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EC number: 931-513-6 | CAS number: 1334422-09-1
- 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
Comprehensive data from animal studies as well as from human data are available. AAPBs are considered to be non sensitising based on the results of reliable animal adjuvant tests. AAPB qualities tested in the past may have, however, contained substantial amounts of impurities meanwhile identified as sensitisers (alkylamidopropylamine and/or 3 -dimethylaminopropylamine), which may explain positive results in human patch tests reported in the literature. However, the production process for AAPBs has been changed since and the level of impurities identified as sensitisers was significantly reduced.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Justification for type of information:
- REPORTING FORMAT FOR THE ANALOGUE APPROACH
see "General Justification for Read-Across" attached to IUCLID section 13
1. HYPOTHESIS FOR THE ANALOGUE APPROACH
Mutual read across from the AAPBs to one another is justified:
a) Based on the information given in section 1, it can be concluded that all AAPBs mentioned above are similar in structure, since they are manufactured from similar resp. identical precursors under similar conditions and all contain the same functional groups. Thus a common mode of action can be assumed.
b) The content of minor constituents in all products are comparable and differ to an irrelevant amount.
c) The only deviation within this group of substances is a minor variety in their fatty acid moiety, which is not expected to have a relevant impact on intrinsic toxic or ecotoxic activity and environmental fate. Potential minor impact on specific endpoints will be discussed in the specific endpoint sections.
The read-across hypothesis is based on structural similarity of target and source substances. Based on the available experimental data, including key physico-chemical properties and data from toxicokinetic, acute toxicity, irritation, sensitisation, genotoxicity and repeated dose toxicity studies, the read-across strategy is supported by a quite similar toxicological profile of all five substances.
The respective data are summarised in the data matrix; robust study summaries are included in the Technical Dossier in the respective sections.
2. SOURCE AND TARGET CHEMICAL(S) (INCLUDING INFORMATION ON PURITY AND IMPURITIES)
see "General Justification for Read-Across" attached to IUCLID section 13
3. ANALOGUE APPROACH JUSTIFICATION
see "General Justification for Read-Across" attached to IUCLID section 13
4. DATA MATRIX
see "General Justification for Read-Across" attached to IUCLID section 13 - Reason / purpose for cross-reference:
- read-across: supporting information
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Reason / purpose for cross-reference:
- read-across source
- Justification for non-LLNA method:
- A valid Guinea pig maximization test conducted comparable to guideline with acceptable restrictions is available, which is reliable with restrictions and adequate for classification and labelling purposes. Potency estimation is not mandatory when existing guideline and GLP conforming data are available, which were conducted before the new annex of the REACH Regulation entered into force. Moreover, no indication for skin sensitisation was observed in this study, thus, no dose response information is needed. For this reason and for reasons of animal welfare no additional LLNA was conducted.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 10 %
- No. with + reactions:
- 2
- Total no. in group:
- 15
- Clinical observations:
- erythema score 1 (Slight erythema (barely perceptible))
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 10 %
- No. with + reactions:
- 0
- Total no. in group:
- 15
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- other: 3rd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 10 %
- No. with + reactions:
- 0
- Total no. in group:
- 15
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- n.a.
- Remarks on result:
- other: No data available
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- positive control
- Dose level:
- n.a.
- Remarks on result:
- other: No data available
- Interpretation of results:
- GHS criteria not met
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
No experimental data on the sensitisation potential of C12-18 AAPB are available. Hoewever, eight reliable adjuvant tests (seven maximization tests according to Magnusson and Kligman, one Draize and one modified Draize test) conducted with the closely related substance C8-18 and C18 unsatd. AAPB (Coco AAPB) are reported. Additionally a skin sensitisation study comparable to OECD Guideline 406 (Guinea pig maximisation test) is available for C12 AAPB. A justification for read-across is given below.
Studies in Animals
Skin sensitisation
None of the studies was performed in full compliance with the current OECD or EU guideline, and information on the purity and impurities of the test materials is available on four studies only. Although the majority of the studies gave no indication of a sensitising potential, the lack of concurrent positive control data, may weaken their reliability. However, the first study selected as a key study on skin sensitisation, has been performed according to OECD Guideline 406 and GLP. As the guideline claims semiannual reliability checks on positive control substances, the missing data on a positive control is probably a deficit in study documentation but not in study conduct. This study (Evonik, 1990) was selected as key study because it is the most recently performed maximisation test available on AAPB. The test AABP in this study was C8-18 and C18 unsatd. AAPB with 30% a.i. in minimum and impurities relevant to sensitisation referred to a.i. of in maximum 1.7% alkylamidopropylamine and 33 ppm DMPA (3-dimethylaminopropylamine). As a second key study (Evonik, 1980), the maximisation test on the test item with the highest amounts of the potentially sensitising impurities alkylamidopropylamine and DMPA was selected. In this study, C8-18 and C18 unsatd. AAPB quality with 8.3% Alkylamidopropylamine and 33 - 50 ppm DMPA based on a.i. has been tested. The results of both key studies as well as further reliable supporting adjuvant tests were all negative. Only in the maximisation study performed by Rantuccio et al. (1983), two out of 20 tested Guinea pigs showed an allergic reaction, whilst the result was ambiguous in four, and clearly negative in 14 animals. Unfortunately, no information on impurities of the test substance, which might have influenced the outcome of the study was provided by the authors of the publication. Furthermore, a second challenge (as recommended in the current OECD TG 406) was not performed that could have helped in the interpretation of the results. Hence, the interpretation of the effects seen in this particular test remains difficult, no firm conclusion about the sensitizing potential of the AAPBs can be drawn from this study. As published results on a further GPMT, and a LLNA are only available as secondary citations, their reliability, relevance and adequacy cannot be judged. It is therefore not possible to draw a firm conclusion about the sensitising potential of the AAPBs from these two studies.
Studies in Humans
The following compilation of studies on human patients and conclusions on photosensitisation and respiratory tract sensitisation is a quotation taken from the OECD SIAR-SIDS Initial Assessment Report on Alkylaminopropyl betaines (remark: Cocamidopropylamine is synonymous to Coco AAPB and amidoamine to alkylaminopropylamine).
(start of quotation)
Skin sensitisation
Patch test results have been reported from several thousands of patients with skin disorders associated with occupational exposure or exposure to cosmetic formulations containing cocamidopropyl betaine.
A complicating factor in most of these studies is the fact that sensitizing impurities and by-products from the manufacturing process, such as amidoamine and 3-dimethylaminopropylamine (DMPA) may have been present in the test formulations, resulting in “false positive” reactions for cocamidopropyl betaine. This is particularly the case for testing performed before the late 90’s when this issue became evident. Furthermore, the patch test reactions to cocamidopropyl betaine (or its impurities) often are irritant in nature, although the morphological picture and crescendo reaction may sometimes suggest a positive allergic reaction (Löffler et al., 2005).
As most of the available reports do not provide information on the purity of the tested material, which appears to have a significant influence on the testing results, they were considered as of limited reliability and are not described in this IUCLID dataset. Only the most relevant and reliable studies are summarized below:
3-Dimethylaminopropylamine and amidoamine have been identified as sensitizing impurities in commercially available cocamidopropyl betaine by several investigators (Pigatto et al., 1995; Angelini et al., 1995, 1996 a, b; Fowler et al., 1997; Hunter and Fowler, 1998; Armstrong et al., 1999; McFadden et al., 2001; Brey and Fowler, 2004; Fowler et al., 2004).
Pigatto et al. (1995) investigated the influence of impurities on patch test results by using cocamidopropyl betaine samples from different manufacturers. In a first study, the authors found that 17 out of 1190 (1.4 %) patients with allergic contact dermatitis were positive to cocamidopropyl betaine (of unknown purity). Subsequently, 15 of these patients were patch tested with cocamidopropyl betaine containing DMPA at concentrations of 200 ppm or below the limit of detection. Whilst all 15 patients showed an allergic reaction to the sample with 200 ppm, only 1 patient reacted to the cocamidopropyl betaine of higher purity. In further tests it was shown that 10 out of 12 patients reacted to DMPA (1 % and 0.1 % aqueous solutions), and 9 out of 13 subjects still reacted to DMPA at 0.05 % (aqueous solution). Two of the 12 patients had irritant reactions to DMPA.
Angelini et al.(1995, 1996a, b) tested 1200 consecutive eczematous patients with a 1 % aqueous solution of cocamidopropyl betaine. Contact allergy was found in 46 subjects (3.8 %), while irritant reactions (i. e., slight erythema only) were observed in 15 cases (1.25 %).30 out of 46 patients with allergic reactions were subsequently tested with the substances used in the synthesis ofcocamidopropyl betaine, together with a sample of cocamidopropyl betaine of a greater purity.In all 30 subjects, positive reactions were obtained to DMPA (1 % aqueous solution), while the cocamidopropyl betaine defined of purer grade, at 0.5 % and 1 %, gave positive reactions in 10 % and 53 % of cases, respectively. According to the study authors, these results suggested that the DMPA present at various levels as an impurity in the commercial product is responsible for cocamidopropyl betaine allergy. Owing to the inconsistency of positive reactions to cocamidopropyl betaine of variable purity, and to the consistency of positive reactions to DMPA, it seems likely that these reactions may also be connected with the presence in the product, defined of purergrade, of unknown amounts of DMPA as impurity.
In product use tests (Fowler et al., 1997; Hunter and Fowler, 1998), amidoamine was shown to be a likely sensitizer in cocamidopropyl betaine formulations. Six out of 9 subjects reacted to amidoamine (0.1 % aqueous solution), none of these individuals reacted to DMPA (0.1 % in petrolatum), and between 1 and 3 subjects reacted to cocamidopropyl betaine (1 % aqueous solution) of different purity grades.
A significant correlation was found between the amidoamine content and the sensitizing potential of “impure” cocamidopropyl betaine (Armstrong et al., 1999; Foti et al., 2003).
McFadden et al. (2001) tested cocamidopropyl betaine of various purity grades. Partially purified cocamidopropyl betaine, i. e., with less than 0.5 percent of amidoamine, resulted in allergic reactions in 3 out of 4 individuals; these three individuals reacted also towards amidoamine (0.1 %), and 1 subject still reacted to amidoamine at 0.01 %. None out of 6 individuals tested with a 1 %aqueous solution of “pure” cocamidopropyl amine (i. e., with < 0.3 % amidoamine, < 10 ppm DMPA) had an allergic reaction. One out of 6 subjects reacted to DMPA (at 1000 ppm on tapestripped skin and 10000 ppm on normal skin), and three of 6 reacted to DMPA (100 - 10 000 ppm) in 0.2 % sodium lauryl sulfate.
Data was collected during 2001 by the North American Contact Dermatitis Group from consecutive patients presenting for patch testing for diagnosis of presumed allergic contact dermatitis (Fowler et al., 2004; Brey and Fowler, 2004). Of 975 patients tested, 15 were patch-test positive to cocamidopropyl betaine, 25 had positive reactions to amidoamine, and 18 had positive reactions to both substances.
In view of the widespread use of cocamidopropyl betaine in personal cleansing products, only relatively few cases of sensitization have been reported. Most cases alleged to have been sensitized by cocamidopropyl betaine were most probably caused by impurities, such as amidoamine and DMPA that may be present in the formulations.
Because of the similar manufacturing method, the impurity profile with regard to the suspected sensitizers is expected to be the same in all AAPB preparations.
Photosensitisation
There is no structural element in alkylamidopropyl betaines present, which could lead to UV absorption and hence photosensitisation.
Respiratory tract sensitisation
No studies were available on the potential of respiratory tract sensitisation.
(end of quotation)
Conclusion
Overall, the sensitising potential of the AAPBs is considered to be low. AAPB qualities tested in the past may have, however, contained substantial amounts of impurities meanwhile identified as sensitisers (amidoamine (also named alkylamidopropylamine or Amides, C8-18 even numbered, N-[3-(dimethylamino) propyl]) and/or DMPA (also named 3-aminopropyldimethylamine or 3–dimethylaminopropylamine)), which may explain positive results in human patch tests reported in the literature. However, the production process for AAPBs has been changed since and the level of impurities identified as sensitisers was significantly reduced. Recent AAPB qualities as defined in the submission substance identity (low levels of amidoamine and DMPA) can be expected to be non sensitising based on reliable animal adjuvant tests. These tests have been performed on AAPB qualities with partial even substantially higher amounts of the potentially sensitising impurities amidoamine and DMPA than defined in the submission substance identity. There is no structural element in alylamidopropyl betaines present, which could lead to UV absorption and hence photosensitization.
The sensitising potential of the whole group of AAPBs is assumed to be similar. As fatty acids independently from their chain length and degree on unsaturation are generally considered to be non-sensitisers, a variability in the fatty acid moiety is not expected to have any influence on the sensitising activity of the AAPBs. Thus, the use of studies performed on individual members of this group of substances as read-across for the whole group is justified.
Justification for read-across
For details on substance identity and detailed toxicological profiles, please refer also to the general justification for read-across attached as pdf document to IUCLID section 13.
This read-across approach is justified based on structural similarities. All AAPBs contain the same functional groups. Thus a common mode of action can be assumed.
The only deviation within this group of substances is a minor variety in their fatty acid moiety (chain length and degree of unsaturation), which may have an influence on the outcome of skin and eye irritation studies. However,as fatty acids independently from their chain length and degree on unsaturation are generally considered to be non-sensitisers, a variability in the fatty acid moiety is not expected to have any influence on the sensitising activity of the AAPBs.
a. Structural similarity and functional groups
Alkylamidopropyl betaines (AAPBs) are – with the exception of C12 AAPB - UVCB substances (Substances of Unknown or Variable composition, Complex reaction products or Biological materials), which are defined as reaction products of natural fatty acids or oils with dimethylaminopropylamine and further reaction with sodium monochloroacetate. AAPBs are amphoteric surfactants, which are characterized by both acidic and alkaline properties.
Their general structure is:
R-C(O)-NH-(CH2)3-(N(CH3)2)+-CH2-C(O)O-
R = fatty acid moiety
The fatty acids have a mixed, slightly varying composition with an even numbered chain length from C8 to C18. Unsaturated C18 may be included. Consequently, the AAPBs differ by their carbon chain length distribution and the degree of unsaturation in the fatty acid moiety. However, Lauramidopropyl betaine (C12 fatty acid derivate) is the major ingredient of all AAPBs covered by this justification as listed in table 1 “Substance identities” of the general justification for read-across.
The substances under evaluation share structural similarities with common functional groups (quaternary amines, amide bonds and carboxymethyl groups), and fatty acid chains with differences in chain length and degree of saturation.
b. Differences
Differences in the sensitising potential of the AAPBs could potentially arise from the following facts:
-Different amounts of different carbon chain lengths (carbon chain length distribution):
Higher amounts of higher chain lengths and corresponding lower amounts of lower chain length could result in a rising average lipophilicity. As fatty acids independently from their chain length are generally considered to be non-sensitisers, a variability in the fatty acid moiety is not expected to have any influence on the sensitising activity of the AAPBs
- Different amounts of unsaturated fatty ester moieties:
Effects may be expected for e.g. physical state and for some toxicological endpoints, mainly local effects (e.g. irritation). However, as fatty acids independently from their degree of unsaturation are generally considered to be non-sensitisers, a variability in the fatty acid moiety is not expected to have any influence on the sensitising activity of the AAPBs
Comparison of sensitisation data
Endpoints
Source substances
Target substance
C8-18 and C18 unsatd. AAPB
C12 AAPB
C12-18 AAPB
Sensitisation,
Animal data
key_GPMT_Skin sensitisation: 61789_40-0_8.3_REWO_1990_OECD 406
key study
OECD TG 406, in vivo, Guinea pig maximisation test, guinea pig33 ppm DMPA
1.7% Alkylamidopropylamine
not sensitising
Reliability: 2 (reliable with restrictions), GLP
Sup_GPMT_Skin sensitisation: 4292-10-8_8.2.1_8.3_Zschimmer_Schwarz_1986_skin sensitization
Supporting study
Similar to OECD TG 406, in vivo, Guinea pig maximisation test, guinea pigNo data on DMPA and Alkylamidopropylamine
not sensitizing
Reliability: 2 (reliable with restrictions), no GLP
No data, read-across
key (highest level of impurities)_Skin sensitisation: 61789-40-0_8.3_THG_1980a
key study
similar to OECD TG 406, in vivo, Guinea pig maximisation test, guinea pig33 – 50 ppm DMPA
8.3% Alkylamidopropylamine
not sensitising
Reliability: 2 (reliable with restrictions), no GLP
Sup_GPMT_Skin sensitisation: 61789-40-0_8.3_THG_1980b
supporting study
similar to OECD TG 406, in vivo, Guinea pig maximisation test, guinea pig
7 ppm DMPA
<0.3% Alkylamidopropylamine
not sensitising
Reliability: 2 (reliable with restrictions), no GLP
Sup_GPMT_Skin sensitisation: 61789-40-0_8.3_REWO_1987_OECD 406
supporting study
OECD TG 406, in vivo, Guinea pig maximisation test, guinea pig
33 ppm DMPA
Max. 1.7% Alkylamidopropylamine
not sensitising
Reliability: 2 (reliable with restrictions), GLP
Sup_GPMT_Skin sensitisation: 61789-40-0_8.3_Arimura et al._1998
Supporting study
Similar to OECD TG 406, in vivo, Guinea pig maximisation test, guinea pig
No data on DMPA andAlkylamidopropylamine
not sensitising
Reliability: 2 (reliable with restrictions), no GLP
Sup_GPMT_Skin sensitisation: 61789-40-0_8.3_Rantuccio et al._ 1983
Supporting study
Similar to OECD TG 406, in vivo, Guinea pig maximisation test, guinea pig
No data on DMPA andAlkylamidopropylamine
ambiguous
Reliability: 2 (reliable with restrictions), no GLP
Sup_ mod Draize Adjuvans Test_Skin sensitisation: 61789-40-0_8.3_Rantuccio et al._1983
supporting study
in vivo, modified Draize test, guinea pig
no data on DMPA andAlkylamidopropylamine
not sensitising
Reliability: 2 (reliable with restrictions), no GLP
Sup_Draize Adjuvans Test_Skin sensitisation: 61789-40-0_8.3_Henkel_1976
Supporting study
in vivo, Draize adjuvans test, guinea pigno data on DMPA and Alkylamidopropylamine
not sensitizing
Reliability: 2 (reliable with restrictions), no GLP
Sensitisation, human data
11 supporting studies:
Human, patch test with Coco AAPB
DMAPA was found to be responsible for sensitization reactions
Reliability: 2 (reliable with restrictions)
No data
No data, read-across
The most recently performed maximisation test available on AAPB was selected as one key study. The test item in this study was C8-18 and C18 unsatd. AAPB with 30% a.i. and 1.7 % alkylamidopropylamine and 33 ppm DMPA (3-dimethylaminopropylamine) as minor constituents relevant to sensitisation.
As a second key study, the maximisation test on the test item with the highest amounts of the potentially sensitising minor constituents alkylamidopropylamine and DMPA was selected. In this study, a C8-18 and C18 unsatd. AAPB quality with 8.3% Alkylamidopropylamine and 33 - 50 ppm DMPA has been tested.
Only in the maximisation study performed by Rantuccio et al.(1983), two out of 20 tested Guinea pigs showed an allergic reaction, whilst the result was ambiguous in four, and clearly negative in 14 animals. No information on impurities of the test substance, which might have influenced the outcome of the study was provided by the authors of the publication. Furthermore, a second challenge (as recommended in the current OECD TG 406) was not performed that could have helped in the interpretation of the results. Hence, the interpretation of the effects seen in this particular test remains difficult, no final conclusion about the sensitizing potential of the AAPBs can be drawn from this study.
Overall, with the exception of one Guinea Pig Maximisation Test with ambiguous results, in all available studies AAPBs were non-sensitisers.
Quality of the experimental data of the analogues:
The available data are adequate and sufficiently reliable to justify the read-across approach.
The key studies were conducted according to (or comparable to) OECD Guideline 406 (Guinea pig maximisation test)and are reliable with restrictions (RL2).
Several supporting studies (RL2) are available, which were conducted according to (or comparable to) OECD Guideline 406 (Guinea pig maximisation test) or according to the modified Draize test protocol or the Draize adjuvans test protocol.
The test materials used in the respective studies represent the source substance as described in the hypothesis in terms of substance identity and minor constituents. A study with the test item containing the minor constituent DMPA (3-dimethylaminopropylamine) in concentrations between 33-50 ppm and thus representing the upper level of the specifications, has been selected as one of the key studies.
Overall, the study results are adequate for the purpose of classification and labelling and risk assessment.
Conclusion
Based on structural similarities of the target and source substancesas presented above and in more detail in the general justification for read across, it can be concluded that the available data from the source substance C8-18 and C18 unsatd. AAPB are also valid for the target substance C12-18 AAPB.
As fatty acids independently from their chain length and degree on unsaturation are generally considered to be non-sensitisers, a variability in the fatty acid moiety is not expected to have any influence on the sensitising activity of the AAPBs. Thus, the use of studies performed on individual members of this group of substances as read-across for the whole group is justified.
Overall, the sensitising potential of the AAPBs is considered to be low. AAPB qualities tested in the past may have, however, contained substantial amounts of impurities meanwhile identified as sensitisers (amidoamine (also named alkylamidopropylamine or Amides, C8-18 even numbered, N-[3-(dimethylamino) propyl]) and/or DMPA (also named 3-aminopropyldimethylamine or 3–dimethylaminopropylamine)), which may explain positive results in human patch tests reported in the literature. However, the production process for AAPBs has been changed since and the level of impurities identified as sensitisers was significantly reduced.
Recent AAPB qualities as defined in the submission substance identity (low levels of amidoamine and DMPA) can be expected to be non-sensitising based on reliable animal adjuvant tests.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Eigth out of nine reliable animal adjuvant tests gave no indication of a sensitising potential of the AAPBs. The ninth study, a Guinea pig maximisation test, gave an ambiguous result. Since this result has been not verified by a second challenge, nor detailed information on the quality of the test item is available, no firm conclusion about the sensitising potential can be drawn from this study. The tested items which gave negative results in animal adjuvant tests included a quality with 8.3 % alkylamidopropylamine and 33 - 50 ppm DMPA based on a.i.. Positive human patch test results have been reported in the literature. AAPB qualities tested in the past may have, however, contained substantially amounts of impurities meanwhile identified as sensitisers (alkylamidopropylamine and/or 3 -dimethylaminopropylamine), which may explain these positive results. However, as the production process for AAPBs has been changed since and the level of impurities identified as sensitisers was significantly reduced. Recent AAPB qualities as defined in the submission substance identity can be expected to be non sensitising based on reliable animal adjuvant tests. These test have been performed on AAPB qualities with partial even substantially higher amounts of the potentially sensitising impurities alkylaminopropylamine and DMPA than defined in the submission substance identity. There is no evidence for a photosensitizing potential.
AAPB qualities as defined in the submission substance identity do not meet the classification criteria regarding sensitisation outlined in regulation (EC) 1272/2008 or the former European directive on classification and labelling 67/548/EEC.
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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