GB/T 35803-2018 PDF English
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| GB/T 35803-2018 | English | 150 |
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Determination of prohibited urocanic acid and its ethyl ester in cosmetics - High performance liquid chromatography
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GB/T 35803-2018: Determination of prohibited urocanic acid and its ethyl ester in cosmetics - High performance liquid chromatography
---This is an excerpt. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.), auto-downloaded/delivered in 9 seconds, can be purchased online: https://www.ChineseStandard.net/PDF.aspx/GBT35803-2018
GB
NATIONAL STANDARD OF THE
PEOPLE’S REPUBLIC OF CHINA
ICS 71.100.70
Y 42
Determination of prohibited urocanic acid and its ethyl
ester in cosmetics - High performance liquid
chromatography
Issued on: FEBRUARY 06, 201
Implemented on: SEPTEMBER 01, 2018
Issued by. General Administration of Quality Supervision, Inspection and
Quarantine;
Standardization Administration of the People's Republic of
China.
Table of Contents
Foreword ... 3
Introduction ... 4
1 Scope ... 5
2 Normative references ... 5
3 Principle ... 5
4 Reagents and materials ... 5
5 Apparatus and equipment ... 6
6 Analysis steps ... 7
7 Result calculation ... 8
8 Detection limit and limit of quantification ... 9
9 Recovery rate and precision ... 9
10 Tolerance ... 9
Annex A (informative) Chinese name, English name, CAS number, molecular
formula, relative molecular mass, structural formula of urocanic acid and its
ethyl ester ... Error! Bookmark not defined.
Annex C (informative) Test of confirmation ... 13
Determination of prohibited urocanic acid and its ethyl
ester in cosmetics - High performance liquid
chromatography
1 Scope
This Standard specifies determination method of high performance liquid
chromatography for prohibited urocanic acid and its ethyl ester in cosmetics.
This Standard is applicable to determination of urocanic acid and its ethyl ester
in cosmetics such as creams, liquids, lipsticks, loose powders, shampoos.
The detection limit of this Standard for urocanic acid and its ethyl ester is 2
mg/kg, and the limit of quantification is 5 mg/kg.
2 Normative references
The following referenced documents are indispensable for the application of
this document. For dated references, only the edition cited applies. For undated
references, the latest edition of the referenced document (including any
amendments) applies.
GB/T 6682, Water for analytical laboratory use - Specification and test
methods
3 Principle
After the specimen is centrifuged by solvent and is centrifuged, after the
supernatant is filtered by nitrogen blowing capacity, use high performance liquid
chromatography to determine, use external standard method to quantify, use
liquid chromatography-mass spectrometry to confirm.
4 Reagents and materials
Unless otherwise stated, the reagents used are analytically pure, the water is
of grade one specified in GB/T 6682.
4.1 Methanol. chromatographically pure.
5.5 Ultrasonic cleaner.
5.6 Nitrogen blower.
5.7 Plugged plastic centrifuge tube. 10mL.
5.8 Graduated nitrogen blow tube. 10mL.
5.9 Microporous membrane. 0.45μm, made of PTFE.
6 Analysis steps
6.1 Sample processing
6.1.1 Cream, liquid, loose powder and shampoo samples
Weigh 0.2g (to the nearest of 0.001g) of specimen in a 10mL plugged plastic
centrifuge tube (5.7). Add into 10mL of methanol (4.1). Shake well. After
performing ultrasonic extraction for 20min, centrifugation at 8000r/min for 15min,
transfer the supernatant to the graduated nitrogen blow tube (5.8). Slow the
nitrogen blowing to 1mL. Add into 9mL of water. Mix well. It is filtered through a
0.45μm microporous membrane for high performance liquid chromatography.
6.1.2 Lipstick sample
Weigh 0.2g (to the nearest of 0.001g) of specimen in a 10mL plugged plastic
centrifuge tube (5.7). Add into 0.5mL of tetrahydrofuran (4.2). Then add into
9.5mL of methanol (4.1). Shake well. Performing ultrasonic extraction for 20min,
centrifugation at 8000r/min for 15min. Transfer the supernatant to the graduated
nitrogen blow tube (5.8). Slow the nitrogen blowing to 1mL. Add into 9mL of
water. Mix well. It is filtered through a 0.45μm microporous membrane for high
performance liquid chromatography.
6.2 Determination conditions
The reference conditions for high performance liquid chromatography are as
follows.
a) Chromatographic column. Xterra MS C18, 5μm, 250mm × 4.6mm (inner
diameter), or the equivalent;
b) Flow rate. 1.0mL/min;
c) Mobile phase. methanol + 0.005mol/L tetrabutylammonium bromide
solution=30+70 (volume ratio);
d) Detection wavelength. 285nm;
Annex C
(informative)
Test of confirmation
C.1 Liquid chromatography conditions
The reference conditions for liquid chromatography determination are as
follows.
a) Chromatographic column. XBridge C18, 3.5μm, 150mm × 2.1mm (inner
diameter);
b) Mobile phase. 0.1% formic acid solution + acetonitrile = 95 + 5 (volume
ratio);
c) Flow rate. 0.3mL/min;
d) Column temperature. 30°C;
e) Injection volume. 5μL.
C.2 Mass spectrometry conditions
The reference conditions for mass spectrometry are as follows.
a) Ion source. electrospray ion source;
b) Ionization mode. positive ion mode;
c) Capillary voltage. 3kV;
d) Extraction voltage. 2.9V;
e) Ion source temperature. 150°C;
f) Desolvation gas temperature. 350°C;
g) Data collection method. multiple reaction monitoring.
C.3 Qualitative determination
When the specimen is measured, the sample solution is appropriately diluted,
and the sample solution and the standard working solution are determined
according to liquid chromatography-mass spectrometry conditions. If the
selected ions are present, and the selected ion ratio is consistent with the
......
Source: Above contents are excerpted from the full-copy PDF -- translated/reviewed by: www.ChineseStandard.net / Wayne Zheng et al.
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