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3,4-Dimethoxybenzyl alcohol (Verapamil Related Compound F - USP)

3,4-Dimethoxybenzyl alcohol (Verapamil Related Compound F - USP)

Product Details:

  • Molecular Formula ‎C9H12O3
  • Melting Point 46-50°C
  • Usage 3,4-Dimethoxybenzyl alcohol is widely used in the synthesis of various cyclotriveratrylenes (CTVs), which are cyclic molecular hosts with a cavity to accommodate guest molecules. It can also be used as a precursor in the total synthesis of salvianolic acid N.
  • Purity 99%
  • Molecular Weight 168.192 Grams (g)
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3,4-Dimethoxybenzyl alcohol (Verapamil Related Compound F - USP) Price And Quantity

  • 1 Kilograms
  • 100 INR

3,4-Dimethoxybenzyl alcohol (Verapamil Related Compound F - USP) Product Specifications

  • 99%
  • 46-50°C
  • 3,4-Dimethoxybenzyl alcohol is widely used in the synthesis of various cyclotriveratrylenes (CTVs), which are cyclic molecular hosts with a cavity to accommodate guest molecules. It can also be used as a precursor in the total synthesis of salvianolic acid N.
  • ‎C9H12O3
  • 168.192 Grams (g)

3,4-Dimethoxybenzyl alcohol (Verapamil Related Compound F - USP) Trade Information

  • Cash in Advance (CID) Cash Advance (CA)
  • 500 Kilograms Per Month
  • 3-4 Week
  • Yes
  • Sample costs shipping and taxes has to be paid by the buyer
  • Western Europe Australia Central America Middle East South America Asia Eastern Europe North America Africa
  • All India

Product Description

3,4-Dimethoxybenzyl alcohol (Verapamil Related Compound F - USP)

pharmaceutical secondary standard; traceable to USP

Synonym: 3,4-Dimethoxybenzyl alcohol, Verapamil related compound F, Veratryl alcohol

  • CAS Number 93-03-8

  • Linear Formula (CH3O)2C6H3CH2OH

  • Molecular Weight 168.19

grade   certified reference material
  pharmaceutical secondary standard
form   neat
refractive index   n20/D 1.552(lit.)
bp   296-297 °C/732 mmHg(lit.)
density   1.157 g/mL at 25 °C(lit.)
format   neat
pharmacopeia traceability   traceable to USP 1711440

Analysis Note

These secondary standards offer multi-traceability to the USP, EP (PhEur) and BP primary standards, where they are available.

General description

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

 

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