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EC number: 236-031-3 | CAS number: 13106-76-8
- 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- secondary literature
- Justification for type of information:
- data is from NTRL reports
Data source
Reference
- Reference Type:
- secondary source
- Title:
- Initial submission: The acute of toxicity certain compounds of molybdenum report to the International Molybdenum Association with attachments and cover letter dated 062891
- Author:
- International Molybdenum association
- Year:
- 1 991
- Bibliographic source:
- NTRL submission report -OTS0000811, last updated 1991
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Principles of method if other than guideline:
- The ocular irritation potential of Ammonium molybdate was assessed in rabbits
- GLP compliance:
- not specified
Test material
- Reference substance name:
- Ammonium molybdate(VI)
- EC Number:
- 236-031-3
- EC Name:
- Ammonium molybdate(VI)
- Cas Number:
- 13106-76-8
- Molecular formula:
- H4N.1/2MoO4
- IUPAC Name:
- ammonium molybdate(VI)
- Test material form:
- solid
- Details on test material:
- - Name of test material (as cited in study report): ammonium molybdate(VI)
- Molecular formula: MoO4.2H4N
- Molecular weight: 196.0132 g/mol
- Smiles notation: [Mo](=O)(=O)([O-])[O-].[NH4+].[NH4+]
- InChl: 1S/Mo.2H3N.4O/h;2*1H3;;;;/q;;;;;2*-1/p+2
- Substance type: Inorganic
- Physical state: Solid
Constituent 1
- Specific details on test material used for the study:
- - Name of test material (as cited in study report): ammonium molybdate(VI)
- Molecular formula: MoO4.2H4N
- Molecular weight: 196.0132 g/mol
- Smiles notation: [Mo](=O)(=O)([O-])[O-].[NH4+].[NH4+]
- InChl: 1S/Mo.2H3N.4O/h;2*1H3;;;;/q;;;;;2*-1/p+2
- Substance type: Inorganic
- Physical state: Solid
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Sex: Male
- Source: A. Smith, Warlingham. Surrey
- Age at study initiation: 12 to 13 week
- Weight at study initiation: 2.8 to 3.1 kg
- Fasting period before study:
- Housing: The rabbits were individually housed in metal cages with perforated floors in Building
- Diet (e.g. ad libitum): SDS Standard Rabbit Diet
- Water (e.g. ad libitum):Tap water
- Acclimation period: The rabbits selected for the study were all acclimated to the laboratory environment
ENVIRONMENTAL CONDITIONS
- Temperature (°C):19 deg C
- Humidity (%):Relative humidity:30-70%
- Air changes (per hr): 19 air changes
per hour
- Photoperiod (hrs dark / hrs light): 12 hours of artificial light in each 24 hour period.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes
- Amount / concentration applied:
- A 100 mg amount of Ammonium molybdate, the weight occupying a volume of 0.1 ml, was placed into the lower everted lid.
- Duration of treatment / exposure:
- single exposure
- Observation period (in vivo):
- Examination of the eyes was made after 1 hour and 1, 2, 3, 4 and.7 days after instillation.
- Duration of post- treatment incubation (in vitro):
- no data available
- Number of animals or in vitro replicates:
- 6 male rabbits
- Details on study design:
- TEST SITE
- Area of exposure: lower everted lid.
SCORING SYSTEM: Grading and scoring of the ocular lesions were performed according to cornea,iris, Conjunctivae ,chemosis and redness in the eye of rabbit
Grading Scale for Eye Irritation:
Cornea Grade
Opacity: degree of density (readings should be taken from most dense area)*
No ulceration or opacity = 0
Scattered or diffuse areas of opacity (other than slight dulling of normal lustre); details of iris slightly obscured = 1*
Easily discernible translucent area; details of iris slightly obscured = 2*
Opalescent area; no details of iris visible; size of pupil barely discernible = 3*
Opaque cornea; iris not discernible through the opacity = 4*
Area of Cornea Involved
One quarter(or less) but not zero = 1
Greater than one quarter, but less than half = 2
Greater than half, but less than three quarters = 3
Greater than three quarters, up to whole area = 4
Iris
Normal = 0
Markedly deepened rugae, congestion, swelling, moderate circumcorneal hyperaemia; or injection; iris reactive to light (a sluggish reaction is considered to be an effect = 1 *
Hemorrhage, gross destruction, or no reaction to light = 2*
Conjunctivae
Redness (refers to palpebral and bulbar conjunctivae; excluding cornea and iris)
Vessels Normal = 0
Some blood vessels definitely hyperaemic (injected) = 1
Diffuse, crimson colour; individual vessels not easily discernible = 2*
Diffuse beefy red = 3 *
Chemosis
Swelling (refers to lids and/or nictating membranes)
No swelling = 0
Any swelling above normal (includes nictating membrane)= 1*
Obvious swelling, with partial eversion of lids = 2*
Swelling, with lids about half closed = 3*
Swelling, with lids more than half closed= 4*
*-interpreted as a positive effect (TSCA test criteria)
Results and discussion
In vitro
- Other effects / acceptance of results:
- no data available
In vivo
Results
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 4 days
- Score:
- 0
- Reversibility:
- fully reversible within: 4 days
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- All conjunctival reactions had resolved one to four days after instillation. No corneal or iridial inflammation was seen throughout the observation period . A diffuse crimson-red colouration of the conjunctivae was evident twenty-four hours after instillation only in one animal. Mild conjunctival inflammation was observed in the remaininq animals.
Any other information on results incl. tables
Ocular reactions elicited by Ammonium molybdate:
Rabbit no. |
Region of eye |
1 hr |
Days after installation |
|||||
1 |
2 |
3 |
4 |
7 |
||||
1 |
Cornea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||
Conjunctivae |
Redness |
1 |
2 |
1 |
1 |
0 |
0 |
|
Chemosis |
1 |
1 |
0 |
0 |
0 |
0 |
||
2 |
Cornea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||
Conjunctivae |
Redness |
1 |
1 |
1 |
1 |
0 |
0 |
|
Chemosis |
1 |
0 |
0 |
0 |
0 |
0 |
||
3 |
Cornea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||
Conjunctivae |
Redness |
1 |
1 |
1 |
0 |
0 |
0 |
|
Chemosis |
1 |
1 |
0 |
0 |
0 |
0 |
||
4 |
Cornea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||
Conjunctivae |
Redness |
1 |
1 |
0 |
0 |
0 |
0 |
|
Chemosis |
1 |
0 |
0 |
0 |
0 |
0 |
||
5 |
Cornea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||
Conjunctivae |
Redness |
1 |
0 |
0 |
0 |
0 |
0 |
|
Chemosis |
1 |
0 |
0 |
0 |
0 |
0 |
||
6 |
Cornea |
Density |
0 |
0 |
0 |
0 |
0 |
0 |
Area |
0 |
0 |
0 |
0 |
0 |
0 |
||
Iris |
0 |
0 |
0 |
0 |
0 |
0 |
||
Conjunctivae |
Redness |
1 |
0 |
0 |
0 |
0 |
0 |
|
Chemosis |
1 |
0 |
0 |
0 |
0 |
0 |
Applicant's summary and conclusion
- Interpretation of results:
- other: not irritating
- Conclusions:
- Instillation of Ammonium molybdate into the rabbit eyes elicited transient and very slight conjunctival inflammation only which were completely resolved after 4 days
The overall irritation scores after 7 days was 0.0
Based on the observations and scores, Ammonium molybdate can be considered not irritating to rabbit eyes. - Executive summary:
The ocular irritation potential of Ammonium molybdate was assessed in rabbits. The study was performed according to OECD 405 Guidelines. 100 mg of 0.1 ml chemical was installed into thelower everted lid of 6 New Zealand White male rabbits. The contralateral eye remained untreated and served as a control. Examination of the eyes was made after 1 hour and 1, 2, 3, 4 and.7 days after instillation. Observation of the eyes was aided by the use of a handheld torch. Grading and scoring of the ocular lesions were performed.
One of the animals gave a "positive" response. No corneal damage or iridial inflammation was seen throughout the observation period. A diffuse crimson-red colouration of the conjunctivae was evident twenty-four hours after instillation only in one animal. Mild conjunctival inflammation was observed in the remaininq animals. All conjunctival reactions had resolved one to four days after instillation.
Instillation of Ammonium molybdate into the rabbit eyes elicited transient and very slight conjunctival inflammation only which were completely resolved after 4 days
The overall irritation scores after 7 days was 0.0
Based on the observations and scores, Ammonium molybdate can be considered not irritating to rabbit eyes.
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