The identity of the other 40% of the material is not determined. Typically, these impurities are other diepoxide isomers, but they may not be the only impurities. For a higher purity 1,4-Butanediol diglycidyl ether, the material listed under product number 220892 is recommended, which has a purity of ≥ 95.0%.
124192
Éther diglycidylique de 1,4-butanédiol
technical grade, 60%
Synonyme(s) :
1,4-Bis(2,3-epoxypropoxy)butane, 1,4-Bis(glycidyloxy)butane, 1,4-Bis(oxiran-2-ylmethoxy)butane, 1,4-Butylene glycol diglycidyl ether, Tetramethylene glycol diglycidyl ether
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100 G
59,10 €
500 G
159,80 €
About This Item
Formule empirique (notation de Hill) :
C10H18O4
Numéro CAS:
Poids moléculaire :
202.25
Beilstein:
115238
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23
Produits recommandés
Qualité
technical grade
Pression de vapeur
~10 mmHg ( 20 °C)
Forme
liquid
Concentration
60%
Indice de réfraction
n20/D 1.453 (lit.)
pb
266 °C (lit.)
Densité
1.1 g/mL at 25 °C (lit.)
Chaîne SMILES
C(CCOCC1CO1)COCC2CO2
InChI
1S/C10H18O4/c1(3-11-5-9-7-13-9)2-4-12-6-10-8-14-10/h9-10H,1-8H2
Clé InChI
SHKUUQIDMUMQQK-UHFFFAOYSA-N
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Catégories apparentées
Description générale
1,4-Butanediol diglycidyl ether(BDDE) is a homobifunctional monomer with two epoxide groups, widely used to modify the viscosity of epoxy resins. It is also used as a cross-linking agent to synthesize polymer networks.
Application
1,4-Butanediol diglycidyl ether can be used:
- As a cross-linking agent to prepare hyaluronic acid dermal fillers This crosslinking process enhances the gel-like consistency of the filler, making it more durable and longer-lasting.[1]
- As a monomer to prepare epoxy-based graphene nanocomposites that have potential applications in the field of flexible electronics, corrosion resistance coatings, and conductive adhesives. BDDE is chosen for its desirable properties such as low viscosity, good reactivity, and compatibility with graphene.
Mention d'avertissement
Danger
Mentions de danger
Classification des risques
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1
Code de la classe de stockage
10 - Combustible liquids
Classe de danger pour l'eau (WGK)
WGK 2
Point d'éclair (°F)
235.4 °F - closed cup
Point d'éclair (°C)
113 °C - closed cup
Équipement de protection individuelle
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Comparative physicochemical analysis among 1, 4-butanediol diglycidyl ether cross-linked hyaluronic acid dermal fillers
Nicola Zerbinati, et al.
Gels, 7, 139-139 (2021)
The new face of fillers: why evidence and experience both count.
Hema Sundaram
Journal of drugs in dermatology : JDD, 10(9), 964-964 (2011-11-05)
P E Morgan et al.
Journal of molecular recognition : JMR, 9(5-6), 394-400 (1996-09-01)
The preparation, characterisation and testing of stable non-porous coated perfluorocarbon supports functionalised with the metal chelate, iminodiacetic acid (IDA) is described. Polyvinyl alcohol (PVA), a neutral hydrophilic polymer was esterified with perfluorooctanoyl chloride and anchored to the surface of solid
David Stocks et al.
Journal of drugs in dermatology : JDD, 10(9), 974-980 (2011-11-05)
Hyaluronic acid (HA) gels are commonly injected into the skin to lift rhytides and to improve facial appearance. The different processes used in their manufacture and formulation yield products with unique physical characteristics that play an important role in predicting
Christopher Pohl et al.
Journal of chromatography. A, 1213(1), 37-44 (2008-11-04)
We have developed a number of new anion exchange stationary phases based on synthesis of hyperbranched condensation polymers prepared in situ on surface sulfonated wide pore, low surface area ethylvinylbenzene-divinylbenzene substrate beads. These new stationary phases are synthesized by exposing
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Product listed as 60%, but what is the make up of the remaining 40%? Is it dissolved in something?
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