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Key Documents

93370

Sigma-Aldrich

1,1,1-Tris(hydroxymethyl)propane

dist., ≥98.0% (GC)

Synonym(s):

2-Ethyl-2-hydroxymethyl-1,3-propanediol, Trimethylolpropane

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About This Item

Linear Formula:
CH3CH2C(CH2OH)3
CAS Number:
Molecular Weight:
134.17
Beilstein:
1698309
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

4.8 (vs air)

Quality Level

vapor pressure

<1 mmHg ( 20 °C)

Assay

≥98.0% (GC)

form

(Powder or Crystals or Granules or Chunks)

autoignition temp.

1301 °F

quality

dist.

bp

159-161 °C/2 mmHg (lit.)

mp

56-58 °C (lit.)
56-61 °C

solubility

H2O: 0.1 g/mL, clear

SMILES string

CCC(CO)(CO)CO

InChI

1S/C6H14O3/c1-2-6(3-7,4-8)5-9/h7-9H,2-5H2,1H3

InChI key

ZJCCRDAZUWHFQH-UHFFFAOYSA-N

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Application

1,1,1-Tris(hydroxymethyl)propane is used as a starting material in the synthesis of a variety of polyglycerols and polylactides. It is also used as a tripodal ligand to construct manganese-based metal-organic complexes as single molecular magnets.

Pictograms

Health hazard

Signal Word

Warning

Hazard Statements

Hazard Classifications

Repr. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

356.0 °F - Cleveland open cup

Flash Point(C)

180 °C - Cleveland open cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Telechelic and star-shaped poly (L-lactide) s by means of bismuth (III) acetate as initiator.
Kricheldorf HR, et al.
Biomacromolecules, 5(2), 492-496 (2004)
A family of manganese rods: Syntheses, structures, and magnetic properties.
Rajaraman G, et al.
Journal of the American Chemical Society, 126(47), 15445-15457 (2004)
Synthesis, characterization, and viscoelastic properties of high molecular weight hyperbranched polyglycerols.
Kainthan RK, et al.
Macromolecules, 39(22), 7708-7717 (2006)
Synthesis, structure, and magnetic properties of a [Mn22] wheel-like single-molecule magnet.
Murugesu M, et al.
Inorganic Chemistry, 43(14), 4203-4209 (2004)
Y Y Linko et al.
Journal of biotechnology, 66(1), 41-50 (1998-12-29)
The interest in the applications of biocatalysis in organic syntheses has rapidly increased. In this context, lipases have recently become one of the most studied groups of enzymes. We have demonstrated that lipases can be used as biocatalyst in the

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