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EC number: 243-900-0 | CAS number: 20592-85-2
- 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
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Endpoint summary
Administrative data
Description of key information
There are no skin sensitisation data available for ATMP-xNa (CAS 20592-85-2, EC No., 243-900-0), therefore data are read-across from the Category members ATMP-xNH4 (CAS 34274-28-7; EC 251-908-0) and ATMP-H (CAS 6419-19-8; EC 229-146-5) and used in a weight of evidence approach.
In the skin sensitisation study, conducted according to OECD Test Guideline 406 and in compliance with GLP, ATMP-xNH4 was not sensitising to the skin of guinea pigs (SafePharm Laboratories, 1995, Reliability 1).
In the skin sensitisation study, conducted according to a protocol similar to OECD Test Guideline 406 but not in compliance with GLP, ATMP-H (without information on active acid content) was not sensitising to the skin of guinea-pigs (Henkel, 1984, Reliability 1).
The key skin sensitisation study on DTPMP acid is included in support of read-across of the reproductive toxicity study on DTPMP (5-7Na) only.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 28.11.1983 to 23.01.1984
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Principles of method if other than guideline:
- Method: Variation of Magnusson and Kligman method.
- GLP compliance:
- no
- Remarks:
- pre-GLP
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- An LLNA study was not performed because there is an existing reliable study for skin sensitisation using the Guinea Pig Maximisation test method.
- Species:
- guinea pig
- Strain:
- Pirbright-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Winkelmann, Borchen
- Weight at study initiation: Average 430 grams for dosed animals, 423 grams for control animals
- Housing: Type 4 Makrolon cages
- Diet: Specialfeed Altromin 3022, ad libitum
- Water: tap water, ad libitum
ENVIRONMENTAL CONDITIONS
- Temperature (°C): ca. 23°C
- Humidity (%): 50-65%
- Photoperiod (hrs dark / hrs light): 12 hours dark / 12 hours light
- Route:
- intradermal
- Vehicle:
- water
- Concentration / amount:
- 5%
- Route:
- other: epicutaneous (need translation)
- Vehicle:
- water
- Concentration / amount:
- 5%
- No. of animals per dose:
- 20
- Details on study design:
- The skin under the shoulder blade was shaved. Only animals with healthy skin were employed. 3 injections were prepared as follows:
A. TEST ANIMALS
1 - Freund's adjuvant, volume: 0.1 mL
2 – 5% test material, volume: 0.1 mL as an aquatic solution
3 – Mixture of Freund’s adjuvant and test material as a 1:1 ratio, final concentration 5%, volume 0.1 mL
B. CONTROL ANIMALS
1 – Freund’s adjuvant, volume 0.1 mL
2 – Aqueous solution, volume 0.1 mL
3 – Mixture of adjuvant/aqueous solution 1:1, volume 0.1 mL
A week after the initial administration, the test material was re-administered epicutaneously further down the torso.
Further sensitization was induced with a patch test. The test material was administered 5% in Vaseline. After 48 hours, the dressings were removed. The control animals were treated with Vaseline only.
14 Days after the induction treatment, a 5x5cm area was shaved in both flanks of each animal. 0.1 mL of 5% test substance in aqueous solution was applied onto the right flank and 0.1 mL of aqueous solution alone to the left flank under a patch for 24 hours. - Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 5% test substance in aqueous solution
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 5% test substance in aqueous solution
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- aqueous solution
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- aqueous solution
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Group:
- positive control
- Dose level:
- N/a
- No. with + reactions:
- 0
- Total no. in group:
- 0
- Remarks on result:
- other: positive control was not specified.
- Reading:
- 2nd reading
- Group:
- positive control
- Dose level:
- N/a
- No. with + reactions:
- 0
- Total no. in group:
- 0
- Remarks on result:
- other: positive control was not specified
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In a skin sensitisation study (Reliability 1), conducted according to a protocol similar to OECD Test Guideline 406 and pre-GLP, ATMP-H (without information on active acid content) was not sensitising to the skin of guinea-pigs. One animal from the control group and the test group respectively died. The Freund’s adjuvant resulted in necrosis and later scar tissue. No sensitising potential was observed in the guinea-pigs.
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 27.03.1995 to 05.05.1995
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- An LLNA study was not performed because there is an existing reliable study for skin sensitisation using the Guinea Pig Maximisation test method.
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- male
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: David Hall Limited, Staffordshire, UK.
- Age at study initiation: 8-12 weeks
- Weight at study initiation: 334-430 g
- Housing: Singly or in pairs in solid-floor polypropylene cages
- Diet: Ad libitum
- Water: Ad libitum
- Acclimation period: Minimum five days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20-28 °C
- Humidity (%): 51-68 %
- Air changes (per hr): 15 per hour
- Photoperiod (hrs dark / hrs light): 12 hours dark / 12 hours light
IN-LIFE DATES: From: 27.03.1995 To 05.05.1995 - Route:
- intradermal and epicutaneous
- Vehicle:
- water
- Concentration / amount:
- Intradermal induction: 10% w/v in distilled water; 10% w/v in a mixture of FCA plus distilled water (1:1).
Topical induction: undiluted.
Topical challenge: 100% and 75% v/v in distilled water. - No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- water
- Concentration / amount:
- Intradermal induction: 10% w/v in distilled water; 10% w/v in a mixture of FCA plus distilled water (1:1).
Topical induction: undiluted.
Topical challenge: 100% and 75% v/v in distilled water. - No. of animals per dose:
- 20 test and 10 control used for the main study.
- Details on study design:
- RANGE FINDING TESTS: Four concentrations of test substance were investigated (1, 5, 10 and 25% w/v in distilled water). A total of four guinea pigs were used, each animal received four 0.1 mL injections of only one concentration of the test substance. The degree of erythema at the injection sites was assessed approximately 24, 48 and 72 hours and 7 days after the injection according to the Draize scale. Oedema was not assessed. Evidence of systemic toxicity was recorded. The highest concentration that caused only mild to moderate skin irritation, and which was well tolerated systemically, was selected for the intradermal induction stage of the main study.
Two guinea pigs (intradermally injected with Freund's Complete Adjuvant 15 days earlier) were treated with the undiluted test substance and three preparations of the test substance (75, 50 and 25%) v/v in distilled water). Applications were made to the clipped flanks under occlusive dressings for an exposure period of 48 hours.The degree of erythema and oedema was evaluated approximately 1, 24 and 48 hours after dressing removal. The highest concentration producing only mild to moderate dermal irritation was selected for the topical induction stage of the main study.
The undiluted test substance and three preparations of the test substance (75, 50 and 25% v/v in distilled water) were applied to the clipped flanks of two guinea pigs under occlusive dressings for 24 hours. The animals did not form part of the main study, but had been treated identically to the controls of the main study up to Day 14. The degree of erythema and oedema was evaluated approximately 1, 24 and 48 hours after dressing removal. The highest non-irritant concentration of test substance and one lower concentration were selected for the topical challenge stage of the main study.
MAIN STUDY
A. INDUCTION EXPOSURE
Shortly before treatment on Day 0 the hair was removed from an area on the shoulder region of each animal. A row of three injections (0.1 mL) each was made on each side of the mid-line. The injections were: a) FCA plus distilled water (1:1); b) a 10% w/v formulation of the test substance in distilled water; c) a 10% w/v formulation of the test substance in a 1:1 preparation of FCA plus distilled water. Approximately 24 and 48 hours after the intradermal injection, the degree of erythema at the injection sites was evaluated. One week later (Day 7), the same area on the shoulder region was clipped again and treated with a topical application of the undiluted test substance (under an occlusive dressing for 48 hours). The degree of erythema and oedema was quantified at one and 24 hours following removal of the patches.
Induction of the control animals used an identical procedure as the test animals, except the injections were: a) FCA plus distilled water in the ratio 1:1; b) distilled water; c) 50% w/v formulation of distilled water in a 1:1 mixture of FCA/distilled water. The topical applications followed the same procedure as for the test animals, but nothing was applied to the patch. Skin reactions were quantified.
B. CHALLENGE EXPOSURE
Shortly before treatment on Day 21, an area of skin on both flanks of each animal was clipped free of hair. A square filter paper patch saturated with the undiluted test substance was applied to the shorn right flank of each animal and was held in place with a strip of surgical adhesive tape. To ensure that the maximum non-irritant concentration was used at challenge, the test substance at a concentration of 75% v/v in distilled water was similarly applied to a skin site on the left shorn flank. The patches were covered with an occlusive dressing. After 24 hours the dressing was removed. The challenge sites were swabbed with cotton wool soaked in distilled water to remove residual material. Prior to the observation period, the flanks were clipped to remove regrown hair.
Approximately 24 and 48 hours after challenge dressing removal, the degree of erythema and oedema was quantified, and any other reactions recorded. The percentage of test animals that showed a more severe reaction at the test substance challenge site than the most severe reaction observed in the control animals, was compared using the scale: 0% = non-sensitiser; >0-8% = weak sensitiser; >8-28 = mild sensitiser; >28-64% = moderate sensitiser; >64-80% = strong sensitiser; >80-100% = extreme sensitiser. - Challenge controls:
- Negative controls only.
- Positive control substance(s):
- no
- Positive control results:
- No positive control.
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 75 and 100%
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- None
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 75 and 100%
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- None
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- distilled water
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- distilled water
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Group:
- positive control
- Dose level:
- N/a
- No. with + reactions:
- 0
- Total no. in group:
- 0
- Remarks on result:
- not measured/tested
- Key result
- Reading:
- 2nd reading
- Group:
- positive control
- Dose level:
- N/a
- No. with + reactions:
- 0
- Total no. in group:
- 0
- Remarks on result:
- not measured/tested
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In the skin sensitisation study (Reliability 1), conducted according to OECD Test Guideline 406 and in compliance with GLP, ATMP-xNH4 was not sensitising to the skin of guinea pigs.
Referenceopen allclose all
Test substance group response:
Following the intracutaneous application, one animal died immediately with bleeding from the nose. No evidence of sensitisation was observed. Necropsy findings included catarrhal enteritis, bulging stomach and cecum (indigestion), pulmonary congestion, enlarged left side of the heart and clear structure of the liver lobules.
CONTROL GROUP RESPONSES
One animal died during the exposure.
No evidence of sensitisation was observed. After removal of the patch, one animal had white dots in the left eye.
During the treatment free period, the Freund’s adjuvant resulted in necrosis and later scar tissue. After the Patch-test of 48 hours, general redness was observed and the injection sites were blood stained. Crust formation was present at injection sites in both the test and control animals.
Further details are available in the study report, however, needs proper translation.
Body weights of the guinea pigs in the test group between Day 0 and 24, were comparable to those observed in the control groups over the same period.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
There are no skin sensitisation data available for ATMP-xNa, therefore data are read-across from the Category members ATMP-xNH4 and ATMP-H and used in a weight of evidence approach. See attachment to IUCLID Section 13 for justification of read-across.
In the skin sensitisation study, conducted according to OECD Test Guideline 406 and in compliance with GLP, ATMP-xNH4 was not sensitising to the skin of guinea pigs (SafePharm Laboratories, 1995, Reliability 1). At induction, shortly before treatment on Day 0 the hair was removed from an area on the shoulder region of each animal. A row of three injections (0.1 ml) each was made on each side of the mid-line. The injections were: a) FCA plus distilled water (1:1); b) a 10% w/v formulation of the test substance in distilled water; c) a 10% w/v formulation of the test substance in a 1:1 preparation of FCA plus distilled water. Approximately 24 and 48 hours after the intradermal injection, the degree of erythema at the injection sites was evaluated. One week later (Day 7), the same area on the shoulder region was clipped again and treated with a topical application of the undiluted test substance under an occlusive dressing for 48 hours. The degree of erythema and oedema was quantified at one and 24 hours following removal of the patches.
Induction of the control animals used an identical procedure as the test animals, except the injections were: a) FCA plus distilled water in the ratio 1:1; b) distilled water; c) 50% w/v formulation of distilled water in a 1:1 mixture of FCA/distilled water. The topical applications followed the same procedure as for the test animals, but nothing was applied to the patch. Skin reactions were quantified.
At challenge, shortly before treatment on Day 21, an area of skin on both flanks of each animal was clipped free of hair. A square filter paper patch saturated with the undiluted test substance was applied to the shorn right flank of each animal and was held in place with a strip of surgical adhesive tape. To ensure that the maximum non-irritant concentration was used at challenge, the test substance at a concentration of 75% v/v in distilled water was similarly applied to a skin site on the left shorn flank. The patches were covered with an occlusive dressing. After 24 hours the dressing was removed. The challenge sites were swabbed with cotton wool soaked in distilled water to remove residual material. Prior to the observation period, the flanks were clipped to remove regrown hair.
Approximately 24 and 48 hours after challenge dressing removal, the degree of erythema and oedema was quantified, and any other reactions recorded. The percentage of test animals that showed a more severe reaction at the test substance challenge site than the most severe reaction observed in the control animals, was compared using the scale: 0% = non-sensitiser; >0-8% = weak sensitiser; >8-28 = mild sensitiser; >28-64% = moderate sensitiser; >64-80% = strong sensitiser; >80-100% = extreme sensitiser.
Neither of the test group animals demonstrated skin reactions indicative of skin sensitisation.
In the skin sensitisation study, conducted according to a protocol similar to OECD Test Guideline 406 but not in compliance with GLP, ATMP-H (without information on active acid content) was not sensitising to the skin of guinea pigs (Henkel, 1984, Reliability 1).
At intradermal induction phase, 3 injections to the skin occurred for 20 female guinea pigs and another 20 guinea pigs which served as a control group. For the test group, the first injection contained 0.1 mL of Freund’s adjuvant, the second injection contained 0.1 mL of the test material (as an aqueous solution) and the third injection contained 0.1 mL of a mixture of Freund’s adjuvant and test material as a 1:1 ratio with a final concentration of 5%. The control animals also received 3 injections, the first injection contained 0.1 mL of Freund’s adjuvant, the second injection contained 0.1 mL of an aqueous solution and the third injection contained 0.1 mL of a mixture of Freund’s adjuvant and the aqueous solution in a 1:1 ratio.
A week after the initial administration and during the epicutaneous induction phase the test material was applied epicutaneously further down the torso at 5% concentration in Vaseline. After 48 hours, the dressings were removed. The control animals were treated with Vaseline only.
14 Days after the induction treatment, challenge was performed on the shaved flanks of each animal. Application of 0.1 mL of the 5% test substance in aqueous solution occurred to the right flank and 0.1 mL of the aqueous solution only was applied to the left flank under a patch for 24 hours. During the treatment free period, the Freund’s adjuvant resulted in necrosis and later scar tissue. After the epicutaneous induction, general redness was observed and the injection sites were blood stained. Crust formation was present at injection sites in both the test and control animals. Moreover, one animal in the control group died. No evidence of sensitisation was observed after challenge. After removal of the patch, one animal had white dots in the left eye (Henkel, 1984, Reliability 1).
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on the available read-across data, no classification is required for ATMP-xNa for skin sensitisation according to Regulation (EC) No 1272/2008.
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.
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