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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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.
EC number: 255-490-0 | CAS number: 41672-81-5
- 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
Toxicity to reproduction
Administrative data
- Endpoint:
- screening for reproductive / developmental toxicity
- Remarks:
- based on test type (migrated information)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012-04-20 to 2012-12-31
- Reliability:
- 1 (reliable without restriction)
Cross-reference
- Reason / purpose for cross-reference:
- reference to other study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 012
- Report date:
- 2012
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)
- Deviations:
- no
- Principles of method if other than guideline:
- Nil
- GLP compliance:
- yes
- Remarks:
- OECD Guideline No. 422
- Limit test:
- no
Test material
- Reference substance name:
- trans-1-(1-oxohexadecyl)-4-[(1-oxohexadecyl)oxy]-L-proline
- EC Number:
- 255-490-0
- EC Name:
- trans-1-(1-oxohexadecyl)-4-[(1-oxohexadecyl)oxy]-L-proline
- Cas Number:
- 41672-81-5
- Molecular formula:
- C37H69NO5
- IUPAC Name:
- 1-palmitoyl-4-(palmitoyloxy)-L-proline
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report): trans-1-(1-oxohexadecyl)-4-[(1-oxohexadecyl)oxy]-L-proline
- Molecular formula (if other than submission substance): NA
- Molecular weight (if other than submission substance): NA
- Smiles notation (if other than submission substance): NA
- InChl (if other than submission substance): NA
- Structural formula attached as image file (if other than submission substance): NA
- Substance type: NA
- Physical state: White powder
- Analytical purity: Consider as 100% (dry extract)
- Impurities (identity and concentrations): NA
- Composition of test material, percentage of components: NA
- Isomers composition: NA
- Purity test date: 2/04/2011
- Lot/batch No.: 1105500007
- Expiration date of the lot/batch: February 23rd 2014
- Radiochemical purity (if radiolabelling): NA
- Specific activity (if radiolabelling): NA
- Locations of the label (if radiolabelling): NA
- Expiration date of radiochemical substance (if radiolabelling): NA
- Stability under test conditions: NA
- Storage condition of test material: Ambient (+ 15 to +25 °C)
- Other: Nil
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Wistar
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Toxicology, Department of Safety Assessment, Advinus Therapeutics Limited, Bangalore 560 058, India
- Age at study initiation: 11 -12 weeks
- Weight at study initiation: Males: 241 to 312g; Females: 171 to 223g
- Fasting period before study: No
- Housing:
Two rats of same sex were housed per cage in sterilized standard polysulfone cages (Size: approximately L 425 x B 266 x H 175 mm), with stainless steel top grill having facilities for pelletted food and drinking water in polycarbonate bottles with stainless steel sipper tubes except for last animal in the recovery group wherein one animal was housed.
- Use of restrainers for preventing ingestion (if dermal): no
- Diet (e.g. ad libitum):
Teklad Certified (2014C) Global 14 % Protein Rodent Maintenance Diet - Pellet (Certified) manufactured by Harlan Laboratories B.V. Maasheseweg 87c PO Box 553, 5800, AN Venray, The Netherlands was provided ad libitum to the animals.
- Water (e.g. ad libitum):
Deep bore-well water passed through activated charcoal filter and exposed to UV rays in ‘Aquaguard’ on-line water filter-cum-purifier manufactured by Eureka Forbes Ltd., Mumbai 400 001, India was provided ad libitum to rats in polycarbonate bottles with stainless steel sipper tubes.
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C):21 to 25°C
- Humidity (%): 65 to 68 %
- Air changes (per hr): 12 - 15
- Photoperiod (hrs dark / hrs light): 12
IN-LIFE DATES: From:20 April 2012 To: 23 June 2012
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- CMC (carboxymethyl cellulose)
- Details on exposure:
- PREPARATION OF DOSING SOLUTIONS:
Following procedure was followed when 100 mL of dose formulation prepared:
The quantities of 1000, 3000 and 10000 mg of test item was weighed on a separate aluminum foil and carefully transferred into separate mortor. Small aliquot of vehicle [0.5%w/v sodium salt of carboxymethyl cellulose (medium viscosity) with 0.1 % Tween 80 in Milli-Q water] was added to each mortar and triturated well to obtain the pasty mass of the suspension. Required aliquot of vehicle was added to the mass and triturated to obtain the suspension and then transferred to separate measuring cylinders. The mortar and pestle was rinsed with vehicle and it was transferred to the respective measuring cylinders. The final volume was made up with the vehicle to get the final concentration of 10, 30 and 100 mg/mL for the G2, G3 and G4/G4R groups, respectively.
DIET PREPARATION
- Rate of preparation of diet (frequency):
- Mixing appropriate amounts with (Type of food):
- Storage temperature of food:
VEHICLE
- Justification for use and choice of vehicle (if other than water):0.5% (w/v) Sodium Carboxymethyl cellulose (medium viscosity) with 0.1% (w/v) Tween® 80 in Milli-Q water was used as vehicle for dose formulation preparation as the same vehicle was used in the dose range finding toxicity study (study no. G8202). Indeed, this vehicle is commonly used for iterative studies, moreover the test item is well solubilized in this matrix. Further the historical data was also available with this vehicle.
- Concentration in vehicle: 0.5 %
- Amount of vehicle (if gavage): 10 mL/Kg body weight
- Lot/batch no. (if required): 039K0149
- Purity: NA - Details on mating procedure:
- - M/F ratio per cage: 1:1
- Length of cohabitation: 21 days
- Proof of pregnancy: [vaginal plug / sperm in vaginal smear] referred to as [day 0 / day 1] of pregnancy
- After 14 days of unsuccessful pairing replacement of first male by another male with proven fertility.
- Further matings after two unsuccessful attempts: no
- After successful mating each pregnant female was caged (how): individually
- Any other deviations from standard protocol: Nil - Analytical verification of doses or concentrations:
- yes
- Details on analytical verification of doses or concentrations:
- For homogeneity and test item concentration (calculated based on determined concentration of DPHP as tracer) analysis, the prepared dose suspension was sampled in duplicate sets from each dose levels (two samples were drawn from each of the top, middle and bottom layers) on Day 1 and during 2nd month of the treatment period. Similarly, one sample from middle layer was drawn from vehicle control. One set of samples was sent to Analytical R&D of Advinus Therapeutics Limited, for analysis and the other set were stored in the refrigerator condition. The sample analysis was done as per the analytical method validated under Advinus Study No.: G8201.
On Day 1, samples corresponding to 10 mg/mL and 30 mg/mL were marginally outside the acceptance criteria of ±15%. Hence back-up samples were analysed. The results indicated that the test item concentrations in solution were within the permissible limits of ± 15 %.from the nominal concentrations. - Duration of treatment / exposure:
- Males: The dose formulation was administered to the rats of the specific groups once daily at approximately the same time each day (varying by ± 2 hours) for 2 weeks prior to mating. Treatment was continued during mating and up to and including the day before sacrifice which was done after the completion of the mating process.
Females: The dose formulations were administered to the specific group of rats once daily at approximately the same time each day (varying by ± 2 hours) throughout the treatment period. Treatment was done 2 weeks prior to the mating period and continued through mating, pregnancy and up to lactation day 4, after which, pups were sacrificed on lactation day 4 and females (dams) were sacrificed on lactation day 5 after overnight fasting (water allowed).
The dose formulations were administered to the high dose recovery group of rats once daily at approximately the same time each day (varying by ± 2 hours).
Similarly, vehicle was administered to rats in the vehicle control and vehicle control recovery groups.
The dose volume administered to each rat was at an equivolume of 10 mL/kg body weight throughout the study. The dose volume was adjusted based on the most recent body weight of individual rat.
The vehicle and the test item was not administered for vehicle control recovery and high dose recovery groups, respectively for 14 days following the treatment period. - Frequency of treatment:
- Daily
- Details on study schedule:
- - Age at mating of the mated animals in the study: 13 - 14 weeks
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
100 mg/kg/day
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
300 mg/kg/day
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
1000 mg/kg/day
Basis:
nominal conc.
- No. of animals per sex per dose:
- Main groups : 10 males+10 females per group
Recovery groups : 5 males + 5 females per group
Total = 100 (50 males + 50 females) - Control animals:
- yes, concurrent vehicle
- Details on study design:
- - Dose selection rationale: The dose levels of 100 (G2), 300 (G3) and 1000 (G4) mg/kg/day were selected for this study based on the results of 14-Day Repeated Dose Oral Toxicity Study in Wistar Rats (Study No.G8202) and in consultation with the Sponsor.
In addition to the test doses, vehicle control and vehicle control recovery groups were included. Animals in the vehicle control and recovery animals were handled in a manner similar to the treatment groups except for test item administration.
- Rationale for animal assignment (if not random): Random
- Other: Nil - Positive control:
- Nil
Examinations
- Parental animals: Observations and examinations:
- CAGE SIDE OBSERVATIONS: Yes
- Time schedule: Once daily
- Cage side observations checked in table [No.?] were included.
DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: Weekly
BODY WEIGHT: Yes
- Time schedule for examinations: Individual body weights of males were recorded initially and at weekly (±1 day) intervals thereafter. Individual body weights of females were recorded initially and at weekly (±1 day) intervals thereafter till cohabitation with males. For recovery groups the individual body weight was recoded initially and weekly (±1 day) intervals thereafter.
All dams were weighed on Gestation Days (GD) 0, 7, 14 and 20 and on lactation days 0 and 4 and weights were recorded.
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: No
WATER CONSUMPTION AND COMPOUND INTAKE (if drinking water study): No
- Time schedule for examinations:
OTHER: Nil - Oestrous cyclicity (parental animals):
- Yes, during cohabitation.
- Sperm parameters (parental animals):
- No
- Litter observations:
- STANDARDISATION OF LITTERS
- Performed on day 4 postpartum: No
PARAMETERS EXAMINED
The following parameters were examined in F1 offspring:
[number and sex of pups, stillbirths, live births, postnatal mortality, presence of gross anomalies, weight gain, physical or behavioural abnormalities, other:]
GROSS EXAMINATION OF DEAD PUPS: Yes, for external and internal abnormalities; possible cause of death was/was not determined for pups born or found dead. - Postmortem examinations (parental animals):
- SACRIFICE
- Male animals: All surviving animals after completion of mating and at least 4 weeks treatment
- Maternal animals: All surviving animals on day 5 of lactation
GROSS NECROPSY
- Gross necropsy consisted of [external and internal examinations including the cervical, thoracic, and abdominal viscera.]
HISTOPATHOLOGY / ORGAN WEIGHTS
The tissues indicated in the Study Plan were prepared for microscopic examination and weighed, respectively. - Postmortem examinations (offspring):
- SACRIFICE
- The offspring were sacrificed on day 4 of lactation.
GROSS NECROPSY
- Gross necropsy consisted of external and internal examinations including the cervical, thoracic, and abdominal viscera. - Statistics:
- The statistical analysis of the experimental data was carried out using the validated package in Excel and also using licensed copies of SYSTAT Statistical package ver.12.0. All quantitative variables like body weight, food intake, haematology, clinical chemistry, organ weights and organ weight ratios were tested for normality (Shapiro-Wilk test) and homogeneity of variances (Levene’s test) within the group before performing a one-factor ANOVA modeling by treatment groups. Non-optimal (non-normal or heteroschedastic) data was transformed, before ANOVA is performed. Comparison of means between treatment groups and control group was done using Dunnett’s test when the overall treatment, ‘F’ test is found to be significant.
Pre-implantation loss (%), post implantation loss (%), no. of corpora lutea and implantations, pre-coital interval and gestation length (days) was analysed after suitable transformation (√ x + ½) of the data. One-way analysis of variance (ANOVA) was carried out for the transformed data. Dunnett’s pair-wise comparison of the treated means with the control mean was done when the group differences are found significant.
Z test was performed for testing the differences in proportions for mating and fertility indices.
All analyses and comparisons were evaluated at the 5% (P≤0.05) level. Statistically significant differences (P≤0.05), indicated by the aforementioned tests were designated by the superscripts throughout the report as stated below:
+/- : Significantly higher (+)/lower (-) than the vehicle control group
a+/a- : Significantly higher (a+)/lower (a-) than the vehicle control recovery group - Reproductive indices:
- a. Male mating index (%)
b. Male fertility index (%)
c. Female mating index (%)
d. Fecundity index (%)
e. Female fertility index (%)
f. Mean number of corpora lutea (CL)/group
g. Mean number of implantations/group
h. Implantation index
i. Percentage of pre-implantation loss per group
j. Post implantation loss (%)
k. Gestation index - Offspring viability indices:
- a. Mean litter size per group
b. Live birth index (%)
c. Day 4 survival index (%)
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:
- no effects observed
- Histopathological findings: non-neoplastic:
- no effects observed
- Other effects:
- not examined
Reproductive function / performance (P0)
- Reproductive function: oestrous cycle:
- no effects observed
- Reproductive function: sperm measures:
- not examined
- Reproductive performance:
- no effects observed
Details on results (P0)
BODY WEIGHT AND FOOD CONSUMPTION (PARENTAL ANIMALS): No
TEST SUBSTANCE INTAKE (PARENTAL ANIMALS): Not done
REPRODUCTIVE FUNCTION: No effects
REPRODUCTIVE FUNCTION: Not examined
REPRODUCTIVE PERFORMANCE (PARENTAL ANIMALS): No effects
ORGAN WEIGHTS (PARENTAL ANIMALS) : No effects
GROSS PATHOLOGY (PARENTAL ANIMALS): No effects
HISTOPATHOLOGY (PARENTAL ANIMALS): No effects
OTHER FINDINGS (PARENTAL ANIMALS): Nil
Effect levels (P0)
- Dose descriptor:
- NOAEL
- Effect level:
- 1 000 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: No significant effect noted
Results: F1 generation
General toxicity (F1)
- Clinical signs:
- no effects observed
- Mortality / viability:
- no mortality observed
- Body weight and weight changes:
- no effects observed
- Sexual maturation:
- not examined
- Organ weight findings including organ / body weight ratios:
- not examined
- Gross pathological findings:
- no effects observed
- Histopathological findings:
- not examined
Details on results (F1)
CLINICAL SIGNS (OFFSPRING): No effects
BODY WEIGHT (OFFSPRING): No effects
SEXUAL MATURATION (OFFSPRING): Not examined
ORGAN WEIGHTS (OFFSPRING): Not examined
GROSS PATHOLOGY (OFFSPRING): No effects
HISTOPATHOLOGY (OFFSPRING): Not examined
OTHER FINDINGS (OFFSPRING): Nil
Effect levels (F1)
- Dose descriptor:
- NOAEL
- Generation:
- F1
- Effect level:
- 1 000 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male/female
- Basis for effect level:
- other: No significant effect noted
Overall reproductive toxicity
- Reproductive effects observed:
- not specified
Any other information on results incl. tables
Nil
Applicant's summary and conclusion
- Conclusions:
- To summarize, oral administration of test item “ trans-1-(1-oxohexadecyl)-4-[(1-oxohexadecyl)oxy]-L-proline” to Wistar rats at the dose levels 100, 300 and 1000 mg/kg Bwt/day had no effects on general health, body weights, food intake, pre-coital time, gestation length, mating and fertility parameters. Functional observations did not reveal any test item related changes at all the tested doses in both sexes. The live birth and survival index was not altered by the treatment at the entire tested dose. The test item administration did not reveal any treatment related changes in the hematology, coagulation and clinical chemistry parameters of both males and females. There were no test item related changes in the terminal body weights, organ weights and organs weight ratios in both males and females. Gross examination of pups on lactation day 4 did not reveal any gross changes.
There were no test item related gross and microscopic changes in both males and females
No Observed Adverse Effect Level (NOAEL):
As there were no adverse effects observed in any parameters up to the highest dose tested, the No Observed Adverse Effect Level (NOAEL) is considered to be 1000 mg/kg Bwt/day. - Executive summary:
Under experimental conditions described in the Material and Method section, the following results were obtained:
No clinical signs or mortality was observed during the course of the study.
No treatment-related neurological abnormalities /dysfunctions were observed at all the doses tested.
The body weights and food consumption were unaffected by the treatment at all the doses tested.
The body weights and food consumption were unaffected during gestation and lactation periods at all the doses tested.
There were no treatment-related changes in the hematology, coagulation and clinical chemistry parameters.
Treatment had no effect on pre-coital time or gestation length, mating and fertility parameters in both sexes.
There were no treatment-related effects on the uterine/implantation data, mean litter size and mean viable litter size.
There were no external abnormalities in live or dead pups in any of the groups.The Day 4 survival index was not altered by the treatment at all the doses tested.
The test item administration did not reveal any treatment related changes in the hematology, coagulation and clinical chemistry parameters of both males and females.
There were no test item related changes in the terminal body weights, organ weights and organs weight ratios in both males and females. Gross examination of pups on lactation day 4 did not reveal any gross changes.
There were no test item related gross and microscopic changes in both males and females.
No Observed Adverse Effect Level (NOAEL): As there were no adverse effects observed in any parameters up to the highest dose tested, the No Observed Adverse Effect Level (NOAEL) is considered to be 1000 mg/kg Bwt/day.
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.