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Pharmacopeial Impurities (EP / USP / BP)

Rosuvastatin EP Impurity L

Reference StandardAvailable on request

Rosuvastatin EP Impurity L (CAS 1347797-73-2) supplier Zemixal. Lab and bulk packs, batch COA, fast global delivery. Exported from India with full paperwork.

Pack sizes
Rosuvastatin EP Impurity L chemical structure
CAS number1347797-73-2
FormulaC44H58CaF2N6O12S2
Molar mass1005.2 g/mol
Physical formSolid
HS code38229090
InChIKeyOUMNOTHSODZWNZ-VKLRDTKISA-L
IUPAC namecalcium bis((3R,5R)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyheptanoate)

About Rosuvastatin EP Impurity L

Rosuvastatin EP Impurity L is supplied by Zemixal as a characterised reference material for Rosuvastatin analysis. Key data (Reference Standard): CAS 1347797-73-2, formula C44H58CaF2N6O12S2 and molar mass 1005.2 g/mol. It is handled as a solid.

Typical applications

  • Pharmacopeial method verification
  • Impurity profiling
  • QC release testing
  • ANDA / DMF filings

Storage and safety notes

Hazard communication follows GHS (Warning: H315, H319 and H335). Our SDS lists exposure controls and first-aid measures.

Available as 10 mg, 25 mg, 50 mg and 100 mg. Larger or split packs can be arranged. Every shipment includes a certificate of analysis with characterisation data. Add it to your quote list and our team replies with price, lead time and shipping options within one business day.

Reference standards for Rosuvastatin

See every impurity, metabolite and related compound we list for this API.

Rosuvastatin standards

Typical uses

  • Pharmacopeial method verification
  • Impurity profiling
  • QC release testing
  • ANDA / DMF filings

Applications

Pharmaceutical Manufacturing and QCResearch Labs and Universities

Grade guides

Ph. Eur. Grade (European Pharmacopoeia)

Specifications and identifiers

Specifications of Rosuvastatin EP Impurity L
Product nameRosuvastatin EP Impurity L
Catalogue numberZX-032296
CAS number1347797-73-2
IUPAC namecalcium bis((3R,5R)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyheptanoate)
Molecular formulaC44H58CaF2N6O12S2
Molar mass1005.2 g/mol
Exact mass1004.3148
GradeReference Standard
Physical formSolid
H-bond donors / acceptors4 / 20
Topological polar surface area304 Ų
HS code38229090
InChIKeyOUMNOTHSODZWNZ-VKLRDTKISA-L
SMILESCC(C)C1=NC(=NC(=C1CC[C@H](C[C@H](CC(=O)[O-])O)O)C2=CC=C(C=C2)F)N(C)S(=O)(=O)C.CC(C)C1=NC(=NC(=C1CC[C@H](C[C@H](CC(=O)[O-])O)O)C2=CC=C(C=C2)F)N(C)S(=O)(=O)C.[Ca+2]
PubChem CID129011612
SynonymsRosuvastatin 6,7-Dihydro Impurity

Lot values are stated on the batch certificate of analysis. Ask for a typical COA with your quotation.

Safety and GHS hazards

GHS07 Irritant or harmful
Irritant or harmful

Signal word Warning

  • H315Causes skin irritation
  • H319Causes serious eye irritation
  • H335May cause respiratory irritation

Precautionary statements P261, P264, P264 + P265, P271, P280, P302 + P352, P304 + P340, P305 + P351 + P338, P319, P321, P332 + P317, P337 + P317, P362 + P364, P403 + P233, P405, P501

Classification summarised from public GHS notifications. It can vary with grade and concentration, so always follow the SDS supplied with your lot.

Pack sizes

Pack sizes of Rosuvastatin EP Impurity L
10 mgQuoted on request
25 mgQuoted on request
50 mgQuoted on request
100 mgQuoted on request

Need a different size? Bulk drums and custom packing are quoted on request through the quote form on this page.

Questions about Rosuvastatin EP Impurity L

Which CAS number identifies Rosuvastatin EP Impurity L?
Rosuvastatin EP Impurity L is registered under CAS 1347797-73-2. You may also see it listed as Rosuvastatin 6,7-Dihydro Impurity. Our catalogue number for this item is ZX-032296.
What are the formula and molar mass of Rosuvastatin EP Impurity L?
For Rosuvastatin EP Impurity L, its formula is C44H58CaF2N6O12S2 and its molar mass is 1005.2 g/mol. The systematic (IUPAC) name is calcium bis((3R,5R)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyheptanoate). InChIKey OUMNOTHSODZWNZ-VKLRDTKISA-L lets you match it in any structure database.
How is Rosuvastatin EP Impurity L used in pharmaceutical QC?
Rosuvastatin EP Impurity L is a characterised reference material linked to Rosuvastatin. Laboratories use it to identify and quantify this impurity during method development and validation, stability work, batch release testing and regulatory submissions.
What grade and pack sizes are available for Rosuvastatin EP Impurity L?
This listing is Reference Standard grade. Standard packs are 10 mg, 25 mg, 50 mg, 100 mg. Larger quantities and custom packing can be quoted on request.
Which documents come with Rosuvastatin EP Impurity L?
Each lot ships with a batch certificate of analysis and a 16-section GHS safety data sheet. A typical COA or specification sheet can be shared with the quotation before you order.
Can Zemixal ship Rosuvastatin EP Impurity L to my country?
Yes. Because Rosuvastatin EP Impurity L is classed as hazardous, it travels in UN-approved packaging as dangerous goods under IATA or IMDG rules, with the export paperwork your broker needs.

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