Registration Dossier
Registration Dossier
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: 215-481-4 | CAS number: 1327-53-3
- 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

Exposure related observations in humans: other data
Administrative data
- Endpoint:
- exposure-related observations in humans: other data
- Type of information:
- other: human data
- Adequacy of study:
- key study
- Study period:
- 2000-10-22 to 2002-05-19
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Arsenic exposure from drinking water and risk of premalignant skin lesions in Bangladesh: Baseline results from the health effects of arsenic longitudinal study
- Author:
- Ahsan, H. et al.
- Year:
- 2 006
- Bibliographic source:
- American Journal of Epidemiology, Vol. 163 (12): 1138-1148
Materials and methods
- Type of study / information:
- This publication describes a cross sectional study.
- Endpoint addressed:
- carcinogenicity
- Principles of method if other than guideline:
- A cross-sectional analysis was conducted to assess the relationship between arsenic exposure in drinking water and premalignant skin lesions involving baseline data from Health Effects of Arsenic Longitudinal Study (HEALS), a prospective cohort study on 11746 participants in Araihazar, Bangladesh in the period between 2000–2002.
- GLP compliance:
- no
Test material
- Reference substance name:
- not applicable (epidemiological investigation based on arsenic exposure via drinking water)
- IUPAC Name:
- not applicable (epidemiological investigation based on arsenic exposure via drinking water)
Constituent 1
Method
- Ethical approval:
- confirmed, but no further information available
- Details on study design:
- TYPE OF EXPOSURE MEASUREMENT:
- Type: Interview
- Details: Well owners were interviewed to create a roster of all users of these wells. Trained study teams and physicians visited directly to participants for interviews. In addition, participants were clinically assessed for skin lesions and other health conditions. Biologic samples (blood and urine) were also collected.
EXPOSURE LEVELS: Drinking water containing 8.1-40:0, 40.1-91.0, 91.1-175.0, and 175.1-864.0 µg/L of arsenic
STUDY PERIOD: From October 22, 2000 to May 19, 2002
STUDY POPULATION
- Total population (Total no. of persons in cohort from which the subjects were drawn): 14828
- Selection criteria: Married (18-75 years); residing in the study area for at least 5 years prior to recruitment; primary user of one of the 5966 tube wells, designated as the ‘index’ well, for at least 3 years.
- Total number of subjects participating in study: 11746 (5042 men and 6704 women)
- Sex/age/race: Male and female / 18-75 years / Asian
- Smoker/nonsmoker: 70.9% smokers/ 29.1% nonsmokers
COMPARISON POPULATION
- Type: Reference group
- Details: Comparing participants with arsenic exposure and more susceptible attribute (e.g., male gender) with the reference group [Reference group: Participants with the lowest arsenic exposure level and a less susceptible attribute (e.g., female gender)]
HEALTH EFFECTS STUDIED
- Disease(s): Arsenicosis (premalignant skin lesions)
- Diagnostic procedure: Total urinary arsenic concentration was measured by graphite furnace atomic absorption using the Analyst 600 graphite furnace system. Urinary creatinine levels were assayed by a colorimetric Sigma Diagnostics Kit (Sigma, St. Louis, USA) for adjustment of urinary total arsenic concentration.
OTHER DESCRIPTIVE INFORMATION ABOUT STUDY:
- Water arsenic concentrations were analysed by graphite furnace atomic absorption or inductively coupled plasma-mass spectrometry.
- Statistics: Data were analysed using GMBO module of the EPICURE software and Statistical Analysis Software, version 8.0 (SAS Institute, Inc., Cary, USA). - Exposure assessment:
- measured
Results and discussion
- Results:
- Discussion: The most relevant and sensitive study is from Ahsan et al. (2006) conducted in Bangladesh, investigating the dose-response relationship between arsenic exposure from drinking water and premalignant skin lesions. 11,746 participants were enrolled in the period 2000-2002. Arsenic exposure was assessed for each participant on the basis of (i) drinking water arsenic concentrations as well as well use patterns, and (ii) creatinine-corrected urinary arsenic excretion. The control population were exposed to drinking water with <8.1 µg/L of arsenic. Drinking water containing 8.1-40:0, 40.1-91.0, 91.1-175.0, and 175.1-864.0 µg/L of arsenic was associated with adjusted prevalence odds ratios (OR) of skin lesions of 1.91 (95% confidence interval (CI): 1.26, 2,89), 3.03 (95% CI: 2.05, 4.50), 3.71 (95% Cl: 2,53, 5.44), and 5.39 (95% CI: 3.69, 7.86), respectively.
Any other information on results incl. tables
Confounding factors
- Age, gender, cigarette smoking, socioeconomic status indicators, sun exposure, and body mass index
Strength and weaknesses
Strengths: (i) addresses a large number of subjects (n=11,746), (ii) covers a wide range of arsenic concentrations in drinking water (0.1-864 ug/L), and (iii) exposure to arsenic was well characterised: not only the arsenic in well water was analysed, but also drinking water consumption monitored and most relevant, creatinine-adjusted urinary arsenic excretion as monitored for each participant enrolling in the study.
Applicant's summary and conclusion
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.

EU Privacy Disclaimer
This website uses cookies to ensure you get the best experience on our websites.