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

Dihydroergotamine EP Impurity E

Synonyms: Dihydro Ergotamine Mesylate Impurity E · Dihydroergocristine · 9,10-Dihydroergocristine · GNF-Pf-3462

CAS No.17479-19-5
FormulaC35H41N5O5
Mol. weight611.70
Catalogue No.VQ-045307
PurityReference Standard
HSN38229090

Dihydroergotamine EP Impurity E (CAS 17479-19-5) – Dihydroergotamine impurity standard. C35H41N5O5, MW 611.7. Vaqora Chemicals: COA, global shipping.

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 Dihydroergotamine EP Impurity E

Dihydroergotamine EP Impurity E (CAS 17479-19-5) is a pharmacopeial impurity of Dihydroergotamine offered by Vaqora Chemicals. Its molecular formula is C35H41N5O5 and its molecular weight is 611.7 g/mol. Alternative names: Dihydro Ergotamine Mesylate Impurity E and Dihydroergocristine.

It is supplied as a solid. Keep the vial tightly closed, protected from light and humidity, at the temperature stated on the Certificate of Analysis. Under GHS it is labelled “Warning”, so handle it with suitable PPE and consult the SDS.

Pharmaceutical QC and development laboratories use this impurity standard of Dihydroergotamine 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

Industries

Related to Dihydroergotamine

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

Dihydroergotamine impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product nameDihydroergotamine EP Impurity E
Catalogue No.VQ-045307
CAS Number17479-19-5
IUPAC name(6aR,9R,10aR)-N-[(1S,2S,4R,7S)-7-benzyl-2-hydroxy-5,8-dioxo-4-propan-2-yl-3-oxa-6,9-diazatricyclo[7.3.0.02,6]dodecan-4-yl]-7-methyl-6,6a,8,9,10,10a-hexahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
Molecular formulaC35H41N5O5
Molecular weight611.7 g/mol
Exact mass611.3108
GradeReference Standard
HSN code38229090
InChIKeyDEQITUUQPICUMR-HJPBWRTMSA-N
SMILESCC(C)[C@@]1(C(=O)N2[C@H](C(=O)N3CCC[C@H]3[C@@]2(O1)O)CC4=CC=CC=C4)NC(=O)[C@@H]5C[C@H]6[C@@H](CC7=CNC8=CC=CC6=C78)N(C5)C
PubChem CID107715
Physical properties
Physical formSolid
LogP (XLogP3)3.3
H-bond donors / acceptors3 / 6
TPSA118 Ų
SynonymsDihydro Ergotamine Mesylate Impurity E, Dihydroergocristine, 9,10-Dihydroergocristine, GNF-Pf-3462, Dihydroergocristin, Ergocristine, 9,10-dihydro-, Diertine, Dihydroergocristine (BAN), 5'-Benzyl-9,10-dihydro-12'-hydroxy-2'-isopropyl-3',6',18-ergotamantrion, 9,10-Dihydro-12'-hydroxy-2'-isopropyl-5'alpha-benzylergotaman-3',6',18-trion, 5'alpha-Benzyl-12'-hydroxy-3',6',18-trioxo-2'-(propan-2-yl)-10alpha-9,10-dihydroergotaman

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed
  • H332Harmful if inhaled

Precautionary statements: P261, P264, P270, P271, P301 + P317, P304 + P340, P317, P330, 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 Dihydroergotamine EP Impurity E?

The CAS Registry Number of Dihydroergotamine EP Impurity E is 17479-19-5. It is also known as Dihydro Ergotamine Mesylate Impurity E, Dihydroergocristine, 9,10-Dihydroergocristine.

What is the molecular formula and molecular weight of Dihydroergotamine EP Impurity E?

Dihydroergotamine EP Impurity E has the molecular formula C35H41N5O5 and a molecular weight of 611.7 g/mol.

What is Dihydroergotamine EP Impurity E used for?

Dihydroergotamine EP Impurity E is supplied as a characterised reference material related to Dihydroergotamine. 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 Dihydroergotamine EP Impurity E can I order?

We supply Dihydroergotamine EP Impurity E 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 Dihydroergotamine EP Impurity E?

Yes. Every lot of Dihydroergotamine EP Impurity E 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 Dihydroergotamine EP Impurity E be shipped internationally?

Yes. Dihydroergotamine EP Impurity E 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.

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