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411744

Sigma-Aldrich

1,4-Butanediol diacrylate

technical grade, contains ~75 ppm hydroquinone as inhibitor

Synonyme(s) :

1,4-Bis(acryloyloxy)butane, Tetramethylene diacrylate

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About This Item

Formule linéaire :
(H2C=CHCO2CH2CH2-)2
Numéro CAS:
1070-70-8
Poids moléculaire :
198.22
Numéro CE :
213-979-6
Numéro MDL:
MFCD00014940
Code UNSPSC :
12162002
ID de substance PubChem :
24865761
Nomenclature NACRES :
NA.23

Qualité

technical grade

Niveau de qualité

200

Essai

87%

Forme

liquid

Contient

~75 ppm hydroquinone as inhibitor

Indice de réfraction

n20/D 1.456 (lit.)

pb

83 °C/0.3 mmHg (lit.)

Densité

1.051 g/mL at 25 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

C=CC(=O)OCCCCOC(=O)C=C

InChI

1S/C10H14O4/c1-3-9(11)13-7-5-6-8-14-10(12)4-2/h3-4H,1-2,5-8H2

Clé InChI

JHWGFJBTMHEZME-UHFFFAOYSA-N

Catégories apparentées

Description générale

1,4-Butanediol diacrylate(BDDA) is an acrylate monomer and a multifunctional crosslinking agent. It ​has a relatively low viscosity and undergoes photopolymerization, initiated by UV radiation. BDDA contributes to the flexibility and elasticity of the cured materials. It is used in optical films,3D printing, tissue engineering, dental composites, UV-curable adhesives, and sealants.

Application

1,4-Butanediol diacrylate can be used:



  • As a precursor to synthesize joint-linker hydrogels with good mechanical strength and used as scaffold materials in bone tissue engineering as biomimetics for natural tissues and also in drug delivery systems.
  • To prepare anti-fouling coating for dental composites.
  • As a crosslinking agent to prepare hydrophobic acrylic intraocular lens(IOL) materials with reduced glistening.
  • As a precursor to fabricate poly(β-amino ester) based solid polymer electrolytefilms for Li-ion batteries. BDDA enhances the ionic conductivity of theelectrolyte films.

Pictogrammes

Skull and crossbonesCorrosion
GHS06,GHS05

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1A

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

>235.4 °F

Point d'éclair (°C)

> 113 °C

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Certificats d'analyse (COA)

Lot/Batch Number
MKCV3758
MKCV4147
MKCV4148
MKCS3273
MKCR2997

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Supramolecular Self-Healing Antifouling Coating for Dental Materials
Qiangwei Xin, et al.
ACS Applied Materials & Interfaces, 15, 41403-41416 (2023)
Preparation of hydrophobic acrylic intraocular lens materials using various crosslinking agents to reduce glistening
Tae Hyoung Kim, et al.
International Journal of Polymeric Materials and Polymeric Biomaterials, 1-10 (2023)
Y Sakai et al.
Bioscience, biotechnology, and biochemistry, 63(4), 688-697 (1999-06-11)
A carboxylesterase that is responsible for conversion of 1,4-butanediol diacrylate (BDA) to 4-hydroxybutyl acrylate (4HBA) was found in Brevibacterium lines IFO 12171, and purified to homogeneity. The purified enzyme was active toward a variety of diesters of ethylene glycol, 1,4-butanediol
Synthesis of joint-linker type gels and porous polymers by addition reactions of multi-functional thiol and alkyl diacrylate, diisocyanate compounds
Naofumi Naga, et al.
Materials Today Communications, 18, 153-162 (2019)
Dan-Li Hao et al.
International journal of nanomedicine, 15, 1771-1786 (2020-03-28)
In this study, pH-sensitive poly(2-ethyl-2-oxazoline)-poly(lactic acid)-poly(β-amino ester) (PEOz-PLA-PBAE) triblock copolymers were synthesized and were conjugated with an antimalaria drug artesunate (ART), for inhibition of a colon cancer xenograft model. The as-prepared polymer prodrugs are tended to self-assemble into polymeric micelles
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