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504-63-2 - 1,3-Propanediol, 99% - 1,3-Dihydroxypropane - Trimethylene glycol - A10829 - Alfa Aesar

A10829 1,3-Propanediol, 99%

Numéro CAS
504-63-2
Synonymes
1,3-Dihydroxypropane
Trimethylene glycol

Dimensions Prix ($) Quantité Disponibilité
250g 53,25
1000g 158,18
5000g 695,25
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1,3-Propanediol, 99%

MDL
MFCD00002949
EINECS
207-997-3

Propriétés chimiques

Formule
HO(CH2)3OH
Poids formulaire
76.10
Point de fusion
-26°
Point d'ébullition
214°
Point d'éclair
140°(174°F)
Densité
1.053
Indice de réfraction
1.4400
Solubilité
Miscible with water and alcohol.

Applications

1,3-Propanediol is used as a solvent for thin film preparations, in the production of polymers such as polytrimethylene terephthalate, adhesives, laminates, coatings, moldings, aliphatic polyesters, as an antifreeze and in wood paint. It also acts as a reagent for vinyl epoxide synthon, for epoxide ring-opening, for polymerization reactions and for natural product syntheses.

Notes

Incompatible with acid chlorides, acid anhydrides, oxidizing agents, chloroformates and reducing agents.

Références bibliographiques

Used for protection of carbonyl groups as their acetals (1,3-dioxane) derivatives, in the presence of a catalyst, e.g. TsOH: J. Chem. Soc. (C), 244 (1962), pyridine hydrochloride: Bull. Soc. Chim. Fr., 2287 (1972), or Amberlyst® 15: J. Chem. Soc. Perkin 1, 158 (1979). Comparative studies have indicated that formation of acetals from this diol is slower than for ethylene glycol, as is acid catalyzed hydrolysis of the resulting 1,3-dioxanes of aldehydes in comparison with the 1,3-dioxolanes, whereas for ketones the reverse applies: J. Am. Chem. Soc., 80, 6350 (1958); 90, 1249, 1253 (1968). For a review of the preparation of acetals, see: Synthesis, 501 (1981). Conditions have been described for the protection of acrolein using anhydrous HBr in dichloromethane: Org. Synth. Coll., 7, 59 (1990). For use in the preparation of the cyclic acetal of cyclopropenone, see: Org. Synth. Coll., 8, 173 (1993). The product behaves as a 1,3-dipole in cycloaddition reactions, see Benzyl­idenemalononitrile, L02426.

/n

Zhang, J.; Zhao, B.; Pan, Z.; Gu, M.; Punnoose, A. Synthesis of ZnO Nanoparticles with Controlled Shapes, Sizes, Aggregations, and Surface Complex Compounds for Tuning or Switching the Photoluminescence. Cryst. Growth Des. 2015, 15 (7), 3144-3149.

Nakagawa, Y.; Tamura, M.; Tomishige, K. Catalytic materials for the hydrogenolysis of glycerol to 1, 3-propanediol. J. Mater. Chem. A 2014, 2 (19), 6688-6702.

Autres références

Merck
14,9714
Beilstein
969155
Code tarifaire harmonisé
2905.39
TSCA
Yes
RTECS
TY2010000

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Analytique et matériel de laboratoire