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Detail of "36001-88-4"

  • CAS Number:
  • 36001-88-4
  • Name:
  • Phosphoramidothioicacid, N-(1-methylethyl)-, O-methyl O-(4-methyl-2-nitrophenyl) ester

  • Molecular Structure:
  • Formula:
  • C11H17 N2 O4 P S
  • Molecular Weight:
  • 304.33
  • Deleted CAS:
  • 55840-20-5
  • Synonyms:
  • Phosphoramidothioicacid, (1-methylethyl)-, O-methyl O-(4-methyl-2-nitrophenyl) ester (9CI);Amiprofos-methyl;Amiprophos-methyl;BAY-NTN 6867;BAY-NTN 80;NSC 313446;NTN6867;NTN 80;O-(2-Nitro-4-methylphenyl) O-methylN-isopropylphosphoramidothioate;O-Methyl O-4-methyl-2-nitrophenylN-isopropylphosphoramidothioate;Tokunol M;
  • EINECS:
  • 252-829-4
  • Density:
  • 1.275g/cm3
  • Melting Point:
  • ~65 °C
  • Boiling Point:
  • 389.9°Cat760mmHg
  • Flash Point:
  • 189.6°C
  • Hazard Symbols:
  • HarmfulXn
  • Risk Codes:
  • 22
  • Safety:
  • A poison by ingestion. Low toxicity by skin contact. When heated to decomposition it emits toxic vapors of NOx, SOx, and POx. Details

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CAS No.36001-88-4 Phosphoramidothioicacid, N-(1-methylethyl)-, O-methyl O-(4-methyl-2-nitrophenyl) ester

Phosphoramidothioicacid, N-(1-methylethyl)-, O-methyl O-(4-methyl-2-nitrophenyl) ester

Supplier:CAPITAL SQUARE INTERNATIONAL INDUSTRIAL LIMITE(SHANGHAI) [ China (Mainland)]

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945Integral
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CAS No.36001-88-4 Phosphoramidothioicacid, N-(1-methylethyl)-, O-methyl O-(4-methyl-2-nitrophenyl) ester

Amiprophos-methyl

Supplier:CHEMOS GmbH [ Germany]

610Integral
610

Tel:+49 9402 9336 0

Address:Werner-von-Siemens Str. 3 D-93128 Regenstauf / Germany

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Reference

Toxicity of agrochemicals to some freshwater organisms
Toxicity of agrochemicals to some freshwater organisms. XXXVI. Nishiuchi, Y. (Japan Aquicult. Res. Group, Hakodate, Japan). Suisan Zoshoku, 24(1), 25-6 (Japanese) 1976. CODEN: SUZOAV. ISSN: 0371-4217. DOCUMENT TYPE: Journal CA Section: 4 (Toxicology) The toxicity of monocrotophos [6923-22-4], Na alginate [9005-38-3], lecithin, 2-(thiocyanomethylthio)benzothiazole [21564-17-0], 4-amino-6-tert-butyl-3-(methylthio)-1,2,4-triazine-5(4H)-one [21087-64-9], O-Me O-(2-nitro-p-tolyl)N-iso-Pr phosphoramidothionate [36001-88-4], and Greener [66106-33-0] (a plant growth regulator) to freshwater organisms (Cyprinus carpio, Oryzias latipes, Misgurnus anguillicaudatus, Daphnia pulex, D. carinata, Moina macrocopa, Indoplanorbis exustus, and Cipangopaludina malleata) was studied. The TLm values ranged from 0.15 to >100 ppm for the agrochems. and organisms tested.
Structure, synthesis and orientation of microfibrils
Structure, synthesis and orientation of microfibrils. III. A survey of the action of microtubule inhibitors on microtubules and microfibril orientation in Oocystis solitaria. Robinson, David G.; Herzog, Wilhelm (Pflanzenphysiol. Inst., Univ. Goettingen, Goettingen, Ger.). Cytobiologie, 15(3), 463-74 (English) 1977. CODEN: CYTZAM. DOCUMENT TYPE: Journal CA Section: 3 (Biochemical Interactions) The action of 15 microtubule inhibitors on cellulose [9004-34-6] microfibril synthesis and orientation in the alga O. solitaria revealed that they could be grouped into 3 classes: (a) those having colchicine [64-86-8]-like effects, podophyllotoxin [518-28-5], oryzalin [19044-88-3], trifluralin [1582-09-8], and aminoprophosmethyl [36001-88-4], (b) those having no effect on cell wall microfibril orientation, lumicolchicine [490-24-4], propyzamide [23950-58-5], isopropyl-N-phenylcarbamate [122-42-9], chloroisopropyl-N-phenylcarbamate [101-21-3], colcemid [477-30-5], dimethyltetrachloroterephthalate [1861-32-1], oncodazole [31430-18-9], and hexanitrodiphenylamine [35860-31-2], (c) those producing unusual colchicine-dissimilar effects on cell wall organization, methylbenzimidazol-2-yl-carbamate [10605-21-7] and griseofulvin [126-07-8]. Whereas a destruction of cortical microtubules was obsd. with compds. of the 1st 2 groups, microtubules were readily seen after treatment with compds. of the 3rd group. The effects of all compds. on the in vitro polymn./depolymn. of pig brain tubulin were investigated. Aminoprophosmethyl and menthylbenzimidazol-2-yl-carbamate caused abnormal wall development in O. solitaria.
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