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EC number: 203-854-4 | CAS number: 111-29-5
- 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
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Endpoint summary
Administrative data
Key value for chemical safety assessment
Effects on fertility
Description of key information
NOAEL (maternal and reproductive toxicity) = 1000 mg/kg/g (OECD 422, BASF SE, 2022 with 1,5-pentandiol; OECD 421, BASF AG (1995), analogue substance 1,6-hexanediol CAS 629-11-8 and OECD 422, BASF SE (2013), metabolite d-valerolactone CAS 542-28-9)
Effect on fertility: via oral route
- Dose descriptor:
- NOAEL
- 1 000 mg/kg bw/day
Additional information
The evaluation of the endpoint toxicity to reproduction for 1,5-pentanediol (CAS 111-29-5) is based on a weight of evidence approach using the toxicological data of 1,5-pentandiol itself and the chemical analogue 1,6-hexanediol (CAS 629-11-8) and main metabolite of 1,5-pentanediol, d-valerolactone (CAS 542-28-9) (for WoE information, see chapter 13.2).
1,5-pentanediol
In a Repeated dose and Reproductive Toxicity Screening study according to OECD 422, the oral administration of 1,5-pentanediol to Han Wistar rats at dose levels of 100, 300 or 1000 mg/kg/day for five weeks to males and for two weeks before pairing, throughout gestation and up to Day 13 of lactation in females was well-tolerated with no adverse findings at any dose level. Reproductive performance, fertility, litter size and offspring survival and growth were unaffected by parental treatment and, in the context of this study, 1,5-pentanediol showed no evidence of being an endocrine disruptor. The no-observed-adverse-effect level (NOAEL) for systemic and reproductive/developmental toxicity was therefore considered to be 1000 mg/kg/day.
1,6-Hexanediol
The Reproduction / Developmental Toxicity Screening Test with 1,6-hexanediol was conducted under GLP according to OECD Guideline 421 to evaluate toxicity to reproduction and development (BASF, 1995).
Thereby, ten male and ten female Wistar rats per dose received 1,6-hexanediol at doses of 100, 400 and 1000 mg/kg/d by gavage. The application period was about four weeks for males and about six weeks for the females starting at least 14 day before mating. After the mating period, the male animals were sacrificed while the females were allowed to litter and rear their pups until day 4 post partum. Thereafter, the pups (F1-generation) and the F0-females were sacrificed. It was found, that the food consumption of F0 males at the 1000 mg/kg bw/day dose level was statistically significantly reduced during study weeks 0 - 1 and 3 – 4 resulting in a statistically significantly reduced mean body weights at the end of the study. The body weight gains of the high dose F0 males were also statistically significantly lower compared to the control F0 males between test weeks 2 - 3 and over the total study period. However, no substance-related effects on organ weights and no gross- and histopathological findings were observed in F0 males and females. As there is no corresponding effects to organ weight nor any histopathologically effect in this study, the observed effect is not considered to be advese. No signs for general toxicity were present in males and in females at 1000, 400 and 100 mg/kg bw/day. In addition, no signs for impairment of reproductive function and no signs of developmental toxicity in the offspring were apparent. Therefore, the NOAEL for parental and F0 toxicity was found to be 1000 mg/kg bw/day for females and for males; the NOAEL for reproductive function and for developmental toxicity was 1000 mg/kg/ bw/day.
d-Valerolactone
Furthermore the data of d-valerolactone from a Combined Repeated Dose Toxicity Study with the Reproduction/Developmental Toxicity Screening Test (according to OECD 422) did not indicate adverse effects on reproductive organs, tissues or behaviour up to the limit dose of 1000 mg/kg bw/day.
Short description of key information:
According to the results of the reproductive toxicity screening studies with 1,5-pentanediol, 1,6-hexanediol and d-valerolactone, the registered substance 1,5-pentanediol is not considered to be a reproductive toxicant. There was no effect at the limit dose of 1000 mg/kg bw/day.
Effects on developmental toxicity
Description of key information
NOAEL (maternal and developmental) = 1000 mg/kg/g (OECD414, BASF SE (2014), analogue substance 1,6-hexanediol CAS 629-11-8 and OECD 414, BASF SE (2016), metabolite d-valerolactone CAS 542-28-9)
Effect on developmental toxicity: via oral route
- Dose descriptor:
- NOAEL
- 1 000 mg/kg bw/day
Additional information
Developmental Toxicity:
In the available OECD 422 study with 1,5-pentandiol, no developmental toxicity was observed up to the limit dose (1000 mg/kg bw). There is no prenatal developmental toxicity study available with the test substance 1,5 -pentanediol. However, the potential of the test substance to induce developmental toxicity can be assessed through the toxicity data of its structural analogue 1,6 -hexandiol and its metabolite d-valerolactone in a weight of evidence approach (for WoE information, see chapter 13.2).
The potential of 1,6 -hexanediol to induce developmental toxicity was assessed in an OECD 414 guideline study (BASF SE, 2014). In this prenatal developmental toxicity study the test compound 1,6 -hexanediol was administered to pregnant Wistar rats daily by gavage from implantation to one day prior to the expected day of parturition (GD 6-19) to evaluate its potential maternal and prenatal developmental toxicity. Generally, clinical observations revealed no toxicologically relevant findings in the animals receiving 100, 400 or 1000 mg/kg bw/d 1,6 -hexanediol. No differences of toxicological relevance between the control and the treated groups (100, 400 or 1000 mg/kg bw/d) were observed for any reproductive parameters, such as conception rate, mean number of corpora lutea, mean number of implantations, as well as pre- and postimplantation loss. Similarly, no influence of the test compound on fetal weight and sex distribution of the fetuses was noted at any dose. Overall, there was no evidence for any toxicologically relevant adverse effect of the test item on fetal morphology at any dose.
Furthermore, the metabolite d-valerolactone was tested in a recent OECD 414 study and no treatment-related adverse systemic effect or developmental toxicity/teratogenicity was observed after oral application up to the limit dose.
Short description of key information:
According to the results of an OECD 422 study with 1,5-pentandiol and the developmental toxicity studies with 1,6 hexanediol and d-valerolactone, 1,5-pentanediol is not considered to be a reproductive toxicant. There was no effect at the limit dose of 1000 mg/kg bw/day.
Justification for classification or non-classification
1,5-Pentandiol is not classified for reproductive/developmental toxicity according to Regulation 1272/2008 (CLP) since the classification criteria are not met.
Additional information
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.
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