442291
Octadecylsilane
97%
Synonym(s):
Octadecyltrihydridosilane
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About This Item
Linear Formula:
CH3(CH2)17SiH3
CAS Number:
Molecular Weight:
284.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
242-453-9
MDL number:
Product Name
Octadecylsilane, 97%
InChI key
YTJSFYQNRXLOIC-UHFFFAOYSA-N
InChI
1S/C18H40Si/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h2-18H2,1,19H3
SMILES string
CCCCCCCCCCCCCCCCCC[SiH3]
assay
97%
bp
195 °C/15 mmHg (lit.)
mp
29 °C (lit.)
density
0.795 g/mL at 25 °C (lit.)
Quality Level
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Application
Octadecylsilane can be used as a modifying agent for montmorillonite clay nanoparticles, which are used as a filler material in the synthesis of poly(methyl methacrylate) (PMMA)/silylated montmorillonite composites.
General description
Octadecylsilane is an organosilicon compound that consists of a long-chain hydrocarbon (18 carbons) bonded to a silicon atom through a carbon-silicon bond. It is widely used in various applications due to its high surface activity, making it an excellent adsorbent for non-polar organic compounds. It is also used as a surface modifier or coating agent.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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Terry Koerner et al.
Analytical chemistry, 79(9), 3312-3319 (2007-03-29)
In this study a nano-electrospray emitter is constructed by precisely positioning entrapped octadecylsilane (ODS) particles within a photoinitiated polymer at the exit aperture of a capillary. Following poly-merization, the microsphere/polymer hybrid material is able to withstand pressures greater than 4000
Oleg V Krokhin
Analytical chemistry, 78(22), 7785-7795 (2006-11-16)
Continued development of a new sequence-specific algorithm for peptide retention prediction in RP HPLC is reported. Our discovery of the large effect on the apparent hydrophobicity of N-terminal amino acids produced by the ion-pairing retention mechanism has led to the
Kajal Chakraborty et al.
Natural product research, 34(12), 1678-1686 (2018-12-26)
The chemical analyses of ethyl acetate-methanol (EtOAc-MeOH) extract of muricid gastropod mollusk, Chicoreus ramosus from the southeastern coast of Indian peninsular led to the identification of unprecedented cembrane-type diterpenoid, which was characterized as (3E, 6E, 10E)-8a-butoxy-17(15→14), 20(12→11)-bis-abeo-cembra-3,6,10,14(17),15-pentaene (1). The structure
Xu Zhang et al.
Analytical chemistry, 79(12), 4507-4513 (2007-05-19)
An integrated microsampling approach based on solid-phase microextraction (SPME) was developed to provide a complete solution to highly efficient and accurate pharmacokinetic studies. The microsampling system included SPME probes that are made of poly(ethylene glycol) (PEG) and C18-bonded silica, a
Tomokazu Hata et al.
PloS one, 12(7), e0180745-e0180745 (2017-07-07)
Gut lumen serotonin (5-hydroxytryptamine: 5-HT) contributes to several gastrointestinal functions such as peristaltic reflexes. 5-HT is released from enterochromaffin (EC) cells in response to a number of stimuli, including signals from the gut microbiota. However, the specific mechanism by which
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