Nonanedioic acid, 1,9-bis(2-octyldodecyl) ester

Repeated dose toxicity: oral

Administrative data

Endpoint:

short-term repeated dose toxicity: oral

Type of information:

migrated information: read-across based on grouping of substances (category approach)

Adequacy of study:

weight of evidence

Reliability:

2 (reliable with restrictions)

Rationale for reliability incl. deficiencies:

other: see 'Remark'

Remarks:

GLP - Guideline study. According to the ECHA guidance document "Practical guide 6: How to report read-across and categories (March 2010)", the reliability was changed from RL1 to RL2 to reflect the fact that this study was conducted on a read-across substance.

Cross-reference

Reason / purpose for cross-reference:

reference to same study

Data source

Reference

Reference 1

Reference Type:

study report

Title:

Unnamed

Year:

2003

Report date:

2003

Reference 2

Reference Type:

publication

Title:

Combined Repeat Dose and Reproductive/Developmental Toxicity Screening Test of Bis(2-ethylhexyl) azelate by Oral Administration in Rats

Author:

Shirota, M.

Year:

2003

Bibliographic source:

Toxicity Testing Reports of Environmental Chemicals, 11, 287-320

Reference 3

Reference Type:

secondary source

Title:

Diesters Category of the Aliphatic Esters Chemicals (Test Plan and Robust Summaries for Substances in the HPV Test Plan)

Author:

US-EPA (American Chemistry Council's Aliphatic Esters Panel)

Year:

2010

Bibliographic source:

High Production Volume (HPV) Chemical Challenge Program (201-16837A and 201-16837B)

Reference 4

Reference Type:

secondary source

Title:

Bis(2-ethylhexyl) azelate

Author:

OECD

Year:

2006

Bibliographic source:

SIDS Initial Assessment Report for SIAM 22, Paris, France, 18-21 April, 2006

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

GLP compliance:

yes

Limit test:

no

Test material

Test material information

Constituent 1

Reference substance name:

103-24-2 (analytical purity 77.2%)

IUPAC Name:

103-24-2 (analytical purity 77.2%)

Details on test material:

- Name of test material (as cited in study report): Bis(2-ethylhexyl)nonanedioate
- Analytical purity: 77.2%
- Impurities (identity and concentrations):
Bis(2-ethylhexyl)glutarate 2.2%,
Bis(2-ethylhexyl)adipate 2.4%,
Bis(2-ethylhexyl)pimelate 2.8%,
Bis(2-ethylhexyl)suberate 3.8%,
Bis(2-ethylhexyl)sebacate 3.3%,
Bis(2-ethylhexyl) 1-,9-nonamethylenedicarboxylate 5.3%,
Bis(2-ethylhexyl)1-,10-decamethylenedicarboxylate 0.6%,
Bis(2-ethylhexyl)1-,11-undecamethylenedicarboxylate 0.3%
- Lot/batch No.: N-31101

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: Charles River Laboratories Japan, Inc., Yokohama, Japan
- Age at study initiation: 10 weeks
- Housing: Metal mesh cage
- Diet: ad libitum, CE-2 from CLEA Japan, Inc., Meguro, Japan
- Water: ad libitum, tap water
- Acclimation period: about 3 weeks

ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22.0 - 25.5
- Humidity (%): 49.5 - 73.0
- Air changes: 15 times/day
- Photoperiod (hrs dark / hrs light): 12/12

Administration / exposure

Route of administration:

oral: gavage

Vehicle:

corn oil

Details on oral exposure:

PREPARATION OF DOSING SOLUTIONS:
Dosing solution was prepared more than once a week and stored at room temperature in the dark for 7 days. The stability for 8 days was verified by GC.

VEHICLE
- Amount of vehicle (if gavage): 5 mL/kg bw

Analytical verification of doses or concentrations:

yes

Details on analytical verification of doses or concentrations:

Dosing solution was mixtured with n-hexane and concentrations were analyzed by GC.

Duration of treatment / exposure:

Males: 14 days before mating, 28 days afterwards
Females: total of 42-53 days beginning 14 days before mating to day 4 of lactation

Frequency of treatment:

7 days/week

Doses / concentrations

Remarks:

Doses / Concentrations:
100, 300, 1000 mg/kg bw/day
Basis:
actual ingested

No. of animals per sex per dose:

13

Control animals:

yes, concurrent vehicle

Examinations

Observations and examinations performed and frequency:

CAGE SIDE OBSERVATIONS: Yes
- Time schedule: twice daily before and after treatment

DETAILED CLINICAL OBSERVATIONS: Yes
- Time schedule: at 13:00-16:00 on Days 7, 14, 21, 28, 35 and 42 of the treatment period using scoring systems.

BODY WEIGHT: Yes
- Time schedule for examinations: Body weights were determined on Days 1, 7, 14, 21, 28, 35, 42 of treatment and prior to necropsy in males and on Days 1, 7, 14 and 21 of treatment, Days 0, 7, 14 and 20 of gestation, Days 0 and 4 of lactation and prior to necropsy in females.

FOOD CONSUMPTION: Yes
- Time schedule: Days 1-2, 7-8, 14-15, 29-30, 35-36 and 41-42 of treatment in males, and on Days 1-2, 7-8 and 14-15 of the treatment period, Days 0-1, 7-8, 14-15 and 20-21 of gestation and day 3-4 of lactation in females. Food consumption was not determined during the mating period in males and females.

WATER CONSUMPTION: No

OPHTHALMOSCOPIC EXAMINATION: No

HAEMATOLOGY: Yes
- Time schedule for collection of blood: Blood samples were collected from the abdominal aorta after overnight starvation on
next day of the last administration.
- Animals fasted: Yes
- How many animals: All
- Following parameters were checked: red blood cell (RBC), hemoglobin, hematocrit, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), white blood cells (WBC), neutrophils, eosinophils, basophils, monocytes, lymphocytes, platelets, prothrombin time (PT), activated partial thromboplastin time (APTT)

CLINICAL CHEMISTRY: Yes
- Time schedule for collection of blood: Blood samples were collected from the abdominal aorta after overnight starvation on
next day of the last administration.
- Animals fasted: Yes
- How many animals: All
- Following parameters were checked: total protein, albumin, albumin/globulin ratio (A/G ratio), blood urea nitrogen (BUN), creatinine, glucose, total cholesterol, triglycerides, alkaline phosphatase (ALP), alanine aminotransferase, aspartate aminotransferase, gamma-glutamyltransferase, total bilirubin, inorganic phosphor, Ca, Na, K, Cl

URINALYSIS: No

NEUROBEHAVIOURAL EXAMINATION: Yes
- Time schedule for examinations: on Day 42 of treatment in males and on Day 4 of lactation in females.
- Dose groups that were examined: 5 animals/sex/dose
- Battery of functions tested: Preyer's reflex, pupillary reflex, pain reaction, withdrawal reflex, eyelid reflex and righting reflex

Sacrifice and pathology:

GROSS PATHOLOGY: Yes
Organ weights: Brain, heart, liver, kidney, spleen, adrenal, thymus, testis and epididymis
HISTOPATHOLOGY: Yes
Testis, epididymis and ovary of all animals at all doses, and
brain, pituitary, thymus, thyroid, parathyroid, adrenal, spleen, heart, stomach,
liver, duodenum, jejunum, ileum, cecum, colon, rectum, trachea, lung, kidney, urinary
bladder, femur, spinal cord, mesentery lymph node, submandibular gland, sciatic nerve,
bone marrow, prostate, seminal vesicle, uterus and vagina of 5 males and females at 0
and 1000 mg/kg bw/day.

Statistics:

Statistical methods: Dunnett's test for continuous data, and Mann-Whitney' U-test and Fisher' test for discrete data.

Results and discussion

Results of examinations

Clinical signs:

no effects observed

Mortality:

no mortality observed

Body weight and weight changes:

effects observed, treatment-related

Description (incidence and severity):

1000 mg/kg bw/day: impaired BW gain in males

Food consumption and compound intake (if feeding study):

no effects observed

Food efficiency:

not specified

Water consumption and compound intake (if drinking water study):

not specified

Ophthalmological findings:

not specified

Haematological findings:

effects observed, treatment-related

Description (incidence and severity):

1000 mg/kg bw: decrease in white blood cells

Clinical biochemistry findings:

effects observed, treatment-related

Description (incidence and severity):

1000 mg/kg bw/day: increase in albumin/globulin ratio in males/females, decrease in total protein and Ca in females; 300 mg/kg bw/day: increase in albumin/globulin ratio in females

Urinalysis findings:

not examined

Behaviour (functional findings):

no effects observed

Organ weight findings including organ / body weight ratios:

effects observed, treatment-related

Description (incidence and severity):

1000 mg/kg bw/day group: increase in rel. liver and kidney weight in males and females (non adverse)

Gross pathological findings:

no effects observed

Histopathological findings: non-neoplastic:

effects observed, treatment-related

Description (incidence and severity):

1000 mg/kg bw:/day: hepatocellular hypertrophy and periportal fatty change in males, (non adverse)

Histopathological findings: neoplastic:

no effects observed

Details on results:

CLINICAL SIGNS AND MORTALITY: There was no mortality related to the test substance treatment. No changes were observed on general clinical observation, nor were scores obtained by detailed clinical observations between control and the test substance-treated groups.

BODY WEIGHT AND WEIGHT GAIN
Body weight gain was suppressed in males of the 1000 mg/kg bw/day-treated group (see Table 1)

FOOD CONSUMPTION
No effects were observed in males and females of the test substance-treated groups.

HAEMATOLOGY
No effects were observed in males of the test substance-treated groups. A decrease in white blood cells (WBC) and a shorter activated partial thromboplastin time were observed in females of the 1000 mg/kg bw/day dose group. But these change were not considered as adverse effects because of no accompanying changes. A decrease in WBC was observed in females of the 1000 mg/kg bw/day dose group.

CLINICAL CHEMISTRY
An increase in albumin/globulin (A/G) ratio was found in males at 1000 mg/kg bw/day and in females at 300 mg/kg bw/day and higher. Decreases in total protein, creatinine and calcium were observed in females at 1000 mg/kg bw/day. The increase in A/G ratio noted in females at 300 mg/kg bw/day was not considered as an adverse effect because of no accompanying changes (see Table 2). Decreases in glucose and alkaline phosphatase observed in females of 100 mg/kg bw/day group and 300 mg/kg bw/day, respectively, were incidential observations and thus considered non-adverse.

NEUROBEHAVIOUR
No neurobehavioural abnormalities were observed in the test substance-treated groups.

ORGAN WEIGHTS
Increases in a relative weight of liver and absolute and relative weights of kidney for males and increases in relative weights of liver and kidney for females were observed in the 1000 mg/kg bw/day group (see Table 3).

GROSS PATHOLOGY
No adverse effects were observed for males and females.

HISTOPATHOLOGY: NON-NEOPLASTIC
Tendency of increase in hypertrophy of centrilobular hepatocytes and a reduction in the grade of periportal fatty change were observed in males of the 1000 mg/kg bw/day group (see Table 4).

Effect levels

1

Dose descriptor:

LOAEL

Remarks:

systemic

Effect level:

1 000 mg/kg bw/day (actual dose received)

Based on:

test mat.

Sex:

male/female

Basis for effect level:

other: clinical chemistry; body weight; organ weight

2

Dose descriptor:

NOAEL

Remarks:

systemic

Effect level:

300 mg/kg bw/day (actual dose received)

Based on:

test mat.

Sex:

male/female

Basis for effect level:

other: clinical chemistry; body weight; organ weight

Target system / organ toxicity

Critical effects observed:

not specified

Any other information on results incl. tables

Table 1: Body weight gain in males

Days of treatment		dose [mg/kg bw/day]
		0	100	300	1000
males		13	13	13	13
1-7	mean	23.6	27.3	19.9	21.5
	SD	10.1	7.5	11.9	4.6
7-14	mean	27.4	26.1	23.4	27.3
	SD	7.9	6.8	6.1	5.6
14-21	mean	20.4	24.1	22.1	21.2
	SD	5.9	4	6.7	8.5
21-28	mean	24.4	25.2	24.1	20.8
	SD	8.8	4	7.9	5.4
28-35	mean	25.4	24.5	22.1	17.3**
	SD	5.3	5	4.3	5
35-42	mean	22.5	22.7	21	13.1**
	SD	6.2	4.7	5.4	6

Table 2: Altered clinical chemistry data

		dose [mg/kg bw/day]
		0	100	300	1000
males		13	13	13	13
A/G ratio	mean	1.18	1.16	1.21	1.28*
	SD	0.09	0.1	0.11	0.09
females		12	10	9	11
A/G ratio	mean	1.26	1.32	1.41*	1.45**
	SD	0.07	0.08	0.16	0.13
Creatinine [mg/dL]	mean	0.7	0.7	0.8	0.6**
	SD	0.1	0	0.1	0.1
T.protein [g/dL]	mean	5.4	5.4	5.5	5.1**
	SD	0.2	0.2	0.3	0.2
Ca [mg/dL]	mean	9.8	9.9	9.8	9.40**
	SD	0.2	0.3	0.4	0.3

 

Table 3: Selected organ weights

			dose [mg/kg bw/day]
			0	100	300	1000
males			13	13	13	13
liver	absolute [g]	mean	14.22	15.07	14.19	15.48
		SD	161.00	1.66	1.14	1.34
	relative [%]	mean	2.86	2.99	2.95	3.27**
		SD	0.16	0.26	0.17	0.21
kidney	absolute [g]	mean	3.23	3.23	3.31	3.64**
		SD	0.29	0.30	0.22	0.29
	relative [%]	mean	0.65	0.64	0.69	0.77**
		SD	0.06	0.07	0.04	0.06
females			12	10	10	11
liver	absolute [g]	mean	11.27	10.71	11.50	12.34
		SD	1.22	0.70	1.69	1.28
	relative [%]	mean	3.53	3.51	3.70	3.92**
		SD	0.31	0.22	0.27	0.24
kidney	absolute [g]	mean	2.09	1.99	2.20	2.28
		SD	0.18	0.21	0.19	0.22
	relative [%]	mean	0.65	0.66	0.72	0.72*
		SD	0.06	0.07	0.12	0.04

 

Table 4: Histopathological changes

			dose [mg/kg bw/day]
			0	100	300	1000
males			5	5	5	12
liver	hypertrophy, hepatocyte, centrilobular	very slight	0	0	0	5*
	Fatty change periportal	very slight	2	2	5	5
		slight	3	2	0	0
		moderate	0	1	0	0
	Total incidence		5/5	5/5	5/5	5/12**

 * significant difference from control; p>0.05

 ** significant difference from control; p>0.01