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236241

Sigma-Aldrich

Pentaerythritol

99%

Sinonimo/i:

2,2-Bis(hydroxymethyl)-1,3-propanediol

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About This Item

Formula condensata:
C(CH2OH)4
Numero CAS:
115-77-5
Peso molecolare:
136.15
Beilstein:
1679274
Numero CE:
204-104-9
Numero MDL:
MFCD00004692
Codice UNSPSC:
12162002
ID PubChem:
24854158
NACRES:
NA.23

Tensione di vapore

<1 mmHg ( 20 °C)

Saggio

99%

P. eboll.

276 °C/30 mmHg (lit.)

Punto di fusione

253-258 °C (lit.)

Stringa SMILE

OCC(CO)(CO)CO

InChI

1S/C5H12O4/c6-1-5(2-7,3-8)4-9/h6-9H,1-4H2
WXZMFSXDPGVJKK-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

Pentaerythritol is acrystalline , odour less white solid. The presence of neopentane core and four terminalhydroxyl groups makes it a versatile substrate for the synthesispolyfunctionalized compounds.

Applicazioni

Pentaerythritol can be used as a starting material to prepare four armed polyurethane prepolymers, which are applicable in the synthesis of UV cured polyurethane dispersions.

It can be used as an additive in the preparation of flame retardant polymers.

It can also be used as a precursor to synthesize polyethylene glycol/4,4′-diphenylmethane diisocyanate/pentaerythritol copolymer which is applicable as heat storage material.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Chin-Wen Chen et al.
Polymers, 12(9) (2020-09-10)
Bio-based unsaturated poly(butylene adipate-co-butylene itaconate) (PBABI) aliphatic copolyesters were synthesized with pentaerythritol (PE) as a modifier, observing the melting point, crystallization, and glass transition temperatures were decreased from 59.5 to 19.5 °C and 28.2 to -9.1 °C as an increase
Zhiming Zhang et al.
Organic & biomolecular chemistry, 9(24), 8220-8223 (2011-10-13)
A trimer of cholic acid made by linking three cholic acid molecules with pentaerythritol via click chemistry serves as the center of an artificial metallohydrolase after the complexation of the triazole groups with a Zn(2+) ion. The invertible amphiphilic cavity
Hussein Al-Mughaid et al.
The Journal of organic chemistry, 71(4), 1390-1398 (2006-02-14)
A nonavalent glycodendrimer bearing terminal alpha-d-mannopyranoside units has been synthesized with a convergent approach. Terminal trivalent mannoside dendrons bearing p-halophenyl ethers were prepared by glycosylation of pentaerythritol derivatives having three 2-hydroxyethyl ether substituents. Two efficient routes were developed for the
Guowei Wang et al.
Macromolecular rapid communications, 32(20), 1658-1663 (2011-08-23)
The eight-shaped poly(ethylene oxide) (PEO) is synthesized by a combination of Glaser coupling with ring-opening polymerization (ROP). Firstly, the star-shaped (PEO-OH)(4) is synthesized by ROP of ethylene oxide (EO) using pentaerythritol as an initiator and diphenylmethyl potassium (DPMK) as a
Tao Tu et al.
The Journal of organic chemistry, 73(14), 5255-5263 (2008-06-19)
Molecular scaffolds that have well-defined geometries, are easy to synthesize and functionalize, and can hold attached sites of molecular recognition in suitable orientations are useful tools in various areas of science and technology. The utility of the tetraphenyl ether of
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