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Pharmacopeial Impurities (EP / USP / BP)

Ranitidine EP impurity A

Reference StandardAvailable on request

Ranitidine EP impurity A (CAS 72126-78-4) supplier Zemixal. Lab and bulk packs, batch COA, fast global delivery. Packs from 10 mg.

Pack sizes
Ranitidine EP impurity A chemical structure
CAS number72126-78-4
FormulaC22H35N5O4S2
Molar mass497.7 g/mol
Physical formSolid
HS code38229090
InChIKeyVTVSRHZKBPARSF-UHFFFAOYSA-N
IUPAC name1-N,1-N'-bis[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-2-nitroethene-1,1-diamine

About Ranitidine EP impurity A

Zemixal lists Ranitidine EP impurity A for laboratories that identify, quantify or control Ranitidine and its related substances. For your records (Reference Standard), the material is defined by CAS 72126-78-4, formula C22H35N5O4S2 and molar mass 497.7 g/mol. It is handled as a solid.

Typical applications

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

Handling and storage

Hazard communication follows GHS (Danger: H317, H334 and H335). Our SDS lists exposure controls and first-aid measures.

Order it in 10 mg, 25 mg, 50 mg and 100 mg packs or ask for a bulk quotation. You receive a certificate of analysis with characterisation data with each order. Request pricing online and we confirm availability, documentation and freight to your country.

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 A
Product nameRanitidine EP impurity A
Catalogue numberZX-026657
CAS number72126-78-4
IUPAC name1-N,1-N'-bis[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-2-nitroethene-1,1-diamine
Molecular formulaC22H35N5O4S2
Molar mass497.7 g/mol
Exact mass497.213
GradeReference Standard
Physical formSolid
XLogP31.4
H-bond donors / acceptors2 / 10
Topological polar surface area153 Ų
HS code38229090
InChIKeyVTVSRHZKBPARSF-UHFFFAOYSA-N
SMILESCN(C)CC1=CC=C(O1)CSCCNC(=C[N+](=O)[O-])NCCSCC2=CC=C(O2)CN(C)C
PubChem CID3055214
SynonymsRanitidine Hydrochloride -Impurity A, Dimethylaminomethylfurylmethylthioethyl Ranitidine, Raniti dine related compound B

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
GHS08 Health hazard
Health hazard

Signal word Danger

  • H317May cause an allergic skin reaction
  • H334May cause allergy or asthma symptoms or breathing difficulties if inhaled
  • H335May cause respiratory irritation

Precautionary statements P233, P260, P261, P271, P272, P280, P284, P302 + P352, P304 + P340, P319, P321, P333 + P317, P342 + P316, P362 + P364, P403, 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 Ranitidine EP impurity A
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 A

Which CAS number identifies Ranitidine EP impurity A?
Ranitidine EP impurity A is registered under CAS 72126-78-4. You may also see it listed as Ranitidine Hydrochloride -Impurity A, Dimethylaminomethylfurylmethylthioethyl Ranitidine, Raniti dine related compound B. Our catalogue number for this item is ZX-026657.
What are the formula and molar mass of Ranitidine EP impurity A?
For Ranitidine EP impurity A, its formula is C22H35N5O4S2 and its molar mass is 497.7 g/mol. The systematic (IUPAC) name is 1-N,1-N'-bis[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-2-nitroethene-1,1-diamine. InChIKey VTVSRHZKBPARSF-UHFFFAOYSA-N lets you match it in any structure database.
How is Ranitidine EP impurity A used in pharmaceutical QC?
Ranitidine EP impurity A 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 A?
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 A?
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 A to my country?
Yes. Because Ranitidine EP impurity A 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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