Preventing the Diseases of Peanuts

Total Page:16

File Type:pdf, Size:1020Kb

Preventing the Diseases of Peanuts 448 YEARBOOK OF AGRICULTURE 1953 labor became scarce, a trend was started toward the use of machine- shelled seed. Poor stands often resulted. Work started by Luther Shaw in North CaroUna in 1939—and later con- Preventing the firmed by research in Virginia, South Carolina, Georgia, Florida, and Ala- bama—showed that machine-shelled Diseases of seeds treated with a seed protectant before planting produced stands com- parable to those obtained by using Peanuts hand-shelled and treated seed. Although seed usually are treated at the time they are shelled because of Coyt Wilson convenience, the treatment may be applied with equal efTectiveness just Prevention, rather than cure, is the before planting. rule with the diseases of peanuts. Several good seed protectants are Some beneficial preventive measures available commercially. Eight materi- are the application of fungicides to seed als were tested in Alabama in 6 years. to prevent seed rot, the use of fungi- Best results were had with Ceresan M cidal dusts or sprays on grovv^ing plants (7.7 percent ethyl mercury /?-toluene to prevent leaf spot, and the treatment sulfonanilide). Phygon (90 percent 2, of soil with chemicals before planting 3-dichloro-i ,4-naphthoquinone), Ara- to control nematodes and soil insects. san (50 percent tetramethyl tbiuram- Prevention involves more than the disulfide), and Spergon (98 percent use of chemicals, however. Manage- tetrachloro-jÉ?-benzoquinone) were ment practices that promote vigorous somewhat less effective. Reasonably growth enable the plants to escape in- good results were obtained with Yellow fection or to survive after infection. Cuprocide (yellow cuprous oxide con- Outstanding are rotations that in- taining 47 percent metallic copper) clude one or two crops of corn, oats, or and Dow 9-B (50 percent zinc trichlo- similar crops before each peanut crop; rophenate). Seedox (50 percent 2,4,5- adequate mineral fertilization; plant- trichlorophenyl acetate) and Merc-O- ing on light-textured, well-drained Dust (a compound of indefinite com- soils; and reduction of mechanical position containing mercury and form- damage by cultivating implements. aldehyde) were ineffective. Similar results have been obtained in other SEED ROT is the most serious of States. the diseases that affect stands of pea- Although the mercurial treatments nuts. It is caused by mildly pathogenic such as Ceresan M are most effective, or saprophytic organisms that live in they are more dangerous to use. Over- the soil—mainly species of Fusarium, dosage results in poor germination. Rhizopus, Mucor, Diplodia, Pénicillium, The radicle of the germinating seed and Aspergillus. Their entrance is facili- does not elongate but becomes thick- tated by broken seed coats and by ened and stubby. If a seedling is pro- other mechanical injuries produced duced, it is stunted and never makes by the sheller. Seed rot is most destruc- normal growth. Therefore—and be- tive under conditions that retard ger- cause of the danger to warm-blooded mination—cool, damp weather, ab- animals that might eat treated seed— normally deep planting, and water- most States recommend one of the logged soils. Most seed rot occurs organic materials such as Arasan or within the first week after planting. Spergon in preference to the mercurial Beginning about 1940, when farm treatments. PREVENTING THE DISEASES OF PEANUTS 449 The organic seed treatments have a tissues and give them a dark gray or tendency to be somewhat erratic in black color on the inside. performance. In tests lasting 6 years Another form of seedling blight is at Auburn, Ala., Ceresan M was the dry rot, caused by Rhizoctonia solani. most consistent of four treatments. It is like charcoal rot in the early Spergon was the best of the four in stages. Lesions develop on the stem 1949 but the poorest in 1947. Dow 9-B near the soil line. The plant may be was practically as good as Arasan or girdled and killed; if the infection Ceresan M in 1946 but was consider- does not spread, the plant may partly ably poorer than either in 1948. recover. The lesions are not likely to Arasan gave less protection than Ce- extend as far below the surface as resan M in 1944, 1946, 1948, and 1949. those caused by Sclerotium baiaticola. Seed protectants are applied as dust There are no specific control meas- treatments at the rate of 2 or 3 ounces ures for seedling blights. Losses may to 100 pounds of seed. Slurry treat- be reduced by planting treated seed ments—liquid suspensions of the fungi- of good quality on a well-prepared cide—have not been popular on pea- seedbed. nuts, probably because of the tendency of the seed coats to peel after the slurry OF THE DISEASES of growing plants, treatments are applied. The tendency leaf spot generally is the most destruc- appears to be more common with tive disease during the growing season. Spanish-type seed than with seed of It is recognized by the brown or runner peanuts. black and somewhat circular spots on the leaves. As the disease pro- SEEDLING BLIGHTS may be destructive gresses, the spots enlarge until the in some localities, but generally they entire leaf is affected. Defoliation do little damage in established stands. follows. The detrimental effects of Damping-off is not a serious disease of leaf spot are threefold: The yield of peanuts. nuts is reduced; the quality of the One of the most common types of peanut hay is lowered; and the fallen seedling blight in peanuts is caused leaves provide organic matter on by Sclerotium baiaticola. This organism which inoculum of other fungi, such causes a disease known as charcoal as Sclerotium rolfsii, is produced. rot in a number of other species of Two species of fungi cause leaf spot. plants during periods of high temper- Each produces characteristic symp- atures. Infections result in the forma- toms. tion of lesions on the succulent stems. Early leaf spot, caused by Cercospora The initial infections usually are near arachidicola, produces spots that are the soil line, but the lesions may ex- light tan at first. With age the spots tend downward some distance into become reddish brown to black on the soil. If plant growth is retarded the lower surface and light brown on by dry weather and if the temperature the upper surface of the leaf. A yellow is high—above 75° F.—the lesion is halo surrounds each spot. Late leaf likely to girdle the stem and kill the spot, caused by C. personata, produces plant. The stem assumes a dull brown dark-brown or black spots on both color and becomes quite dry. Some- surfaces of the leaf. The spots usually times the progress of the disease is are somewhat smaller than those of stopped and the seedling is stunted early leaf spot and there is no distinct rather than killed. Then the plant is halo. The fungi can be distinguished made more susceptible to other dis- by microscopic examination of the eases later in the season. Charcoal conidia. rot in peanuts can be recognized by The conidia of Cercospora arachidicola the many small, irregular, black are colorless to pale olive green and sclerotia that develop in the affected often curved. According to measure- YEARBOOK OF AGRICULTURE 1953 ments made by W. A. Jenkins in carbamate fungicides have not come 1938, they are 37-108 by 2.7-5.4 into general use on peanuts, probably microns and contain 3 to 12 septations. because of their higher cost. Increases The conidia of C. personata are much in yield resulting from dusting depend shorter and considerably thicker; upon the fertility of the soil on which they measure 18-60 by 5-11 microns, the crop is grown, the prevalence and with I to 8 septations. They are gen- severity of leaf spot, and the type of erally cylindrical and seldom curved. peanuts being grown. Highest returns Both leaf spots attack the leaves, have been obtained on runner pea- petioles, pegs, and pods of Spanish, nuts growing on fertile sandy loam bunch, and runner peanuts. No host soils in the Southeast. Increases of plants other than Arachis hypogaea are 1,000 pounds an acre have been re- known for them. ported by the Alabama Agricultural Primary infections of leaf spot are Experiment Station. The increases caused by ascospores formed in the generally amount to 500 pounds an spring on overwintered peanut leaves. acre or less. Secondary infections result from co- nidia. Although the fungus has been SOUTHERN BLIGHT, caused by Sclero- reported to be seed-borne, this method tium rolfsii^ is more destructive on Span- of overwintering is of minor impor- ish and bunch types of peanuts than on tance. The principal means of dis- runners. It may appear on the plants semination is by wind-borne inocu- at any time during the growing season lum. The ascospores or conidia ger- but is more likely to cause damage in minate within a few hours and pene- late summer and early fall as the trate the leaf directly through the plants approach maturity. The fungus, epidermal cells or through stomata. soil-borne, attacks the plants near the In both species, the mycelium is inter- soil line. It causes wilting and eventual cellular at first. Branched haustoria death of the part of the plant above are soon formed by the mycelium of the infection. It may attack the cen^ Cercospora personata and the host cells tral stem and affect the entire plant, are not killed outright. C. arachidicola or the infection may be limited to one does not form haustoria; the host cells or more branches. Diseased plants are killed in advance and the invading wilt; the leaves gradually turn brown germ tubes enter dead cells.
Recommended publications
  • INDEX to PESTICIDE TYPES and FAMILIES and PART 180 TOLERANCE INFORMATION of PESTICIDE CHEMICALS in FOOD and FEED COMMODITIES
    US Environmental Protection Agency Office of Pesticide Programs INDEX to PESTICIDE TYPES and FAMILIES and PART 180 TOLERANCE INFORMATION of PESTICIDE CHEMICALS in FOOD and FEED COMMODITIES Note: Pesticide tolerance information is updated in the Code of Federal Regulations on a weekly basis. EPA plans to update these indexes biannually. These indexes are current as of the date indicated in the pdf file. For the latest information on pesticide tolerances, please check the electronic Code of Federal Regulations (eCFR) at http://www.access.gpo.gov/nara/cfr/waisidx_07/40cfrv23_07.html 1 40 CFR Type Family Common name CAS Number PC code 180.163 Acaricide bridged diphenyl Dicofol (1,1-Bis(chlorophenyl)-2,2,2-trichloroethanol) 115-32-2 10501 180.198 Acaricide phosphonate Trichlorfon 52-68-6 57901 180.259 Acaricide sulfite ester Propargite 2312-35-8 97601 180.446 Acaricide tetrazine Clofentezine 74115-24-5 125501 180.448 Acaricide thiazolidine Hexythiazox 78587-05-0 128849 180.517 Acaricide phenylpyrazole Fipronil 120068-37-3 129121 180.566 Acaricide pyrazole Fenpyroximate 134098-61-6 129131 180.572 Acaricide carbazate Bifenazate 149877-41-8 586 180.593 Acaricide unclassified Etoxazole 153233-91-1 107091 180.599 Acaricide unclassified Acequinocyl 57960-19-7 6329 180.341 Acaricide, fungicide dinitrophenol Dinocap (2, 4-Dinitro-6-octylphenyl crotonate and 2,6-dinitro-4- 39300-45-3 36001 octylphenyl crotonate} 180.111 Acaricide, insecticide organophosphorus Malathion 121-75-5 57701 180.182 Acaricide, insecticide cyclodiene Endosulfan 115-29-7 79401
    [Show full text]
  • Synthesis and Herbicidal Activity of Sulfonanilides Having a Pyrimidinyl-Containing Group at the 2-Position
    J. Pestic. Sci., 36(2), 212–220 (2011) DOI: 10.1584/jpestics.G10-87 Original Article Synthesis and herbicidal activity of sulfonanilides having a pyrimidinyl-containing group at the 2؅-position Takumi YOSHIMURA,†* Masao NAKATANI,† Sohei ASAKURA,†† Ryo HANAI,†† Manabu HIRAOKA††† and Shigefumi KUWAHARA†††† † K-I Chemical Research Institute Co., Ltd., Iwata, Shizuoka 437–1213, Japan †† Life Science Research Institute, Kumiai Chemical Industry Co., Ltd., Kikugawa, Shizuoka 439–0031, Japan ††† Formulation Technology Institute, Kumiai Chemical Industry Co., Ltd., Shimizu, Shizuoka 424–0053, Japan †††† Graduate School of Agricultural Science, Tohoku University, Aoba-ku, Sendai 981–8555, Japan (Received October 27, 2010; Accepted November 16, 2010) A novel series of sulfonanilides having a pyrimidinyl-containing group at the 2Ј-position was prepared and their herbicidal activities against paddy weeds and selectivity against rice plants were assessed. The structure-activity relationships were probed by substitution of the sulfonyl group, bridge and benzene ring. Among the sulfon- amides, difluoromethyl compound showed comparatively high activity and a broad spectrum to control weeds, including Echinochloa oryzicola. The most preferable substitution position on the benzene ring was in the 6-po- sition and the lower alkyl group showed high herbicidal activity and a broad weed control spectrum, and among the compounds tested, the methoxymethyl group was the best. In respect of the bridge moiety, the hydroxyl group was the best. Among the compounds examined, 2Ј-[(4,6-dimethoxypyrimidin-2-yl)(hydroxy)methyl]-1,1- difluoro-6Ј-(methoxymethyl)methanesulfonanilide, applied at rates between 4 to 16 g a.i./ha, showed excellent pre-emergence herbicidal activity with a broad spectrum against grass, sedge and broadleaf weeds without injury to rice plants.
    [Show full text]
  • IUPAC Provisional Recommendations
    Preferred IUPAC Names 177 Chapter 6, Sect 66 September, 2004 P-66 Amides, imides, hydrazides, nitriles, aldehydes, their chalcogen analogues and derivatives P-66.0 Introduction P-66.1 Amides P-66.2 Imides P-66.3 Hydrazides P-66.4 Amidines, amidrazones, hydrazidines P-66.5 Nitriles P-66.6 Aldehydes P-66.0 Introduction The classes dealt with in this Section have in common the fact that their retained names are derived from those of acids by changing the ‘ic acid’ ending to a class name, for example ‘amide’, ‘ohydrazide’, ‘nitrile’ or ‘aldehyde’. Their systematic names are formed substitutively by the suffix mode using one of two types of suffix, one that includes the carbon atom, for example, ‘carbonitrile’ for −CN, and one that does not, for example, ‘-nitrile’ for −(C)N,. Amidines are named as amides, hydrazidines as hydrazides, and amidrazones as amides or hydrazides. P-66.1 Amides P-66.1.0 Introduction P-66.1.1 Primary amides P-66.1.2 Secondary and tertiary amides P-66.1.3 Chalcogen analogues of amides P-66.1.4 Lactams, lactims, sultams and sultims P-66.1.5 Amides of carbonic, oxalic, cyanic, and polycarbonic acids P-66.1.6 Polyfunctional amides P-66.1.0 Introduction Amides are derivatives of oxoacids in which each hydroxy group has been replaced by an amino or substituted amino group. Chalcogen replacement analogues are called thio-, seleno- and telluroamides. Compounds having one, two or three acyl groups on a single nitrogen atom are generically included and may be designated as primary, secondary and tertiary amides, respectively.
    [Show full text]
  • Standard X-Ray Diffraction Powder Patterns NATIONAL BUREAU of STANDARDS
    NATIONAL INSTITUTE OF STANDARDS & TECHNOLOGY Research Information Center Gaithersburg, MD 20899 NATL INST OF STANDARDS & TECH R.I.C. A1 11 00988606 /NBS monograph QC100 .U556 V25-12;1975 C.1 NBS-PUB-C 19 NBS MONOGRAPH 25 " SECTION 12 U.S. DEPARTMENT OF COMMERCE / National Bureau of Standards Standard X-ray Diffraction Powder Patterns NATIONAL BUREAU OF STANDARDS 1 The National Bureau of Standards was established by an act of Congress March 3, 1901. The Bureau's overall goal is to strengthen and advance the Nation's science and technology and facilitate their effective application for public benefit. To this end, the Bureau conducts research and provides: (1) a basis for the Nation's physical measurement system, (2) scientific and technological services for industry and government, (3) a technical basis for equity in trade, and (4) technical services to promote public safety. The Bureau consists of the Institute for Basic Standards, the Institute for Materials Research, the Institute for Applied Technology, the Institute for Computer Sciences and Technology, and the Office for Information Programs. THE INSTITUTE FOR BASIC STANDARDS provides the central basis within the United States of a complete and consistent system of physical measurement; coordinates that system with measurement systems of other nations; and furnishes essential services leading to accurate and uniform physical measurements throughout the Nation's scientific community, industry, and commerce. The Institute consists of a Center for Radiation Research, an Office of Meas- urement Services and the following divisions: Applied Mathematics — Electricity — Mechanics — Heat — Optical Physics — Nuclear Sciences 2 — Applied Radiation 2 — Quantum Electronics 3 — Electromagnetics 3 — Time 3 3 3 and Frequency — Laboratory Astrophysics — Cryogenics .
    [Show full text]
  • Sulfonanilide Compounds
    ~" ' Nil II II II Nil 1 1 Nil II MINI II J European Patent Office o «i -» © Publication number: 0 31/ 332 B1 Office europeen* des.. brevets , © EUROPEAN PATENT SPECIFICATION © Date of publication of patent specification: 19.05.93 © Int. CI.5: C07C 311/08, C07D 309/12, C07D 211/46, C07C 317/14, © Application number: 88310899.5 C07C 323/18, C07D 335/02, A61K 31/18, A61K 31/33 (5)nn, Date of filing: 18.11.88AOAAOO ' © Sulfonanilide compounds. ® Priority: 19.11.87 JP 292856/87 Urawa-shi(JP) Inventor: Ohuchi, Yutaka @ Date of publication of application: Azumaso 101, 12-11 Oyaba-2-chome 24.05.89 Bulletin 89/21 Urawa-shl(JP) Inventor: Sekluchl, Kazuto © Publication of the grant of the patent: 2716-4-1-204 Oaza Kawarabukl 19.05.93 Bulletin 93/20 Ageo-shl(JP) Inventor: Salto, Shlujl © Designated Contracting States: Pakusaldo Maehara 202 31-12, Torocho- AT BE CH DE FR GB IT LI LU NL SE 1 - chome Omlya-shl(JP) © References cited: Inventor: Hatayama, Katsuo EP-A- 0 093 591 Danchl 35-3 1200-215, Horlsaklcho FR- A- 2 244 473 Omlya- shl(JP) US- A- 3 725 451 Inventor: Sota, Kaoru US-A- 3840 597 1158- 11, Shlmotoml US- A- 3 856 859 Tokorozawa- shl(JP) © Proprietor: TAISHO PHARMACEUTICAL CO. LTD © Representative: Colelro, Raymond et al 00 24- 1 Takata 3- chome Toshlma- ku MEWBURN ELLIS & CO. 2/3 Cursltor Street CM Tokyo 1 71 (JP) London EC4A 1BQ (GB) CO CO @ Inventor: Yoshlkawa, Kensel IV 2878, Dalmon CO Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted.
    [Show full text]
  • Light in Gold Catalysis Sina Witzel, A
    pubs.acs.org/CR Review Light in Gold Catalysis Sina Witzel, A. Stephen K. Hashmi, and Jin Xie* Cite This: https://dx.doi.org/10.1021/acs.chemrev.0c00841 Read Online ACCESS Metrics & More Article Recommendations ABSTRACT: Within the wide family of gold-catalyzed reactions, gold photocatalysis intrinsically features unique elementary steps. When gold catalysis meets photocatalysis, a valence change of the gold center can easily be achieved via electron transfer and radical addition, avoiding the use of stoichiometric sacrificial external oxidants. The excellent compatibility of radicals with gold catalysts opens the door to a series of important organic transformations, including redox-neutral C−C and C−X coupling, C−H activation, and formal radical−radical cross-coupling. The photocatalysis with gold complexes nicely complements the existing photoredox catalysis strategies and also opens a new avenue for gold chemistry. This review covers the achieved transformations for both mononuclear gold(I) catalysts (with and without a photosensitizer) and dinuclear gold(I) photocatalysts. Various fascinating methodologies, their value for organic chemists, and the current mechanistic understanding are discussed. The most recent examples also demonstrate the feasibility of both, mononuclear and dinuclear gold(I) complexes to participate in excited state energy transfer (EnT), rather than electron transfer. The rare applications of gold(III) photocatalysts, both homogeneous and heterogeneous, are also summarized. CONTENTS Authors AZ Notes AZ 1. Introduction A Biographies AZ 1.1. Redox Au(I)/Au(III) Catalysis A Acknowledgments AZ 1.2. Gold Photoredox Catalysis B References AZ 2. Mononuclear Gold(I) Complexes D 2.1. Dual Gold/Photoredox Catalysis D 2.1.1.
    [Show full text]
  • Korea Industrial Tariff Schedule
    DRAFT Subject to Legal Review for Accuracy, Clarity, and Consistency Annex 2-B Industrial Schedule for the Republic of Korea Staging HSK 10 Description Base Rate Category 0301101000 Gold carp 10 C 0301102000 Tropical fish 10 C 0301109000 Other 10 A 0301911000 Salmo trutta, Oncorhynchus mykiss,Oncorhynchus clarki, Oncorhynchus 10 C aguabonita,Oncorhynchus gilae 0301912000 Oncorhynchus apache and Oncorhynchus chrysogaster 10 C 0301921000 Glass eel 10 A 0301929000 Other 30% or I ₩1,908/kg 0301930000 Carp 10 C 0301992000 Yellow tail 10 A 0301994000 Sea-bream 45% or G ₩3,292/kg 0301995000 Conger eel 10 G 0301996000 Sharp toothed eel 10 G 0301997000 Salad eel 10 C 0301998000 Flat fish 10 C 0301999010 True bass 10 G 0301999020 Puffers 10 G 0301999030 Tilapia 10 C 0301999040 Rock fish(including pacific ocean perch) 10 C 0301999050 Sea bass 40 C 0301999060 Mullets 10 C 0301999070 Loaches 10 C 0301999080 Cat fishes 10 A 0301999091 Rock Trout(Hexagrammos spp., Agrammus spp.) 10 C 0301999092 Crusian carp 10 C 0301999093 Salmon 10 A 0301999094 Grass carp 10 A 0301999095 Croakers 36 G 0301999099 Other 10 G 0302111000 Salmo trutta, Oncorhynchus mykiss, Oncorhynchus clarki,Oncorhynchus 20 G aquabonita, Oncorhynchus gilae 0302112000 Oncorhynchus apache and Oncorhynchus chrysogaster 20 A 0302120000 Pacific salmon(Oncorhynchus nerka, Oncorhynchus gorbuscha, Oncorhynchus 20 A keta, Oncorhynchus tschawytscha, Oncorhynchus kisutch, Oncorhynchus masou and Oncorhynchus rhodurus), Atlantic salmon(Salmo salar)and Danube salmon(Hucho hucho) 0302190000 Other 20
    [Show full text]
  • Alkyl Mercury-Induced Toxicity: Multiple Mechanisms of Action
    Alkyl Mercury-Induced Toxicity: Multiple Mechanisms of Action John F. Risher and Pamela Tucker Contents 1 Preface 1.1 How Alkyl Mercury Compounds Get into the Food Web 2 Introduction 3 Methylmercury: Mechanisms of Toxic Action 3.1 Altered Membrane Permeability 3.2 Altered Intracellular Calcium Homeostasis 3.3 Oxidative Stress/Reactive Oxygen Species (ROS) 3.4 Effects on Receptor Binding/Neurotransmitter Release 3.5 Effects Involving Arachidonic Acid 3.6 Effects on Cell Cycle/Cell Division 3.7 Effects on Glutathione (GSH) Activity 3.8 Involvement with Nitric Oxide Synthetase 3.9 Effects on Glial Cells and Glutamate-Glutamine Uptake and Homeostasis 3.10 Other Mechanisms 4 Ethylmercury: Mechanisms of Toxic Action 4.1 Mobilization of Intracellular Ca++ 4.2 Effects on Mitochondria (Membrane and ROS) 4.3 Effects on Arachidonic Acid, Leukotriene Synthesis, and Membrane Integrity 4.4 Effects on Glutathione (GSH) 4.5 Effects on Glutamate Transport 4.6 Effects on Neurotransmitter Availability 5 Summary and Conclusions References J.F. Risher (*) • P. Tucker Division of Toxicology and Human Health Sciences, Agency for Toxic Substances and Disease Registry, 1600 Clifton Road (MS F-58), Atlanta, GA 30333, USA e-mail: [email protected]; [email protected] © Springer International Publishing 2016 Reviews of Environmental Contamination and Toxicology, DOI 10.1007/398_2016_1 J.F. Risher and P. Tucker Abstract There are a number of mechanisms by which alkylmercury compounds cause toxic action in the body. Collectively, published studies reveal that there are some similarities between the mechanisms of the toxic action of the mono-alkyl mercury compounds methylmercury (MeHg) and ethylmercury (EtHg).
    [Show full text]
  • (12) United States Patent (10) Patent No.: US 8,298,992 B2 Stern Et Al
    US008298.992B2 (12) United States Patent (10) Patent No.: US 8,298,992 B2 Stern et al. (45) Date of Patent: Oct. 30, 2012 (54) LOW ODOR, LOW VOLATILITY SOLVENT (56) References Cited FOR AGRICULTURAL CHEMICALS U.S. PATENT DOCUMENTS (75) Inventors: Alan J. Stern, Magnolia, TX (US); 2,778,826 A * 1/1957 Schmidle ...................... 546,192 David Ferguson, Spring, TX (US); 3,074,940 A * 1/1963 Benzing ............. ... 544,178 Howard Stridde, George West, TX (US) 3,342,673 A * 9, 1967 Kaufman et al. ............. 514,443 5,283,229 A 2/1994 Narayanan et al. (73) Assignee: Huntsman Petrochemical LLC. The 2005, 0137091 A1 6, 2005 Herold et al. Woodlands, TX (US) 2005/0215433 A1 9, 2005 Benitez et al. (*) Notice: Subject to any disclaimer, the term of this OTHER PUBLICATIONS patent is extended or adjusted under 35 Masuyama A. Preparation and Surface Active Properties of Terminal U.S.C. 154(b) by 743 days. Amide Type of Alcohol Ethoxylates, Jun. 1989, JAOCS, vol. 66, No. (21) Appl. No.: 12/300,482 6, pppp. 834-837.* * cited by examiner (22) PCT Filed: May 25, 2007 86) PCT No.: PCT/US2007/069793 Primary Examiner — Brian-Yong S Kwon (86) O Assistant Examiner — Andriae M Holt S371 (c)(1), (74) Attorney, Agent, or Firm — Huntsman International (2), (4) Date: Nov. 12, 2008 LLC (87) PCT Pub. No.: WO2007/140332 (57) ABSTRACT PCT Pub. Date: Dec. 6, 2007 A composition includes an agricultural component in an (65) Prior Publication Data amount of at least about 27% by weight and a solvent com position in an amount not greater than about 55% by weight.
    [Show full text]
  • The Preparation of Derivatives Related to Novocain
    University of Louisville ThinkIR: The University of Louisville's Institutional Repository Electronic Theses and Dissertations 1-1927 The preparation of derivatives related to novocain. Helen Peil University of Louisville Follow this and additional works at: https://ir.library.louisville.edu/etd Recommended Citation Peil, Helen, "The preparation of derivatives related to novocain." (1927). Electronic Theses and Dissertations. Paper 1108. https://doi.org/10.18297/etd/1108 This Master's Thesis is brought to you for free and open access by ThinkIR: The University of Louisville's Institutional Repository. It has been accepted for inclusion in Electronic Theses and Dissertations by an authorized administrator of ThinkIR: The University of Louisville's Institutional Repository. This title appears here courtesy of the author, who has retained all other copyrights. For more information, please contact [email protected]. UNIVERSITY OF LOUISVILLE THE PREPARATION OF DERIVATIVES RELATED TO NOVOCAIN A Dissertation Submitted to the Faculty Of the Graduate School of the College of Liberal Arts In Partial Fulfillment of the Requirements for the Degree Of Master of Science Department of Chemistry By Helen Peil 1927 COYTENTS Part 1 THE PREP RATION OF DERIVA.TIVES REUTED TO NOVOCAIN Page 1 . Introduction 1 2. Experiments 7 3 . Conclusions 17 4. Bibliography 18 Part 2 THE OXIDII. TION OF n- BUTYL THIOCYA.NA TE WITH NITRIC ACID Page 1. Introduction 19 2. Experiments 20 3. Conclusions 28 4. BIbliography 29 INTRODUCTION \ I • 1. PREP/~RA'l'IUN OF DlillIVATIV.I!:S REL.A,Tl.;D TO NOVOCAIN The study of the relationship between chemica.l constitution - snd physiological effect emb~ cas m~ ny very interesting pro­ blems which are, however, frequently difficuJt to solve In the investigation of any dru the first step i s to determine the princ~ple to which the physiological effect is due, and then b:' ane.lysis and synthesis assign t 1e correct chemic" 1 constitution t o this principle.
    [Show full text]
  • Korea Tariff Schedule
    Annex 2-B Tariff Schedule of Korea HSK Description Base rate Staging Category Safeguard 0101101000 Horses 8 D 0101109000 Other 8 D 0101901010 Horses for racing 8 D 0101901090 Other 8 D 0101909000 Other 8 G 0102101000 Milch cows 89.1 A 0102102000 Beef cattle 89.1 A 0102109000 Other 89.1 A 0102901000 Milch cows 40 M 0102902000 Beef cattle 40 H 0102909000 Other 0 K 0103100000 1. Pure-bred breeding animals 18 A 0103910000 Weighing less than 50kg 18 G 0103920000 Weighing 50kg or more 18 G 0104100000 Sheep 8 A 0104201000 Milch goats 8 G 0104209000 Other 8 A 0105111000 Pure-bred breeding animals 9 A 0105119000 Other 9 A 0105120000 B. Turkeys 9 A 0105191000 Ducks 18 G 0105199000 Other 9 A 0105921000 (1) Pure-bred breeding animals 9 A 0105929000 (2)Other 9 A 0105931000 (1) Pure-bred breeding animals 9 A 0105939000 (2) Other 9 A 0105991000 Ducks 18 G 0105992000 Turkeys 9 A 0105999000 Other 9 A 0106110000 Primates 8 A Whales, dolphins and porpoises(mammals 0106120000 of the order Cetacea); manatees and 8A dugongs(mammals of the order Sirenia) 0106191000 Dogs 8 D 0106192000 Rabbits and hares 8 D 0106193000 Deer 8 G 0106194000 Bears 8 A 0106199000 Other 8 D 0106201000 Snakes 8 A 0106202000 Fresh-water tortoises 8 D 0106203000 Turtles 8 A 0106209000 Other 8 A 0106310000 Birds of prey 8 D Psittaciformes (including parrots, 0106320000 8D parakeets, macaws and cockatoos) 0106390000 Other 8 A 0106901000 Amphibia 8 A 0106902010 Honey bees 8 D 0106902090 Other 8 A 0106903010 Lug worms 8 A 0106903020 Yarn earth worms 8 A 0106903090 Other 8 A 0106909000 Other
    [Show full text]
  • Multidirectional Efficacy of Biologically Active Nitro Compounds Included in Medicines
    Review Multidirectional Efficacy of Biologically Active Nitro Compounds Included in Medicines Dorota Olender, Justyna Żwawiak * and Lucjusz Zaprutko Department of Organic Chemistry, Pharmaceutical Faculty, Poznan University of Medical Sciences, Grunwaldzka 6, 60-780 Poznan, Poland; [email protected] (D.O.); [email protected] (L.Z.) * Correspondence: e-mail: [email protected]; Tel.: +48-618-546-678 Received: 8 May 2018; Accepted: 25 May 2018; Published: 29 May 2018 Abstract: The current concept in searching for new bioactive products, including mainly original active substances with potential application in pharmacy and medicine, is based on compounds with a previously determined structure, well-known properties, and biological activity profile. Nowadays, many commonly used drugs originated from natural sources. Moreover, some natural materials have become the source of leading structures for processing further chemical modifications. Many organic compounds with great therapeutic significance have the nitro group in their structure. Very often, nitro compounds are active substances in many well-known preparations belonging to different groups of medicines that are classified according to their pharmacological potencies. Moreover, the nitro group is part of the chemical structure of veterinary drugs. In this review, we describe many bioactive substances with the nitro group, divided into ten categories, including substances with exciting activity and that are currently undergoing clinical trials. Keywords: nitro group; nitro compounds; drugs with the nitro group; veterinary medicines with the nitro group 1. Introduction Drugs exert a local action, or, after being absorbed into the body, a general effect. The chemical structure of the active substance is fundamental because of its therapeutic effect on the body.
    [Show full text]