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1,1,1-Tris-(p-hydroxyphenyl)ethane enhances thermal stability and mechanical strength.
1,1,1-Tris-(p-hydroxyphenyl)ethane improves adhesion and chemical resistance.
1,1,1-Tris-(p-hydroxyphenyl)ethane provides durability and resistance to environmental factors.
CAS Number: 27955-94-8
EC Number: 405-800-7
MDL number: MFCD00012180
Linear Formula: CH3C(C6H4OH)3
Molecular Formula: C20H18O3
Molecular Weight: 306.36 g/mol
SYNONYMS:
1,1,1-TRIS(P-HYDROXYPHENYL)ETHANE, TIMTEC-BB SBB006476, LABOTEST-BB LT00159983, TRIS-HYDROXYPHENYLETHANE, Tri(4-hydroxyphenyl)ethane, 4,4',4''-Ethylidynetriphenol, 4,4’,4’’-ethylidynetri-pheno, 4,4’,4’’-ethylidynetrisphenol, 4,4',4''-(ethan-1,1,1-triyl)triphenol, 4,4',4''-(Ethane-1,1,1-triyl)triphenol, Phenol, 4,4',4''-ethylidynetris-, 4,4,4-(Ethylidene)trisphenol, tris(4-hydroxyphenyl)ethane, LABOTEST-BB LT00159983, 4,4',4''-(ETHYLIDENE)TRISPHENOL, 1,1,1-TRIS(P-HYDROXYPHENYL)ETHANE, 4,4',4''-ethane-1,1,1-triyltriphenol, 1,1,1-This(4-hydroxyphenyl)ethane, Phenol, 4,4',4''-ethylidynetri- (8CI), 4,4',4''-Ethylidynetris[phenol], 1,1,1-Tri(4-hydroxyphenyl)ethane, 1,1,1-Tris(4-hydroxyphenyl)ethane, 1,1,1-[Tris(p-hydroxyphenyl)]ethane, 4,4',4''-Ethane-1,1,1-triyltriphenol, Tris(4-hydroxyphenyl)ethane, TrisP-HAP, Phenol, 4,4′,4′′-Ethylidynetrisphenol, THPE, 1,1,1-Tris(4-hydroxyphenyl)ethane, 27955-94-8, Phenol, 4,4',4''-ethylidynetris-, Tris(4-hydroxyphenyl)ethane, 4,4',4''-Ethylidynetrisphenol, Phenol, 4,4',4''-ethylidynetri-, DTXSID2037712, 4,4',4''-Ethane-1,1,1-triyltriphenol, TRISP-HAP, 25K43J16E2, 4,4',4''-(ethan-1,1,1-triyl)triphenol, DTXCID0017712, EC 405-800-7, 1,1,1-(TRIS(P-HYDROXYPHENYL))ETHANE, Tris(phydroxyphenyl)ethane, Tris(4hydroxyphenyl)ethane, Tris(parahydroxyphenyl)ethane, 4,4',4''Ethylidynetrisphenol, 1,1,1Tris(phydroxyphenyl)ethane, Phenol, 4,4',4''ethylidynetri, Phenol, 4,4',4''ethylidynetris, 4,4',4''(Ethan1,1,1triyl)triphenol, Phenol, 4,4',4''ethylidynetri (8CI), Phenol, 4,4',4''-ethylidynetri-(8CI), 405-800-7, 608-155-1, 4,4',4''-(ethane-1,1,1-triyl)triphenol, 4-[1,1-bis(4-hydroxyphenyl)ethyl]phenol, 4,4',4"-(Ethylidene)trisphenol, 4,4',4"-Ethane-1,1,1-triyltriphenol, UNII-25K43J16E2, MFCD00012180, SCHEMBL18750, triphenylmethane derivative, 7, CHEMBL491936, BDBM29335, BP_12, 1,1,1-Tris(p-hydroxyphenyl)ethane, 1,1,1tris(4-hydroxy-phenyl)ethane, Tox21_300402, 1,1,1-tri-(4-hydroxyphenyl)ethane, 1,1,1 tris(4-hydroxy-phenyl)ethane, 1,1,1-tris(4'-hydroxyphenyl)ethane, 1,1,1-tris(4-hydroxy phenyl)ethane, 1,1,1-tris(4-hydroxyphenyl) ethane, 1,1,1-tri-(4-hydroxyphenyl)-ethane, AKOS015856425, 1,1,1 -tris(4'-hydroxyphenyl)ethane, 1,1,1 tris(4-hydroxy-phenyl) ethane, 1,1,1-tris-(4-hydroxyphenyl)-ethane, 1,1,1 tris (4-hydroxy-phenyl) ethane, 1,1,1-tris-(4'-hydroxyphenyl)-ethane, NCGC00164142-01, NCGC00164142-02, NCGC00254528-01, AC-24003, AS-15139, 1,1,1-Tris(4-hydroxyphenyl)ethane, 99%, CAS-27955-94-8, CS-0132357, NS00019386, T1254, D78151, Q24849250, 1,1,1-Tris(4-hydroxyphenyl)ethane 100 microg/mL in Acetonitrile, 4,4',4''- ethylidyne trisphenol, 4,4',4''- ethylidynetrisphenol, 4-[1,1-bis(4- hydroxyphenyl)ethyl]phenol, phenol, 4,4',4''-ethylidynetris-, 4,4',4''-ethylidynetris-, 4,4,4-(Ethylidene)trisphenol, 4,4a ,4a a -ethylidynetri-pheno, 4,4a ,4a a -ethylidynetris-pheno, 4,4a ,4a a -ethylidynetrisphenol, tris(4-hydroxyphenyl)ethane, LABOTEST-BB LT00159983, 4,4',4''-(ETHYLIDENE)TRISPHENOL, 1,1,1-TRIS(P-HYDROXYPHENYL)ETHANE, LABOTEST-BB LT00159983, tris(4-hydroxyphenyl)ethane, 4,4',4''-ethylidynetri-pheno, 4,4',4''-ethylidynetri-pheno, 4,4,4-(Ethylidene)trisphenol, 4,4',4''-ethylidynetrisphenol, 4,4',4''-ethylidynetrisphenol, 4,4',4''-ethylidynetris-pheno, 4,4',4''-ethylidynetris-pheno, 4,4',4''-(ETHYLIDENE)TRISPHENOL, 1,1,1-TRIS(4-HYDROXYPHENYL)ETHANE, 1,1,1-TRIS(P-HYDROXYPHENYL)ETHANE, 1,1,1-This(4-hydroxyphenyl)ethane, 1,1,1-tris(4-hydroxyphenyl)ethane, 4,4',4''-ethane-1,1,1-triyltriphenol, 4-[1,1-bis(4-hydroxyphenyl)ethyl]phenol, 3,5-dichloro-N-diethoxyphosphoryl-2-(trichloromethyl)-4-pyridinamine, 1,1,1-Tris-(p-hydroxyphenyl) ethane glycidyl ether, 2-[[4-[1,1-Bis[4-(oxiran-2-ylmethoxy)phenyl]ethyl]phenoxy]methyl]oxirane, Oxirane, 2,2',2''-(ethylidynetris(4,1-phenyleneoxymethylene))tris-
1,1,1-Tris-(p-hydroxyphenyl)ethane is a white Powder.
1,1,1-Tris-(p-hydroxyphenyl)ethane is a three-functional phenolic compound that can be used as a variety of polymers (such as polycarbonate, epoxy resin, polyaryl ester, adhesive and coating, etc.)
Crosslinking agent or branching agent, 1,1,1-Tris-(p-hydroxyphenyl)ethane can also be used as an intermediate for preparing antioxidants.
1,1,1-Tris-(p-hydroxyphenyl)ethane is an organic compound widely utilized in polymer chemistry and materials science.
1,1,1-Tris-(p-hydroxyphenyl)ethane is a precursor for epoxy formulations.
1,1,1-Tris-(p-hydroxyphenyl)ethane is a trifunctional aromatic triol with the molecular formula C₂₀H₁₈O₃ and a molecular weight of 306.36 g/mol.
1,1,1-Tris-(p-hydroxyphenyl)ethane consists of an ethane core substituted with three 4-hydroxyphenyl groups, making it a versatile building block in polymer chemistry and coordination chemistry.
1,1,1-Tris-(p-hydroxyphenyl)ethane is synthesized via the acid-catalyzed condensation of 4-hydroxyacetophenone and phenol, often requiring purification steps to remove impurities like isomers and residual reactants .
USES and APPLICATIONS of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
1,1,1-Tris-(p-hydroxyphenyl)ethane is used Electronic Materials
This special molecule, 1,1,1-Tris-(p-hydroxyphenyl)ethane, is used as cross-linking or branching agent for polymers like polycarbonates, epoxies, and polyesters.
Given its “tri” functionality, 1,1,1-Tris-(p-hydroxyphenyl)ethane finds applications in hyperbranched systems suitable for adhesive and coating applications.
Additionally unique properties like low viscosity and high thermal resistance make 1,1,1-Tris-(p-hydroxyphenyl)ethane an ideal candidate for demanding applications.
1,1,1-Tris-(p-hydroxyphenyl)ethane yields polymers with a wide range starting from soft materials to hard highly crosslinked materials.
1,1,1-Tris-(p-hydroxyphenyl)ethane is primarily used as a cross-linking or branching agent in various polymer applications.
Polycarbonates: 1,1,1-Tris-(p-hydroxyphenyl)ethane enhances thermal stability and mechanical strength.
Epoxy Resins: 1,1,1-Tris-(p-hydroxyphenyl)ethane improves adhesion and chemical resistance.
Adhesives and Coatings: 1,1,1-Tris-(p-hydroxyphenyl)ethane provides durability and resistance to environmental factors.
Antioxidants: 1,1,1-Tris-(p-hydroxyphenyl)ethane acts as a stabilizer in polymer formulations.
Additionally, 1,1,1-Tris-(p-hydroxyphenyl)ethane is utilized as an indirect food additive in adhesives and components of coatings, though it is not approved for direct use in flavors or fragrances .
1,1,1-Tris-(p-hydroxyphenyl)ethane is widely utilized in the synthesis of hyperbranched polycarbonates (HBPCs), where its trifunctional structure enables controlled branching (degree of branching: 0.5–0.7) and terminal functional group customization.
1,1,1-Tris-(p-hydroxyphenyl)ethane also serves as a precursor for trisphosphinite ligands in trimetallic complexes and is incorporated into vitrimers as a safer alternative to toxic bisphenol-A.
1,1,1-Tris-(p-hydroxyphenyl)ethane obviates the need to work with epichlorohydrin.
1,1,1-Tris-(p-hydroxyphenyl)ethane can be used for high temperature applications.
SCIENTIFIC RESEARCH APPLICATIONS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Chemical Applications:
Branching Agent in Polymer Chemistry
1,1,1-Tris-(p-hydroxyphenyl)ethane is primarily utilized as a branching agent in the synthesis of polycarbonates and epoxy resins.
Its trifunctional nature allows 1,1,1-Tris-(p-hydroxyphenyl)ethane to create cross-linked structures that enhance the mechanical properties and thermal stability of polymers.
*Synthesis of Hyperbranched Polymers:
Recent studies have demonstrated the successful synthesis of hyperbranched polycarbonates using 1,1,1-Tris-(p-hydroxyphenyl)ethane.
The incorporation of 1,1,1-Tris-(p-hydroxyphenyl)ethane leads to materials with superior properties compared to linear counterparts.
For instance, a study highlighted the polymerization of di-tert-butyl tricarbonate with 1,1,1-Tris-(p-hydroxyphenyl)ethane, resulting in a hyperbranched structure that exhibited improved thermal properties and processability.
BIOLOGICAL APPLICATIONS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Drug Delivery Systems:
1,1,1-Tris-(p-hydroxyphenyl)ethane has been investigated for its potential in drug delivery systems due to its ability to form stable complexes with various pharmaceuticals.
This property enhances the solubility and bioavailability of drugs, making 1,1,1-Tris-(p-hydroxyphenyl)ethane a promising candidate for developing advanced drug formulations.
*Antioxidant Properties:
The antioxidant capabilities of 1,1,1-Tris-(p-hydroxyphenyl)ethane are being explored for therapeutic applications.
Research indicates that compounds with similar structures exhibit significant free radical scavenging activity, suggesting that 1,1,1-Tris-(p-hydroxyphenyl)ethane could be developed into new therapeutic agents for oxidative stress-related diseases.
INDUSTRIAL APPLICATIONS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Adhesives and Coatings:
In the industrial sector, 1,1,1-Tris-(p-hydroxyphenyl)ethane is employed in the production of adhesives and coatings.
1,1,1-Tris-(p-hydroxyphenyl)ethane's role as a branching agent contributes to the formulation of products that require high durability and resistance to environmental factors.
*Intermediate for Antioxidants:
1,1,1-Tris-(p-hydroxyphenyl)ethane serves as an intermediate in synthesizing various antioxidants used in plastics and rubber industries.
1,1,1-Tris-(p-hydroxyphenyl)ethane's incorporation into formulations helps improve the longevity and performance of materials exposed to oxidative degradation.
FUNCTIONS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Photosensitive Material
*Photoinitiators
FEATURES OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Chemical Resistance
*Weather Resistant
PREPARATION METHODS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Synthetic Routes and Reaction Conditions:
1,1,1-Tris-(p-hydroxyphenyl)ethane can be synthesized through several methods. One common method involves the reaction of phenol with 2,4-pentanedione in the presence of sulfuric acid and a mercapto sulfonic acid such as 3-mercaptopropanesulfonic acid as a promoter.
This reaction yields high product yields in relatively short times .
Another method involves the reaction of phenol with p-hydroxyacetophenone in the presence of acetic acid as a catalyst.
The reaction is carried out at 65-75°C with nitrogen introduction, followed by vacuum filtration to obtain the crude product .
*Industrial Production Methods:
In industrial settings, the production of 1,1,1-Tris-(p-hydroxyphenyl)ethane typically involves the use of phenol and 2,4-pentanedione under acidic conditions.
The reaction is promoted by mercapto compounds to enhance yield and reduce reaction time .
CHEMICAL REACTIONS ANALYSIS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Types of Reactions:
1,1,1-Tris-(p-hydroxyphenyl)ethane undergoes various chemical reactions, including:
*Oxidation:
The hydroxy groups can be oxidized to form quinones.
*Reduction:
1,1,1-Tris-(p-hydroxyphenyl)ethane can be reduced to form corresponding alcohols.
*Substitution:
The hydroxy groups can participate in substitution reactions to form ethers or esters.
COMMON REAGENTS AND CONDITIONS OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Oxidation:
Common oxidizing agents include potassium permanganate and chromium trioxide.
*Reduction:
Reducing agents such as sodium borohydride or lithium aluminum hydride are used.
*Substitution:
Reagents like alkyl halides or acyl chlorides are used for etherification or esterification reactions.
*Major Products:
Oxidation: Quinones.
*Reduction:
Alcohols.
*Substitution:
Ethers and esters
ADDITIONAL INFORMATION OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Incompatibilities:
Avoid 1,1,1-Tris-(p-hydroxyphenyl)ethane contact with oxidizing agents.
*Storage Recommendations:
Store 1,1,1-Tris-(p-hydroxyphenyl)ethane in a cool, dry, and well-ventilated area away from incompatible substances.
*First Aid Measures:
In case of contact 1,1,1-Tris-(p-hydroxyphenyl)ethane with eyes or skin, rinse immediately with plenty of water and seek medical advice.
MECHANISM OF ACTION OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
The mechanism of action of 1,1,1-Tris-(p-hydroxyphenyl)ethane involves its ability to form stable complexes with various molecules.
The hydroxy groups can participate in hydrogen bonding and other interactions, making 1,1,1-Tris-(p-hydroxyphenyl)ethane a versatile compound in various applications.
In polymer synthesis, 1,1,1-Tris-(p-hydroxyphenyl)ethane acts as a branching agent, enhancing the mechanical properties and thermal stability of the resulting polymers
BIOLOGICAL ACTIVITY OF 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
*Chemical Structure and Properties
1,1,1-Tris-(p-hydroxyphenyl)ethane is a trifunctional phenolic compound with the chemical formula C2020H1818O33.
1,1,1-Tris-(p-hydroxyphenyl)ethane's structure consists of three hydroxyphenyl groups attached to a central ethane core, which imparts unique chemical properties that contribute to its biological activity.
1,1,1-Tris-(p-hydroxyphenyl)ethane is known for its antioxidant properties and potential role as a coactivator in estrogen receptor signaling.
*Antioxidant Activity
1,1,1-Tris-(p-hydroxyphenyl)ethane exhibits strong antioxidant properties due to its phenolic structure, which allows it to scavenge free radicals effectively.
This activity can protect cells from oxidative stress, which is linked to various diseases including cancer and neurodegenerative disorders.
Research indicates that 1,1,1-Tris-(p-hydroxyphenyl)ethane can reduce oxidative damage in cellular models, suggesting its potential as a therapeutic agent in oxidative stress-related conditions.
*Estrogen Receptor Modulation
Studies have shown that 1,1,1-Tris-(p-hydroxyphenyl)ethane acts as a modulator of estrogen receptors (ERs), particularly ERβ.
In vitro assays demonstrated that 1,1,1-Tris-(p-hydroxyphenyl)ethane binds to ERβ with higher affinity compared to ERα, functioning as a partial agonist.
This selective activation may have implications for hormone-related therapies, particularly in conditions such as breast cancer where estrogen signaling plays a critical role
PHYSICAL and CHEMICAL PROPERTIES of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
EINECS (EC#): 405-800-7
Molecular Formula: C20H18O3 (Products with the same molecular formula)
Molecular Weight: 306.35
Inchi: InChI=1/C20H18O3/c1-20(14-2-8-17(21)9-3-14,15-4-10-18(22)11-5-15)16-6-12-19(23)13-7-16/h2-13,21-23H,1H3
InChIKey: BRPSWMCDEYMRPE-UHFFFAOYSA-N
Canonical SMILES: CC(C1=CC=C(C=C1)O)(C2=CC=C(C=C2)O)C3=CC=C(C=C3)O
MOL File: 27955-94-8.mol
Chemical and Physical Properties
Density: 1.252 g/ml
Melting Point: 246-248
Boiling Point: 531.8 °C
Vapor: 6.3E-12 mmHg at 25 °C
Refractive Index: 1.655
Flash Point: 251 °C
Computed Properties: Molecular Weight: 306.35512 [g/mol]
Molecular Formula: C20H18O3
Molecular Formula / Molecular Weight: C20H18O3 = 306.36
Physical State (20 °C): Solid
Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN: 27955-94-8
Reaxys Registry Number: 2141621
PubChem Substance ID: 87577029
SDBS (AIST Spectral DB): 9753
MDL Number:
MFCD: MFCD00012180
CAS: 27955-94-8
EINECS: 405-800-7
InChI: InChI=1/C20H18O3/c1-20(14-2-8-17(21)9-3-14,15-4-10-18(22)11-5-15)16-6-12-19(23)13-7-16/h2-13,21-23H,1H3
Molecular Formula: C20H18O3
Molar Mass: 306.36
Density: 1.252±0.06 g/cm3 (Predicted)
Melting Point: 246-248 °C (lit.)
Boiling Point: 531.8±45.0 °C (Predicted)
Flash Point: 251 °C
Water Solubility: 25.1 mg/L at 20 °C
Solubility: 241 in mg/100g standard fat at 20 °C
Vapor Pressure: 0 Pa at 25 °C
Appearance: White powder
Color: White to Almost white
pKa: 10.02±0.10 (Predicted)
Storage Condition: Sealed in dry, Room Temperature
Refractive Index: 1.655
MDL: MFCD00012180
Compound Canonicalized: Yes
Physical state: Powder
Color: Off-white
Odor: No data available
Melting point/freezing point: Melting point/range: 246 - 248 °C - lit.
Initial boiling point and boiling range: No data available
Flammability (solid, gas): No data available
Upper/lower flammability or explosive limits: No data available
Flash point: No data available
Autoignition temperature: > 400 °C at 1.013 hPa
Decomposition temperature: No data available
pH: No data available
Viscosity:
Viscosity, kinematic: No data available
Viscosity, dynamic: No data available
Water solubility: 0.0251 g/l at 20 °C
Partition coefficient: n-octanol/water: log Pow: 3.88 at 20 °C
Vapor pressure: No data available
Density: No data available
Relative density: 1.23 at 20 °C
Relative vapor density: No data available
Particle characteristics: No data available
Explosive properties: No data available
Oxidizing properties: None
Other safety information
Surface tension: 76.6 mN/m at 25.5 °C
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
Water, 7.795 mg/L @ 25 °C (est)
IUPAC Name: 1,1,1-Tris(4-hydroxyphenyl)ethane
CAS Number: 27955-94-8
EC Number: 405-800-7
Molecular Formula: C₂₀H₁₈O₃
Molecular Weight: 306.36 g/mol
Structure: A central ethane carbon bonded to three para-hydroxyphenyl groups.
Appearance: White to almost white crystalline powder
Melting Point: 246–248 °C
Boiling Point: Approximately 531.8 °C (predicted)
Density: ~1.252 g/cm³
Water Solubility: 25.1 mg/L at 20 °C
LogP (octanol/water): 3.88
pKa: 10.02 (predicted)
Vapor Pressure: Negligible at 25 °C
Storage Conditions: Store in a sealed container at room temperature, in a cool and dark place
Molecular Formula / Molecular Weight: C20H18O3 = 306.36
Physical State (20 deg.C): Solid
Storage Temperature: Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN: 27955-94-8
Reaxys Registry Number: 2141621
PubChem Substance ID: 87577029
SDBS (AIST Spectral DB): 9753
MDL Number:
MFCD: MFCD00012180
Compound Canonicalized: Yes
Linear Formula: CH3C(C6H4OH)3
CAS Number: 27955-94-8
Molecular Weight: 306.36
EC Number: 405-800-7
MDL number: MFCD00012180
UNSPSC Code: 12162002
PubChem Substance ID: 24859624
NACRES: NA.23
Molecular Weight: 306.4 g/mol
XLogP3: 4.1
Hydrogen Bond Donor Count: 3
Hydrogen Bond Acceptor Count: 3
Rotatable Bond Count: 3
Exact Mass: 306.125594432 Da
Monoisotopic Mass: 306.125594432 Da
Topological Polar Surface Area: 60.7 Ų
Heavy Atom Count: 23
Formal Charge: 0
Complexity: 304
Isotope Atom Count: 0
Defined Atom Stereocenter Count: 0
Undefined Atom Stereocenter Count: 0
Defined Bond Stereocenter Count: 0
Undefined Bond Stereocenter Count: 0
Covalently-Bonded Unit Count: 1
Compound Is Canonicalized: Yes
FIRST AID MEASURES of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
-Description of first-aid measures:
*If inhaled:
After inhalation:
Fresh air.
*In case of skin contact:
Wash off with soap and plenty of water.
*In case of eye contact:
Remove contact lenses.
*If swallowed:
Never give anything by mouth to an unconscious person.
Rinse mouth with water.
-Indication of any immediate medical attention and special treatment needed:
No data available
ACCIDENTAL RELEASE MEASURES of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
-Environmental precautions:
Do not let product enter drains.
-Methods and materials for containment and cleaning up:
Keep in suitable, closed containers for disposal.
FIRE FIGHTING MEASURES of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
-Extinguishing media:
*Suitable extinguishing media:
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
-Further information:
No data available
EXPOSURE CONTROLS/PERSONAL PROTECTION of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
-Control parameters:
--Ingredients with workplace control parameters:
-Exposure controls:
--Personal protective equipment:
*Eye/face protection:
Use equipment for eye protection.
*Skin protection:
Handle with gloves.
Wash and dry hands.
*Body Protection:
Impervious clothing
*Respiratory protection:
Respiratory protection not required.
-Control of environmental exposure:
Do not let product enter drains.
HANDLING and STORAGE of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
-Conditions for safe storage, including any incompatibilities:
*Storage conditions:
Store in cool place.
Keep container tightly closed in a dry and well-ventilated place.
Containers which are opened must be carefully resealed and kept upright to prevent leakage.
STABILITY and REACTIVITY of 1,1,1-TRIS-(p-HYDROXYPHENYL)ETHANE:
-Reactivity:
No data available
-Chemical stability:
Stable under recommended storage conditions.
-Possibility of hazardous reactions:
No data available
-Conditions to avoid:
No data available
