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EC number: 201-550-6 | CAS number: 84-66-2
- 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
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- Nanomaterial pour density
- Nanomaterial photocatalytic activity
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- 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
Toxicity to reproduction
Administrative data
- Endpoint:
- two-generation reproductive toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Experimental result published in peer reveiwed journal. Some details on methods / results not available
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 2 005
- Report date:
- 2005
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 416 (Two-Generation Reproduction Toxicity Study)
- GLP compliance:
- yes
- Limit test:
- no
Test material
- Reference substance name:
- Diethyl phthalate
- EC Number:
- 201-550-6
- EC Name:
- Diethyl phthalate
- Cas Number:
- 84-66-2
- Molecular formula:
- C12H14O4
- IUPAC Name:
- .
- Details on test material:
- - Name of test material (as cited in study report): diethyl phthalate
- Physical state: liquid
- Analytical purity: 99.8%
- Lot/batch No.: SEM5441
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: Crj:CD (SD) IGS
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Tsukuba breeding Center Charles River japan Inc
- Age at study initiation: (P) x wks; (F1) x wks: P 4 weeks
- Weight at study initiation: (P) Males: x-x g; Females: x-x g; (F1) Males: x-x g; Females: x-x g
- Fasting period before study: no
- Housing: individually except during acclimatisation (1 or 2 animals same sex)
- Use of restrainers for preventing ingestion (if dermal): yes/no: N/A
- Diet (e.g. ad libitum): NIH-07M Clea Japan Inc Tokyo Japan
- Water (e.g. ad libitum): tap water
- Acclimation period: 1 week
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 23+/- 3degrees C
- Humidity (%): 50 +/- 20
- Air changes (per hr): 10-15
- Photoperiod (hrs dark / hrs light): 12
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- other: basal diet
- Details on exposure:
- DIET PREPARATION
- Mixing appropriate amounts with (Type of food): basal NIH-07M diet
VEHICLE
- Justification for use and choice of vehicle (if other than water): dietary study; in addition DEP is poorly soluble in water
- Concentration in vehicle: 600, 3000 & 5000 ppm - Details on mating procedure:
- - M/F ratio per cage: 1:1
- Length of cohabitation: until the day of sucessful copulation
- Proof of pregnancy: [vaginal plug / sperm in vaginal smear] referred to as [day 0 / day 1] of pregnancy: vaginal plug/sperm; day 0
- After ... days of unsuccessful pairing replacement of first male by another male with proven fertility. Not reported
- Further matings after two unsuccessful attempts: [no / yes (explain)]: procedure repeated until pregnancy resulted for 3 week mating period
- After successful mating each pregnant female was caged (how): singly
- Any other deviations from standard protocol: not reported - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- Not reported
- Duration of treatment / exposure:
- Approximately 15 weeks for male and 17 weeks for female parents of the F0 & F1 generations.
- Frequency of treatment:
- Continuously via the diet
- Details on study schedule:
- - F1 parental animals not mated until 10 weeks after selected from the F1 litters.
- Selection of parents from F1 generation when pups were 21-25 days of age.
- Age at mating of the mated animals in the study: 15 weeks
Doses / concentrations
- Remarks:
- Doses / Concentrations:
0 (control) 600, 3000 & 15000 ppm
Basis:
nominal in diet
- No. of animals per sex per dose:
- 24
- Control animals:
- yes, plain diet
- Details on study design:
- - Dose selection rationale: selected on basis of results of a preliminary study
- Rationale for animal assignment (if not random): assigned on the basis of weight so that the 4 groups had similar group mean and SD values - Positive control:
- No
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes
- Time schedule: twice daily for clinical signs & mortality
DETAILED CLINICAL OBSERVATIONS: No data
- Time schedule:Not reported
BODY WEIGHT: Yes
- Time schedule for examinations: weekly
FOOD CONSUMPTION AND COMPOUND INTAKE (if feeding study):
- Food consumption for each animal determined and mean daily diet consumption calculated as g food/kg body weight/day: Yes
- Compound intake calculated as time-weighted averages from the consumption and body weight gain data: Yes - Oestrous cyclicity (parental animals):
- yes,see table below
- Sperm parameters (parental animals):
- Sperm parameters were measured in all F0 & F1 males surviving to scheduled terminal kill. The right cauda epididymis was weighed & used for sperm analysis. Right testis was also used used for counting homogenisation resistant testicular spermatids.
- Litter observations:
- STANDARDISATION OF LITTERS
- Performed on day 4 postpartum: yes
- If yes, maximum of 8 pups/litter (4/sex/litter as nearly as possible); excess pups were killed and discarded.
PARAMETERS EXAMINED
The following parameters were examined in [F1 / F2 / F3] offspring:
[number and sex of pups, stillbirths, live births, postnatal mortality, presence of gross anomalies, weight gain, physical or behavioural abnormalities, other:] seee table below
GROSS EXAMINATION OF DEAD PUPS:
[no / yes, for external and internal abnormalities; possible cause of death was/was not determined for pups born or found dead.] yes gross examination - Postmortem examinations (parental animals):
- SACRIFICE
- Male animals: All surviving animals [describe when, e.g. as soon as possible after the last litters in each generation were produced.]: after weaning of their F1 & F2 offspring as appropriate
- Maternal animals: All surviving animals [describe when, e.g. after the last litter of each generation was weaned.]: after weaning of their F1 & F2 offspring as appropriate
GROSS NECROPSY
- Gross necropsy consisted of [external and internal examinations including the cervical, thoracic, and abdominal viscera.]: yes
HISTOPATHOLOGY / ORGAN WEIGHTS
Selected tissues were prepared for microscopic examination and weighed, respectively. - Postmortem examinations (offspring):
- SACRIFICE
- The F1 offspring not selected as parental animals and all F2 offspring were sacrificed at [26] days of age.
- These animals were subjected to postmortem examinations (macroscopic and/or microscopic examination) as follows: macroscopic & microscopic examination
GROSS NECROPSY
- Gross necropsy consisted of [external and internal examinations including the cervical, thoracic, and abdominal viscera.]: yes
HISTOPATHOLOGY / ORGAN WEIGTHS
Selected tissues were prepared for microscopic examination and weighed, respectively.For control & 15000 ppm groups all F0 & F1 parental animals were examined for abnormalities of the reproductive organs. In the low dose group the same organs were examined in female animals with abnormal oestrus cycles, males with sperm abnormality & pairs of animals that failed to mate or produce offspring. In addition the kidneys of F1 parental females in control & 15000 groups were examined due to the significant increase in weight noted when compared with controls.
In F1& F2 weanlings the thymus of 6 of each of the males & females & the spleen of 6 F2 males in the control & 15000 ppm groups were examined as the weights were significantly decreased in the 15000 group compared with controls. - Statistics:
- For body weights, body weight gain, food consumption, oestrus cyle length, number of implants & pups delivered, delivery index sperm parameters ormone levels, absolute & relative organ weights, time of reflex response completion, pinna detachment, eye opening, incisor eruption, age & body weights at sexual maturation, AGD & and pup viability homogeneity of variance was evaluated using Bartlett's test then if homogeneous one way analysis of variance was used to determine if there were statistical differences between the groups and their counterparts in the controls.If the analysis of variance gave a significant result , Dunnetts test was performed to detect the differences between controls & the DEP groups.
When Bartlett's test detected non homogeneous results Kruskal-Wallis test was used to detect significant differences and then the Mann Whitney U test was performed to detect any significant differences between the DEP groups and the corresponding control group.
Statistical aanalyses was performed using litter means for body weights and the AGDs of pups /sex before weaning.
The completion of physical development of pups was assessed by the Wilcoxon rank test on the litter data,
The Chi squared /Fishers exact probability tests were used to analyse incidence of females with normal oestrus cycles & indices of copulation, fertility & gestation, & sex ratios of pups. - Reproductive indices:
- See table below
- Offspring viability indices:
- See table below
Results and discussion
Results: P0 (first parental generation)
General toxicity (P0)
- Clinical signs:
- no effects observed
- Body weight and weight changes:
- no effects observed
- Food consumption and compound intake (if feeding study):
- no effects observed
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Histopathological findings: non-neoplastic:
- no effects observed
- Other effects:
- no effects observed
Reproductive function / performance (P0)
- Reproductive function: oestrous cycle:
- no effects observed
- Reproductive function: sperm measures:
- effects observed, treatment-related
- Description (incidence and severity):
- Incidences of abnormal sperm & tailess spermwere significantly increased in males of F0 generation given 3000 ppm DEP and in males of the F1 generation given 3000 and 15000 ppm.
- Reproductive performance:
- no effects observed
Details on results (P0)
Effect levels (P0)
open allclose all
- Dose descriptor:
- NOAEL
- Effect level:
- 15 000 ppm (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: No adverse effects were observed on systemic & reproductive parameters at dietary levels of up to 15000 ppm.
- Remarks on result:
- other: Generation: F0 & F1 in parents (migrated information)
- Dose descriptor:
- NOAEL
- Effect level:
- 3 000 ppm (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: In terms of development and growth pup body weight gain before weaning was reduced in the 15000 ppm group.
- Remarks on result:
- other: Generation: F1 & F2 pups (migrated information)
Results: F1 generation
General toxicity (F1)
- Clinical signs:
- no effects observed
- Mortality / viability:
- no mortality observed
- Body weight and weight changes:
- effects observed, treatment-related
- Sexual maturation:
- effects observed, treatment-related
- Organ weight findings including organ / body weight ratios:
- not examined
- Gross pathological findings:
- no effects observed
- Histopathological findings:
- no effects observed
- Description (incidence and severity):
- examination limited to thymus & spleen
Details on results (F1)
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
Reproductive data for F0 and F1 parental animals
|
DEP (ppm) Administered |
|||
|
0 (control) |
600 |
3000 |
15000 |
F0 parental animals |
|
|
|
|
No. of pairs |
24 |
24 |
24 |
24 |
Precoital interval (days) |
3.4±3.8a |
2.7±1.5 |
3.7±3.5 |
2.4±1.2 |
Copulation index (%)b |
|
|
|
|
Male |
95.8 |
95.8 |
100 |
100 |
Female |
100 |
95.8 |
100 |
100 |
Fertility index (%)c |
|
|
|
|
Male |
95.7 |
95.7 |
100 |
95.8 |
Female |
95.8 |
95.7 |
100 |
95.8 |
Gestation index (%)d |
95.7 |
100 |
100 |
95.7 |
Gestation length (days) |
22.3±0.5 |
22.3±0.5 |
22.3±0.5 |
22.1±0.3 |
No. of implantations |
14.7±1.8 |
15.0±1.7 |
14.9±2.0 |
14.8±2.1 |
Delivery index (%)e |
94.3±6.7 |
91.3±8.8 |
93.8±5.0 |
94.9±7.2 |
No. of pups delivered |
13.9±2.0 |
13.7±2.0 |
14.0±2.1 |
14.0±2.2 |
F1 parental animals |
|
|
|
|
No. of pairs |
24 |
24 |
24 |
24 |
Precoital interval (days) |
2.5±1.6 |
2.8±1.2 |
4.3±4.7 |
3.8±3.8 |
Copulation index (%) |
|
|
|
|
Male |
100 |
100 |
87.5 |
95.8 |
Female |
100 |
100 |
95.8 |
100 |
Fertility index (%) |
|
|
|
|
Male |
95.8 |
95.8 |
95.2 |
95.7 |
Female |
95.8 |
95.8 |
95.7 |
95.8 |
Gestation index (%) |
100 |
100 |
100 |
100 |
Gestation length (days) |
22.4±0.5 |
22.3±0.5 |
22.3±0.6 |
22.1±0.3* |
No. of implantations |
14.3±2.5 |
14.3±3.2 |
14.9±2.7 |
14.7±2.5 |
Delivery index (%) |
91.3±11.1 |
93.7±8.4 |
91.8±13.2 |
98.8±17.9 |
No. of pups delivered |
13.0±2.8 |
13.5±3.5 |
13.9±3.1 |
13.3±3.5 |
a Mean±SD; b Copulation index (%) = (No. of rats with successful copulation/no. of rats paired) x100; cFertility index (%) = (No. of females pregnant or no. of males sired/no. of rats with successful copulation) x100; d Gestation index (%) = (No. of females with parturition/no. of females pregnant) x100; e Delivery index (%) = (No. of pups delivered/no. of implantations) x100; * Significantly different from the control, p≤0.05
Litter data on reproductive parameters for F1 and F2 offspring
|
DEP (ppm) |
|||
|
0 (control) |
600 |
3000 |
15000 |
F1 offspring |
|
|
|
|
No. of litters examined |
22 |
22 |
24 |
22 |
Sex ratio of pupsb |
0.544 |
0.465 |
0.507 |
0.490 |
Viability index before weaning (%)cde |
|
|
|
|
Day 0 |
97.6 |
98.8 |
97.8 |
97.2 |
Day 4 |
97.8 |
96.2 |
97.2 |
97.7 |
Day 21 |
97.7 |
95.5 |
90.6 |
88.1 |
Male pup weight before weaning (g) |
|
|
|
|
Day 0 |
6.9±0.7a |
7.0±0.6 |
7.0±0.7 |
6.7±0.7 |
Day 4 |
10.6±1.4 |
10.1±1.4 |
10.5±1.9 |
9.7±1.4 |
Day 21 |
59.0±7.7 |
56.8±6.6 |
55.1±9.5 |
48.1±4.8f** |
Female pup weight before weaning (g) |
|
|
|
|
Day 0 |
6.5±0.7 |
6.5±0.7 |
6.5±0.7 |
6.3 b±0.6 |
Day 4 |
10.2±1.4 |
9.6±1.5 |
9.9±1.6 |
9.1±1.1* |
Day 21 |
56.3±6.6 |
55.4±7.0 |
53.8±7.2 |
45.8±4.5f** |
Anogenital distance (mm) |
|
|
|
|
Male Day 0 |
3.67±0.31 |
3.72±0.29 |
3.83±0.35 |
3.56±0.28 |
Day 4 |
5.66±0.50 |
5.46±0.44 |
5.54±0.69 |
5.54±0.55 |
Female Day 0 |
1.76±0.21 |
1.67±0.22 |
1.67±0.23 |
1.77±0.22 |
Day 4 |
2.77±0.34 |
2.70±0.25 |
2.72±0.34 |
2.74±0.33 |
F2 offspring |
|
|
|
|
No. of litters examined |
23 |
23 |
22 |
23 |
Sex ratio of pups |
0.510 |
0.510 |
0.523 |
0.482 |
Viability index before weaning (%) |
|
|
|
|
Day 0 |
96.2 |
98.6 |
97.9 |
98.6 |
Day 4 |
96.3 |
97.8 |
99.4 |
98.1 |
Day 21 |
94.0 |
96.7 |
98.9 |
99.5 |
Male pup weight before weaning (g) |
|
|
|
|
Day 0 |
7.1±0.5 |
7.0±0.7 |
6.9±0.7 |
6.8±0.6 |
Day 4 |
11.4±1.8 |
10.6±1.5 |
10.7±1.2 |
10.8±1.6 |
Day 21 |
60.9±9.5 |
61.4±6.9 |
60.6±4.5 |
53.8±4.8** |
Female pup weight before weaning (g) |
|
|
|
|
Day 0 |
6.6±0.6 |
6.5±0.7 |
6.4±0.5f |
6.3±0.4g |
Day 4 |
10.8±2.1 |
9.9±1.4 |
10.0±0.9f |
10.0±1.1g |
Day 21 |
58.2±9.4 |
58.7±6.2 |
58.2±4.2f |
51.5±4.2g ** |
Anogenital distance (mm) |
|
|
|
|
Male Day 0 |
3.63±0.29 |
3.59±0.17 |
3.64±0.20 |
3.65±0.24 |
Day 4 |
5.78±0.42 |
5.66±0.39 |
5.73±0.36 |
5.77±0.49 |
Female Day 0 |
1.76±0.11 |
1.73±0.09 |
1.76±0.09f |
1.74±0.09g |
Day 4 |
2.93±0.23 |
2.89±0.22 |
2.90±0.21f |
2.88±0.20g |
a Mean±SD; b Sex ratio of pups = No. of male pups/total no. of pups; c Viability index on postnatal day 0 (%) = (No. of live pups delivered/total no. of pups delivered) x100
d Viability index on postnatal day 4 (%) = (No. of live pups on postnatal day 4/no. of live pups delivered) x100 ; e Viability index on postnatal day 21 (%) = (No. of live pups on postnatal day 21/no. of live pups on postnatal day 4 after cull) x100; f and g Values obtained from 21 and 22 litters, respectively; * Significantly different from the control, p≤0.05; ** Significantly different from the control, p≤0.01
Hepatic microsomal cytochrome P450 isozyme contents in F0 parental males
|
DEP (ppm) |
|||
|
0 (control) |
600 |
3000 |
15000 |
No. of F0 parental males examined |
6 |
6 |
6 |
6 |
CYP3A2 (p mol/mg protein) |
55.6±20.5 |
62.2±18.5 |
33.2±13.1 |
92.0±15.4** |
CYP4A1 (p mol/mg protein) |
13.7±3.1 |
15.0±6.9 |
11.5±2.6 |
62.8±19.2* |
a Mean±SD; * Significantly different from the control, p≤0.05; ** Significantly different from the control, p≤0.01
Serum hormone levels in F0 parental males
|
DEP (ppm) |
|||
|
0 (control) |
600 |
3000 |
15000 |
No. of F0 parental males examined |
6 |
6 |
6 |
6 |
Testosterone (ng/mL) |
2.63±1.23a |
1.81±0.46 |
0.50±0.26** |
1.26±0.66* |
Progesterone (ng/mL) |
2.66±2.51 |
3.61±2.50 |
5.98±3.00 |
3.08±0.94 |
a Significantly different from the control, p≤0.05; ** Significantly different from the control, p≤0.01
Applicant's summary and conclusion
- Conclusions:
- Following dietary administration to rats through 2 successive generations, the NOAEL for general toxicity and reproductive performance in parental animals is considered to be 15000 ppm as there were no adverse effects on these parameters.
For development and growth of pups the NOAEL is considered to be 3000 ppm due to decreased body weight gain in those given 15000 ppm. - Executive summary:
Reproductive toxicity has been investigated in a 2 -generation study in rats using methods in accordance with OECD test methods. The the NOAEL for general toxicity and reproductive performance in parental animals was considered to be 15000 ppm (equivalent to a mean intake of 1016 -1297 mg/kg/day) as there were no adverse effects on these parameters. For development and growth of pups the NOAEL was considered to be 3000 ppm (equivalent to a mean intake of 222 -267 mg/kg/day) due to decreased body weight gain in those given 15000 ppm (equivalent to a mean intake of 1150 -1375 mg/kg/day).
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