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Safety Information

462373

Sigma-Aldrich

Hexyl methacrylate

98%, contains 100 ppm MEHQ

Synonym(s):

n -Hexyl methacrylate, Hexyl 2-methyl-2-propenoate, Hexyl methacrylate

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About This Item

Linear Formula:
C6H13OCOCCH2CH3
CAS Number:
142-09-6
Molecular Weight:
170.25
EC Number:
205-521-9
MDL number:
MFCD00015283
UNSPSC Code:
12162002
PubChem Substance ID:
24869970
NACRES:
NA.23

Assay

98%

contains

100 ppm MEHQ

refractive index

n20/D 1.432 (lit.)

bp

203 °C (lit.)

density

0.863 g/mL at 25 °C (lit.)

SMILES string

CCCCCCOC(=O)C(C)=C

InChI

1S/C10H18O2/c1-4-5-6-7-8-12-10(11)9(2)3/h2,4-8H2,1,3H3

InChI key

LNCPIMCVTKXXOY-UHFFFAOYSA-N

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Application


  • Fabrication and evaluation of an organic monolithic column based upon the polymerisation of hexyl methacrylate with 1, 6-hexanediol ethoxylate diacrylate for the capillary electrochromatography of small molecules: This study details the fabrication of a novel monolithic column for capillary electrochromatography, showcasing the application of hexyl methacrylate in advanced analytical techniques (W Alshitari et al., Talanta, 2015).

  • Tunable mechanical properties of core‐shell polymers of poly (hexyl methacrylate) and poly (methyl methacrylate) by semicontinuous heterophase polymerization: The article discusses the synthesis of core-shell polymers with adjustable mechanical properties, illustrating the versatility of hexyl methacrylate in creating tailored polymeric materials (LO Sahagún Aguilar et al., Polymer Engineering & Science, 2019).

  • Supramolecular cross-links in poly (alkyl methacrylate) copolymers and their impact on the mechanical and reversible adhesive properties: This paper evaluates the mechanical and adhesive properties of poly(hexyl methacrylate) copolymers, highlighting the role of supramolecular cross-links in enhancing material performance (C Heinzmann et al., ACS Applied Materials & Interfaces, 2015).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H317,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

172.0 °F - closed cup

Flash Point(C)

77.8 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

462373-VAR:
462373-BULK:
462373-1KG:
462373-500G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS9535
MKCN6475
MKCN4492
MKCK7119
MKCK0895

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J A Navarro-Huerta et al.
Analytica chimica acta, 1086, 142-155 (2019-09-29)
The development of methacrylate-based monolithic columns was studied for the separation of pharmaceutical hydrophilic compounds in nano-liquid chromatography. The selected polymerisation mixture consisted of 7.5% hexyl methacrylate, 4.5% methacrylic acid and 18.0% ethylene dimethacrylate (w/w), in a binary porogenic solvent
Mutaz E Salih et al.
Journal of chromatographic science, 56(9), 819-827 (2018-06-20)
Recently, analytical separation techniques have the potential toward green approaches to reduce the environmental impact. This study focuses on the development of an analytical method for the determination of paracetamol and chlorzoxazone in their pharmaceutical combination. The separation was achieved
Hiroyuki Hoshina et al.
Polymers, 12(11) (2020-11-15)
A nonwoven fabric adsorbent loaded with 2-ethylhexyl hydrogen-2-ethylhexylphosphonate (EHEP) was developed for the separation and recovery of dysprosium (Dy) and neodymium (Nd) from an aqueous solution. The adsorbent was prepared by the radiation-induced graft polymerization of a methacrylate monomer with
Shufeng Li et al.
Biomaterials, 53, 95-106 (2015-04-22)
Cell processes, including growth cones, respond to biophysical cues in their microenvironment to establish functional tissue architecture and intercellular networks. The mechanisms by which cells sense and translate biophysical cues into directed growth are unknown. We used photopolymerization to fabricate
D S Spencer et al.
International journal of pharmaceutics, 588, 119691-119691 (2020-07-30)
Cationic polymers have garnered significant interest for their utility in intracellular drug delivery and gene therapy. However, due to their associated toxicities, novel synthesis approaches must be explored to develop materials that are biocompatible. The novel library of nanoparticles synthesized
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