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Detail of "534-52-1"

  • MSDS Download
  • CAS Number:
  • 534-52-1
  • Name:

  • Phenol,2-methyl-4,6-dinitro-

  • Superlist Name:
  • 2-Methyl-4,6-dinitrophenol
  • Molecular Structure:
  • Formula:
  • C7H6 N2 O5
  • Molecular Weight:
  • 198.15
  • Synonyms:
  • o-Cresol,4,6-dinitro- (8CI);2,4-Dinitro-6-methylphenol;2-Methyl-4,6-dinitrophenol;3,5-Dinitro-2-hydroxytoluene;4,6-Dinitro-2-methylphenol;4,6-Dinitro-o-cresol;6-Methyl-2,4-dinitrophenol;Antinonin;Antinonnin;Arborol;DNOC;Degrassan;Dekrysil;Detal;Dillex;Dinitro;Dinitrocresol;Dinitrodendtroxal;Dinitrol;Dinoc;Dinurania;Ditrosol;Effusan;Effusan 3436;Elgetol;Elgetol 30;Elipol;Extrar;Flavin-Sandoz;Hedolit;Hedolite;K III;KIV;Kreozan;Krezotol 50;Lipan;NSC 2082;Neudorff DN 50;Nitrofan;Prokarbol;Rafex;Rafex 35;Raphatox;Sandolin;Sandolin A;Selinon;Sinox;Winterwash;
  • EINECS:
  • 208-601-1
  • Density:
  • 1.55 g/cm3
  • Melting Point:
  • 83-85 ºC
  • Boiling Point:
  • 332.4 °C at 760 mmHg
  • Flash Point:
  • 149.2 °C
  • Solubility:
  • slightly soluble
  • Appearance:
  • straw yellow to yellow crystal
  • Hazard Symbols:
  • Risk Codes:
  • R26/27/28;R38;R40;R41;R43;R44;R50/53   
  • Safety:
  • 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, cardiac and gastrointestinal changes. Mutation data reported. An eye and skin irritant. Less toxic than the para form, but is still highly toxic. A pesticide. See also NITRO COMPOUNDS of AROMATIC HYDROCARBONS and 3,5-DINITRO-o-CRESOL; 3,5-DINITRO-p-CRESOL; 2,6-DINITRO-p-CRESOL; 4,6-DINITRO-m-CRESOL; 4,6-DINITRO-o-CRESOL AMMONIUM SALT; 4,6-DINITRO-o-CRESOL BARIUM DERIVATIVE; 4,6-DINITRO-o-CRESOL DIETHYLAMINE SALT; 4,6-DINITRO-o-CRESOL METHYLAMINE (1:1); 4,6-DINITRO-o-CRESOL MORPHOLINE (1:1); 4,6-DINITRO-o-CRESOL SODIUM SALT.

    Analytical Methods:

       

    For occupational chemical analysis use NIOSH: Dinitro-o-cresol S166. Details

  • Transport Information:
  • UN 1598
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CAS No.534-52-1 2-Methyl-4,6-dinitrophenol

Assay:99%  Appearance:yellow to ye...  Package:1KG, 5KG, 10...Storage:0-6°C

Chemical Properties yellow to yellow-green crystals or cryst. powder mp 83-85 °C(lit.) bp 196°C 1012mm Fp 11 °C storage temp. 0-6°C Water Solubility slightly soluble Merck 3279 Product Name: 2-Methyl-4,6-dinitrophenol CAS: 534-52-1 MF: C7H6N2O5 MW: 1

Min. Order:1Gram

Supplier:shijiazhuang dunao chemical co.,ltd [ China (Mainland)]

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Reference

Methods of applying postemergence herbicides to cotton and soybeans for cocklebur control
Methods of applying postemergence herbicides to cotton and soybeans for cocklebur control. Mullins, J. A. (Dep. Agric. Eng., Univ. Tennessee, Knoxville, Tenn., USA). Tenn. Farm Home Sci., Prog. Rep., 99, 34-6 (English) 1976. CODEN: TFHSAT. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemicals) Paraquat (I) [4685-14-7] (1/8 pound/acre), 2,4-DB [94-82-6] (0.2 pound/acre), Tenoran [1982-47-4] (1 pound/acre), and Dinitro [534-52-1] (1.5 pound/acre) applied by the off-center, directed, and overtop methods gave excellent cocklebur control in soybeans and had little adverse effect on soybean yields. However, in cotton treated with Dinitro (1.5 pound/acre), MSMA [2163-80-6] (1 pound/acre), Cotoran [2164-17-2] (1 pound/acre), the 2-year mean total seed-cotton yields were 350 and 275 pounds/acre higher when the herbicides were applied by the direct method as compared with the off-center and overtop methods, resp.In this experiment, several chemicals are used like 2163-80-6 and 2164-17-2 Mean 1st-pick yields were 475 and 550 pounds/acre higher when the herbicides were applied by the direct as compared with the off-center and overtop methods, resp. Few differences were seen in herbicide effectiveness. .
Effect of herbicides on photosynthetic electron transport and on the growth of the alga Scenedesmus quadricauda
Effect of herbicides on photosynthetic electron transport and on the growth of the alga Scenedesmus quadricauda. Hendrich, Waclaw; Kubiak, Z.; Jurajda, K.; Pawlaczyk-Szpilowa, M. (Inst. Biochem., Univ. Wroclaw, Wroclaw, Pol.). Acta Soc. Bot. Pol., 45(1-2), 101-10 (English) 1976. CODEN: ASBNA2. DOCUMENT TYPE: Journal CA Section: 5 (Agrochemicals) Section cross-reference(s): 11 2,4-D [94-75-7] at 5-500 mg/L stimulated the growth of the title alga, without affecting the Hill reaction. Kresamone (2,4-dinitro-o-cresol) [534-52-1] at 0.05-0.5 mg/L inhibited the growth without affecting the Hill reaction, whereas CIPC [101-21-3] stimulated the growth but inhibited the Hill reaction. Afalon [330-55-2] at 10-6 M inhibited the growth and Hill reaction by 50%, without distorting the cell shape. Simazine [122-34-9] at 1.2 .times. 10-8-1.2 .times. 10-5 M and Gramoxone [4685-14-7] at 2 . 330-55-2 and 101-21-3 which are cas registry numbers of substances are two of reagents here.times. 10-5-8 .times. 10-5 M inhibited the Hill reaction in a concn.-dependent manner, inhibited growth, and induced formation of distorted cells. .
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