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Merck
CN

93370

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
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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

functional group

hydroxyl

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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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)
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)
M Y Bekkedal et al.
Neurotoxicology and teratology, 20(3), 307-316 (1998-06-25)
A potent convulsant, trimethylolpropane phosphate (TMPP), was evaluated for long-term effects on measures of social behaviors and anxiety in Long-Evans rats. Animals received three to four daily treatments of TMPP (0.1 mg/kg/ml) beginning at age 23 days in Experiment 1
Synthesis, characterization, and viscoelastic properties of high molecular weight hyperbranched polyglycerols.
Kainthan RK, et al.
Macromolecules, 39(22), 7708-7717 (2006)
Vita Kiriliauskaitė et al.
Journal of industrial microbiology & biotechnology, 38(9), 1561-1566 (2011-02-18)
The ability of the commercial lipolytic enzyme Lipoprime 50T to catalyze the biotechnologically important synthesis of the biodegradable and environmentally acceptable trimethylolpropane (2-ethyl-2-(hydroxymethyl)-1,3-propanediol) ester of oleic acid was investigated. Simple and accurate thin-layer chromatography and computer analysis methods were used

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