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USP Monograph for Caffeine Analysis

The document provides the official monograph for caffeine, detailing its chemical composition, identification methods, assay procedures, and impurity limits. It specifies the acceptance criteria for caffeine content and impurities, as well as storage and labeling requirements. The monograph is currently official as of February 14, 2025, and includes references for further information.

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0% found this document useful (0 votes)
10 views2 pages

USP Monograph for Caffeine Analysis

The document provides the official monograph for caffeine, detailing its chemical composition, identification methods, assay procedures, and impurity limits. It specifies the acceptance criteria for caffeine content and impurities, as well as storage and labeling requirements. The monograph is currently official as of February 14, 2025, and includes references for further information.

Uploaded by

Muhammad Nadeem
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© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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2/14/25, 2:04 AM USP-NF Caffeine

[Link]
Status: Currently Official on 14-Feb-2025
Official Date: Official as of 01-May-2020
Document Type: USP Monographs
DocId: GUID-A1199B07-4EA5-476C-ADC6-EF9D4E9231B1_4_en-US
DOI: [Link]
DOI Ref: dn2lv

© 2025 USPC
Do not distribute

Caffeine

C8H10N4O2 · H2O 212.21


C8H10N4O2 194.19
1H-Purine-2,6-dione, 3,7-dihydro-1,3,7-trimethyl-;
1,3,7-Trimethylxanthine CAS RN®: 58-08-2; UNII: 3G6A5W338E.
Monohydrate CAS RN®: 5743-12-4.

DEFINITION
Caffeine is anhydrous or contains one molecule of water of hydration. It contains NLT 98.5% and NMT 101.0% of C8H10N4O2, calculated on the

anhydrous basis.

IDENTIFICATION
Change to read: L
• A. ▲Spectroscopic Identification Tests 〈197〉, Infrared Spectroscopy: 197M▲ (CN 1-May-2020)
IA
• B. The retention time of the caffeine peak of the Sample solution corresponds to that of the Standard solution, as obtained in the Assay.

ASSAY
• Procedure
IC

Buffer: 0.82 g/L of anhydrous sodium acetate


Mobile phase: Acetonitrile, tetrahydrofuran, and Buffer (25:20:955). Adjust with glacial acetic acid to a pH of 4.5.
System suitability solution: 0.02 mg/mL of theophylline in Mobile phase. Shake, and sonicate if necessary, to dissolve.
Standard solution: Transfer 5.0 mg of USP Caffeine RS to a 25-mL volumetric flask. Add 5.0 mL of the System suitability solution and 10 mL
FF

of Mobile phase. Shake, and sonicate if necessary. Dilute with Mobile phase to volume, and filter.
Sample solution: 0.2 mg/mL of Caffeine in Mobile phase. [Note—Shake, and sonicate if necessary, to dissolve.]
Chromatographic system
(See Chromatography 〈621〉, System Suitability.)
Mode: LC
O

Detector: UV 275 nm
Column: 4.6-mm × 15-cm; packing L1
Flow rate: 1 mL/min
Injection size: 10 µL
System suitability
Sample: Standard solution
[Note—The relative retention times for theophylline and caffeine are 0.69 and 1.0, respectively.]
Suitability requirements
Resolution: NLT 6.0 between theophylline and caffeine
Tailing factor: NMT 2.0 for theophylline and caffeine peaks
Relative standard deviation: NMT 2.0%
Analysis
Samples: Standard solution and Sample solution
Calculate the percentage of caffeine (C8H10N4O2) in the portion of Caffeine taken:

Result = (rU/rS) × (CS/CU) × 100

rU = peak response of caffeine from the Sample solution

[Link]
2/14/25, 2:04 AM USP-NF Caffeine
[Link]
rS = peak response of caffeine from the Standard solution

CS = concentration of USP Caffeine RS in the Standard solution (mg/mL)

CU = concentration of Caffeine in the Sample solution (mg/mL)

Acceptance criteria: 98.5%–101.0% on the anhydrous basis

IMPURITIES
• Residue on Ignition 〈281〉: NMT 0.1%
• Organic Impurities
Mobile phase, Standard solution, Sample solution, Chromatographic system, and System suitability: Proceed as directed in the Assay.
Analysis
Sample: Sample solution
Calculate the percentage of each impurity in the portion of Caffeine taken:

Result = (rU/rT) × 100

rU = peak response for each impurity from the Sample solution

rT = sum of the responses of all the peaks from the Sample solution

Acceptance criteria
Individual impurities: NMT 0.1%
Total impurities: NMT 0.1%

SPECIFIC TESTS
• Water Determination, Method III〈921〉: Dry a sample at 80° for 4 h: the anhydrous form loses NMT 0.5% of its weight, and the hydrous form
loses NMT 8.5% of its weight.

ADDITIONAL REQUIREMENTS
L
• Packaging and Storage: Preserve hydrous Caffeine in tight containers. Preserve anhydrous Caffeine in well-closed containers.
IA
• Labeling: Label it to indicate whether it is anhydrous or hydrous.
• USP Reference Standards 〈11〉
USP Caffeine RS
IC

Auxiliary Information - Please check for your question in the FAQs before contacting USP.

Topic/Question Contact Expert Committee

CAFFEINE Documentary Standards Support SM52020 Small Molecules 5


FF

Chromatographic Database Information: Chromatographic Database


O

Most Recently Appeared In:


Pharmacopeial Forum: Volume No. 49(2)

Current DocID: GUID-A1199B07-4EA5-476C-ADC6-EF9D4E9231B1_4_en-US


DOI: [Link]
DOI ref: dn2lv

[Link]

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