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PHR1927

Supelco

Lopinavir

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(s):

Lopinavir

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50 ML
CN¥902.44
100 ML
CN¥1,530.28
250 ML
CN¥2,602.91
500 ML
CN¥3,473.26
1 L
CN¥4,893.91

CN¥902.44

Estimated to ship onApril 07, 2025Details

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All Photos(1)

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50 ML
CN¥902.44
100 ML
CN¥1,530.28
250 ML
CN¥2,602.91
500 ML
CN¥3,473.26
1 L
CN¥4,893.91

About This Item

Empirical Formula (Hill Notation):
C37H48N4O5
CAS Number:
192725-17-0
Molecular Weight:
628.80
UNSPSC Code:
41116107
NACRES:
NA.24

CN¥902.44

Estimated to ship onApril 07, 2025Details

Request a Bulk Order

biological source

synthetic

Quality Level

300

grade

certified reference material
pharmaceutical secondary standard

Agency

BP
EP
USP
traceable to Ph. Eur. Y0001498
traceable to USP 1370101

API family

lopinavir

form

powder

CofA

current certificate can be downloaded

packaging

pkg of 1 g

storage condition

protect from light

color

white to off-white

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assay

≥99.9%

assay

-

assay

≥99.5%

assay

-

technique(s)

DNA sequencing: suitable, transfection: suitable, PCR: suitable

technique(s)

cell culture | hybridoma: suitable, cryopreservation: suitable

technique(s)

PCR: suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

Quality Level

200

Quality Level

400

Quality Level

200

Quality Level

300

solubility

H2O: miscible (completely)

solubility

H2O: miscible (completely)

solubility

H2O: miscible (completely)

solubility

-

form

liquid

form

liquid

form

liquid

form

-

General description

Lopinavir is an antiretroviral agent and a protease inhibitor indicated for the management of human immunodeficiency virus (HIV) infection.[1][2] It is a key component of Kaletra, the co-formulation of lopinavir and ritonavir.[3]
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.

Application

Lopinavir may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations[1] and clinical plasma samples[4] by chromatography techniques.
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Analysis Note

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

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Footnote

To see an example of a Certificate of Analysis for this material enter LRAB1665 in the Documents slot below. This is an example certificate only and may not be the lot that you receive.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

  • Specification Sheet

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number

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    Determination of 19 antiretroviral agents in pharmaceuticals or suspected products with two methods using high-performance liquid chromatography
    Rebiere H, et al.
    Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 850(1-2), 376-383 (2007)
    Simultaneous determination of indinavir, ritonavir and lopinavir (ABT 378) in human plasma by high-performance liquid chromatography
    Ray J, et al.
    Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 775(2), 225-230 (2002)
    Validation and application of a high-performance liquid chromatography-tandem mass spectrometric method for simultaneous quantification of lopinavir and ritonavir in human plasma using semi-automated 96-well liquid-liquid extraction
    Wang PG, et al.
    Journal of Chromatography A, 1130(2), 302-307 (2006)
    Therapeutic drug monitoring of lopinavir/ritonavir in pregnancy
    Lambert JS, et al.
    HIV Medicine, 12(3), 166-173 (2011)

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