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Trimethoprim EP Impurity H

Methyl Eudesmate; Methyl Gallate Trimethyl Ether; Trimethylgallic Acid Methyl Ester; 3,4,5-Trimethoxybenzoic Acid Methyl Ester; Methyl Tri-O-methylgallateMethyl 3,4,5-Trimethoxybenzoate;

Trimethoprim EP Impurity H | 1916-07-0 | Trimethoprim

Specifications:

CAS No.

: 1916-07-0

Mol F.

: C11H14O5

Mol W.

: 226.23

Cat No.

: SA27108

Appearance

Pack Size Price Availability
25 mg $79 In Stock
50 mg $95 In Stock
100 mg $115 In Stock
200 mg $155 In Stock
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Product Name

: Trimethoprim EP Impurity H

CAS No.

: 1916-07-0

Mol F.

: C11H14O5

Mol W.

: 226.23

Cat No.

: SA27108

Appearance

Synonyms

: Methyl Eudesmate; Methyl Gallate Trimethyl Ether; Trimethylgallic Acid Methyl Ester; 3,4,5-Trimethoxybenzoic Acid Methyl Ester; Methyl Tri-O-methylgallateMethyl 3,4,5-Trimethoxybenzoate;

Related API

: Trimethoprim

Category

Order Trimethoprim EP Impurity H impurity standard with CAS: 1916-07-0 and speed up your Trimethoprim project. This product is also known as 3,4,5-Trimethoxybenzoic Acid Methyl Ester; Methyl Eudesmate and can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Trimethoprim and its related formulations. Moreover, 3,4,5-Trimethoxybenzoic Acid Methyl Ester is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

Product quantity / packs as per your requirement, just let us know!

Please contact us or email us at enquiry@synthinkchemicals.com

Product Name

: Trimethoprim EP Impurity H

CAS No.

: 1916-07-0

Mol F.

: C11H14O5

Mol W.

: 226.23

Cat No.

: SA27108

Appearance

Synonyms

: Methyl Eudesmate; Methyl Gallate Trimethyl Ether; Trimethylgallic Acid Methyl Ester; 3,4,5-Trimethoxybenzoic Acid Methyl Ester; Methyl Tri-O-methylgallateMethyl 3,4,5-Trimethoxybenzoate;

Related API

: Trimethoprim

Category

Order Trimethoprim EP Impurity H impurity standard with CAS: 1916-07-0 and speed up your Trimethoprim project. This product is also known as 3,4,5-Trimethoxybenzoic Acid Methyl Ester; Methyl Eudesmate and can be used as a working standard or secondary reference standard. Additional internal validation as per respective FDA regulations/guidelines may require. This compound is generally used for Quality Control (QC), Quality Assurance (QA) during commercial production of Trimethoprim and its related formulations. Moreover, 3,4,5-Trimethoxybenzoic Acid Methyl Ester is also used in the process of Abbreviated New Drug Application (ANDA) filing to FDA and toxicity study of respective drug formulation.

Product quantity / packs as per your requirement, just let us know!

Please contact us or email us at enquiry@synthinkchemicals.com

Terms and Conditions

CoA & Characterization Data At no extra cost, we provide: 1H-NMR, Mass, HPLC, IR, TGA and Certificate of Analysis (with Purity and Potency.) In rare cases for purity and mass, we need to rely on alternative methods like 1H-NMR, ELSD, GC, GCMS etc. (Applicable for products under ‘Impurities’ category). Additional data will be provided upon request for an additional fee.
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Delivery Timeline India: 2 to 3 business days
International: 5 to 8 business days
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Incoterms CPT (Incoterms® 2020) or as mutually agreed upon
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Payment Terms Regular/returning customers: Due 30 days from invoice date
New customers: 100% payment in advance
After Sales Support Please write to us. Our R&D team will provide all possible support.

Please check detailed terms and conditions.

Certificate of Analysis (CoA) & Characterization Data

With every product in impurity category, we provide comprehensive characterization data and a Certificate of Analysis (CoA) wherever possible. The data package typically includes:

  • 1H-NMR (Proton Nuclear Magnetic Resonance)
  • Mass Spectrometry (MS)
  • High-Performance Liquid Chromatography (HPLC)
  • Infrared Spectroscopy (IR)
  • Thermogravimetric Analysis (TGA)
  • CoA (detailing Purity and Potency)

In rare cases, for purity estimations and mass alternative validated methods such as 1H-NMR, ELSD (Evaporative Light Scattering Detection), GC (Gas Chromatography) or GCMS may be used when standard tests are not feasible.

Additional data such as C-NMR, 13C-DEPT, HMBC-NMR, HMQC-NMR, COSY-NMR, NOESY-NMR, NOE-NMR, CHN analysis, Water Content, Structure Elucidation Reports, and more will be provided upon request for an additional fee.

For other categories like Building blocks, intermediates we provide, CoA with HPLC purity on request

This ensures you have all the necessary analytical data to verify the quality and identity of your impurity standards.

Retest CoA: We also offer retest Certificates of Analysis (CoA). To request a retest CoA, please submit your batch number through the ‘Request CoA’ form.

Request CoA or Retest CoA of this product:

This material is intended for use as a reference standard, working standard, or secondary reference standard, provided it has been properly characterized, identified, and qualified for its specific application. Additional internal validation may be necessary to comply with relevant FDA regulations and guidance.

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Disclaimer

The product information provided on this webpage is based on the best available knowledge at the time of publication. However, accuracy and completeness are not guaranteed. The purchaser, user, or importer of record is responsible for verifying the product specifications and details at the time of ordering, as they may change without prior notice.

This product is intended strictly for research purposes and is not approved for animal or human consumption.

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