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Merck

C0614

(±) Clopidogrel hydrogensulfate

≥98% (HPLC), ADP-induced platelet aggregation inhibitor, powder

Synonym(s):

Methyl (2-chlorophenyl)(6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl)acetate hydrogen sulfate, SR-25990

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About This Item

Empirical Formula (Hill Notation):
C16H16ClNO2S · H2SO4
CAS Number:
135046-48-9
Molecular Weight:
419.90
UNSPSC Code:
51111800
PubChem Substance ID:
329774806
NACRES:
NA.77
MDL number:
MFCD05865229

Key Documents

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Product Name

(±) Clopidogrel hydrogensulfate, ≥98% (HPLC), powder

SMILES string

OS(O)(=O)=O.COC(=O)C(N1CCc2sccc2C1)c3ccccc3Cl

InChI

1S/C16H16ClNO2S.H2O4S/c1-20-16(19)15(12-4-2-3-5-13(12)17)18-8-6-14-11(10-18)7-9-21-14;1-5(2,3)4/h2-5,7,9,15H,6,8,10H2,1H3;(H2,1,2,3,4)

InChI key

FDEODCTUSIWGLK-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

storage condition

desiccated

color

white

solubility

DMSO: ~26 mg/mL

originator

Bristol-Myers Squibb

storage temp.

2-8°C

Quality Level

100

Related Categories

Biochem/physiol Actions

Inhibits ADP-induced platelet aggregation; anti-thrombotic drug.

Features and Benefits

This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the P2 Receptors: P2Y G-Protein Family page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Bristol-Myers Squibb. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Packaging

Store under desiccant

pictograms

CorrosionEnvironment
GHS05,GHS09

signalword

Danger

hcodes

H314,H411

Hazard Classifications

Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000500417
0000500417
0000389516
0000389516
0000295952

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Yong Wang et al.
Nature protocols, 6(7), 935-942 (2011-07-02)
We describe an effective and simple protocol that uses click chemistry to attach native β-cyclodextrin (β-CD) to silica particles, resulting in a chiral stationary phase (CCNCSP) that can be used for the enantioseparation of chiral drugs by high-performance liquid chromatography

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