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    Heptachlor exo-epoxide

    Available from stock

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      Heptachlor exo-epoxide

      SKU
      H0237

      Category: Insecticides

      Synonyms
      exo-1,4,5,6,7,8,8-Heptachloro-2,3-epoxy-4,7-methano-3a,4,7,7a-tetrahydroindane, Epoxyheptachlor, HCE, HSDB 6182
      1024-57-3
      CAS-Number
      C10H5Cl7O
      Molecular Formula
      389.32
      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 to off-white powder or crystals
      Identity
      1H-NMR
      Water content (K.F.)
      ≤1.0%
      Melting Point
      156 - 163 °C

      Properties

      Solvents
      Soluble in chloroform.
      Melting Point
      156-163 °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
      H300 - H351 - H373 - H410
      Precautionary statements
      P201 - P202 - P260 - P264 - P273 - P301 + P310
      GHS Symbol
      GHS06+GHS08+GHS09
      Signal word
      Danger
      RIDADR
      UN2811
      Transportation
      Packing Group II
      Description
      Naphthofluorescein-diacetate is a non-fluoresent compound that is hydrolyzed by esterases to the fluorescent compound Naphthofluorescein. Spectral data: λex 594 nm; λem 663 nm in 0.1 M Tris pH 9.0 (esterase). The fluorescent naphthofluorescein has been shown to be an inhibitor of furin.
      Smiles
      ClC1=C(Cl)[C@]2(Cl)[C@@H]([C@H](O3)[C@@H]3[C@@H]4Cl)[C@@H]4[C@]1(Cl)C2(Cl)Cl
      InChi Key
      ZXFXBSWRVIQKOD-QXTGVUBQSA-N
      References
      (1) L.G. Lee, et al.; Cytometry 10, 151 (1989) , (2) J.M. Coppola, et al.; Neoplasia 10, 363 (2008)
      InChi
      (1) W.D. Basson, et al.: Analyst 94, 1135 (1969) , (2) R.R. Spencer & D.E. Erdmann , Environ. Sci. Technol. 13, 954 (1979) , (3) R.A. Edwards , Analyst 105, 139 (1980) , (4) M. Zenki, et al.: Fresenius J. Anal. Chem. 334, 238 (1989) , (5) J. Ciba & A. Chrusciel , Fresenius J. Anal. Chem. 342, 147 (1992) , (6) E.L. Novelli, et al.: Free Radic. Res. 26, 319 (1997) , (7) A. Gross, et al.: Chemosphere 72, 400 (2008) , (8) E. Merdivan, et al.: Spectrochim. Acta A Mol. Biomol. Spectrosc. 71, 2045 (2009)

      Naphthofluorescein-diacetate is a non-fluoresent compound that is hydrolyzed by esterases to the fluorescent compound Naphthofluorescein. Spectral data: λex 594 nm; λem 663 nm in 0.1 M Tris pH 9.0 (esterase). The fluorescent naphthofluorescein has been shown to be an inhibitor of furin.

      SKU: H0237 Category: Insecticides
      • Additional information

      Additional information

      Synonyms

      exo-1,4,5,6,7,8,8-Heptachloro-2,3-epoxy-4,7-methano-3a,4,7,7a-tetrahydroindane, Epoxyheptachlor, HCE, HSDB 6182

      Purity

      ≥98% (HPLC)

      Appearance

      White to off-white powder or crystals

      CAS-Number

      1024-57-3

      Molecular Formula

      C10H5Cl7O

      Molecular Weight

      389.32

      Identity

      1H-NMR

      Solvents

      Soluble in chloroform.

      Melting Point

      156-163 °C

      Smiles

      ClC1=C(Cl)[C@]2(Cl)[C@@H]([C@H](O3)[C@@H]3[C@@H]4Cl)[C@@H]4[C@]1(Cl)C2(Cl)Cl

      InChi Key

      ZXFXBSWRVIQKOD-QXTGVUBQSA-N

      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

      H300 – H351 – H373 – H410

      Precautionary statements

      P201 – P202 – P260 – P264 – P273 – P301 + P310

      GHS Symbol

      GHS06+GHS08+GHS09

      Signal word

      Danger

      RIDADR

      UN2811

      Transportation

      Packing Group II

      References

      (1) L.G. Lee, et al.; Cytometry 10, 151 (1989), (2) J.M. Coppola, et al.; Neoplasia 10, 363 (2008)

      InChi

      (1) W.D. Basson, et al.: Analyst 94, 1135 (1969), (2) R.R. Spencer & D.E. Erdmann, Environ. Sci. Technol. 13, 954 (1979), (3) R.A. Edwards, Analyst 105, 139 (1980), (4) M. Zenki, et al.: Fresenius J. Anal. Chem. 334, 238 (1989), (5) J. Ciba & A. Chrusciel, Fresenius J. Anal. Chem. 342, 147 (1992), (6) E.L. Novelli, et al.: Free Radic. Res. 26, 319 (1997), (7) A. Gross, et al.: Chemosphere 72, 400 (2008), (8) E. Merdivan, et al.: Spectrochim. Acta A Mol. Biomol. Spectrosc. 71, 2045 (2009)

      Quantity

      50 mg, Bulk

      cdx-Water content (K.F.)

      ≤1.0%

      cdx-Melting Point

      156 – 163 °C

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