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EC number: 700-363-1 | CAS number: 1335203-20-7
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2010-02-01 to 2010-02-1
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 010
- Report date:
- 2010
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 429 (Skin Sensitisation: Local Lymph Node Assay)
- Version / remarks:
- Method B42 Skin Sensitisation
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- mouse local lymph node assay (LLNA)
Test material
- Reference substance name:
- (6E)-3,13-diethylpentadec-6-ene; (6E)-tetradec-6-ene; (7E)-hexadec-7-ene; (8E)-nonadec-8-ene; 2-[(6E)-3,13-diethylpentadec-6-en-8-yl]butanedioic acid; 2-[(8E)-nonadec-8-en-7-yl]butanedioic acid; 2-[(8E)-tetradec-8-en-7-yl]butanedioic acid; 2-[(9E)-hexadec-9-en-8-yl]butanedioic acid
- EC Number:
- 700-363-1
- Cas Number:
- 1335203-20-7
- IUPAC Name:
- (6E)-3,13-diethylpentadec-6-ene; (6E)-tetradec-6-ene; (7E)-hexadec-7-ene; (8E)-nonadec-8-ene; 2-[(6E)-3,13-diethylpentadec-6-en-8-yl]butanedioic acid; 2-[(8E)-nonadec-8-en-7-yl]butanedioic acid; 2-[(8E)-tetradec-8-en-7-yl]butanedioic acid; 2-[(9E)-hexadec-9-en-8-yl]butanedioic acid
- Details on test material:
- - Name of test material : Hydrolysed reaction products of furan-2,5-dione and C15-18-(linear and branched)-alkenes
- Physical state: Amber coloured extremely viscous liquid
- Lot/batch No.: AF405
- Expiration date of the lot/batch: 31 December 2010
- Storage condition of test material: room temperature in the dark
Constituent 1
In vivo test system
Test animals
- Species:
- mouse
- Strain:
- other: CBA/CaOlaHsd
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Harlan Laboratories UK Limited, Bicester, Oxon, UK
- Age at study initiation: 15 - 23 g
- Weight at study initiation: 8 - 12 weeks old
- Housing: Individually housed in suspended solid floor polypropylene cages furnished with softwood woodflakes
- Diet (e.g. ad libitum): 2014 Teklad Global Rodent diet
- Water (e.g. ad libitum): Tap water
- Acclimation period:at least five days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 19 - 25°C
- Humidity (%): 30 - 70%
- Air changes (per hr): 15 changes per hour
- Photoperiod (hrs dark / hrs light): 12 hour light/ 12 hour dark
IN-LIFE DATES: From: February 2010 To: 17 February 2010
Study design: in vivo (LLNA)
- Vehicle:
- acetone/olive oil (4:1 v/v)
- Concentration:
- 0, 10, 25 and 50% in acetone/olive oil 4:1
- No. of animals per dose:
- Preliminary dose: one mouse
Main test: four mice/dose - Details on study design:
- RANGE FINDING TESTS:
- Compound solubility: The test substance is expected to be soluble in acetone/olive oil
- Irritation: Clinical observations, bodyweight and mortality were recorded
MAIN STUDY
ANIMAL ASSIGNMENT AND TREATMENT
- Name of test method:
- Criteria used to consider a positive response: Sensitiser if at least one concentration of the test material results in a threefold or greater increase in 3HTdR incorporation compared to control values. Any test material failing to produce a threefold or greater increase in 3HTdR incorporation will be classified as a "non sensitiser".
- Lymph node proliferation response: Number of radioactive disintegration per minute per lymph node and as the ratio of 3HTdR incorporation into lymph node cells of test nodes relative to that recorded for the control nodes (Stimulation Index)
TREATMENT PREPARATION AND ADMINISTRATION:
Groups of four mice were treated with the test material at concentrations of 50%, 25% or 10% w/w in acetone/olive oil 4:1. The mice were treated by daily application of 25 µl of the appropriate concentration of the test material to the dorsal surface of each ear for three consecutive days (Days 1, 2, 3). Five days following the first topical application of the test material or vehicle (Day 6) the surviving mice were injected via the tail vein with 250 µl of phosphate buffered saline (PBS) containing 3H methyl thymidine (3HTdR: 80 µCi/ml, specific activity 2.0 Ci/mmol, ARC UK Ltd) giving a total of 20 µCi to each mouse. Five hours later, the mice were killed and the draining auricular lymph nodes from the surviving mice were excised, collected and prepared for analysis of the disintegration per minute of 3H-methyl thymidine by scintillation counting. - Positive control substance(s):
- hexyl cinnamic aldehyde (CAS No 101-86-0)
- Statistics:
- Not applicable
Results and discussion
- Positive control results:
- The Stimulation Index expressed as the mean radioactive incorporation for the treatment group divided by the mean radioactive incorporation of the vehicle control group is 3.12 for Hexylcinnamaldehyde, tech., 85% in acetone/olive oil (4:1). Based on this result, it is concluded that it is a sensitiser.
In vivo (LLNA)
Resultsopen allclose all
- Parameter:
- SI
- Value:
- 6.65
- Test group / Remarks:
- 10% DCI-30.n w/w in acetone/olive oil (4:1)
- Parameter:
- SI
- Value:
- 7.2
- Test group / Remarks:
- 25% DCI-30.n w/w in acetone/olive oil (4:1)
- Parameter:
- SI
- Value:
- 9.02
- Test group / Remarks:
- 50% DCI-30.n w/w in acetone/olive oil (4:1)
- Parameter:
- other: disintegrations per minute (DPM)
- Value:
- 64 063.33
- Test group / Remarks:
- 10% DCI-30.n w/w in acetone/olive oil (4:1)
- Parameter:
- other: disintegrations per minute (DPM)
- Value:
- 52 001.84
- Test group / Remarks:
- 25% DCI-30.n w/w in acetone/olive oil (4:1)
- Parameter:
- other: disintegrations per minute (DPM)
- Value:
- 86 798.47
- Test group / Remarks:
- 50% DCI-30.n w/w in acetone/olive oil (4:1)
Any other information on results incl. tables
During the preliminary screening test, no signs of systemic toxicity were noted. Mild redness to the ears and neck was reported on Day 3 and on Day 4. Based on this information the dose levels selected for the main test were 50%, 25% and10% w/w in acetone/olive oil 4:1.
During the main study, one animal in the 25% w/w in actone/olive oil group died on day 6. No signs of toxicity were reported in any of the remaining animals. Mild redness to the ears and neck was noted in animals treated with the test material at concentrations of 50% or 25% w/w in acetone/olive oil 4:1.
Applicant's summary and conclusion
- Interpretation of results:
- Category 1 (skin sensitising) based on GHS criteria
- Conclusions:
- The Stimulation Index for the 10% w/w, 25% w/w and 50% w/w Hydrolysed reaction products of furan-2,5-dione and C15-18-(linear and branched)-alkenes concentration in olive oil groups were reported to be 6.65, 7.20 and 9.02. The test is considered to be a sensitiser since the Stimulation Index is greater than 3. It is classified as a skin sensitiser Category 1 and assigned the hazard statement H317 "May cause an allergic skin reaction" according to Regulation (EC) No 1272/2008.
- Executive summary:
In a preliminary study, one mouse was treated with a 50% w/w Hydrolysed reaction products of furan-2,5-dione and C15-18-(linear and branched)-alkenes in acetone/olive oil (4:1). No clinical signs were reported and this dose was selected as the highest dose in the main test of the Local Lymph Node Assay. Hydrolysed reaction products of furan-2,5-dione and C15-18-(linear and branched)-alkenes was applied to the dorsal surface of each ear of three groups of four mice at the following concentration 50% w/w, 25% w/w and 10% w/w Hydrolysed reaction products of furan-2,5-dione and C15-18-(linear and branched)-alkenes in acetone/olive oil (4:1). A negative control was only treated with acetone/olive oil (4:1).
The applications were made for three consecutive days (Days 1, 2 and 3). Five days after the first topical application, the mice were injected 250 µl of phosphate buffered saline (PBS) containing3H-methyl thymidine. Five hours later, the mice were killed and the draining auricular lymph nodes from the surviving mice were excised, collected and prepared for analysis of the disintegration per minute of 3H-methyl thymidine by scintillation counting. The proliferation of lymph node cells was expressed as the number of radioactive disintegrations per minute per lymph node (disintegration perminute/node) and as the ration of 3HTdR incorporation into lymph node cells of test nodes relative to that recorded for the control nodes (Stimulation Index).
During the preliminary screening test, no signs of systemic toxicity were noted. Mild redness to the ears and neck was reported on Day 3 and on Day 4. Based on this information the dose levels selected for the main test were 50%, 25% and10% w/w in acetone/olive oil 4:1. During the main study, one animal in the 25% w/w in acetone/olive oil group died on day 6. No signs of toxicity were reported in any of the remaining animals.Mild redness to the ears and neck was noted in animals treated with the test material at concentrations of 50% or 25% w/w in acetone/olive oil 4:1. Bodyweight changes of the test animals between Day 1 and Day 6 were comparable to those observed in the corresponding control group animals over the same period.
The Stimulation Index for the 10% w/w, 25% w/w and 50% w/w Hydrolysed reaction products of furan-2,5-dione and C15-18-(linear and branched)-alkenes concentration in olive oil groups were reported to be 6.65, 7.20 and 9.02. The test is considered to be a sensitiser since the Stimulation Index is greater than 3. It is classified as a skin sensitiser Category 1 and assigned the hazard statement H317 "May cause an allergic skin reaction" according to Regulation (EC) No 1272/2008.
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