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EC number: 215-183-4 | CAS number: 1310-65-2
- 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
- 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
Endpoint summary
Administrative data
Description of key information
In accordance with column 2 of REACH Regulation 1907/2006/EC Annex VII section 8.1 and 8.2 in-vitro studies for skin corrosion/ irritation and eye irritation do not need to be conducted if the available information indicates that the criteria are met for classification as corrosive to the skin and eyes. Lithium hydroxide anhydrous and its monohydrate are corrosive due to their chemical properties (strong alkaline substances). Thus, respective studies are not required.
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 2009-10-06
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 435 (In Vitro Membrane Barrier Test Method for Skin Corrosion)
- Principles of method if other than guideline:
- Corrositex TM is a quantitative in vitro corrosivity test. The model is based on the time required for the test substance to pass through a biobarrier membrane and produce a change in a chemical detection system.
- GLP compliance:
- yes
- Test system:
- artificial membrane barrier model
- Details on test system:
- SOURCE AND COMPOSITION OF MEMBRANE BARRIER USED
- Was the Corrositex® test kit used: Yes
WAS THE COMPATIBILITY TEST PERFORMED: Yes, test substance produced a change in colour when applied directly into the vial with CDS.
WAS THE TIMESCALE CATEGORY TEST PERFORMED: The test substance was placed into Vial A (containing an acid buffer) and Vial B (containing a base buffer), and the vials were observed for a colour change. A colour change observed in either vial is matched to a colour chart. Vial A showed a yellow color and vial B a grey colour. Based on the colour the substance was considered as category 2 substance and therefore was tested according to Category 2 test criteria.
METHOD OF DETECTION
- Indicator solution: Chemical Detection System (CDS) is composed of water and pH indicator dyes.
NUMBER OF REPLICATES: 4
PREDICTION MODEL / DECISION CRITERIA (choose relevant statement)
- The test substance is considered to be corrosive to skin if the test substances penetrates the membrane barrier in up to 60 min.
- The test substance is considered to be non-corrosive to skin if the penetration time is below 60 min.
- Justification for the selection of the cut-off point(s): According to Corrositex packing group assignment (please also refer to "any other information on materials and methods incl. tables") - Control samples:
- yes, concurrent vehicle
- yes, concurrent positive control
- Details on study design:
- The international Corrositex assay kit is an In vitro method for determining the corrosive potential of chemical substances. The results of this assay were used to determine the United Nations Transport Regulations Packaging Group. For detailed test procedure see Sect. "Any other information on materials and methods incl. tables"
- Irritation / corrosion parameter:
- penetration time (in minutes)
- Run / experiment:
- A
- Value:
- 21.93
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Remarks on result:
- positive indication of irritation
- Irritation / corrosion parameter:
- penetration time (in minutes)
- Run / experiment:
- B
- Value:
- 19.88
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Remarks on result:
- positive indication of irritation
- Interpretation of results:
- Category 1B (corrosive) based on GHS criteria
- Conclusions:
- A Corrositex TM Assay with Lithium hydroxide monohydrate was performed. Lithium hydroxide monohydrate was found to be corrosive.
- Executive summary:
The potential of lithium hydroxide monohydrate to cause dermal corrosion was assessed by a single topical application of the test substance to the Corrositex® Biobarrier Membrane (Corrositex® assay) equivalent or similar to OECD guideline 435. The Corrositex® Biobarrier Membrane is a test system consisting of a reconstituted collagen matrix. The assay is based on the time that is required for the test substance to penetrate through the Corrositex® Biobarrier Membrane and produce a change in the Chemical Detection System (CDS). In addition to the test substance a positive and a negative control were assessed. The Corrositex® assay showed the following results: The qualification screen demonstrated that the test substance is able to react with the CDS and produce a visible color change. Therefore the membrane barrier test method was determined to be suitable for the evaluation of the corrosive potential of the test substance. In each test run four Corrositex® Biobarrier Membranes were treated with the test substance. The mean breakthrough time of the test substance was below 30 min. Based on the observed results it was concluded, that lithium hydroxide monohydrate was found to be corrosive. Lithium hydroxide monohydrate has to be classified as corrosive Cat . 1B (H314) according to Regulation (EC) No 1272/2008 (CLP).
- Endpoint:
- skin corrosion: in vitro / ex vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 2009-10-06
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 435 (In Vitro Membrane Barrier Test Method for Skin Corrosion)
- Principles of method if other than guideline:
- Corrositex TM is a quantitative in vitro corrosivity test. The model is based on the time required for the test substance to pass through a biobarrier membrane and produce a change in a chemical detection system.
- GLP compliance:
- yes
- Test system:
- artificial membrane barrier model
- Details on test system:
- SOURCE AND COMPOSITION OF MEMBRANE BARRIER USED
- Was the Corrositex® test kit used: Yes
WAS THE COMPATIBILITY TEST PERFORMED: Yes, test substance produced a change in colour when applied directly into the vial with CDS.
WAS THE TIMESCALE CATEGORY TEST PERFORMED: The test substance was placed into Vial A (containing an acid buffer) and Vial B (containing a base buffer), and the vials were observed for a colour change. A colour change observed in either vial is matched to a colour chart. Vial A showed a yellow color and vial B a grey colour. Based on the colour the substance was considered as category 2 substance and therefore was tested according to Category 2 test criteria.
METHOD OF DETECTION
- Indicator solution: Chemical Detection System (CDS) is composed of water and pH indicator dyes.
NUMBER OF REPLICATES: 4
PREDICTION MODEL / DECISION CRITERIA (choose relevant statement)
- The test substance is considered to be corrosive to skin if the test substances penetrates the membrane barrier in up to 60 min.
- The test substance is considered to be non-corrosive to skin if the penetration time is below 60 min.
- Justification for the selection of the cut-off point(s): According to Corrositex packing group assignment (please also refer to "any other information on materials and methods incl. tables") - Control samples:
- yes, concurrent vehicle
- yes, concurrent positive control
- Details on study design:
- The international Corrositex assay kit is an in vitro method for determining the corrosive potential of chemical substances. The results of this assay were used to determine the United Nations Transport Regulations Packaging Group. For detailed test procedure see Sect. "Any other information on materials and methods incl. tables"
- Irritation / corrosion parameter:
- penetration time (in minutes)
- Run / experiment:
- A
- Value:
- 25.42
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Remarks on result:
- positive indication of irritation
- Irritation / corrosion parameter:
- penetration time (in minutes)
- Run / experiment:
- B
- Value:
- 21
- Vehicle controls validity:
- valid
- Negative controls validity:
- not examined
- Positive controls validity:
- valid
- Remarks on result:
- positive indication of irritation
- Interpretation of results:
- Category 1B (corrosive) based on GHS criteria
- Conclusions:
- A Corrositex TM Assay with lithium hydroxide anhydrous was performed. Lithium hydroxide anhydrous was found to be corrosive. Based on this data, this substance is found to be classified.
- Executive summary:
The potential of lithium hydroxide anhydrous to cause dermal corrosion was assessed by a single topical application of the test substance to the Corrositex® Biobarrier Membrane (Corrositex® assay) equivalent or similar to OECD guideline 435. The Corrositex® Biobarrier Membrane is a test system consisting of a reconstituted collagen matrix. The assay is based on the time that is required for the test substance to penetrate through the Corrositex® Biobarrier Membrane and produce a change in the Chemical Detection System (CDS). In addition to the test substance a positive and a negative control were assessed. The Corrositex® assay showed the following results: The qualification screen demonstrated that the test substance is able to react with the CDS and produce a visible color change. Therefore the membrane barrier test method was determined to be suitable for the evaluation of the corrosive potential of the test substance. In each test run four Corrositex® Biobarrier Membranes were treated with the test substance. The mean breakthrough time of the test substance was below 30 min. Based on the observed results it was concluded, that lithium hydroxide anhydrous was found to be corrosive. Lithium hydroxide anhydrous has to be classified as corrosive Cat . 1B (H314) according to Regulation (EC) No 1272/2008 (CLP).
Referenceopen allclose all
Two runs have been performed:
Run C:
Sample Nr. |
1 |
2 |
3 |
4 |
Detection Time hr:min:sec |
00:21:55 |
00:22:27 |
00:22:07 |
00:22:13 |
Start Time |
00:00:00 |
00:00:10 |
00:00:20 |
00.00:30 |
CORROSITEX Time |
00:21:55 |
00:22:17 |
00:21:47 |
00:21:43 |
Convert to Minutes |
21.92 |
22.28 |
21.78 |
21.72 |
Mean of 4 Replicates |
21.93 |
Run D:
Sample Nr. |
1 |
2 |
3 |
4 |
Detection Time hr:min:sec |
00:23:10 |
00:24:24 |
00:22:22 |
00:25:52 |
Start Time |
00:03:45 |
00:03:58 |
00:04:08 |
00.04:25 |
CORROSITEX Time |
00:19:25 |
00:20:26 |
00:18:14 |
00:21:27 |
Convert to Minutes |
19.42 |
20.43 |
18.23 |
21.45 |
Mean of 4 Replicates |
19.88 |
According to the results of the Corrositex TM Assay, the test article, lithium hydroxide monohydrate, has to be classified as corrosive and allocated to packing group II according to the UN Dangerous Goods Transport Regulations
Two runs have been performed:
Run A:
Sample Nr. |
1 |
2 |
3 |
4 |
Detection Time hr:min:sec |
00:25:50 |
00:25:50 |
00:25:50 |
00:25.50 |
Start Time |
00:00:00 |
00:00:48 |
00:01:55 |
00.02:57 |
CORROSITEX Time |
00:25.50 |
00:25:02 |
00:23:55 |
00:22:53 |
Convert to Minutes |
25.83 |
25.03 |
23.92 |
22.88 |
Mean of 4 Replicates |
24.42 |
Run B:
Sample Nr. |
1 |
2 |
3 |
4 |
Detection Time hr:min:sec |
00:26:00 |
00:28:30 |
00:28:30 |
00:26.00 |
Start Time |
00:04:36 |
00:05:43 |
00:06:52 |
00.07:50 |
CORROSITEX Time |
00:21:24 |
00:22:47 |
00:21:38 |
00:18:10 |
Convert to Minutes |
21.40 |
22.78 |
21.63 |
18.17 |
Mean of 4 Replicates |
21.00 |
According to the results of the Corrositex TM Assay, the test article, lithium hydroxide anhydrous, has to be classified as corrosive and allocated to packing group II according to the UN Dangerous Goods Transport Regulations
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
In accordance with column 2 of REACH Regulation 1907/2006/EC Annex VII section 8.1 and 8.2 in-vitro studies for skin corrosion/ irritation and eye irritation do not need to be conducted if the available information indicates that the criteria are met for classification as corrosive to the skin and eyes.
Lithium hydroxide anhydrous and its monohydrate are corrosive. Thus, respective studies are not required.
For classification, the results of CORROSITEX assays with lithium hydroxide anhydrous and lithium hydroxide monohydrate were considered.
Based on this data, lithium hydroxide anhydrous and lithium hydroxide are to be classified
- corrosive: Cat . 1B (H314 - causes severe skin burns and eye damage) according to Regulation (EC) No 1272/2008 (CLP)
Lithium hydroxide anhydrous and its monohydrate were found to be corrosive to skin and eye and assigned to packing group II.
Justification for classification or non-classification
Based on the available data, lithium hydroxide anhydrous and lithium hydroxide monohydrate are to be classified as
- corrosive to skin: Cat . 1B (H314) according to Regulation (EC) No 1272/2008 (CLP) and
- corrosive to eyes: Cat 1 (H318) according to Regulation (EC) No 1272/2008 (CLP) and
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.