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    Clopidogrel bisulfate

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      Clopidogrel bisulfate

      SKU
      D0505

      Category: API's & Intermediates

      Synonyms
      Clopidogrel bisulfate , Clopidogrel Hemisulfate , SR 25990C , (S)-Methyl (2-chlorophenyl)(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)acetate hydrogensulfate
      120202-66-6
      CAS-Number
      C16H16ClNO2S · H2SO4
      Molecular Formula
      419.90
      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
      Identity
      1H-NMR

      Properties

      Solvents
      DMSO (>30mg/ml), methanol, water (>30mg/ml)
      Shipping
      AMBIENT
      Short Term Storage
      +4°C
      Long Term Storage
      +4°C
      Handling Advice
      Protect from light and moisture.
      Use / Stability
      Stable for at least 2 years after receipt when stored at +4°C.
      Hazard statements
      H300-H314-H411
      Precautionary statements
      P260-P280-P303 + P361 + P353-P304 + P340 + P310-P305 + P351 + P338
      GHS Symbol
      GHS05+GHS06+GHS09
      Signal word
      Danger
      RIDADR
      2928 6.1(8)
      Transportation
      Packing Group I
      Description
      (S)-(+)-Clopidogrel is a prodrug that is metabolized by cytochrome P450 isoforms to produce an active metabolite, which is a selective, irreversible high-affinity antagonist of the platelet purinergic P2Y12 receptor. Potent antithrombotic antiplatelet agent. By inhibiting the Purinoceptor P2Y12 subtype it consequently inhibits ADP-induced platelet aggregation. (S)-(+)-Clopidogrel hydrogen sulfate is the active isomer. Compound can be used as analytical reference material.
      Smiles
      ClC1=CC=CC=C1[C@H]([NH+]2CCC(SC=C3)=C3C2)C(OC)=O.[O-]S(=O)(O)=O
      InChi Key
      FDEODCTUSIWGLK-UHFFFAOYSA-N
      References
      (1) D.C.B. Mills, et al., Arterioscler. Thromb. 12, 430 (1992) , (2) G. Feuerstein, et al., Exp. Opin. Invest. Drugs 4, 425 (1995) , (3) P. Savi, et al., BBRC 283, 379 (2001) , (4) P. Savi & J.M. Herbert, Se≥ Thromb. Haemostas. 31, 174 (2005) , (5) I. von Kugelgen, Pharmacol.Ther. 110, 415 (2006) , (6) N. Ferri, et al., Drugs 73, 1681 (2013)

      (S)-(+)-Clopidogrel is a prodrug that is metabolized by cytochrome P450 isoforms to produce an active metabolite, which is a selective, irreversible high-affinity antagonist of the platelet purinergic P2Y12 receptor. Potent antithrombotic antiplatelet agent. By inhibiting the Purinoceptor P2Y12 subtype it consequently inhibits ADP-induced platelet aggregation. (S)-(+)-Clopidogrel hydrogen sulfate is the active isomer. Compound can be used as analytical reference material.

      SKU: D0505 Category: API's & Intermediates
      • Additional information

      Additional information

      Synonyms

      Clopidogrel bisulfate, Clopidogrel Hemisulfate, SR 25990C, (S)-Methyl (2-chlorophenyl)(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)acetate hydrogensulfate

      Purity

      ≥98% (HPLC)

      Appearance

      White to off-white powder

      CAS-Number

      120202-66-6

      Molecular Formula

      C16H16ClNO2S · H2SO4

      Molecular Weight

      419.90

      Identity

      1H-NMR

      Solvents

      DMSO (>30mg/ml), methanol, water (>30mg/ml)

      Smiles

      ClC1=CC=CC=C1[C@H]([NH+]2CCC(SC=C3)=C3C2)C(OC)=O.[O-]S(=O)(O)=O

      InChi Key

      FDEODCTUSIWGLK-UHFFFAOYSA-N

      Shipping

      AMBIENT

      Short Term Storage

      +4°C

      Long Term Storage

      +4°C

      Handling Advice

      Protect from light and moisture.

      Use / Stability

      Stable for at least 2 years after receipt when stored at +4°C.

      Hazard statements

      H300-H314-H411

      Precautionary statements

      P260-P280-P303 + P361 + P353-P304 + P340 + P310-P305 + P351 + P338

      GHS Symbol

      GHS05+GHS06+GHS09

      Signal word

      Danger

      RIDADR

      2928 6.1(8)

      Transportation

      Packing Group I

      References

      (1) D.C.B. Mills, et al., Arterioscler. Thromb. 12, 430 (1992), (2) G. Feuerstein, et al., Exp. Opin. Invest. Drugs 4, 425 (1995), (3) P. Savi, et al., BBRC 283, 379 (2001), (4) P. Savi & J.M. Herbert, Se≥ Thromb. Haemostas. 31, 174 (2005), (5) I. von Kugelgen, Pharmacol.Ther. 110, 415 (2006), (6) N. Ferri, et al., Drugs 73, 1681 (2013)

      Quantity

      250 mg, Bulk

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