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240117

Sigma-Aldrich

1,6-Hexanediol

99%

Sinonimo/i:

Hexamethylene glycol

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About This Item

Formula condensata:
HO(CH2)6OH
Numero CAS:
Peso molecolare:
118.17
Beilstein:
1633461
Numero CE:
Numero MDL:
Codice UNSPSC:
12162002
ID PubChem:
NACRES:
NA.23

Tensione di vapore

0.53 mmHg ( 20 °C)

Livello qualitativo

Saggio

99%

Temp. autoaccensione

608 °F

Limite di esplosione

16 %

P. eboll.

250 °C (lit.)

Punto di fusione

38-42 °C (lit.)

Stringa SMILE

OCCCCCCO

InChI

1S/C6H14O2/c7-5-3-1-2-4-6-8/h7-8H,1-6H2
XXMIOPMDWAUFGU-UHFFFAOYSA-N

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Descrizione generale

1,6-hexanediol is a versatile chemical compound commonly used in the polymer industry. It is used as a building block or monomer for the synthesis of various polymers and polymer-based materials. For instance, it can be used in the production of polyesters, polyurethanes, and polyamides, among others. These polymers find applications in a wide range of industries, including automotive, textiles, coatings, adhesives, and sealants.

Applicazioni

1,6-Hexanediol can be used for a variety of applications such as:
  • a structure-directing agent for the synthesis of ZSM-5 zeolite
  • a solvent for titanium tetra-isopropoxide to form titanium oxide (TiO2) nanocrystals
  • a phase change material in combination with lauric acid for thermal energy storage applications
1,6-hexanediol can also be used in the synthesis of a specific type of biopolymer called poly(3-hydroxybutyrate-co-4-hydroxybutyrate) (PHB4HB) which is used for some medical applications. It is also used as a component in the formulation of the gel polymer electrolyte. It may act as a crosslinking agent or a plasticizer to facilitate the formation of a stable and conductive gel polymer electrolyte for sodium metal batteries.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

215.6 °F - closed cup

Punto d’infiammabilità (°C)

102 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)


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We reported previously that 2,5-hexanedione (2,5-HD), the neurotoxic metabolite of methyl-n-butylketone (MnBK) and n-hexane, induced aggregation of intermediate filaments of the vimentin type in cultured fibroblasts. To determine if these findings have relevance to the mechanism by which these hexacarbons
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A crucial feature of differentiated cells is the rapid activation of enhancer-driven transcriptional programs in response to signals. The potential contributions of physicochemical properties of enhancer assembly in signaling events remain poorly understood. Here we report that in human breast

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