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EC number: 203-232-2 | CAS number: 104-74-5
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Sensitisation data (human)
Administrative data
- Endpoint:
- sensitisation data (humans)
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1987
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 987
- Report date:
- 1987
Materials and methods
- Type of sensitisation studied:
- skin
- Study type:
- case report
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Case report. Patch test with the European standard series (ICDRG) and lauryl pyridinium chloride 0.1% aqueous solution, amongst other substances (ingredients of a hair conditioner).
- GLP compliance:
- no
Test material
- Reference substance name:
- 1-dodecylpyridinium chloride
- EC Number:
- 203-232-2
- EC Name:
- 1-dodecylpyridinium chloride
- Cas Number:
- 104-74-5
- Molecular formula:
- C17H30N.Cl
- IUPAC Name:
- 1-dodecylpyridin-1-ium chloride
- Test material form:
- solid
Constituent 1
Method
- Type of population:
- general
- Ethical approval:
- not specified
- Subjects:
- - Number of subjects exposed: 1
- Sex: male
- Age: 28 - Clinical history:
- - History of allergy or casuistics for study subject or populations:
- Symptoms: recurrent itchy dermatitis on the left side of the chest and adjacent area of the arm.
- Exposure history: the patient had noted that the eruption alsways developed after his wife had used a hair conditioner and rested hear head in the area when sleeping. - Controls:
- 23 healthy patients
- Route of administration:
- dermal
- Details on study design:
- TYPE OF TEST(S) USED: patch test (epicutaneous test). No further details.
Results and discussion
- Results of examinations:
- SYMPTOMS
- Frequency, level, duration of symptoms observed: recurrent itchy dermatitis, that disappeared after exposure was discontinued.
NO. OF PERSONS WITH/OUT REACTIONS COMPARED TO STUDY POPULATION
- Number of subjects with positive reactions: the test subject and 1/23 control patients
- Number of subjects with negative reactions: 16/23 control patients
- Number of subjects with equivocal reactions: 6/23 control patients
RESULT OF CASE REPORT: In the tes subject, a positive reaction was found to lauryl pyridinium chloride 0.1% aq. (48h +, 72h ++), but not to 0.01% aq. Of 23 controls tested with lauryl pyridinium chloride 0.1% aq., 16 were negative, 6 had an equivocal reaction, and 1 had a positive reaction. Control tests indicated a delayed time course of irritation. The strength and appearance of the patch test reaction compared to the controls, and the patient's clinical features favoured an allergic mechanism.
Applicant's summary and conclusion
- Conclusions:
- Based on the available data, the test item may cause allergic contact dermatitis.
- Executive summary:
A 28-year-old male presented recurrent itchy dermatitis on the left side of the chest and adjacent area of the arm, where his wife usually rested her head when sleeping. The patient had noted that the eruption always developed after his wife had used a hair conditioner. The patient was subjected to patch tests with the European standard series (ICDRG), the hair conditioner, and later, its ingredients, separately. A positive reaction was found to lauryl pyridinium chloride 0.1% aq. (48h +, 72h ++), but not to 0.01% aq. Of 23 controls tested with lauryl pyridinium chloride 0.1% aq., 16 were negative, 6 had an equivocal reaction, and 1 had a positive reaction. Control tests indicated a delayed time course of irritation. The strength and appearance of the patch test reaction compared to the controls, and the patient's clinical features favoured an allergic mechanism. Based on the available data, the test item may cause allergic contact dermatitis.
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