ASTM D6512 - 07(2014)

    Standard Practice for Interlaboratory Quantitation Estimate

    Active Standard ASTM D6512 | Developed by Subcommittee: D19.02

    Book of Standards Volume: 11.01


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    ASTM D6512

    Significance and Use

    5.1 Appropriate application of this practice should result in an IQE achievable by most laboratories properly using the test method studied. That is, most laboratories should be capable of measuring concentrations greater than IQEZ % with RSD = Z % or less. The IQE provides the basis for any prospective use of the test method by qualified laboratories for reliable quantitation of low-level concentrations of the same analyte as the one studied in this practice, and same media (matrix).

    5.2 The IQE values may be used to compare the quantitation capability of different methods for analysis of the same analyte in the same matrix. The IQE is not an indicator of individual laboratory performance.

    5.3 The IQE procedure should be used to establish the interlaboratory quantitation capability for any application of a method where interlaboratory quantitation is important to data use. The intent of the IQE is not to set reporting limits.

    1. Scope

    1.1 This practice establishes a uniform standard for computing the interlaboratory quantitation estimate associated with Z % relative standard deviation (referred to herein as IQEZ %), and provides guidance concerning the appropriate use and application. The calculations involved in this practice can be performed with DQCALC, Microsoft Excel-based software available from ASTM.2

    1.2 IQEZ % is computed to be the lowest concentration for which a single measurement from a laboratory selected from the population of qualified laboratories represented in an interlaboratory study will have an estimated Z % relative standard deviation (Z % RSD, based on interlaboratory standard deviation), where Z is typically an integer multiple of 10, such as 10, 20, or 30, but Z can be less than 10. The IQE10 % is consistent with the quantitation approaches of Currie (1)3 and Oppenheimer, et al. (2).

    1.3 The fundamental assumption of the collaborative study is that the media tested, the concentrations tested, and the protocol followed in the study provide a representative and fair evaluation of the scope and applicability of the test method as written. Properly applied, the IQE procedure ensures that the IQE has the following properties:

    1.3.1 Routinely Achievable IQE Value—Most laboratories are able to attain the IQE quantitation performance in routine analyses, using a standard measurement system, at reasonable cost. This property is needed for a quantitation limit to be feasible in practical situations. Representative laboratories must be included in the data to calculate the IQE.

    1.3.2 Accounting for Routine Sources of Error—The IQE should realistically include sources of bias and variation that are common to the measurement process. These sources include, but are not limited to: intrinsic instrument noise, some “typical” amount of carryover error; plus differences in laboratories, analysts, sample preparation, and instruments.

    1.3.3 Avoidable Sources of Error Excluded—The IQE should realistically exclude avoidable sources of bias and variation; that is, those sources that can reasonably be avoided in routine field measurements. Avoidable sources would include, but are not limited to: modifications to the sample; modifications to the measurement procedure; modifications to the measurement equipment of the validated method, and gross and easily discernible transcription errors, provided there was a way to detect and either correct or eliminate them.

    1.4 The IQE applies to measurement methods for which calibration error is minor relative to other sources, such as when the dominant source of variation is one of the following:

    1.4.1 Sample Preparation, and calibration standards do not have to go through sample preparation.

    1.4.2 Differences in Analysts, and analysts have little opportunity to affect calibration results (as is the case with automated calibration).

    1.4.3 Differences in Laboratories  (for whatever reasons), perhaps difficult to identify and eliminate.

    1.4.4 Differences in Instruments  (measurement equipment), such as differences in manufacturer, model, hardware, electronics, sampling rate, chemical processing rate, integration time, software algorithms, internal signal processing and thresholds, effective sample volume, and contamination level.

    1.5 Data Quality Objectives—Typically, one would compute the lowest % RSD possible for any given dataset for a particular method. Thus, if possible, IQE10 % would be computed. If the data indicated that the method was too noisy, one might have to compute instead IQE20 %, or possibly IQE30 %. In any case, an IQE with a higher % RSD level (such as IQE50 %) would not be considered, though an IQE with RSD <10 % (such as IQE1 % ) would be acceptable. The appropriate level of % RSD may depend on the intended use of the IQE.


    2. Referenced Documents (purchase separately) The documents listed below are referenced within the subject standard but are not provided as part of the standard.

    ASTM Standards

    D2777 Practice for Determination of Precision and Bias of Applicable Test Methods of Committee D19 on Water

    D6091 Practice for 99 %/95 % Interlaboratory Detection Estimate (IDE) for Analytical Methods with Negligible Calibration Error

    E1763 Guide for Interpretation and Use of Results from Interlaboratory Testing of Chemical Analysis Methods


    ICS Code

    ICS Number Code 03.120.20 (Product and company certification. Conformity assessment)

    UNSPSC Code

    UNSPSC Code


    DOI: 10.1520/D6512

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