tripropylene glycol

propanol, ((1-methyl-1,2-ethanediyl)bis(oxy))bis-

CAS: 24800-44-0 C9 H20 O4 MW: 192.25520000

Identification

Nametripropylene glycol
IUPAC2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol
CAS Number24800-44-0
EINECS246-466-0
FDA UNII3C8845E7C1
Molecular FormulaC9 H20 O4
Molecular Weight192.25520000
MDL NumberMFCD00014405
Nikkaji NumberJ47.851B
Beilstein2235421
XlogP3-0.40 (est)

Regulatory

FDA/DG SANTE Petitions, Reviews, NoticesFCN 1071
DG SANTE Food Contact Materialstripropyleneglycol
FDA Mainterm (IAUFC)24800-44-0 ; TRIPROPYLENE GLYCOL

Physical Properties

Appearance colorless to pale yellow clear liquid (est)
Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Specific Gravity 1.01700 to 1.02200 @ 20.00 °C.
Pounds per Gallon - (est). 8.472 to 8.514
Refractive Index 1.44200 to 1.44700 @ 20.00 °C.
Boiling Point 271.00 °C. @ 760.00 mm Hg
Vapor Density 6.63 ( Air = 1 )
Flash Point > 230.00 °F. TCC ( > 110.00 °C. )
logP (o/w) -0.586 (est)
Soluble in water, 1.269e+005 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesantioxidants

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityoral-rat LD50 3000 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categoryemulsifiers, humectants
Recommendation for tripropylene glycol usage levels up tonot for fragrance use.
Recommendation for tripropylene glycol flavor usage levels up tonot for flavor use.

TCI AMERICA

Moving Your Chemistry Forward

We continuously strive to advance our technology.

View All Website 1-800-423-8616 Sales-US@TCIchemicals.com;

Potential Uses

None Found

Natural Occurrence

not found in nature

Synonyms

2-(2-(2- hydroxypropoxy)propoxy)-1-propanol 2-[2-(2- hydroxypropoxy)propoxy]propan-1-ol ((1- methyl-1,2-ethanediyl)bis(oxy))bispropanol propanol, ((1-methyl-1,2-ethanediyl)bis(oxy))bis- 1- propanol, 2-[2-(2-hydroxypropoxy)propoxy]- tri(propylene glycol) 1,4,7- trimethyl-3,6-dioxaoctane-1,8-diol tripropyleneglycol PubMed: Synthesis of Fullerene-Fused Dioxanes/Dioxepanes: Ferric Perchlorate-Mediated One-Step Reaction of [60]Fullerene with Diols. PubMed: Photoswitchable hydrogel surface topographies by polymerisation-induced diffusion. PubMed: A toxicological review of the propylene glycols. PubMed: Safety assessment of propylene glycol, tripropylene glycol, and PPGs as used in cosmetics. PubMed: Shear and dielectric responses of propylene carbonate, tripropylene glycol, and a mixture of two secondary amides. PubMed: Dermal penetration of propylene glycols: measured absorption across human abdominal skin in vitro and comparison with a QSAR model. PubMed: Effects of water contamination on the supercooled dynamics of a hydrogen-bonded model glass former. PubMed: Polymerization of electric field-centered double emulsion droplets to create polyacrylate shells. PubMed: Electrochemical sensor for parabens based on molecular imprinting polymers with dual-templates. PubMed: Final report on the safety assessment of PPG-2 methyl ether, PPG-3 methyl ether, and PPG-2 methyl ether acetate. PubMed: Paramagnetic ultrasmall gadolinium oxide nanoparticles as advanced T1 MRI contrast agent: account for large longitudinal relaxivity, optimal particle diameter, and in vivo T1 MR images. PubMed: A novel polyurethane-based root canal-obturation material and urethane-acrylate-based root canal sealer-part 2: evaluation of push-out bond strengths. PubMed: A novel polyurethane-based root canal-obturation material and urethane acrylate-based root canal sealer--part I: synthesis and evaluation of mechanical and thermal properties. PubMed: Bio-oxidation of tripropylene glycol under aerobic conditions. PubMed: Dielectric secondary relaxations in polypropylene glycols. PubMed: Water dynamics in n-propylene glycol aqueous solutions. PubMed: Dielectric and shear mechanical alpha and beta relaxations in seven glass-forming liquids. PubMed: Dielectric relaxation processes in water mixtures of tripropylene glycol. PubMed: Soot emissions from spherical droplet flames for mixtures of JP8 and tripropylene glycol monomethyl ether. PubMed: Minimal model for Beta relaxation in viscous liquids. PubMed: Biodegradation of potential diesel oxygenate additives: dibutyl maleate (DBM), and tripropylene glycol methyl ether (TGME). PubMed: Binding efficiency and transport properties of molecularly imprinted polymer thin films. PubMed: A method for measuring dermal exposure to multifunctional acrylates. PubMed: Comparative in vitro cytotoxicity of ethyl acrylate and tripropylene glycol diacrylate to normal human skin and lung cells. PubMed: A tape-stripping method for measuring dermal exposure to multifunctional acrylates. PubMed: Workers' dermal exposure to UV-curable acrylates in the furniture and Parquet industry. PubMed: Occupational dermatitis to ultraviolet-cured acrylic-based inks in computer hard disc manufacturing. PubMed: Tripropylene glycol diacrylate but not ethyl acrylate induces skin tumors in a twenty-week short-term tumorigenesis study in Tg.AC (v-Ha-ras) mice. PubMed: Absence of systemic in vivo genotoxicity after dermal exposure to ethyl acrylate and tripropylene glycol diacrylate in Tg.AC (v-Ha-ras) mice. PubMed: Occupational allergic contact dermatitis caused by photobonded sculptured nails and a review of (meth) acrylates in nail cosmetics. PubMed: Occupational allergic contact dermatitis caused by epoxy diacrylate in ultraviolet-light-cured paint, and bisphenol A in dental composite resin. PubMed: Lemna minor membranes affected by adjuvants. PubMed: Allergic contact dermatitis due to an amino-substituted diacrylate in a UV-cured lacquer. PubMed: Allergic contact dermatitis to ultra violet cured inks. PubMed: The sensitizing capacity of multifunctional acrylates in the guinea pig. PubMed: The pharmacology of the mono methyl ethers of mono-, di-, and tripropylene glycol in the dog with observations on the auricular fibrillation produced by these compounds.