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2-METHYL-4'-(METHYLTHIO)-2-MORPHOLINOPROPIOPHENONE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 71868-10-5 | |
EINECS NO. | ||
FORMULA | C15H21O2NS | |
MOL WT. | 279.41 | |
H.S. CODE | ||
TOXICITY |
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SYNONYMS |
2-Methyl-1-(4-Methylthio)phenyl-2-Morpholinyl-1-Propanon; | |
2-Methyl-1-4-(methylthio)pheny-2-morpholino-propan-1-one; CS CURE-105; | ||
SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | white to yellow powder | |
MELTING POINT | 72 - 75 C | |
BOILING POINT | ||
SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | Insoluble | |
AUTOIGNITION | ||
pH | ||
VAPOR DENSITY | ||
NFPA RATINGS | Health: 1; Flammability: 0; Reactivity: 0 | |
FLASH POINT |
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STABILITY | Stable under ordinary conditions | |
APPLICATIONS |
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Polymerization is initiated generally by free radical. There are four types of
free radical initiators which initiate polymerization.
The main advantage of polymerization started by photoinitiators is temperature-independence and easy control. It can be conducted at very low temperatures and can be stopped simply by removing the light source. Photoinitiators are compounds that break down into free radicals upon exposure to ultraviolet radiation. Photoinitiators undergo a unimolecular bond cleavage upon irradiation to yield free radicals (benzoin esters; benzil ketals; alpha-dialkoxy acetophenones; alpha-hydroxy-alkylphenones; alpha-amino alkyl- phosphine; acylphosphine oxides). Another type of photoinitiators undergo a bimolecular reaction where the excited state of the photoinitiator interacts with a second molecule (a coinitiator) to generate free radicals(benzo phenones,amines; thioxanthones,amines; titanocenes). Photoinitiators are widely applied in UV curing inks, wood coatings, paper coatings, optical fiber, PCB, screen printing , paper varnish and other surface coatings. |
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SALES SPECIFICATION | ||
APPEARANCE |
White to yellow powder | |
ASSAY |
98.0% min | |
MELTING POINT | 72 - 75 C | |
VOLATILES |
0.3% max | |
CLARITY OF SOLUTION |
Clear ( 10g in 100ml acetone) | |
TRANSMITTANCE |
70% min (425nm) , 85% min (500nm) | |
TRANSPORTATION | ||
PACKING | 50kgs in Fiber drum | |
HAZARD CLASS | ||
UN NO. | ||
OTHER INFORMATION | ||
Morpholine is a
hygroscopic, weak basic, oily and volatile liquid; with a characteristic amine
odor; melting point -5 C, boiling point at 129 C; miscible with water and with
many alcohol organic solvents such methanol, ethanol, acetone, ethers, BTX (it
is used as a solvent itself), but has limited solubility in alkaline solutions.
It decomposes on heating resulting toxic nitrogen oxides and violently reacts
with strong oxidants resulting fire hazard and attacking copper and its
compounds. It can be prepared by the reductive ammonation of diethylene glycol
with hydrogen, by the dehydration of diethanolamine with a strong acid (oleum)
and by heating bis(chloroethyl)ether with excess ammonia. It is a cyclic amino
ether as well as a secondary amine. 1,4-Dioxane is the form which nitrogen atom
is replaced by oxygen. The ether property of morpholine is typically inert. The
secondary amine property involves in the most chemical reactions. Morpholine is
a versatile chemical. It is used as a solvent itself for resins, dyes, and
waxes. Its alkyl derivatives (e.g. N-methylmorpholine, N-ethylmorpholine) are
used as a catalyst for the production of polyurethane foams. Nitrogen in ring
system involves in the introduction
of sterically demanding asymmetric center to achieve
effective stereocontrol. Morpholine has a
similar volatility with water. It is used as a pH adjustment additive in fossil
fuel and steam systems as a corrosion inhibitor. The most important use is as a
chemical intermediate to prepare below compounds:
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