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

Tamsulosin EP Impurity I

Synonyms: Tamsulosin Hydrochloride - Impurity I · 2-(2-Ethoxyphenoxy)ethyl Bromide · Benzene, 1-(2-bromoethoxy)-2-ethoxy- · 2-(2-Bromoethoxy)-ethoxybenzene

CAS No.3259-03-8
FormulaC10H13BrO2
Mol. weight245.11
Catalogue No.VQ-023836
PurityReference Standard
HSN38229090

Tamsulosin EP Impurity I (CAS 3259-03-8) – Tamsulosin impurity standard. C10H13BrO2, MW 245.11. Request a quote: COA, bulk packs and worldwide export.

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 Tamsulosin EP Impurity I

Listed under CAS 3259-03-8, Tamsulosin EP Impurity I is a pharmacopeial impurity of Tamsulosin available from Vaqora Chemicals. Formula C10H13BrO2, molecular weight 245.11 g/mol. The IUPAC name is 1-(2-bromoethoxy)-2-ethoxybenzene. It is also known as Tamsulosin Hydrochloride - Impurity I or 2-(2-Ethoxyphenoxy)ethyl Bromide.

The product is provided as a solid. Store the standard in its sealed vial, protected from light and moisture, and follow the storage condition printed on the COA. It carries the GHS signal word “Warning” with 4 hazard statements. Review the Safety Data Sheet before use.

As a characterised impurity of Tamsulosin, it is used for analytical method development, method validation (AMV) and routine quality-control testing, and it supports ANDA and DMF regulatory filings. Buyers come mainly from pharmaceutical manufacturing and academic and industrial research.

Available in 10 mg, 25 mg, 50 mg and 100 mg packs, Tamsulosin EP Impurity I is dispatched with a Certificate of Analysis (COA) to destinations worldwide.

Typical applications

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

Industries

Related to Tamsulosin

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

Tamsulosin impurities

Grade guides

Specifications & identifiers

Chemical identifiers
Product nameTamsulosin EP Impurity I
Catalogue No.VQ-023836
CAS Number3259-03-8
IUPAC name1-(2-bromoethoxy)-2-ethoxybenzene
Molecular formulaC10H13BrO2
Molecular weight245.11 g/mol
Exact mass244.0099
GradeReference Standard
HSN code38229090
InChIKeyIOYHGBZPUZBUTJ-UHFFFAOYSA-N
SMILESCCOC1=CC=CC=C1OCCBr
PubChem CID7010183
Physical properties
Physical formSolid
LogP (XLogP3)2.8
H-bond donors / acceptors0 / 2
TPSA18.5 Ų
SynonymsTamsulosin Hydrochloride - Impurity I, 2-(2-Ethoxyphenoxy)ethyl Bromide, Benzene, 1-(2-bromoethoxy)-2-ethoxy-, 2-(2-Bromoethoxy)-ethoxybenzene, 2-(2-Ethoxyphenoxy) ethyl bromide, 2-(2-ethoxyphenoxy)ethylbromide, 1-(2-bromoethoxy)-2-ethoxy-benzene, 2-bromo-1-(2-ethoxyphenoxy)ethane, 2-(2-Bromoethoxy)phenetole, Tamsulosin Impurity 48, 2-(o-ethoxyphenoxy)ethyl bromide

Safety & hazard information (GHS)

GHS07 Harmful / irritant
Harmful / irritant

Signal word: Warning

Hazard statements

  • H302Harmful if swallowed
  • H315Causes skin irritation
  • H319Causes serious eye irritation
  • H335May cause respiratory irritation

Precautionary statements: P261, P264, P264 + P265, P270, P271, P280, P301 + P317, P302 + P352, P304 + P340, P305 + P351 + P338, P319, P321, P330, P332 + P317, P337 + P317, P362 + P364, P403 + P233, 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 Tamsulosin EP Impurity I?

The CAS Registry Number of Tamsulosin EP Impurity I is 3259-03-8. It is also known as Tamsulosin Hydrochloride - Impurity I, 2-(2-Ethoxyphenoxy)ethyl Bromide, Benzene, 1-(2-bromoethoxy)-2-ethoxy-.

What is the molecular formula and molecular weight of Tamsulosin EP Impurity I?

Tamsulosin EP Impurity I has the molecular formula C10H13BrO2 and a molecular weight of 245.11 g/mol. Its IUPAC name is 1-(2-bromoethoxy)-2-ethoxybenzene.

What is Tamsulosin EP Impurity I used for?

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

We supply Tamsulosin EP Impurity I 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 Tamsulosin EP Impurity I?

Yes. Every lot of Tamsulosin EP Impurity I 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 Tamsulosin EP Impurity I be shipped internationally?

Yes. Tamsulosin EP Impurity I 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 Tamsulosin EP Impurity I

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Why buyers choose Vaqora

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