Category: multi-functional cosmetic ingredient for skin and hair care
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Physical Properties:
Appearance: | colorless clear liquid (est) |
Assay: | 95.00 to 100.00 %
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Food Chemicals Codex Listed: | No |
Specific Gravity: | 0.96500 to 0.97500 @ 25.00 °C.
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Pounds per Gallon - (est).: | 8.030 to 8.113
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Refractive Index: | 1.43400 to 1.44400 @ 20.00 °C.
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Boiling Point: | 198.00 to 199.00 °C. @ 760.00 mm Hg (est)
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Vapor Pressure: | 0.057000 mmHg @ 25.00 °C. (est) |
Flash Point: | 220.00 °F. TCC ( 104.40 °C. ) (est)
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logP (o/w): | 0.011 (est) |
Soluble in: |
| water, 7.664e+004 mg/L @ 25 °C (est) |
Organoleptic Properties:
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Odor and/or flavor descriptions from others (if found). |
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Cosmetic Information:
Suppliers:
BASF |
1,2-Pentanediol
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BOC Sciences |
For experimental / research use only. |
1,2-Pentanediol 95%
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Connect Chemicals |
Bio-pentylene glycol
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ECSA Chemicals |
PENTYLENE GLYCOL
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ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY |
Kingyoung Bio Technical |
Pentylene Glycol
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Minasolve |
MinaCare Pentiol (Pentylene glycol)
Odor: characteristic Use: Pentylene glycol is a very widely used moizturing agent, also showing interesting antimicrobial boosting properties.
Minasolve is a large producer of synthetic pentylene glycol of odouless and colourless quality for the cosmetic industry.
Its quality is recognized by small, medium and large companies all over the world, including the luxury brands. |
Minasolve |
MinaCare Pentiol Green ECOCERT (Pentylene Glycol)
Odor: characteristic Use: Pentylene Glycol is a very widely used moizturing agent, also showing interesting antimicrobial boosting properties.
Minasolve is a large producer of synthetic Pentylene Glycol of odouless and colourless quality for the cosmetic industry.
Its quality is recognized by small, medium and large companies all over the world, including the luxury brands. |
Santa Cruz Biotechnology |
For experimental / research use only. |
1,2-Pentanediol
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Sigma-Aldrich: Aldrich |
For experimental / research use only. |
1,2-Pentanediol 96%
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Symrise |
Hydrolite® 5 green
Odor: characteristic Use: Hydrolite® 5 green perfectly fits into the sustainability strategy of Symrise. Within the context of this strategy, the company emphasizes the importance of comprehensive transparency that benefits customers and end consumers. In 2018 the company won several awards for its exceptional global environmental protection efforts (Carbon Disclosure Project) and climate targets as well as for its environmental and social engagement (Ethibel Sustainability Index). The company currently assesses 80 percent of its main suppliers according to sustainability criteria. “Every time we use raw materials in our product development, we look at their sustainability as well as their social and environmental added value,” said Eder Ramos Global President Cosmetic Ingredients Division of Symrise. “With Hydrolite® 5 green we have reached a further milestone, because it is entirely made from byproducts of a renewable source, the sugar cane.” |
Symrise |
Hydrolite® 5
Odor: characteristic Use: Hydrolite® 5 is 1,2-pentanediol. Hydrolite® 5 is a colorless liquid with a charateristic intrinsic odor. Due to its chemical properties, Hydrolite® 5 is readily soluble in water and oil.
Hydrolite® 5 improves the water-binding capability of the skin and increases the degree of hydration. Hydrolite® 5 is also outstanding for its antimicrobial properties. |
TCI AMERICA |
For experimental / research use only. |
1,2-Pentanediol >98.0%(GC)
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Vigon International |
Hydrolite-5 (Pentylene Glycol)
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Vigon International |
HYDROLITE® 5 GREEN
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Safety Information:
Preferred SDS: View |
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Hazards identification |
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Classification of the substance or mixture |
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS) |
None found. |
GHS Label elements, including precautionary statements |
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Pictogram | |
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Hazard statement(s) |
None found. |
Precautionary statement(s) |
None found. |
Oral/Parenteral Toxicity: |
oral-rat LD50 12700 mg/kg BEHAVIORAL: EXCITEMENT
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
BEHAVIORAL: MUSCLE WEAKNESS Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 38(9), Pg. 14, 1973.
oral-rabbit LD50 3700 mg/kg BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
BEHAVIORAL: EXCITEMENT
BEHAVIORAL: MUSCLE WEAKNESS Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 38(9), Pg. 14, 1973.
oral-mouse LD50 7400 mg/kg BEHAVIORAL: EXCITEMENT
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
BEHAVIORAL: MUSCLE WEAKNESS Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 38(9), Pg. 14, 1973.
oral-guinea pig LD50 5200 mg/kg BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)
BEHAVIORAL: EXCITEMENT
BEHAVIORAL: MUSCLE WEAKNESS Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 38(9), Pg. 14, 1973.
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Dermal Toxicity: |
Not determined
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Inhalation Toxicity: |
Not determined
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Safety in Use Information:
Category: | multi-functional cosmetic ingredient for skin and hair care |
Recommendation for pentylene glycol usage levels up to: | | not for fragrance use.
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Recommendation for pentylene glycol flavor usage levels up to: |
| not for flavor use.
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Safety References:
References:
Other Information:
Potential Blenders and core components note
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
| hydrolite 5 (Symrise) | | hydrolite 5 green (Symrise) | 1,2- | pentane diol | | pentane-1,2-diol | 1,2- | pentanediol |
Articles:
PubMed: | Effect of hydrocarbon chain length in 1,2-alkanediols on percutaneous absorption of metronidazole: toward development of a general vehicle for controlled release. |
PubMed: | Safety assessment of 1,2-glycols as used in cosmetics. |
PubMed: | Dermal peptide delivery using enhancer molecules and colloidal carrier systems--part I: carnosine. |
PubMed: | The influence of alkane chain length on the skin irritation potential of 1,2-alkanediols. |
PubMed: | Preservative system development for argan oil-loaded nanostructured lipid carriers. |
PubMed: | Allergic contact dermatitis to propyl gallate and pentylene glycol in an emollient cream. |
PubMed: | Allergic contact dermatitis to ethylhexylglycerin and pentylene glycol. |
PubMed: | The influence of alcohol, propylene glycol and 1,2-pentanediol on the permeability of hydrophilic model drug through excised pig skin. |
PubMed: | Dermal and transdermal targeting of dihydroavenanthramide D using enhancer molecules and novel microemulsions. |
PubMed: | Contact dermatitis to pentylene glycol in a prescription cream for atopic dermatitis: case report. |
PubMed: | Modulation of dihydroavenanthramide D release and skin penetration by 1,2-alkanediols. |
PubMed: | Allergic contact dermatitis to pentylene glycol in a cosmetic cream. |
PubMed: | A novel TEM contrasting technique for extracellular polysaccharides in in vitro biofilms. |
PubMed: | Contact allergy to pentylene glycol. |
PubMed: | Purification, characterization, and gene cloning of glycerol dehydrogenase from Hansenula ofunaensis, and its expression for production of optically active diol. |
PubMed: | A family of nanoporous materials based on an amino acid backbone. |
PubMed: | Heat capacity studies of formation of micelle-like structure in aqueous solutions of some alkane polyols. |
PubMed: | Synthesis and properties of an acetaldehyde-derived oligonucleotide interstrand cross-link. |
PubMed: | Stereoselective oxidation of aliphatic diols and reduction of hydroxy-ketones with galactitol dehydrogenase from Rhodobacter sphaeroides D. |
PubMed: | Structures of carbohydrate-boronic acid complexes determined by NMR and molecular modelling in aqueous alkaline media. |
PubMed: | Allergic contact dermatitis from pentylene glycol in an emollient cream, with possible co-sensitization to resveratrol. |
PubMed: | In vitro induction of apoptosis vs. necrosis by widely used preservatives: 2-phenoxyethanol, a mixture of isothiazolinones, imidazolidinyl urea and 1,2-pentanediol. |
PubMed: | Stereospecific synthesis of oligonucleotides containing crotonaldehyde adducts of deoxyguanosine. |
PubMed: | Effects of alcohols and diols on the phase behaviour of quaternary systems. |
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