1 2 propanediol
Some substance identifiers may have been claimed confidential, 1 2 propanediol may not have been provided, and therefore not be displayed. More information about the EC Inventory can be found here.
Propylene glycol IUPAC name : propane-1,2-diol is a viscous, colorless liquid, which is nearly odorless but possesses a faintly sweet taste. As it contains two alcohol groups, it is classed as a diol. It is miscible with a broad range of solvents, including water , acetone , and chloroform. In general, glycols [5] are non-irritating and have very low volatility. It is produced on a large scale primarily for the production of polymers. In the European Union, it has E-number E for food applications.
1 2 propanediol
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For a detailed overview on identified uses and environmental releases, please consult the registered substance factsheet.
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Propanediol PDO is a common ingredient in cosmetics and personal care products such as lotions, cleansers, and other skin treatments. PDO is a chemical substance either derived from corn or petroleum. It can be clear or very slightly yellow. PDO has many household and manufacturing uses. It can help your skin quickly absorb other ingredients in your product of choice. It can also help dilute other active ingredients. But you can also find it in other personal care products, including:. There are actually two distinct forms of PDO: 1,3-propanediol and 1,2-propanediol, also known as propylene glycol PG. PG has recently received some negative press as a skin care ingredient. Consumer protection groups have raised concerns that PG can irritate eyes and skin, and is a known allergen to some.
1 2 propanediol
Propylene glycol IUPAC name : propane-1,2-diol is a viscous, colorless liquid, which is nearly odorless but possesses a faintly sweet taste. As it contains two alcohol groups, it is classed as a diol. It is miscible with a broad range of solvents, including water , acetone , and chloroform.
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Release to the environment of this substance can occur from industrial use: in processing aids at industrial sites, for thermoplastic manufacture, of substances in closed systems with minimal release and as processing aid. Responses may include CNS depression, "hypotension, bradycardia , QRS and T abnormalities on the ECG, arrhythmia , cardiac arrhythmias, seizures, agitation, serum hyperosmolality , lactic acidosis , and haemolysis ". Substance Information Data platform availability banner - infocard, search, nanomaterias. January CAS number. If the substance was not covered by the EC Inventory, ECHA attributes a list number in the same format, starting with the numbers 6, 7, 8 or 9. Thank you We will respond to your enquiry shortly. We are passionate about supporting your science for a safer world. When information is available in all sources, the first two are displayed as a priority. Wikimedia Commons. Article service life Release to the environment of this substance can occur from industrial use: industrial abrasion processing with low release rate e. PMID The source of the information is mentioned in the introductory sentence of the hazard statements.
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Harmonised classification and labelling CLH Harmonised classification and labelling is a legally binding classification and labelling for a substance, agreed at European Community level. The freezing point of water is depressed when mixed with propylene glycol. The use information is displayed per substance life cycle stage consumer use, in articles, by professional workers widespread uses , in formulation or re-packing, at industrial sites or in manufacturing. Your punchout session will expire in 1 min 59 sec. Petrochemical Processes. Estimates on the prevalence of propylene glycol allergy range from 0. Mono Propylene Glycol. For a detailed overview on identified uses and environmental releases, please consult the registered substance factsheet. Contact Dermatitis. Cochrane Database Syst Rev. Manufacture Release to the environment of this substance can occur from industrial use: manufacturing of the substance and formulation of mixtures.
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