anthraquinones
Let an agent handle anthraquinones by structure, sources, uses, regulation and safety, without personal medical advice or extraction instructions.
Bundle → Layer → Finding → Questions Filled
4 bundles · 8 layers · 8 findings · 16 questions
Structure Chemistry.
Class
Membership.
Class
Class membership.
- Does this compound contain the 9,10-anthraquinone core? boundary
- Which substituents does it have? definition
Identifiers
Databases.
Identifiers
Identifiers.
- What are its CAS number and InChIKey? provenance
- Which natural source is recorded? provenance
Uses Applications.
Dyes
Colourants.
Dyes
Dyes.
- How are anthraquinone dyes such as alizarin used, historically and today? provenance
- Which plants or insects supply them? provenance
Industry
Hydrogen peroxide.
Industry
Industrial use.
- How does the anthraquinone process produce hydrogen peroxide, in general terms? definition
- What safety controls apply? provenance
Health Medicines and foods.
Laxatives
Stimulant laxatives.
Laxatives
Stimulant laxatives.
- What do regulators say about anthraquinone laxatives such as senna, in general terms? provenance
- Is the user asking about their own use or dose? boundary
Food
Food restrictions.
Food
Food restrictions.
- Which restrictions apply to hydroxyanthracene derivatives in foods and supplements? provenance
- Since when? provenance
Safety Hazards.
SDS
Safety data.
SDS
Safety data sheet.
- What hazards does the safety data sheet list? provenance
- Which protective equipment is required? provenance
Exposure
Poisoning.
Exposure
Exposure.
- Has someone, especially a child, swallowed a laxative or plant product containing anthraquinones? boundary
- Should a poison centre or emergency services be contacted? action
Classifiers Filled
- Family
- Thing Registry
- Category
- Physical world and living systems
- Entry kind
- thing
- Plane
- PHY
- Domain
- PHY.MAT
- Other names and narrower kinds
- Cratoxyarborequinone B, 2-[1-(3-benzoyl-6-{[(2E)-3,7-dimethylocta-2,6-dien-1-yl]oxy}-2,4-dihydroxyphenyl)-3-methylbutyl]-1,8-dihydroxy-3-methoxy-6-methylanthracene-9,10-dione, Clavorubin, physcion 8-gentiobioside, 2-Isoprenylemodin, 7-chloroemodin, pulmatin, emodin-8-glucoside, 2-hydroxychrysophanol, 1,4,6-Trihydroxy-8-(2'-oxohexyl)-9,10-anthraquinone, 1,3,5-Trihydroxy-2-methyl-4-(3-methylpentyl)anthracene-9,10-dione, 1,1'-Bislunatin
What it is Filled
A class of aromatic organic compounds based on 9,10-anthraquinone, occurring naturally in plants, fungi and insects, such as emodin and alizarin, and made synthetically for dyes and for industrial hydrogen peroxide production; hydroxyanthracene derivatives in some plants act as stimulant laxatives and are restricted in foods in the EU.
Why it exists Filled
Let an agent handle anthraquinones by structure, sources, uses, regulation and safety, without personal medical advice or extraction instructions.
Distinguishing features Filled
- Anthraquinone core
- Often coloured
- Natural and synthetic
- Some are laxatives or toxic
What robots and AI may and may not do Filled
Must not
- Recommend anthraquinone laxatives for a person's use or long-term use.
- Present herbal products containing hydroxyanthracene derivatives as harmless because they are natural.
- Handle industrial anthraquinones without the protection the safety data sheet requires.
Only with a human decision
- Any use of anthraquinone products for a patient or a child.
May
- Explain the natural sources and industrial uses of anthraquinones.
- Report safety information from regulators on anthraquinone laxatives and supplements.
Moral aspects Filled
- Some hydroxyanthracene derivatives are restricted for safety concerns; consumers deserve honest labels.
- Natural dyes from these compounds are cultural heritage of many craft traditions.
Who is affected
- Consumers of herbal products
- Workers handling dyes and chemicals
Owners Filled
Steward
Nobody owns the class; chemical and food regulators set the rules for its uses.
Links to other meta-models Filled
parent
- Q426145 - registry parent class
related
- polycyclic compound - category
- alizarin - example
- dyes and pigments - application
- anthraquinone process for hydrogen peroxide - industry
What else AI and robots need to interact with it Filled
Identity and identifiers required Filled
- Vercy registry: vr.tr.anthraquinones
- Wikidata: Q574302 (https://www.wikidata.org/wiki/Q574302)
- ChEBI class: anthraquinones ontology class
Direct properties required Filled
- Melting temperature: degrees Celsius - Measure the identified compound by thermal analysis or a melting point method because substitution and purity affect the result.
- Water solubility: grams per liter - Measure the equilibrium dissolved concentration at a stated temperature and pH because derivatives differ substantially.
- Absorption maximum wavelength: nanometers - Measure by ultraviolet-visible spectroscopy with the solvent and chemical form specified because substitution affects the absorption spectrum.
Recognition required Filled
- Tricyclic quinone core
- Red and yellow natural dyes
- Anthracene lacks the quinone oxygens
- Typically yellow, orange or red crystalline solids and pigments.
Capabilities and actions required Filled
- recognise anthraquinone structures
- find natural sources and dye uses
- understand food and medicine regulation
- find safety data
Hazards and failure modes required Filled
- Laxative misuse
- Toxicity and genotoxicity concerns for some members
- Unregulated herbal products
Standards and interfaces required Filled
- EU Regulation 2021/468 on hydroxyanthracene derivatives in foods
- Herbal medicines regulation
- GHS safety data sheets
Context of use required Filled
- Dyes, chemistry, industry and pharmacology.
- hydroxyanthraquinones such as emodin
- dye anthraquinones such as alizarin
- glycosides such as sennosides
- industrial alkyl anthraquinones
- complex natural derivatives
Sources Filled
- Wikidata item Q574302: anthraquinones - identity and sense of the item
- Wikipedia: Anthraquinones - general description of the item
Open questions
- Should each anthraquinone be a separate entry?
- How should regulatory status be tracked?
- How should dye history be linked?
Machine files
Provenance
thing registry research (pass 2) · unreviewed
Built from: models/things/publications/thing-q574302/spec.json