77-85-0 Usage
Description
1,1,1-Tris(hydroxymethyl)ethane, also known as Glycerol, is a trihydric alcohol compound with three hydroxyl groups attached to a central carbon atom. It is a colorless, odorless, and viscous liquid that is soluble in water and has a sweet taste. Glycerol is a versatile chemical with a wide range of applications in various industries due to its unique properties, such as its ability to form hydrogen bonds and its compatibility with other chemicals.
Uses
Used in Cosmetics and Personal Care Industry:
1,1,1-Tris(hydroxymethyl)ethane is used as a conditioning agent for hair and skin care products, providing moisture retention and improving the texture and appearance of the skin and hair.
Used in Paints and Coatings Industry:
1,1,1-Tris(hydroxymethyl)ethane is used as an intermediate in the production of alkyd and polyester resins, which are used as binders in paints, varnishes, and coatings. These resins provide excellent adhesion, durability, and resistance to chemicals and weathering.
Used in Plastics and Polymers Industry:
1,1,1-Tris(hydroxymethyl)ethane is used as an intermediate in the production of powder coating resins, synthetic lubricants based on polyol esters, stabilizers for plastics, and plasticizers. These applications improve the performance and properties of plastics and polymers, such as flexibility, durability, and resistance to heat and chemicals.
Used in Textile Industry:
1,1,1-Tris(hydroxymethyl)ethane is used in the manufacturing process of synthetic drying oils, which are used to treat textiles to improve their water resistance, durability, and appearance.
Used in Energy Storage Industry:
1,1,1-Tris(hydroxymethyl)ethane is used in some phase change materials, which are substances that absorb and release thermal energy during phase transitions. These materials have potential applications in thermal energy storage and temperature regulation systems.
Purification Methods
Dissolve it in hot tetrahydrofuran, filter and precipitate it with hexane. It has also been crystallised from acetone/water (1:1). Dry it in a vacuum. [Beilstein 1 H 520, 1 IV 2780.]
Check Digit Verification of cas no
The CAS Registry Mumber 77-85-0 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 7 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77-85:
(4*7)+(3*7)+(2*8)+(1*5)=70
70 % 10 = 0
So 77-85-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H12O3/c1-5(2-6,3-7)4-8/h6-8H,2-4H2,1H3
77-85-0Relevant articles and documents
A gold(I) complex based on 1,8-naphthyridine functionalized N-heterocyclic carbene (NHC) and its catalytic activity
Liu, Zu-Yin,Liu, Shiuh-Tzung
, p. 321 - 323 (2012)
A gold complex containing 2,7-bis(mesitylimidazolylidenyl)naphthyridine (NHC-NP) has been synthesized. Thus, reaction of [{Ag3(NHC-NP) 2}(PF6)3] with [Au(Me2S)Cl] provided an unusual digold complex bridged by two NHC-NP, forming a 20-membered dinuclear metallacycle [{Au2 (NHC-NP) 2Cl2}-(PF 6)2] (2) in high yield. This complex was characterized by spectroscopic and elemental analysis. This gold complex is active for the hydrolysis of 2,2,5-trimethyl-1,3-dioxane-5-methanol and can be recycled without losing the activity.
Precise Steric Control over 2D versus 3D Self-Assembly of Antimony(III) Alkoxide Cages through Strong Secondary Bonding Interactions
Moaven, Shiva,Yu, Jingze,Yasin, Jason,Unruh, Daniel K.,Cozzolino, Anthony F.
supporting information, p. 8372 - 8380 (2017/07/22)
Antimony(III) alkoxide cages were designed as building blocks for predictable supramolecular self-assembly. Supramolecular synthons featuring two Sb···O secondary bonding interactions (SBIs), each SBI stronger than 30 kJ/mol, were used to drive the formation of the supramolecular architectures. Judicious choice of pendant groups provided predictable control over the formation of self-assembled 3D columnar helices, which crystallized with hollow morphologies, or a self-assembled 2D bilayer. The Sb-O stretching frequency provides a spectroscopic signature of Sb···O SBI formation.
NOVEL HYDROGEN PEROXIDE-ACTIVABLE, ANTI-OXIDANT COMPOUNDS AND METHODS USING SAME
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Page/Page column 21; 22; 27, (2016/06/01)
The present invention includes 4-(hydroxymethyl)phenylboronic esters, which react with hydrogen peroxide to form 4-hydroxybenzyl alcohol, which is an anti-inflammatory and/or anti-oxidant compound. In certain embodiments, the compositions of the invention may be used to treat or prevent oxidative stress and/or inflammation, including ischemic disease.