Trimellitic anhydride chloride
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Trimellitic anhydride chloride
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CAS No:
1204-28-0
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Formula:
C9H3ClO4
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Chemical Name:
Trimellitic anhydride chloride
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Synonyms:
5-Isobenzofurancarbonyl chloride,1,3-dihydro-1,3-dioxo-;Phthalic anhydride,4-(chloroformyl)-;1,3-Dihydro-1,3-dioxo-5-isobenzofurancarbonyl chloride;Trimellitic anhydride monoacid chloride;Trimellitic anhydride chloride;4-(Chloroformyl)phthalic anhydride;Trimellitic anhydride acid chloride;4-(Chlorocarbonyl)phthalic anhydride;Trimellitic acid anhydride 4-monoacid chloride;1,3-Benzofurandione-5-carbonyl chloride;Trimellitic acid anhydride chloride;Anhydrotrimellitic acid chloride;Trimellitic anhydride monochloride;1,3-Dioxo-1,3-dihydro-2-benzofuran-5-carbonyl chloride;NSC 89728;1,3-Dioxo-2-benzofuran-5-carbonyl chloride;1,3-Dioxo-1,3-dihydro-isobenzofuran-5-carbonyl chloride
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CAS No:
Trimellitic anhydride chloride Basic Attributes
210.57
210.57
214-874-8
56231EU26X
89728
DTXSID9061621
29173990
Characteristics
60.4
1.37620
PelletsLargeCrystals
1.5015 (rough estimate)
68 °C @ Solvent: Hexane
162-164 °C @ Press: 1 Torr
186.3ºC
1.4571 (estimate)
decomposes
2-8ºC
Safety Information
II
8
UN 3261 8/PG 2
3
R29; R34
26-36/37/39-45
C
Stable at room temperature in closed containers under normal storage and handling conditions.
P280; P303 + P361 + P353; P304 + P340 + P310; P305 + P351 + P338
H314
|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 64 companies from 7 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Trimellitic anhydride chloride Use and Manufacturing
50g of trimellitic anhydride, and45mL of cyclohexane was added dimethylaminopyridine 0.05g4- reaction flask washeated to 90 ° C, Was slowly added dropwise 37.2g of thionyl chloride (TMA /SOCl 2 molar ratio of 1: 1.2), the reaction was refluxed for 6h, until no gasevolution, The reaction solution obtained at the end the reaction, the reactionsolution was -0.085MPa recovered by distillation at 90 ° C the remainingcyclohexane and excess thionyl chloride, And then by vacuum distillation(degree of vacuum of 750 mm Hg) collected 180 ~ 190 ° C fraction obtained in47.6 g of trimellitic anhydride acid chloride, cooled After it is a whitecrystalline solid, mp 67.5~ 68.8 ° C, HPLC chromatography 99.5percent, yield 86.9percent.200 g of trimellitic anhydride, 120 mL of ethyl acetate and 0.02 g of tri-n-butylphosphine were added to the reaction flask, and the temperature was raised to 80 ° C.156 g of thionyl chloride was slowly added dropwise, and the reaction was refluxed for 6 hours until no gas evolved, and the reaction was completed to obtain a reaction solution.The reaction solution was distilled at -0.085 MPa at 80 ° C to recover residual benzene and excess thionyl chloride, and then vacuum distilled through a thin film evaporator.The degree of vacuum was 660 mmHg and the temperature was 130 °C.Collect 180-190 ° C fractions, Obtained 150.6 g of trimellitic anhydride acid chloride, After cooling, it was a white solid crystal with a melting point of 68.1 ° C and an HPLC chromatographic content of 99.25percent.
Plasticizers
Plastic material and resin manufacturing|5-Isobenzofurancarbonyl chloride, 1,3-dihydro-1,3-dioxo-: ACTIVE
Computed Properties
Molecular Weight:210.57
XLogP3:1.8
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:209.9719863
Monoisotopic Mass:209.9719863
Topological Polar Surface Area:60.4
Heavy Atom Count:14
Complexity:312
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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