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VAQORACHEMICALS
Pharmacopeial Impurities (EP / USP / BP)Reference StandardAvailable on request

Lisinopril EP Impurity F

Synonyms: Lisinopril Dihydrate - Impurity F · Lisinopril specified impurity F · N2-((1S)-1-Carboxy-3-cyclohexylpropyl)-L-lysyl-L-proline · N2-[(1S)-1-Carboxy-3-cyclohexylpropyl]-L-lysyl-L-proline

CAS No.1132650-67-9
FormulaC21H37N3O5
Mol. weight411.50
Catalogue No.VQ-031599
PurityReference Standard
HSN38229090

Lisinopril EP Impurity F (CAS 1132650-67-9) – Lisinopril impurity standard. C21H37N3O5, MW 411.5. Order from Vaqora Chemicals with COA and global delivery.

Pack sizesPrice on quotation · bulk available
10 mg
25 mg
50 mg
100 mg
Bulk / custom pack · kg to MT
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Batch COA with every lot
16-section GHS SDS
Export to 120+ countries
DG-compliant packing

About Lisinopril EP Impurity F

Lisinopril EP Impurity F (CAS 1132650-67-9) is a pharmacopeial impurity of Lisinopril offered by Vaqora Chemicals. Formula C21H37N3O5, molecular weight 411.5 g/mol. Systematically, it is named (2S)-1-[(2S)-6-amino-2-[[(1S)-1-carboxy-3-cyclohexylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid. Common synonyms include Lisinopril Dihydrate - Impurity F and Lisinopril specified impurity F.

The product is provided as a solid. Reference materials should be stored sealed and away from light and moisture, as specified on the accompanying COA. The GHS classification uses the signal word “Danger”, so appropriate gloves, eye protection and ventilation are recommended.

Pharmaceutical QC and development laboratories use this impurity standard of Lisinopril to develop and validate HPLC methods, to set specification limits and to document impurity profiles in ANDA and DMF submissions. Typical end-use sectors are pharmaceutical manufacturing and academic and industrial research.

Standard pack sizes are 10 mg, 25 mg, 50 mg and 100 mg, and every batch ships with a Certificate of Analysis (COA) and we export worldwide.

Typical applications

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

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Related to Lisinopril

View every impurity, metabolite and intermediate we list for Lisinopril.

Lisinopril impurities

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Specifications & identifiers

Chemical identifiers
Product nameLisinopril EP Impurity F
Catalogue No.VQ-031599
CAS Number1132650-67-9
IUPAC name(2S)-1-[(2S)-6-amino-2-[[(1S)-1-carboxy-3-cyclohexylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid
Molecular formulaC21H37N3O5
Molecular weight411.5 g/mol
Exact mass411.2733
GradeReference Standard
HSN code38229090
InChIKeyQYSKCMYFYQRFSL-BZSNNMDCSA-N
SMILESC1CCC(CC1)CC[C@@H](C(=O)O)N[C@@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)O
PubChem CID71587933
Physical properties
Physical formSolid
LogP (XLogP3)-1.7
H-bond donors / acceptors4 / 7
TPSA133 Ų
SynonymsLisinopril Dihydrate - Impurity F, Lisinopril specified impurity F, N2-((1S)-1-Carboxy-3-cyclohexylpropyl)-L-lysyl-L-proline, N2-[(1S)-1-Carboxy-3-cyclohexylpropyl]-L-lysyl-L-proline, L-Proline, N2-((1S)-1-carboxy-3-cyclohexylpropyl)-L-lysyl-, N~2~-[(1S)-1-Carboxy-3-cyclohexylpropyl]-L-lysyl-L-proline

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant
GHS08 Health hazard
Health hazard

Signal word: Danger

Hazard statements

  • H319Causes serious eye irritation
  • H360May damage fertility or the unborn child

Precautionary statements: P203, P264 + P265, P280, P305 + P351 + P338, P318, P337 + P317, P405, P501

Classification is indicative (aggregated GHS notifications) and may vary by grade and concentration. Always refer to the SDS supplied with your lot.

Documents

Frequently asked questions

What is the CAS number of Lisinopril EP Impurity F?

The CAS Registry Number of Lisinopril EP Impurity F is 1132650-67-9. It is also known as Lisinopril Dihydrate - Impurity F, Lisinopril specified impurity F, N2-((1S)-1-Carboxy-3-cyclohexylpropyl)-L-lysyl-L-proline.

What is the molecular formula and molecular weight of Lisinopril EP Impurity F?

Lisinopril EP Impurity F has the molecular formula C21H37N3O5 and a molecular weight of 411.5 g/mol. Its IUPAC name is (2S)-1-[(2S)-6-amino-2-[[(1S)-1-carboxy-3-cyclohexylpropyl]amino]hexanoyl]pyrrolidine-2-carboxylic acid.

What is Lisinopril EP Impurity F used for?

Lisinopril EP Impurity F is supplied as a characterised reference material related to Lisinopril. It is used for analytical method development and validation (AMV), impurity profiling, stability studies and quality control, and in ANDA/DMF regulatory filings.

Which grade and pack sizes of Lisinopril EP Impurity F can I order?

We supply Lisinopril EP Impurity F in Reference Standard grade, in 10 mg, 25 mg, 50 mg, 100 mg packs. Larger bulk quantities and custom packing are quoted on request.

Do you provide a COA and SDS with Lisinopril EP Impurity F?

Yes. Every lot of Lisinopril EP Impurity F is shipped with a batch-specific Certificate of Analysis, and a 16-section GHS Safety Data Sheet is provided with the quotation and the shipment.

Can Lisinopril EP Impurity F be shipped internationally?

Yes. Lisinopril EP Impurity F is classified as hazardous, so it is packed in UN-approved packaging and shipped as dangerous goods under IATA/IMDG rules. We export worldwide on EXW, FOB, CIF and DAP terms.

Enquire about Lisinopril EP Impurity F

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Why buyers choose Vaqora

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  • R&D packs to multi-tonne supply
  • IATA / IMDG dangerous-goods packing
  • EXW, FOB, CIF, DAP Incoterms
  • Custom synthesis & sourcing
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