Tridecyl methacrylate
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Tridecyl methacrylate
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CAS No:
2495-25-2
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Formula:
C17H32O2
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Chemical Name:
Tridecyl methacrylate
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Synonyms:
2-Propenoic acid,2-methyl-,tridecyl ester;Methacrylic acid,tridecyl ester;1-Tridecanol,methacrylate;Tridecyl methacrylate;1-Tridecyl methacrylate;SR 493;Light Ester TD;SR 493D;Acryester TD
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CAS No:
Tridecyl methacrylate Basic Attributes
268.43500
268.43
219-671-8
71FJI2DJAW
DTXSID8029236
2916140000
Characteristics
26.30000
5.41670
Liquid
0.8740 g/cm3 @ Temp: 20 °C
118 °C @ Press: 1 Torr
>230 °F
n20/D 1.45(lit.)
Temp during storage must be kept low to minimize formation of peroxides and other oxidation products. ... Storage temp below 30 deg C are recommended for the polyfunctional methacrylates. ... The methacrylate monomers should not be stored for longer than one year. Shorter storage times are recommended for the aminomethacrylates, ie, three months, and the polyfunctional methacrylates, ie, six months. Many of these cmpd are sensitive to UV light and should, therefore, be stored in the dark. The me
9.45E-05mmHg at 25°C
Safety Information
3
R36/37/38
S26-S36
Xi: Irritant;
P261, P264, P271, P272, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, P501
H315
|Warning|H315 (99.6%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P272, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 498 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
SUITABLE PROTECTIVE CLOTHING & SELF-CONTAINED RESP PROTECTIVE APPARATUS SHOULD BE AVAILABLE FOR USE OF THOSE WHO MAY HAVE TO RESCUE PERSONS OVERCOME BY FUMES. /ACRYLIC ACID & DERIVATIVES/
... Hazard is the generation of considerable exothermic heat in some of the reactions, so that high pressures & temp may develop. This danger ... should be borne in mind when designing plant. Awareness of the dangers and of good engineering design are essential to safety. Employees should be instructed about the necessity of cleansing the skin if it is contaminated by materials which are irritants or skin-absorbed. With careful design, however, and complete enclosure of those processes where toxic chemicals or intermediates occur, dangerous exposures can be avoided. /Acrylic acid & derivatives/|SRP: Contaminated protective clothing should be segregated in such a manner so that there is no direct personal contact by personnel who handle, dispose, or clean the clothing. Quality assurance to ascertain the completeness of the cleaning procedures should be implemented before the decontaminated protective clothing is returned for reuse by the workers. Contaminated clothing should not be taken home at end of shift, but should remain at employee's place of work for cleaning.|SRP: The scientific literature for the use of contact lenses in industry is conflicting. The benefit or detrimental effects of wearing contact lenses depend not only upon the substance, but also on factors including the form of the substance, characteristics and duration of the exposure, the uses of other eye protection equipment, and the hygiene of the lenses. However, there may be individual substances whose irritating or corrosive properties are such that the wearing of contact lenses would be harmful to the eye. In those specific cases, contact lenses should not be worn. In any event, the usual eye protection equipment should be worn even when contact lenses are in place.
Methacrylates ... produce slight to moderate skin and eye irritation ... depending upon volatility, these materials also may be sensory irritants. /Methacrylic acid & derivatives/
Drug Information
SMALL QUANTITIES OF METHACRYLATES MAY READILY BE METABOLIZED BY SAPONIFICATION INTO THE ALCOHOL AND METHACRYLIC ACID. THE LATTER MAY FORM AN ACETYL-COENZYME A DERIVATIVE, WHICH THEN ENTERS THE NORMAL LIPID METABOLISM. /METHACRYLATES/
BIOLOGICALLY, METHACRYLATES RESEMBLE ACRYLATES, EXCEPT FOR LOWER REACTIVITY & THUS DECR TOXICITY. THIS IS PROBABLY DUE TO STERIC HINDRANCE BY ITS METHYL GROUP & IN TURN DECR RATES OF MEMBRANE TRANSPORT & SYSTEMIC TRANSLOCATION. /METHACRYLIC ESTERS/
Tridecyl methacrylate Use and Manufacturing
The methacrylates can be synthesized by catalytic oxidation of isobutylene and subsequent esterification with the appropriate alcohol, or by reacting acetone with hydrocyanic acid and subsequent esterification in sulfuric acid with the appropriate alcohol. /Methacrylic esters/|TRANSESTERIFICATION OF TRIDECYL ALCOHOL WITH METHYL METHACRYLATE
Intermediates
Adhesives and sealants
1,000,000 - 10,000,000 lb|NO EVIDENCE OF COMMERCIAL PRODN IN USA
Adhesive manufacturing|2-Propenoic acid, 2-methyl-, tridecyl ester: ACTIVE|NO EVIDENCE OF CURRENT COMMERCIAL PRODN IN USA|METHYL METHACRYLATE, AND IN GENERAL THE METHACRYLIC ESTERS, POLYMERIZE MUCH LESS READILY THAN THE CORRESPONDING ORDINARY ACRYLATES. NONE THE LESS, THEY ARE STABILIZED BY ADDING HYDROQUINONE OR PYROGALLOL, PARTICULARLY IN THE PRESENCE OF METALLIC COPPER. /METHACRYLATES/
Thin-layer chromatography (TLC), polarography, and spectrometry are used for soln measurements. Methacrylates in air have been analyzed by TLC, polarography, and colorimetry. Polarography has been used for dtermination of any residual monomer in the polymer. /Methacrylic acid & derivatives/
Computed Properties
Molecular Weight:268.4
XLogP3:7.8
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:14
Exact Mass:268.240230259
Monoisotopic Mass:268.240230259
Topological Polar Surface Area:26.3
Heavy Atom Count:19
Complexity:233
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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