534-52-1 Usage
Chemical Properties
yellow to yellow-green crystals or cryst. powder
Uses
Different sources of media describe the Uses of 534-52-1 differently. You can refer to the following data:
1. 2-Methyl-4,6-dinitrophenol can be used as dormant ovicidal spray for fruit trees (highly phytotoxic and cannot be used successfully on actively growing plants); herbicide; insecticide.
2. 4,6-Dinitro-o-cresol is used as a selective herbicide as well as an insecticide.
3. DNOC is a dinitrophenolic compound which exhibits insecticidal,
acaricidal and herbicidal activities. It is a non-selective insecticide
and controls aphids, Lepidoptera larva and scale insects on pome fruits
and stone fruit trees.
Definition
ChEBI: A hydroxytoluene that is o-cresol carrying nitro substituents at positions 4 and 6.
General Description
A yellow solid. Emits toxic oxides of nitrogen fumes when heated to decomposition. Toxic by skin absorption, inhalation or ingestion. Soluble in alcohol, acetone, ether and solutions of sodium or potassium hydroxides.
Air & Water Reactions
Slightly soluble in water.
Health Hazard
Different sources of media describe the Health Hazard of 534-52-1 differently. You can refer to the following data:
1. Extremely toxic material; probable oral lethal dose is 5-50 mg/kg in humans or between 7 drops and 1 teaspoonful for a 70 kg (150 lb.) person.
2. 4,6-Dinitro-o-cresol exhibits cumulative toxicity in humans; the symptoms of poisoning are manifested when the blood levels of this compound exceeds 15–20 μg/g (ACGIH 1986). Thus chronic exposure to this compound can cause serious health hazard. The signs of toxicity in humans are headache, fever, profuse sweating, rapid pulse and respiration, cough, shortness of breath, and coma. Other symptoms noted are a decrease in hemoglobin, an increase in blood sugar, a loss of muscle tone, dyspnea, kidney and liver injury, and edema of the lung and brain.LD50 value, oral (mice): 47 mg/kg LD50 value, skin (rats): 200 mg/kg.
Fire Hazard
Combustible material: may burn but does not ignite readily. When heated, vapors may form explosive mixtures with air: indoors, outdoors and sewers explosion hazards. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated. Runoff may pollute waterways. Substance may be transported in a molten form.
Agricultural Uses
Herbicide, Fungicide, Pesticide: DNOC is widely used in agriculture as a herbicide and pesticide; it is also used in the dyestuff industry. Although 4,6-dinitro-o-cresol (DNOC) is no longer
registered for use in the United States, it was used as a
blossom-thinning agent on fruit trees and as a fungicide,
insecticide, and miticides on fruit trees during the dormant
season. It is used in mushroom houses to control foreign
fungi; to kill locusts and other insects; and as a pre-harvest
desiccant of potatoes and leguminous seed crops. DNOC
is used as free radical polymerization inhibitor and agricultural chemical intermediate; widely used in agriculture
as a herbicide and pesticide; Hence, individuals formulating or spraying the compound incur the highest risk of
exposure to the compound. Not approved for use in EU
countries. DNOC’s registration in the U.S. as a pesticide was canceled in 1991. Currently, there are 39 global
suppliers.
Trade name
ANTINONIN?; ANTINONNIN?;
ARBOROL?; DEGRASSAN?; DEKRYSIL?; DETAL?;
DILLEX?; DINOC?; DINURANIA?; DITROSOL?;
DNOC?[C]; EFFUSAN?; EFFUSAN 3436?;
ELGETOL?; ELGETOL 30?; ELIPOL?; EXTRAR?;
FLAVIN-SANDOZ?; HEDOLIT?; HEDOLITE?; K
III?; K IV?; KREOZAN?; KREZOTOL 50?; LIPAN?;
NEUDORFF DN 50?; NITROFAN?; PROKARBOL?;
RAFEX?; RAFEX 35?; RAPHATOX?; SANDOLIN?;
SANDOLIN A?; SELINON?; SINOX?;
WINTERWASH?
Safety Profile
Human poison by
unspecified route. Experimental poison by
ingestion, inhalation, skin contact,
intraperitoneal, and intravenous routes.
Human systemic effects by ingestion and
inhalation: somnolence, headache, abnormal
brain recordings from specific areas of the
central nervous system, cardlac and
gastrointestinal changes. Mutation data
reported. An e~7e and skin irritant. Less toxic
than the para form, but is still highly toxic.
A pesticide. See also NITRO
COMPOUNDS of AROMATIC
HYDROCARBONS and other dinitrocresol
entries.
Carcinogenicity
In one chronic feeding study in rats
DNOC did not cause an increased incidence
of any type of tumor. DNOC was clastogenic,
increasing the frequency of chromosomal aberrations
both in vivo and in vitro. Conflicting
results for mutagenicity have been obtained in
bacterial assays.
The 2003 ACGIH threshold limit valuetime-
weighted average (TLV-TWA) for
dinitro-o-cresol is 0.2mg/m3 with a notation
for skin absorption.
Environmental Fate
Soil/Plant. In plants and soils, the nitro groups reduced to amino groups (Hartley and Kidd, 1987). When 4,6-dinitro-o-cresol was statically incubated in the dark at 25°C with yeast extract and settled domestic wastewater inoculum, no signi?cant biodegradation and necessary acclimation for optimum biooxidation within the 4-week incubation period was observed (Tabak et al., 1981).Chemical/Physical. 4,6-Dichloro-o-cresol will react with amines and alkali metals forming water-soluble salts which are indicative of phenols (Morrison and Boyd, 1971).
Metabolic pathway
DNOC is metabolised in soils, plants and animals via common metabolic
pathways. The primary reaction is the reduction of the nitro groups
to the corresponding amino-analogues. Acetylation and deamination
via hydroxylation/elimination follow. N- and O-Conjugation as glucosides
and glucuronides occurred in plants and animals. The metabolic
pathways of DNOC are presented in Scheme 1.
Purification Methods
The cresol crystallises from aqueous EtOH. [Beilstein 6 H 369, 6 III 1276.]
Degradation
DNOC (1) is stable to hydrolytic and photolytic degradation at acidic pH
and is readily degraded under alkaline conditions (Molnar, 1935).
Check Digit Verification of cas no
The CAS Registry Mumber 534-52-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,3 and 4 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 534-52:
(5*5)+(4*3)+(3*4)+(2*5)+(1*2)=61
61 % 10 = 1
So 534-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O5/c1-4-2-5(8(11)12)6(9(13)14)3-7(4)10/h2-3,10H,1H3
534-52-1Relevant articles and documents
-
Pfister
, p. 375 (1921)
-
Highly efficient catalytic nitration of phenolic compounds by nitric acid with a recoverable and reusable Zr or Hf oxychloride complex and KSF
Shi, Min,Cui, Shi-Cong,Yin, Wan-Po
, p. 2379 - 2384 (2007/10/03)
Phenolic compounds can be nitrated with 60% nitric acid (1.2 equiv.) in the presence of catalytic amounts of a Zr or Hf oxychloride complex and montmorillonite KSF to give the corresponding nitrated products in good yields in a heterogeneous catalytic system. The co-catalyst and montmorillon ite can be easily recovered and reused in the next batch of nitration. This is a practical process for the nitration of phenolic compounds in a clean way. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.
Highly efficient nitration of phenolic compounds in solid phase or solution using Bi(NO3)3·5H2O as nitrating reagent
Sun, Hong-Bin,Hua, Ruimao,Yin, Yingwu
, p. 9071 - 9073 (2007/10/03)
Bi(NO3)3·5H2O was used as an efficient nitrating reagent in the nitration of phenolic compounds to give nitrated phenols in good to high yields. The nitration reaction proceeded smoothly by grinding 1 equiv of phenol, 2-methylphenol, 4-methylphenol, or 4-chlorophenol and Bi(NO3)3· 5H2O, and the nitration of other phenolic compounds could be performed in acetone at ambient temperature (22-30 °C).
