Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
Reaction mass of [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aR,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate and [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
EC number: 953-451-9 | CAS number: -
- 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 (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2002-08-05 to 2002-09-19
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 002
- Report date:
- 2002
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Test performed in 2002.
LLNA method (OECD 442 B) was adopted in 2010.
Test material
- Reference substance name:
- Reaction mass of [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aR,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate and [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
- EC Number:
- 953-451-9
- Molecular formula:
- C48H78O20
- IUPAC Name:
- Reaction mass of [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aR,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate and [(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
- Details on test material:
- Container: plastic box (n=6)
Form: powder
Quantity: 180.19g (Container + Content)
Colour: white
Batch: 001
Storage: room temperature
Purity: 99.8% · CAS n°: 34540-22-2
Code number: PH-02/0203
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- male
- Details on test animals and environmental conditions:
- 15 male albino guinea pigs of Dunkin-Hartley strain, supplied by Centre de Production Animale (F-
45160 Olivet) were exposed to the test product after a 5-day acclimatisation period. For the main study, the animals weighted between 275g and 342g at the beginning of the test.
The environmental parameters were:
- Temperature: between 19 °C and 23°C
- Relative humidity: between 47% and 60%
Study design: in vivo (non-LLNA)
Induction
- Route:
- intradermal and epicutaneous
- Vehicle:
- other:
- Concentration / amount:
- 1st induction:
- 2 intradermal injections of the product diluted at 20% in an ethanol/distilled water (20/80: v/v) solution.
- 2 intradermal injections of Freund’s Complete Adjuvant diluted at 50% in a physiological saline solution.
- 2 intradermal injections of a mixture with equal volumes - Freund’s Complete Adjuvant at 50% and the product diluted at 40% in a ethanol/distilled water (20/80: v/v) solution.
Weighing of animals.
2nd induction: topical application, on the same zone, with the product at 100%, 24 hours after brushing with 0.5 ml of a solution of Sodium lauryl sulfate at 10%.
Challenge
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- water
- Concentration / amount:
- Challenge phase: topical application under occlusive dressing at the following concentrations : 100% and 50%.
- No. of animals per dose:
- Negative control: 5 mal guinea pigs identified n°C7276 to C7280
Treated: 10 male guinea pigs identified n°C7281 to C7290 - Details on study design:
- 1) Preliminary studies:
- Maximum Non Necrotizing Concentration (M.N.N.C.) determination:
2 female guinea pigs identified n°C7259 to C7260 were used.
The test product was injected by intradermal route at the following concentrations: 25%, 12.5%, 6.25% and 3.125% diluted in distilled water, 12.5% and 6.25% diluted in paraffin oil and 20% and 10% diluted in ethanol/distilled water (20/80; v/v).
- Pre-Maximum Non Irritant Concentration (M.N.I.C.) determination:
2 female guinea pigs identified n°C7259 to C7260 were used.
The product was applied under an occlusive dressing during 24 hours, at the following concentrations pure and diluted 50%, 25% and 12.5% in distilled water.
- Maximum Non Irritant Concentration (M.N.I.C.) determination:
3 female guinea pigs identified n° C7265 to C7267 were used.
After induction by intradermal injection with ethanol/distilled water (20/80: v/v) solution and by topical application with ethanol/distilled water (20/80: v/v) solution and a 17-days rest phase, the challenge phase under occlusive dressing for 24 hours consists in a single topical application of the test product at the following concentrations: 100%, diluted 50%, 25% and 12.5% in ethanol/distilled water (20/80: v/v) solution.
2) Main study
GROUP 1 (negative control) : 5 male guinea pigs identified n° C7276 to C7280;
GROUP 2 (treated) : 10 male guinea pigs identified n° C7281 to C7290;
Note : The results of the 3 latest positive group (Reference substance : neomycin sulfate Test 6 and benzocaïne Test 4 and 5) carried out as method sensibility, were presented in appendix.
The environmental parameters were :
- Temperature : between 19 °C and 23°C
- Relative humidity : between 47% and 60%
* Chronological development:
a) Preliminary studies:
2002/08/01: Arrival of animals.
2002/08/05 to 2002/09/04: Preliminary tests : pre MNIC, MNNC, and MNIC determinations.
b) Main study:
2002/08/20: Arrival of animals.
Induction phase
2002/08/25: 1st induction:
- 2 intradermal injections of the product diluted at 20% in an ethanol/distilled water (20/80: v/v) solution.
- 2 intradermal injections of Freund’s Complete Adjuvant diluted at 50% in a physiological saline solution.
- 2 intradermal injections of a mixture with equal volumes - Freund’s Complete Adjuvant at 50% and the product diluted at 40% in a ethanol/distilled water (20/80: v/v) solution.
2002/08/25: Weighing of animals.
2002/08/30: 2nd induction: topical application, on the same zone, with the product at 100%, 24 hours after brushing with 0.5 ml of a solution of Sodium lauryl sulfate at 10%.
2002/09/01 to 2002/09/16: Rest phase: 15 days
2002/09/1:6 Challenge phase: topical application under occlusive dressing at the following concentrations : 100% and 50%.
2002/09/17: 24-hours reading time.
2002/09/18: 48-hours reading time and weighing. - Challenge controls:
- Main study:
2002/08/20: Arrival of animals.
Induction phase
2002/08/25: 1st induction:
- 2 intradermal injections of the product diluted at 20% in an ethanol/distilled water (20/80: v/v) solution.
- 2 intradermal injections of Freund’s Complete Adjuvant diluted at 50% in a physiological saline solution.
- 2 intradermal injections of a mixture with equal volumes - Freund’s Complete Adjuvant at 50% and the product diluted at 40% in a ethanol/distilled water (20/80: v/v) solution.
2002/08/25: Weighing of animals.
2002/08/30: 2nd induction: topical application, on the same zone, with the product at 100%, 24 hours after brushing with 0.5 ml of a solution of Sodium lauryl sulfate at 10%.
2002/09/01 to 2002/09/16: Rest phase: 15 days
2002/09/1:6 Challenge phase: topical application under occlusive dressing at the following concentrations : 100% and 50%.
2002/09/17: 24-hours reading time.
2002/09/18: 48-hours reading time and weighing. - Positive control substance(s):
- yes
- Remarks:
- Neomycin sulfate Benzocaine
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 100%
- No. with + reactions:
- 1
- Total no. in group:
- 5
- Clinical observations:
- Skin reaction
Score 1: 1
Score 2: 0
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 100%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 5
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 100%
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction
Score 1: 1
Score 2: 0
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 100%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 50%
- No. with + reactions:
- 3
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction
Score 1: 3
Score 2: 0
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 50%
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 25%
- No. with + reactions:
- 9
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 6th test)
Score 1: 4
Score 2: 5
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 25%
- No. with + reactions:
- 7
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 6th test)
Score 1: 2
Score 2: 5
Score 3: 0
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 12.5%
- No. with + reactions:
- 9
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 4th test)
Score 1: 4
Score 2: 5
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 12.5%
- No. with + reactions:
- 7
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 4th test)
Score 1: 2
Score 2: 5
Score 3: 0
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 12.5%
- No. with + reactions:
- 9
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 5th test)
Score 1: 5
Score 2: 4
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 12.5%
- No. with + reactions:
- 8
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 5th test)
Score 1: 3
Score 2: 5
Score 3: 0
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 6.25%
- No. with + reactions:
- 9
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 5th test)
Score 1: 5
Score 2: 4
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 6.25%
- No. with + reactions:
- 8
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 5th test)
Score 1: 3
Score 2: 5
Score 3: 0
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 75%
- No. with + reactions:
- 6
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 6th test)
Score 1: 2
Score 2: 4
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 75%
- No. with + reactions:
- 5
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 6th test)
Score 1: 1
Score 2: 4
Score 3: 0
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- 38%
- No. with + reactions:
- 6
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 6th test)
Score 1: 3
Score 2: 3
Score 3: 0
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- 38%
- No. with + reactions:
- 6
- Total no. in group:
- 10
- Clinical observations:
- Skin reaction (treated group 6th test)
Score 1: 2
Score 2: 4
Score 3: 0
Any other information on results incl. tables
Concentrations selected
Preliminary studies:
- MNNC determination :
No necrosis has been observed since the concentrations of 20% (dilution in ethanol/distilled water (20/80: v/v) solution), the first induction has been carried out by intradermal injection at the same concentration.
-Pre MNIC determination :
24 hours after the removal of the occlusive dressings, no macroscopic cutaneous reaction was recorded.
In view of these results, the concentrations selected were pure for the 2nd induction of the main study and the MNIC began at the concentration of 100%.
- MNIC determination :
24 hours after removal of the occlusive dressings, no cutaneous reaction was recorded.
In view of this result, the concentrations selected were 100% (MNIC) and 50% (1/2 MNIC) for the challenge phase.
Main study :
- induction phase :
The induction phase was performed by intradermal injection at D0 with the test product diluted at 20% in an ethanol/distilled water (20/80: v/v) solution and by topical application at D7 with the test product at 100%, after brushing with a solution of sodium lauryl sulfate.
- challenge phase :
The test product has been used pure and diluted at 50% in an ethanol/distilled water (20/80: v/v) solution (1/2 MNIC).
Sensitising potential assessment
No macroscopic cutaneous reactions attributable to allergy was recorded during the examinationfollowing the removal of the occlusive dressings (challenge phase) from the animals of the treated group with the test product.
No cutaneous intolerance reaction was recorded in animals from the negative control group.
Weight evolution
Not any abnormality was recorded in the weight growth of both groups.
Applicant's summary and conclusion
- Interpretation of results:
- other: not classified
- Conclusions:
- In view of these results, under these experimental conditions, the product MADECASSOSIDE, in accordance with the criteria for classification, packaging and labelling of dangerous substances of the E.E.C. Directives 67/548 and 99/45, must not be classified.
- Executive summary:
After induction (intradermic injection and topical application) of 10 animals (male) of treated group with the test product MADECASSOSIDE and a 15-days rest phase, the challenge phase, under occlusive dressing for 24 hours, consisted to a single topical application of the test product at 100% and diluted at 50% in an ethanol/distiller water solution (20/80, v/v), according to the experimental
protocol established from the O.E.C.D. guideline n°406 dated July 17th, 1992 and the method B.6 of the E.E.C. n°96/54 dated July 30th, 1996.No macroscopic cutaneous reactions attributable to allergy was recorded during the examinationfollowing the removal of the occlusive dressing (challenge phase) from the animals of the treated group with the test product.
No cutaneous intolerance reaction was recorded in animals from the negative control group.
In conclusion, in view of these results, under these experimental conditions, the product MADECASSOSIDE, must not be classified and in accordance with the criteria for classification, packaging and labelling of dangerous substances of the E.E.C. Directives 67/548 and 99/45.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.