ChemicalBook--->CAS DataBase List--->4704-94-3

4704-94-3

4704-94-3 Structure

4704-94-3 Structure
IdentificationMore
[Name]

2-(HYDROXYMETHYL)-1,3-PROPANEDIOL
[CAS]

4704-94-3
[Synonyms]

2-(HYDROXYMETHYL)-1,3-PROPANEDIOL
TRIMETHYLOLMETHANE
TRIS(HYDROXYMETHYL)METHANE
Propane, 1,3-dihydroxy-2-hydroxymethyl-
2-(hydroxymethyl)propane-1,3-diol
2-HYDROXYMETHYL-1,3-PROPANEDIOL, POLYME&
2-(HYDROXYMETHYL)-1,3-PROPANEDIOL 97+%
trihydroxymethylmethane
Trimethylolmethane, Tris(hydroxymethyl)methane
(Methanetriyl)trimethanol
Methylidynetrismethanol
[EINECS(EC#)]

225-187-8
[Molecular Formula]

C4H10O3
[MDL Number]

MFCD00192217
[Molecular Weight]

106.12
[MOL File]

4704-94-3.mol
Chemical PropertiesBack Directory
[Melting point ]

63-68 °C (dec.) (lit.)
[Boiling point ]

158 °C(Press: 1.5 Torr)
[density ]

1.213±0.06 g/cm3(Predicted)
[Fp ]

89 °C
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

solid
[pka]

14.10±0.10(Predicted)
[Appearance]

Off-white to light yellow Solid
[BRN ]

1733340
[InChI]

InChI=1S/C4H10O3/c5-1-4(2-6)3-7/h4-7H,1-3H2
[InChIKey]

SFRDXVJWXWOTEW-UHFFFAOYSA-N
[SMILES]

C(O)C(CO)CO
[CAS DataBase Reference]

4704-94-3(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Safety Statements ]

S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

3
[F ]

3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

2-(Hydroxymethyl)propane-1,3-diol is a useful reactant for the preparation of tetracyanocyclopentadienide amine salts.
[Synthesis Reference(s)]

Synthesis, p. 742, 1987 DOI: 10.1055/s-1987-28072
[Synthesis]

1,3-Propanediol, 2-[(benzoyloxy)methyl]-, 1,3-dibenzoate

113967-50-3

2-(HYDROXYMETHYL)-1,3-PROPANEDIOL

4704-94-3

The general procedure for the synthesis of 2-hydroxymethyl-1,3-propanediol using the compound (CAS:113967-50-3) as starting material was as follows: the white powder (360 g, 0.86 mol) obtained in step (2) was dissolved in methanol (2L), followed by the addition of sodium methanolate (139 g, 2.58 mol). The reaction mixture was heated to reflux and kept for 20 hours. After completion of the reaction, the solvent was removed by evaporation. The residue was washed twice with chloroform and the organic phases were combined. The organic phase was dried over anhydrous sodium sulfate and concentrated. The concentrated product was crystallized in isobutanol to give 82 g of white powdered 2-hydroxymethyl-1,3-propanediol in 90% yield.

[References]

[1] Synthesis, 1987, # 8, p. 742 - 744
[2] Patent: CN108440455, 2018, A. Location in patent: Paragraph 0066; 0076-0078; 0100; 0122
Spectrum DetailBack Directory
[Spectrum Detail]

2-(HYDROXYMETHYL)-1,3-PROPANEDIOL(4704-94-3)1HNMR
2-(HYDROXYMETHYL)-1,3-PROPANEDIOL(4704-94-3)1HNMR
2-(HYDROXYMETHYL)-1,3-PROPANEDIOL(4704-94-3)Raman
2-(HYDROXYMETHYL)-1,3-PROPANEDIOL(4704-94-3)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

4704-94-3(sigmaaldrich)
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