Skip to Content
Merck

113360

3,4,5-Trimethoxyphenylacetonitrile

97%

Synonym(s):

3,4,5-Trimethoxybenzyl cyanide

Slide 1 of 1
Sign In to View Organizational & Contract Pricing.

Select a Size

10 G

$222.00

$222.00

Please contact Customer Service for Availability
Request a Bulk Order

About This Item

Linear Formula:
(CH3O)3C6H2CH2CN
CAS Number:
13338-63-1
Molecular Weight:
207.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24846877
EC Number:
236-388-5
Beilstein/REAXYS Number:
2214548
MDL number:
MFCD00001912

Key Documents

View All Documentation

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

3,4,5-Trimethoxyphenylacetonitrile, 97%

InChI key

ACFJNTXCEQCDBX-UHFFFAOYSA-N

InChI

1S/C11H13NO3/c1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3/h6-7H,4H2,1-3H3

SMILES string

COc1cc(CC#N)cc(OC)c1OC

assay

97%

form

solid

mp

77-79 °C (lit.)

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
331384141704PHR2619
3,4,5-Trimethoxyphenylacetonitrile 97%

Sigma-Aldrich

113360

3,4,5-Trimethoxyphenylacetonitrile

3,4,5-Trimethylphenol 97%

Sigma-Aldrich

331384

3,4,5-Trimethylphenol

2,4,5-Tribromoimidazole 97%

Sigma-Aldrich

141704

2,4,5-Tribromoimidazole

3,4-Dimethoxyphenylacetonitrile Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR2619

3,4-Dimethoxyphenylacetonitrile

assay

97%

assay

97%

assay

97%

assay

-

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

300

mp

77-79 °C (lit.)

mp

-

mp

217-220 °C (dec.) (lit.)

mp

62-63.5 °C (lit.)

form

solid

form

-

form

-

form

solid

Application

3,4,5-Trimethoxyphenylacetonitrile is used as an internal standard during the determination of vancomycin in serum. The method used involved a direct and rapid solvent precipitation of protein[1].

General description

3,4,5-Trimethoxyphenylacetonitrile is synthesized by the condensation of 3 : 4 : 5-trimethoxybenzaldehyde with hippuric acid[2].

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK4648
STBJ9678
STBJ6143
STBD9148V
S24549

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

A F Rosenthal et al.
Clinical chemistry, 32(6), 1016-1019 (1986-06-01)
We simplified determination of vancomycin in serum by using a direct and rapid solvent precipitation of protein and by using a simple organic compound as internal standard. Reproductibility of the vancomycin retention time was improved by modifying the mobile phase.
XXII.?Synthetical experiments in the isoflavone group.Part IV. A synthesis of 2-methylirigenol.
Baker W and Robinson R.
Journal of the Chemical Society, 152-161 (1929)

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service