguanidine salts ... are highly effective for agricultural applications, particularly in the control of apple scab and cherry leaf spot. They are also effective algal growth inhibitors, useful in the manufacture of microorganisms-stable oil and water emulsions and in treatment of saline process water. /Dodecylguanidine salts/

Fungicide

Consumption Patterns

Related reactions

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Food Contact Substances
FCS -> FDA Inventory of Food Contact Substances Listed in 21 CFR
Physical Description · 2 items

Dodine is a white crystalline solid. Used as a fungicide.

Colorless solid; [HSDB]; [MSDSonline] White solid; [CAMEO]

Stability/Shelf LifeAT ORDINARY TEMP CMPD IS STABLE AS SOLID OR IN SOLN; STABLE UNDER MODERATELY ALKALINE OR ACID CONDITIONS.
Dissociation ConstantspKa = 9
Other Experimental Properties · 2 items

FREE BASE, REG NUMBER (112-25-2), IS LIBERATED BY CONCENTRATED ALKALI.

CMPD IS SURFACE-ACTIVE; SALT OF STRONG BASE & WEAK ACID.

Physicochemical properties

Melting point
136 °C · 136°C
Boiling point
429.73 °C · 429.73°C (rough estimate)
Density
0.9636 · 0.9636 (rough estimate)
vapor pressure
5 x · 5 x 10-6 Pa (20 °C, est.)
refractive index
1.65 · 1.6500 (estimate)
Flash point
100 °C · >100 °C
storage temp.
0 · 0-6°C
solubility
DMSO (Slightly, Heated), Methanol (Slightly)
pka
13 · >13 (strong base)
Water Solubility
630 mg · 630 mg l-1(25 °C)
Merck
13 · 13,3442
BRN
6546960 · 6546960
Henry's Law Constant
1.1 · 1.1×105 mol/(m3Pa) at 25℃, Duchowicz et al. (2020)
Major Application
agricultureenvironmental
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
1.15 · 1.150
CAS DataBase Reference
2439 · 2439-10-3(CAS DataBase Reference)
Indirect Additives used in Food Contact Substances
N-DODECYLGUANIDINE ACETATE
FDA 21 CFR
176.17 · 176.170
EWG's Food Scores
1 · 1-2
FDA UNII
259 C423Y98 · 259C423Y98
NIST Chemistry Reference
1 · 1-dodecylguanidinium acetate(2439-10-3)
EPA Substance Registry System
Dodine (2439-10-3)
Pesticides Freedom of Information Act (FOIA)
Dodine
UNSPSC Code
41116107 · 41116107
NACRES
24 · NA.24
Symbol(GHS)
7 · GHS07,GHS09
Signal word
Warning
Hazard statements
302 · H302-H315-H319-H410
Precautionary statements
264 · P264-P270-P273-P301+P312-P302+P352-P305+P351+P338
PPE
95 · dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Hazard Codes
Xn;N,N,Xn
Risk Statements
22 · 22-36/38-50/53
Safety Statements
26 · 26-60-61
RIDADR
3077 · UN 3077
WGK Germany
3 · 3
RTECS
1750000 · MF1750000
TSCA
TSCA listed
HS Code
29252900 · 29252900
Storage Class
11 · 11 - Combustible Solids
Hazard Classifications
4 OralAquatic · Acute Tox. 4 OralAquatic Acute 1Aquatic Chronic 1Eye Irrit. 2Skin Irrit. 2
Hazardous Substances Data
2439 · 2439-10-3(Hazardous Substances Data)
Toxicity
50 in · LC50 in harlequin fish: 0.6 mg/l (Hourdakis)
Reactive GroupSalts, Acidic
FIFRA Requirements · 3 items

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their future use. Under this pesticide reregistration program, EPA examines health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether they are eligible for reregistration. In addition, all pesticides must meet the new safety standard of the Food Quality Protection Act of 1996. Dodine is found on List A, which contains most food use pesticides and consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA, as amended in 1988. Case No: 0161; Pesticide type: fungicide, antimicrobial; Registration Standard Date: 02/26/87; Case Status:OPP is reviewing data from the pesticide's producers regarding its human health and/or environmental effects, or OPP is determining the pesticide's eligibility for reregistration and developing the Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): Dodine; Data Call-in (DCI) Date(s): 12/09/91, 06/16/92, 10/13/95; AI Status: The producers of the pesticide has made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.

Tolerances are established for residues of the fungicide dodine (n-dodecylguanidine acetate) in or on the following raw agricultural commodities: apples; cherries, sour; cherries, sweet; meat; milk; peaches; pears; pecans; strawberries; and walnuts.

Tolerances with regional registration, as defined in 180.1(n), are established for residues of dodine in or on the following raw agricultural commodities: spinach.

Reactivity Profile · 1 item

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.

Air and Water ReactionsSoluble in hot water.
Hazard Classes and Categories · 5 items

Acute Tox. 4 (100%)

Acute toxicity - category 4

Acute toxicity (Oral) - Category 4

Acute toxicity (Oral) - Category 4

Acute Tox. 4 *

Skin, Eye, and Respiratory Irritations · 3 items

Strong irritant to eyes and skin over 50% concentration.

It ... is irritating to skin, eyes, and gastrointestinal tract.

Cause severe irritation of the skin and eyes when there is contact with strong solutions.

Safety & protection

Fire FightingExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
First AidExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
Storage ConditionsKEEP CONTAINER CLOSED WHEN NOT IN USE. ... STORE THIS PRODUCT AWAY FROM FOOD OR FEED.
Nonfire Spill ResponseExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
Disposal Methods · 2 items

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Recommendable methods: Incineration. Peer-review: Large amt: Incinerate in a unit equipped with effluent gas scrubbing. (Peer-review conclusions of an IRPTC expert consultation (May 1985))

Preventive Measures · 2 items

SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.

TRANSFER OR MIX /PRODUCT/ WITH ADEQUATE VENTILATION ... .

Isolation and EvacuationExcerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:
Allowable Tolerances · 2 items

Tolerances are established for residues of the fungicide dodine (n-dodecylguanidine acetate) in or on the following raw agricultural commodities: apples, 5.0 ppm; cherries, sour, 5.0 ppm; cherries, sweet, 5.0 ppm; meat, 0 ppm; milk, 0 ppm; peaches, 5.0 ppm; pears, 5.0 ppm; pecans, 0.3 ppm; strawberries, 5.0 ppm; and walnuts, 0.3 ppm.

Tolerances with regional registration, as defined in 180.1(n), are established for residues of dodine in or on the following raw agricultural commodities: spinach, 12.0 ppm.

Personal Protective Equipment (PPE) · 2 items

Excerpt from ERG Guide 171 [Substances (Low to Moderate Hazard)]:

Protective clothing: goggles, face shield, rubber gloves when handling.

Toxicology

Interactions · 5 items

MICE WERE TREATED INTRAGASTRICALLY DURING LAST WEEK OF PREGNANCY WITH DODINE & SODIUM NITRITE 0.05%. MALIGNANT LYMPHOMAS, LUNG ADENOMAS & HEPATOMAS OCCURRED IN 30-70%. IN PARENT GENERATION TUMORS APPEARED 4 MO AFTER DELIVERY & AT 6-7 MO IN F1 GENERATION. SPONTANEOUS TUMORS IN CONTROLS WERE 6%. DODINE ALONE HAD NO EFFECT ON CANCER INCIDENCE.

Dodine at 60 mg/kg for 8 days and sodium nitrite at 22.5 mg/kg alone or in combination altered liver structure in male rats. The liver alterations incl reduced granular endoplasmic reticulum, incr smooth endoplasmic reticulum, polymorphism and mitochondrial edema, incr lysosome numbers, glycogen reduction, collagen proliferation, incr Kupffer cell numbers. The alterations were more marked by the combination of the chemicals, the endoplasmic reticulum being particularly affected.

Oral admin of 1/10 LD50 sodium nitrite and dodine, individually or in combination, to rats enhanced the activity of glutamic-oxaloacetic transaminase, glutamic-pyruvic transaminase, lactate dehydrogenase, glucose 6-phosphate dehydrogenase, isocitrate dehydrogenase, and succinate dehydrogenase, reduced the activity of cholinesterase, and decr the concn of total protein, all in the blood serum. Quant estimation of the results from liver functional investigations revealed a summation of the toxic effect, tending to potentiation with combined exposure of the two agents.

A single oral admin of 22.5 mg/kg of sodium nitrite (0.1 LD50) alone or in combination with 60 mg dodine (0.1 LD50) inhibited mixed-function oxidase of rat liver microsomes by 28.7-36 and 64-68.6%, respectively, whereas dodine alone was ineffective. The dodine addition also prolonged the enzyme depression. Within 30 days the enzyme activities approached the normal level. Only dodine-sodium nitrite lowered the microsomal protein by 15.5-21.6% on days 2, 4, and 15 after the administration. Nitrosation of dodine by sodium nitrite potentiates the effect of sodium nitrite.

Experiments were carried out on albino rats in which 1/10 LD50 sodium nitrite and dodecylguanidineacetate were given orally & in combination. The activity of mixed function oxidases was determined at 2 levels of biological organization: the intact organism after loading with aminopyrine & subsequent determination of its basic metabolites in the urine; subcellular level (microsomal liver fraction) by the velocity of N-demethylation of aminopyrine, hydroxylation of aniline and by the cytochrome p450 content. The combined action of the 2 agents caused considerable mixed function oxidases inhibition (63-67%) on the 1st, 2nd, 4th and 15th days at both levels. A new compound is apparently formed under the conditions of the experiment, probably through in vivo nitrosification of the pesticide. This is testified by the established qualitatively different effects of the preliminary induction of mixed function oxidases with phenobarbital on the acute toxicity of the noxae studied: lack of effect for dodecyclguanidineacetate, increase for sodium nitrite and decrease for their combination.

Target OrgansEndocrine
Ecotoxicity Values · 2 items

LC50 Gammarus fasciatus 1.1 mg/l/96 hr. Static bioassay without aeration, pH 7.2-7.5, water hardness 40-50 mg/l as calcium carbonate and alkalinity of 30-35 mg/l.

LD50 Mallard duck oral 1142 mg/kg

Environmental Fate · 3 items

TERRESTRIAL FATE: Based on a classification scheme(1), a Koc value of 1X10+5 measured in soil(2), indicates that cyprex is expected to be immobile in soil(SRC). The pKa of cyprex is 9(3), indicating that this compound will primarily exist as the cation in the environment. Cyprex is also a salt and will be dissociated in the environment. Volatilization from moist soil surfaces is not expected to be an important fate process for cyprex because cations and salts are not expected to volatilize(SRC). When river mud from the Denver area was treated with 14C-labeled cyprex, only five percent of the fungicide was degraded in 68 days(4), which suggests biodegradation will occur slowly in soils(SRC).

AQUATIC FATE: Based on a classification scheme(1), a Koc value of 1X10+5 measured in soil(2), indicates that cyprex is expected to adsorb to suspended solids and sediment(SRC). A pKa of 9(4) indicates that cyprex will exist almost entirely in the ionized form at environmental pH values and therefore volatilization from water surfaces is not expected to be an important fate process, particularly in acid to neutral environments. In addition, cyprex is a salt and will exist in the dissociated form in the environment; therefore, volatilization from water surfaces is not expected to occur. According to a classification scheme(5), an estimated BCF of 16(SRC), calculated from its water solubility of 630 mg/l(6) and a regression-derived equation(3), suggests the potential for bioconcentration in aquatic organisms is low (SRC). When river mud from the Denver area was treated with 14C-labeled cyprex, only five percent of the fungicide was degraded in 68 days(7), which suggests biodegradation will occur slowly in water(SRC).

ATMOSPHERIC FATE: Since cyprex is an acetate salt of dodecylguanidine, it will not be found in the vapor phase in the atmosphere; cyprex will exist solely in the particulate phase in the ambient atmosphere. Particulate-phase cyprex may be removed from the air by wet and dry deposition. (SRC)

Acute Toxicity LinkChemical: DODINE
EPA IRIS Information · 3 items

Dodine

Endocrine

4 x 10 ^-3 mg/kg-day

Soil Adsorption/Mobility · 1 item

Cyprex is an organic base that has a pKa of 9(1), which indicates that cyprex will exist primarily as a cation in moist soils and cations adsorb strongly to soils(SRC). The Koc of cyprex measured in soil is 1X10+5(2). According to a classification scheme(3), this Koc value suggests that cyprex is expected to be immobile in soil(SRC).

Atmospheric ConcentrationsCyprex was not found in ambient air during a nationwide air monitoring program operated during 1970 and 1971 by the USEPA(1).
Human Toxicity Excerpts · 3 items

INGESTION CAUSES VOMITING, DIARRHEA.

ENVIRONMENTAL CHEMICALS INCL PESTICIDES CARRYING SECONDARY AND TERTIARY AMINO GROUPS ARE SUGGESTED TO BE A HEALTH HAZARD TO MAN SINCE POTENTIALLY CARCINOGENIC NITROSO COMPOUNDS MAY BE FORMED IN THE PRESENCE OF NITRITE AT LOW pH VALUES RESEMBLING CONDITIONS IN THE HUMAN STOMACH.

Cause severe irritation of the skin and eyes when there is contact with strong solutions.

Artificial Pollution SourcesCyprex's production and use as a fungicide(1) will result in its direct release to the environment through various waste streams(SRC).
Environmental Biodegradation · 1 item

Achromobacter and Flavobacterium species, both common to soil, can grow with cyprex as the sole source of carbon(1). When river mud from the Denver area was treated with 14C-labeled cyprex, five percent of the fungicide was degraded in 68 days(1).

Environmental Bioconcentration · 1 item

Cyprex, an acetate salt of dodecylguanidine, is expected to exist in the dissociated form in aquatic environments. An estimated BCF value of 16 was calculated for non-dissociated cyprex(SRC), using a water solubility of 630 mg/l(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is low(SRC).

Regulatory information

FIFRA Requirements · 3 items

As the federal pesticide law FIFRA directs, EPA is conducting a comprehensive review of older pesticides to consider their health and environmental effects and make decisions about their future use. Under this pesticide reregistration program, EPA examines health and safety data for pesticide active ingredients initially registered before November 1, 1984, and determines whether they are eligible for reregistration. In addition, all pesticides must meet the new safety standard of the Food Quality Protection Act of 1996. Dodine is found on List A, which contains most food use pesticides and consists of the 194 chemical cases (or 350 individual active ingredients) for which EPA issued registration standards prior to FIFRA, as amended in 1988. Case No: 0161; Pesticide type: fungicide, antimicrobial; Registration Standard Date: 02/26/87; Case Status:OPP is reviewing data from the pesticide's producers regarding its human health and/or environmental effects, or OPP is determining the pesticide's eligibility for reregistration and developing the Reregistration Eligibility Decision (RED) document.; Active ingredient (AI): Dodine; Data Call-in (DCI) Date(s): 12/09/91, 06/16/92, 10/13/95; AI Status: The producers of the pesticide has made commitments to conduct the studies and pay the fees required for reregistration, and are meeting those commitments in a timely manner.

Tolerances are established for residues of the fungicide dodine (n-dodecylguanidine acetate) in or on the following raw agricultural commodities: apples; cherries, sour; cherries, sweet; meat; milk; peaches; pears; pecans; strawberries; and walnuts.

Tolerances with regional registration, as defined in 180.1(n), are established for residues of dodine in or on the following raw agricultural commodities: spinach.

Safety data

PPE
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
wgk
3
tsca
TSCA listed
rtecs
MF1750000
ridadr
UN 3077
hs_code
29252900
Toxicity
LC50 in harlequin fish: 0.6 mg/l (Hourdakis)
risk_code
22-36/38-50/53
Signal word
Warning
Symbol(GHS)
GHS07,GHS09
hazard_code
Xn;N,N,Xn
safety_code
26-60-61
Storage Class
11 - Combustible Solids
Hazard statements
H302-H315-H319-H410
Hazard Classifications
Acute Tox. 4 OralAquatic Acute 1Aquatic Chronic 1Eye Irrit. 2Skin Irrit. 2
Precautionary statements
P264-P270-P273-P301+P312-P302+P352-P305+P351+P338
Hazardous Substances Data
2439-10-3(Hazardous Substances Data)
FUNGICIDE, OF WHICH APPROXIMATELY 64% IS USED ON APPLES AND 36% ON OTHER DECIDUOUS FRUITS AND NUTS (1975).
Methods of Manufacturing · 1 item

Dodine may be made by the reaction of dodecyl chloride with sodium cyanamide followed by treatment of the product of the first reaction with ammonia. Dodine may also be made by the reaction of dodecyl amine with cyanamide in the presence of acetic acid.

Formulations/Preparations · 3 items

USEPA/OPP Pesticide Code 044301; Trade Names: Cytox 2160; Cyprex; AC 5223; Melprex.

... Include wettable powder (650 and 800 ai/kg); liquid (200 and 250 g/l); dust (750 g/kg).

A COMBINATION OF DODINE & CAPTAN HAS ALSO SHOWN PROMISE, PARTICULARLY IN PREVENTING FRUIT INFECTION.

Use Classification · 2 items

Fungicides

FUNGICIDES

General Manufacturing Information · 6 items

Guanidine, N-dodecyl-, acetate (1:1): ACTIVE

Discontinued by American Cyanamide Co.

... PERFORM DOUBLE ROLE OF RESIDUAL PROTECTION & PARTIAL THERAPY OF ESTABLISHED INFECTIONS. FUNGUS IS NOT KILLED BUT IS INHIBITED FROM DEVELOPING FURTHER. THIS INCLUDES LARGE GROUP OF POPULAR FUNGICIDES SUCH AS ... DODINE ... .

... Is an effective contact fungicide against early infections of the apple scabfungus and destroys the fungus effectively because it invades only the superficial epidermal layer of the apple leaf ... . Even though the fungus /Diplocarpon earliana/ is very susceptible to the fungitoxicity of dodine, the fungicide functions only as a residual or contact protectant to destroy the spores before they can become established. /Monilinia fructicola/ infects the acid tissues of fruits ... dodine loses its fungitoxicity as the medium becomes acid. The brown rot fungus is inhibited at very low concn, near 5 ppm, by dodine in spore germination tests, but will not affect fungal growth on the peach fruit at 1600 ppm.

CLASSIFICATION OF SOME OF COMMON FUNGICIDES INDICATING THEIR CHARACTERISTICS AS OBSERVED FROM FIELD EXPT: DODINE; RESIDUAL 3, CONTACT 2, TOPICAL THERAPY 2, FUNGICIDAL 3, FUNGISTATIC 1. 1= LIGHTLY EFFECTIVE OR RESPONSIVE; 2= MODERATELY EFFECTIVE OR RESPONSIVE; 3= STRONGLY EFFECTIVE OR RESPONSIVE. /FROM TABLE/

For more General Manufacturing Information (Complete) data for CYPREX (12 total), please visit the HSDB record page.

Applications · 4 items

DescriptionDodine is a guanidine fungicide which is currently approved for use in both the UK and the EU. It is moderately soluble in water but not most organic solvents. It tends not to be persistent in soil and is non-mobile. Based on its physico-chemical parameters, dodine is not expected to leach to groundwater. It demonstrates a moderate toxicity to mammals, birds and fish but is highly toxic to aquatic invertebrates and algae. It is less toxic to bees. Limited data is available on its toxicity to humans it is considered moderately toxic via the oral route.

UsesDodine 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.

UsesUsed as agricultural fungicide.

General DescriptionWhite crystalline solid. Used as a fungicide.

Upstream & downstream products

Upstream raw materials

CyanamideDodecylamineAcetic acid

Suppliers88 total

湖北永阔科技有限公司027-59223108 15972152991 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
湖南韵邦生物科技股份有限公司0731-88532326 13319508186 · [email protected]
湖北万得化工有限公司15377098680 15377098680 · [email protected]
Hebei Chuanghai Biotechnology Co., Ltd+86-17732866630 · [email protected]
湖北威德利化学试剂有限公司186-02735115 18062128043 · [email protected]
艾吉析科技(上海)有限公司17717235263 · [email protected]
杭州品高化工有限公司0571-87658025 · [email protected]
江苏普乐司生物科技有限公司0513-66017706 18551496367 · [email protected]
安耐吉化学&3A(安徽泽升科技有限公司)021-58432009 400-005-6266 · [email protected]
湖北兴琰新材料科技有限公司13129948835 · [email protected]
梯希爱(上海)化工贸易有限公司021-61109150 · [email protected]
上海艾梯西生物科技有限公司18721763493 · [email protected]
湖北广奥生物科技有限公司027-02702759223056 18162699093 · [email protected]
佛山宝诺生物科技有限公司0757-85921206 18520245316 · [email protected]
湖北成海化工有限公司027-59220433 18327245847 · [email protected]
湖北扬信医药科技有限公司0714-3999001 19171453112 · [email protected]
上海毕楷科技有限公司18516304666 · [email protected]
四川库利南科技有限公司400-1166-196 18981987031 · [email protected]
ZHEJIANG JIUZHOU CHEM CO., LTD+86-0576225566889 +86-13454675544 · [email protected];[email protected];[email protected]
艾科试剂4008-755-333 18080918076 · [email protected]
上海湄水化工科技有限公司021-60549325 18616193163
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天津普西唐生物医药科技有限公司010-60605840 · [email protected]
Xiamen Eagle Chemical Limited Corporation+86-18900207489 · [email protected]
LUYUNJIA CHEMISTRY XIAMEN LIMITED+86-592-5360779 +86-13055435203
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湖北巨胜科技有限公司027-59599241 18871490274 · [email protected]
池州凯隆进出口贸易有限公司[email protected]
TargetMol中国(陶术生物)021-021-33632979 15002134094 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
Henan Alfa Chemical Co., Ltd+8618339805032 · [email protected]
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上海珈得尔化学技术有限公司13564435016 13564435016 · [email protected]
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成都华纯科技有限公司400-1166-196 15982826727 · [email protected]
上海煜柯化学品有限公司13391486464 · [email protected]
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上海贤鼎生物科技有限公司021-021-52271985 17721149837 · [email protected]
武汉弘德悦欣医药科技有限公司027-83850116 18164090116 · [email protected]
浙江麦格生物医药有限公司4000-156-528 13355733872 · [email protected]
盼得(上海)国际贸易有限公司80159919 18662931292 · [email protected]
深圳市丽晶生化科技有限公司0755-85201366 18938635012 · [email protected]
江苏艾康生物医药研发有限公司025-58859352 19370895928 · [email protected]

Additional notes

DefinitionChEBI: 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.