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    Flupyrsulfuron methyl sodium

    Available from stock

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      Flupyrsulfuron methyl sodium

      SKU
      F0083

      Category: Fungicides

      Synonyms
      Methyl 2-[(4,6-dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl]-6-(trifluoromethyl)nicotinate monosodium salt
      144740-54-5
      CAS-Number
      C15H13F3N5NaO7S
      Molecular Formula
      487.34
      Molecular Weight

      For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

      • Product Data
      • Handling
      • Safety Information
      • Details

      Specifications

      Purity
      ≥98% (HPLC)
      Appearance
      White powder
      Identity
      1H-NMR

      Properties

      Solvents
      water, methanol, acetone
      Melting Point
      165-170°C
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      -20°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at -20°C.
      Hazard statements
      H410
      Precautionary statements
      P273-P391-P501
      GHS Symbol
      GHS09
      Signal word
      Warning
      RIDADR
      UN3077 9
      Transportation
      Packing Group III
      Description
      Systemic and slective herbicide. Mode of action is through inhibition of acetolactate synthase ALS (acetohydroxyacid synthase AHAS), which causes a blockade of the biosynthesis of amino acids with branched side chains, such as L-Leucin, L-Isoleucin and L-Valin. Compound can be used as analytical reference material.
      Smiles
      O=C([N-]S(C1=NC(C(F)(F)F)=CC=C1C(OC)=O)(=O)=O)NC2=NC(OC)=CC(OC)=N2.[Na+]
      InChi Key
      JKPSVOHVUGMYGH-UHFFFAOYSA-M
      References
      (1) J. Rouchaud, et al. , Pest Manag. Sci. 59, 940 (2003) , (2) E.M. Desmet, et al. , Commun. Agric. Appl. Biol. Sci. 69, 83 (2004)
      InChi
      InChI=1S/C15H14F3N5O7S.Na/c1-28-9-6-10(29-2)21-13(20-9)22-14(25)23-31(26,27)11-7(12(24)30-3)4-5-8(19-11)15(16,17)18 , /h4-6H,1-3H3,(H2,20,21,22,23,25) , /q , +1/p-1

      Systemic and slective herbicide. Mode of action is through inhibition of acetolactate synthase ALS (acetohydroxyacid synthase AHAS), which causes a blockade of the biosynthesis of amino acids with branched side chains, such as L-Leucin, L-Isoleucin and L-Valin. Compound can be used as analytical reference material.

      SKU: F0083 Category: Fungicides
      • Additional information

      Additional information

      Synonyms

      Methyl 2-[(4,6-dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl]-6-(trifluoromethyl)nicotinate monosodium salt

      Purity

      ≥98% (HPLC)

      Appearance

      White powder

      CAS-Number

      144740-54-5

      Molecular Formula

      C15H13F3N5NaO7S

      Molecular Weight

      487.34

      Identity

      1H-NMR

      Solvents

      water, methanol, acetone

      Melting Point

      165-170°C

      Smiles

      O=C([N-]S(C1=NC(C(F)(F)F)=CC=C1C(OC)=O)(=O)=O)NC2=NC(OC)=CC(OC)=N2.[Na+]

      InChi Key

      JKPSVOHVUGMYGH-UHFFFAOYSA-M

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      -20°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at -20°C.

      Hazard statements

      H410

      Precautionary statements

      P273-P391-P501

      GHS Symbol

      GHS09

      Signal word

      Warning

      RIDADR

      UN3077 9

      Transportation

      Packing Group III

      References

      (1) J. Rouchaud, et al., Pest Manag. Sci. 59, 940 (2003), (2) E.M. Desmet, et al., Commun. Agric. Appl. Biol. Sci. 69, 83 (2004)

      InChi

      InChI=1S/C15H14F3N5O7S.Na/c1-28-9-6-10(29-2)21-13(20-9)22-14(25)23-31(26,27)11-7(12(24)30-3)4-5-8(19-11)15(16,17)18, /h4-6H,1-3H3,(H2,20,21,22,23,25), /q, +1/p-1

      Quantity

      10 mg, 25 mg, 50 mg, Bulk

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