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Phenolic Acids & Alcohols Standard Mixture - 1

TABLE OF COMPOSITION

CAS
Verified Purity
RT
Mass
Comp
7400-08-0
99.1%
14.484
164.0473
1.0 mM (0.016%)
530-59-6
99.1%
19.131
224.0685
1.0 mM (0.022%)
501-36-0
99.9%
23.416
228.0786
1.0 mM (0.023%)
140-10-3
99.9%
25.362
148.0524
1.0 mM (0.015%)
87-66-1
99.8%
2.442
126.0317
1.0 mM (0.013%)
303-38-8
98.8%
9.111
154.0266
1.0 mM (0.015%)
530-57-4
97.9%
11.375
198.0528
1.0 mM (0.02%)
1135-24-6
99.8%
18.065
194.0579
1.0 mM (0.019%)
1948-33-0
97%
166.0994
0.5 mM
Methanol
67-56-1
32.0262
99.857%

ANALYSIS RESULTS

Analysis method
Instrument

Agilent HPLC 1290 Series

UV Detector: Agilent 1260 Infinity II Diode Array

ELSD Detector: 1260 Infinity II Evaporative Light Scattering Detector.

MSD: Agilent 6460C QQQ

Column

InfinityLab Poroshell 120 EC-C18, 2.1 x 150 mm, 1.9 µm, narrow bore LC column

Chromatography method
  A: 0.1% Formic acid in H2O
B: 0.1% Formic acid in Acetonitrile  
Time (min) A (%) B (%) Flow (mL/min)
0 95 5 0.3
2 95 5 0.3
15 88 12 0.3
35 45 55 0.3
36 0 100 0.3
38 0 100 0.3
39 95 5 0.3
40 95 5 0.3
Chromatogram
Note

All signals in the above chromatogram are recorded at 220nM.

Note

A peak at 13.7 belongs to 0.5mM TBHQ (tert-butylhydroquinone, CAS# 1948-33-0) which is used as an internal standard. The TBHQ in all solutions comes from the same stock mix and is comparable ampule to ampule.

MS Spectra
To view the spectra

Please refer to the online version of the Certificate of Analysis by scanning the QR code on the product label. Click on the name of the corresponding compound in the Sec 3. Table of composition to view the compound specification.

STABILITY

Shelf life and storage
Shelf-life

A shelf life of at least 2 years has been established for this product. 

Your product expires no eariler than Feb 2025

Real-time Stability Test

No data is available at this moment. For the latest stability results, please visit our website (www.metasci.ca)

Additional Methods

MS2 Transitions for MS/MS
Instrument

Agilent QQQ 6460C - ESI

Column

InfinityLab Poroshell 120 EC-C18, 2.1 x 150 mm, 1.9 µm, narrow bore LC column

Analysis Method
  Name Polarity Exact Mass CAS# Fragmentor Precursor Ion Product Ion CE CAV Abundance
1 p-Coumaric acid Negative 164.0473 7400-08-0 104 163 119.1 10 4 46359
1 p-Coumaric acid Negative 164.0473 7400-08-0 104 163 93.1 38 4 2651
1 p-Coumaric acid Negative 164.0473 7400-08-0 104 163 117.1 34 4 1238
1 p-Coumaric acid Positive 164.0473 7400-08-0 100 165.1 91.1 26 4 7725
1 p-Coumaric acid Positive 164.0473 7400-08-0 100 165.1 147.1 10 4 13449
2 Sinapic acid Negative 224.0685 530-59-6 108 223.1 93.1 38 4 4480
2 Sinapic acid Negative 224.0685 530-59-6 108 223.1 208.1 10 4 8377
2 Sinapic acid Negative 224.0685 530-59-6 108 223.1 121 30 4 5166
2 Sinapic acid Positive 224.0685 530-59-6 88 225.1 91.2 30 4 8325
2 Sinapic acid Positive 224.0685 530-59-6 88 225.1 207.1 2 4 28368
3 Resveratrol Negative 228.0786 501-36-0 141 227.1 143.1 26 4 5649
3 Resveratrol Negative 228.0786 501-36-0 141 227.1 185.1 18 4 4331
3 Resveratrol Negative 228.0786 501-36-0 141 227.1 41.2 34 4 936
4 trans-Cinnamic acid Negative 148.0524 140-10-3 84 147 96.6 10 4 52
4 trans-Cinnamic acid Negative 148.0524 140-10-3 82 147 103.1 10 4 761
4 trans-Cinnamic acid Positive 148.0524 140-10-3 42 149.1 85 10 4 7807
4 trans-Cinnamic acid Positive 148.0524 140-10-3 42 149.1 77.2 38 4 3290
5 Pyrogallol Negative 126.0317 87-66-1 128 125 79.2 18 4 433
5 Pyrogallol Negative 126.0317 87-66-1 128 125 51.2 30 4 250
5 Pyrogallol Positive 126.0317 87-66-1 42 149 85.1 10 4 8003
6 2,3-Dihydroxybenzoic acid Negative 154.0266 303-38-8 94 153 109.1 14 4 8946
6 2,3-Dihydroxybenzoic acid Negative 154.0266 303-38-8 94 153 108 26 4 2839
6 2,3-Dihydroxybenzoic acid Positive 154.0266 303-38-8 76 155 107.2 22 4 115
6 2,3-Dihydroxybenzoic acid Positive 154.0266 303-38-8 76 155 63.1 34 4 345
7 Syringic acid Negative 198.0528 530-57-4 106 197 129.3 10 4 66
7 Syringic acid Negative 198.0528 530-57-4 108 197 182.1 10 4 2999
7 Syringic acid Negative 198.0528 530-57-4 108 197 123 22 4 2452
7 Syringic acid Negative 198.0528 530-57-4 108 197 95.1 34 4 1152
7 Syringic acid Positive 198.0528 530-57-4 42 199.1 85 18 4 3044
7 Syringic acid Positive 198.0528 530-57-4 42 199.1 117 10 4 1339
8 Ferulic acid Negative 194.0579 1135-24-6 98 193.1 178.1 10 4 6900
8 Ferulic acid Negative 194.0579 1135-24-6 98 193.1 149.1 10 4 3196
8 Ferulic acid Negative 194.0579 1135-24-6 98 193.1 134.1 14 4 14447
8 Ferulic acid Positive 194.0579 1135-24-6 82 195.1 85.1 18 4 3558
8 Ferulic acid Positive 194.0579 1135-24-6 82 195.1 177.1 10 4 4037
*CE: Collision energy **CAV: Capillary Accelerator Voltage
Notes

- Solvent system used (refer to the ANALYSIS RESULTS -> Chromatography method):

A: 0.1% Formic acid in H2O

B: 0.1% Formic acid in Acetonitrile

- Experimental: Adding 10-100mM ammonium formate to the solvent system may increase the ionization and the signal of the analytes

- Depending on the ion source and the instrument setup, alcohols generally yield lower signal and fragmentation. In such a case, higher injection volume may improve the signal. When the ionization is too week, the sodium adduct (M+Na) is more prominent.

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