ENDOCRINE DISRUPTING CHEMICALS

Environmental Hormones Panel

Endocrine Disrupting Chemicals — Targeted Quantification

Environmental hormones (endocrine disruptors)—represented by phthalate metabolites, bisphenols and phenolic compounds—enter the human body through plastics, personal-care products and food packaging; urinary metabolite concentrations are a common exposure metric. This service absolutely quantifies 15+ endocrine-disruptor metabolites for research on reproductive development, metabolic disruption and population exposure assessment.

15+
exposure metabolites
TARGET COMPOUNDS
2
matrices: urine / serum
SAMPLE TYPES
MRM
Isotope-IS Absolute Quantification
ABSOLUTE QUANTIFICATION

Targeted List & Analysis Examples

Targeted List & Analysis Examples
Targeted List (partial)
NO.Chinese NameAbbr.English NameCAS No.
1单甲基酯MMPMonomethylPhthalate4376-18-5
2单乙基酯MEPMonoethylphthalate2306-33-4
3单丁基酯MnBPMonobutylphthalate131-70-4
4单乙基己基酯MEHPMonoethylhexylPhthalate4376-20-9
5单苄基酯MBzPMonobenzylphthalate2528-16-7
6邻苯二甲酸单(3-羧基丙基)酯MCPPMono(3-carboxypropyl)phthalate66851-46-5
7邻苯二甲酸单(2-乙基-5-羟基己基)酯MEHHPMono(2-ethyl-5-hydroxyhexyl)Phthalate40321-99-1
8邻苯二甲酸单(2-乙基-5-酮-己基)酯MEОHPMono(2-ethyl-5-oxohexyl)phthalate40321-98-0
Full list available on request — contact our team.

Technical Specifications

TECHNICAL SPECIFICATIONS
PlatformUHPLC coupled with triple-quadrupole MS (UHPLC-MS/MS)
Ion ModePositive/negative ion switching acquisition
Quantification UnitStandard-curve absolute quantification, ng/mL or ng/g
QCPooled QC samples inserted across the batch to monitor signal drift and stability

Sample Requirements

SAMPLE REQUIREMENTS
Serum / Plasma
50 μL
Tissue
30 mg
Cells
1–5 × 10⁶ cells
Feces / Gut Content
100 mg fresh / 20 mg lyophilized
Urine
50 μL
Exosomes
50 μL
Replicates: cell / microbial samples ≥6 replicates per group; animal samples ≥10 per group; clinical samples ≥50 per group with strictly controlled inclusion criteria. Sampling site, timing and handling must be consistent between experimental and control groups.
Shipping notes: applicable to serum/plasma, various tissues, feces and gut content, urine, saliva, cells / cell culture medium and more. Recommended amounts are for a single experiment — please ship 2–3× the recommended amount; keep sampling sites consistent across groups for tissue samples; ship on dry ice or cold chain.

Workflow

WORKFLOW
1
Consultation
Study goals / panel selection
2
Proposal & Quote
Targets / timeline / agreement
3
Sample Intake
Cold chain / pre-check / labeling
4
Experiment
Acquisition / QC
5
Delivery
Quantification + interpretation + raw data
Deliverables: exposure-metabolite concentrations, detection rates and population-stratified statistics · absolute-quantification table for each metabolite (concentration + units) · group-wise T-test and fold-change analysis · PCA / PLS-DA modeling and hierarchical clustering · KEGG annotation and pathway enrichment · full analysis report and raw data.

Analysis Examples

ANALYSIS EXAMPLES
Example figures are generated from real project data; actual figures and analyses depend on the detection panel and study plan.
T-test Bar Chart
T-test Bar Chart
All metabolites sorted by ascending p-value; grouped bars show group means ± SD with p-values annotated beside the bars.
Hierarchical Clustering Heatmap
Hierarchical Clustering Heatmap
Z-score normalized abundance patterns of all metabolites; rows ordered by hierarchical clustering — red for high, blue for low abundance.
Disease Association Bar Chart
Disease Association Bar Chart
Known metabolite–disease associations mined from HMDB and other databases, ranked by the number of associated metabolites.
Metabolite Abundance Analysis
Metabolite Abundance Analysis
Faceted boxplots of significantly different metabolites between groups; intergroup comparison by Welch's t-test.
Bar Chart Analysis
Bar Chart Analysis
Per-sample bar charts of differential metabolites, visualizing group differences and individual dispersion.

References

REFERENCES
[1] 'T MANNETJE A, COAKLEY J, DOUWES J. Levels and determinants of urinary phthalate metabolites in New Zealand children and adults[J]. International Journal of Hygiene and Environmental Health, 2021, 238: 113853.
[2] LIAO K W, CHANG W H, CHOU W C, et al. Human biomonitoring reference values and characteristics of Phthalate exposure in the general population of Taiwan[J]. International Journal of Hygiene and Environmental Health, 2021, 235: 113769.

Applications

APPLICATIONS
Endocrine-disruptor exposure assessmentEnvironmental-risk research for reproductive healthFood-packaging migrant testingEnvironmental-epidemiology researchChildhood-exposure health effects

FAQ

FAQ
How long does a Environmental Hormones Panel project take?
Mature targeted panels typically take 1-3 weeks; untargeted projects take 2-4 weeks (counted from sample receipt and QC approval). The exact timeline is confirmed in writing before project start, and progress is trackable on the OmicsHub cloud platform.
What if my sample amount is below the recommendation?
Please do not dilute your samples. Low-input samples can often be accommodated by adjusting the preparation workflow — tell us the actual amount and our technical team will assess feasibility and note adjustments in the study plan.
Can I add targets to an existing panel?
Yes. Mature panels support on-demand additions; novel analytes outside the list can be implemented through custom method development (requires standards and extra validation time) — see our Custom Targeted Metabolomics service.
What samples do you need for Environmental Hormones Panel?
Serum/plasma ≥100 μL (fasting, no haemolysis), tissue ≥50 mg (snap-frozen), cells ≥1×10⁶ (medium washed off), urine ≥200 μL. Keep fasting time consistent, aliquot into single-use volumes and avoid freeze–thaw. Full guidance: Technical Resources → Sample Guide.

Delivery timing: sample shipping, customs declaration and similar steps may extend turnaround; actual project timelines prevail.

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