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Pharmacopeial Impurities (EP / USP / BP)

Ranitidine EP Impurity I

Reference StandardAvailable on request

Buy Ranitidine EP Impurity I (CAS 207592-21-0) from Zemixal: C27H44N8O6S2, COA and SDS with every lot, worldwide shipping.

Pack sizes
Ranitidine EP Impurity I chemical structure
CAS number207592-21-0
FormulaC27H44N8O6S2
Molar mass640.8 g/mol
Physical formSolid
HS code38229090
InChIKeyDHFGZFWSNTVORH-UHFFFAOYSA-N
IUPAC name1-N',5-N'-bis[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-N,5-N-dimethyl-2,4-dinitropenta-1,4-diene-1,1,5,5-tetramine

About Ranitidine EP Impurity I

Zemixal lists Ranitidine EP Impurity I for laboratories that identify, quantify or control Ranitidine and its related substances. Identity at a glance (Reference Standard): CAS 207592-21-0, formula C27H44N8O6S2 and molar mass 640.8 g/mol. It is handled as a solid.

Typical applications

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

Handling and storage

It carries the GHS signal word Warning (H302), so wear gloves and eye protection and work with good ventilation.

Order it in 10 mg, 25 mg, 50 mg and 100 mg packs or ask for a bulk quotation. 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 Ranitidine

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

Ranitidine 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 Ranitidine EP Impurity I
Product nameRanitidine EP Impurity I
Catalogue numberZX-026665
CAS number207592-21-0
IUPAC name1-N',5-N'-bis[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-N,5-N-dimethyl-2,4-dinitropenta-1,4-diene-1,1,5,5-tetramine
Molecular formulaC27H44N8O6S2
Molar mass640.8 g/mol
Exact mass640.2825
GradeReference Standard
Physical formSolid
XLogP33.3
H-bond donors / acceptors4 / 14
Topological polar surface area223 Ų
HS code38229090
InChIKeyDHFGZFWSNTVORH-UHFFFAOYSA-N
SMILESCNC(=C(CC(=C(NC)NCCSCC1=CC=C(O1)CN(C)C)[N+](=O)[O-])[N+](=O)[O-])NCCSCC2=CC=C(O2)CN(C)C
PubChem CID72941760
SynonymsRanitidine Hydrochloride -Impurity I, Ranitidine hydrochloride specified impurity I, 2,2 inverted exclamation mark -Methylene Bis[Ranitidine]

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

  • H302Harmful if swallowed

Precautionary statements P264, P270, P301 + P317, P330, 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 Ranitidine EP Impurity I
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 Ranitidine EP Impurity I

Which CAS number identifies Ranitidine EP Impurity I?
Ranitidine EP Impurity I is registered under CAS 207592-21-0. You may also see it listed as Ranitidine Hydrochloride -Impurity I, Ranitidine hydrochloride specified impurity I, 2,2 inverted exclamation mark -Methylene Bis[Ranitidine]. Our catalogue number for this item is ZX-026665.
What are the formula and molar mass of Ranitidine EP Impurity I?
For Ranitidine EP Impurity I, its formula is C27H44N8O6S2 and its molar mass is 640.8 g/mol. The systematic (IUPAC) name is 1-N',5-N'-bis[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-N,5-N-dimethyl-2,4-dinitropenta-1,4-diene-1,1,5,5-tetramine. InChIKey DHFGZFWSNTVORH-UHFFFAOYSA-N lets you match it in any structure database.
How is Ranitidine EP Impurity I used in pharmaceutical QC?
Ranitidine EP Impurity I is a characterised reference material linked to Ranitidine. 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 Ranitidine EP Impurity I?
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 Ranitidine EP Impurity I?
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 Ranitidine EP Impurity I to my country?
Yes. Because Ranitidine EP Impurity I 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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