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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Workers - Hazard via inhalation route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
43.8 mg/m³
Most sensitive endpoint:
repeated dose toxicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
10
Modified dose descriptor starting point:
NOAEC
Value:
438 mg/m³
Explanation for the modification of the dose descriptor starting point:
As no inhalation study is available an reliable subchronic oral study is considered appropriate for the estimation of an inhalative DNEL.
AF for dose response relationship:
1
Justification:
true NOAEC applied
AF for differences in duration of exposure:
2
Justification:
correction for duration from sub-chronic to chronic
AF for interspecies differences (allometric scaling):
1
Justification:
already considered in route correction
AF for intraspecies differences:
5
Justification:
ECHA default assessment factor
AF for the quality of the whole database:
1
Justification:
good quality for database
Acute/short term exposure
Hazard assessment conclusion:
hazard unknown (no further information necessary)
DNEL related information

Local effects

Acute/short term exposure
Hazard assessment conclusion:
hazard unknown (no further information necessary)
DNEL related information

Workers - Hazard via dermal route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
125 mg/kg bw/day
Most sensitive endpoint:
repeated dose toxicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
40
Modified dose descriptor starting point:
NOAEL
Value:
5 000 mg/kg bw/day
Explanation for the modification of the dose descriptor starting point:
The dermal route is typically covered by oral route information in the absence of data for this administration route.
AF for dose response relationship:
1
Justification:
true NOAEL used
AF for differences in duration of exposure:
2
Justification:
correction for duration from sub-chronic to chronic
AF for interspecies differences (allometric scaling):
4
Justification:
allometric scaling rat to human
AF for intraspecies differences:
5
Justification:
default factor
AF for the quality of the whole database:
1
Justification:
good quality database
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified

Workers - Hazard for the eyes

Local effects

Hazard assessment conclusion:
no hazard identified

Additional information - workers

DNEL acute

A DNELacuteshould be established for substances if an acute hazard toxicity (leading to C&L) has been identified and a potential for high peak exposures exists.

RRR-(alpha-, beta-, gamma-, delta)-tocopherol does not have to be labelled for acute toxicity and therefore, a derivation of a DNELacuteis not necessary.

 

DNEL long-term systemic

RRR-(alpha-, beta-, gamma-, delta)-tocopherol isnot classified for any endpoint related to systemic toxicity.

For the DNEL-derivation a NOAEL of 500 mg/kg bw was used derived from the 90-day repeated dose oral, basedon hemorrhagic diathesis in males and females (an increase in APTT, PT and fibrinogen at 2000 mg/kg).

The dermal DNELfor long-term exposure - systemic effects for workers is derived as follows:

Description

Value

Remark

Step 1) Relevant dose-descriptor

NOAEL: 500 mg/kg bw/day

Based on hemorrhagic diathesis in males and females

Step 2) Modification of starting point

 

x 50/5

 

 

50% for oral absorption, and 5% absorption is assumed for dermal absorption

Modified dose-descriptor

500 mg/kg bw/d x 50/5 = 5000 mg/kg bw/day

Step 3) Assessment factors

 

 

Interspecies

4

 

Allometric scaling for the rat, the additional factor of 2.5 is omitted.

Intraspecies

5

Default assessment factor

Exposure duration

2

A correction for duration from sub-chronic to chronic is required

Dose response

1

 NOAEL used

Quality of database

1

 good quality database

DNEL

Value

 5000 mg/kg bw/d/ (4 x 5 x 2 x 1 x 1)=125 mg/kg bw/d

The inhalative DNELfor long-term exposure - systemic effects for workers is derived as follows:

Description

Value

Remark

Step 1) Relevant dose-descriptor

NOAEL: 500 mg/kg bw/d

Based on hemorrhagic diathesis in males and females

Step 2) Modification of starting point

/0.38 m3/kg bw

  

 x 6.7 m3/10 m3

 

 

 

 

x50/100

 

8 h respiratory volume for rat.

 

Correction for activity driven differences of respiratory volumes in workers compared to workers in rest.

 

 

Default 50% for oral absorption, and 100% absorption is assumed for inhalation.

Modified dose-descriptor

500 x 0.67 x 0.5 / 0.38 = 440 mg/m3

Step 3) Assessment factors

 

 

Interspecies

1.0

 

The allometric scaling is already considered in the starting point correction. The additional factor of 2.5 is omitted.

Intraspecies

5

Default assessment factor

Exposure duration

2

A correction for duration from sub-chronic to chronic is required

Dose response

1

 NOAEL used

Quality of database

1

 good quality database

DNEL

Value

 

 440 mg/m3/ (1.0 x 5 x 2 x 1 x 1)=44 mg/m3

 

 

The dermal DNELfor long term exposure - local effects for workers should be established for substances if a local toxicity (leading to C&L) has been identified and a potential for long term risks exists. RRR-(alpha-, beta-, gamma-, delta)-tocopherol does not have to be labelled for local toxicity, including irritation and skin sensitisation and therefore, a derivation of a DNELacute is not necessary.

General Population - Hazard via inhalation route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
10.8 mg/m³
Most sensitive endpoint:
repeated dose toxicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
20
Modified dose descriptor starting point:
NOAEC
Value:
217 mg/m³
Explanation for the modification of the dose descriptor starting point:
As no inhalation study is available an reliable subchronic oral study is considered appropriate for the estimation of a inhalative DNEL.
AF for dose response relationship:
1
Justification:
true NOAEL used
AF for differences in duration of exposure:
2
Justification:
correction fro duration from subchronic to chronic
AF for interspecies differences (allometric scaling):
1
Justification:
already considered in rout correction
AF for intraspecies differences:
10
Justification:
default value
AF for the quality of the whole database:
1
Justification:
good quality databse
Acute/short term exposure
Hazard assessment conclusion:
hazard unknown (no further information necessary)
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
hazard unknown (no further information necessary)
Acute/short term exposure
Hazard assessment conclusion:
hazard unknown (no further information necessary)
DNEL related information

General Population - Hazard via dermal route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
62.5 mg/kg bw/day
Most sensitive endpoint:
repeated dose toxicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
40
Modified dose descriptor starting point:
LOAEL
Value:
5 000 mg/kg bw/day
Explanation for the modification of the dose descriptor starting point:
The dermal route is typically covered by oral route information in the absence of data for this administration route.
AF for dose response relationship:
1
Justification:
true NOAEL used
AF for differences in duration of exposure:
2
Justification:
correction factor for duration from sub-chronic to chronic
AF for interspecies differences (allometric scaling):
4
Justification:
allometric scaling for the rat
AF for intraspecies differences:
10
Justification:
default value
AF for the quality of the whole database:
1
Justification:
good quality database
Acute/short term exposure
Hazard assessment conclusion:
low hazard (no threshold derived)
Route of original study:
Dermal
DNEL related information

Local effects

Long term exposure
Hazard assessment conclusion:
no hazard identified
Acute/short term exposure
Hazard assessment conclusion:
hazard unknown (no further information necessary)

General Population - Hazard via oral route

Systemic effects

Long term exposure
Hazard assessment conclusion:
DNEL (Derived No Effect Level)
Value:
6.25 mg/kg bw/day
Most sensitive endpoint:
repeated dose toxicity
Route of original study:
Oral
DNEL related information
DNEL derivation method:
ECHA REACH Guidance
Overall assessment factor (AF):
80
Modified dose descriptor starting point:
NOAEL
Value:
500 mg/kg bw/day
Explanation for the modification of the dose descriptor starting point:
not necessary as key study uses oral administration
AF for dose response relationship:
1
Justification:
true NOAEL used
AF for differences in duration of exposure:
2
Justification:
correction factor for duration from sub-chronic to chronic is required
AF for interspecies differences (allometric scaling):
4
Justification:
allometric scaling for rat
AF for intraspecies differences:
10
Justification:
default value
AF for the quality of the whole database:
1
Justification:
good quality database
Acute/short term exposure
Hazard assessment conclusion:
no hazard identified
Route of original study:
Oral
DNEL related information

General Population - Hazard for the eyes

Local effects

Hazard assessment conclusion:
no hazard identified

Additional information - General Population

DNEL acute

ADNELacuteshould be established for substances if an acute hazard toxicity (leading to C&L) has been identifiedanda potential for high peak exposures exists. RRR-(alpha-, beta-, gamma-, delta)-tocopherol does not have to be labelled for acute toxicity and therefore, a derivation of a DNELacuteis not necessary.

DNEL long-term systemic

RRR-(alpha-, beta-, gamma-, delta)-tocopherol is not classified for systemic target organ toxicitity

For the DNEL-derivation a NOAEL of 500 mg/kg bw/d was used derived from the 90 -day repeated dose oral, based on hemorrhagic diathesis in males and females (an increase in APTT, PT and fibrinogen at 2000 mg/kg).

The dermal DNEL for long-term exposure - systemic effects for general population is derived as follows:

Description

Value

Remark

Step 1) Relevant dose-descriptor

NOAEL: 500 mg/kg bw/d

Based on hemorrhagic diathesis

Step 2) Modification of starting point

 

x 50/5

 

 

50% for oral absorption and 5% absorption is assumed for dermal absorption.

Modified dose-descriptor

500 mg/kg bw/d x 50/5 = 5000 mg/kg bw/day

Step 3) Assessment factors

 

 

Interspecies

4

 

Allometric scaling for the rat

Intraspecies

10

Default assessment factor

Exposure duration

2

A correction for duration from sub-chronic to chronic is required

Dose response

1

 

Quality of database

1

 good quality database

DNEL

Value

5000 mg/kg bw/d/ (4 x 10 x 2 x 1 x 1)=62.5 mg/kg bw/d

The inhalation DNEL for long-term exposure - systemic effects for general population is derived as follows:

Description

Value

Remark

Step 1) Relevant dose-descriptor

NOAEL: 500 mg/kg bw/d

Based on hemorrhagic diathesis

Step 2) Modification of starting point

/ 1.15 m3/kg bw

 

 

x 50/100

 

24 h respiratory volume for rats.

 

 

50% for oral absorption and 100% absorption is assumed for inhalation.

Modified dose-descriptor

500 / 1.15 x 0.5 = 217 mg/m3

Step 3) Assessment factors

 

 

Interspecies

1.0

 

Allometric scaling already considered in starting point correction.

Intraspecies

10

Default assessment factor

Exposure duration

2

A correction for duration from sub-chronic to chronic is required.

Dose response

1

 

Quality of database

1

 

DNEL

Value

*DNEL using ECETOC AF

217 mg/m3/ (1.0 x 10 x 2 x 1 x 1)=10.8 mg/m3

The oral DNEL for long-term exposure - systemic effects for general public is derived as follows:

Description

Value

Remark

Step 1) Relevant dose-descriptor

NOAEL: 500 mg/kg bw/d

Based on hemorrhagic diathesis

Step 2) Modification of starting point

Not required

 

 

 

 

 

Step 3) Assessment factors

 

 

Interspecies

4

 

Allometric scaling for the rat.

Intraspecies

10

Default assessment factor

Exposure duration

2

A correction for duration from sub-chronic to chronic is required

Dose response

1

 

Quality of database

1

 

DNEL

Value

500 mg/kg bw/d/ (4 x 10 x 2 x 1 x 1)=6.25 mg/kg bw/d

 

The dermal DNEL for long-term local effects should be established for substances if a local toxicity (leading to C&L) has been identified and a potential for long term risks exists. RRR-(alpha-, beta-, gamma-, delta)-tocopherol does not have to be labelled for local toxicity, including irritation and skin sensitisation and therefore, a derivation of a DNELacute is not necessary.