Detail of "78-51-3"

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CAS Number:
78-51-3
Name:
Tris(2-butoxyethyl) phosphate
Molecular Structure:
Formula:
C₁₈H₃₉O₇P
Molecular Weight:
398.54
Deleted CAS:
119166-98-2|19040-50-7|31227-66-4
Synonyms:
Ethanol,2-butoxy-, phosphate (3:1) (7CI,8CI,9CI);Phosphoric acid, tris(2-butoxyethyl)ester (6CI);2-Butoxyethanol phosphate;Amgard TBEP;Hostaphat B310;Ethanol, 2-butoxy-,1,1',1''-phosphate;Phosflex T-BEP;Tris(2-n-butoxyethyl) phosphate;tris-2-Butoxyethyl phosphate;Tri(butoxyethyl)phosphate;TBEP;Tris(2-butoxyethyl) phosphate(TBEP);
EINECS:
201-122-9
Density:
1.027 g/cm³
Melting Point:
-70 ºC
Boiling Point:
413.9 ºC at 760 mmHg
Flash Point:
241.5 ºC
Solubility:
soluble in water
Appearance:
viscous colourless or slightly yellow liquid
Hazard Symbols:
Xn
Risk Codes:
20/21/22-36/37/38
Safety:
26-37/39 Details

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One-component sealing compositions: One-component sealing compositions. (Toray Thiokol Co., Ltd., Japan). Jpn. Kokai Tokkyo Koho JP 58187452 A2 1 Nov 1983 Showa, 5 pp. (Japanese). (Japan).There are some reagents with their cas registry numbers 2432-87-3 and 1314-22-3 are used in this study. CODEN: JKXXAF. CLASS: IC: C08L081-00; C08G075-00. APPLICATION: JP 82-70649 27 Apr 1982. DOCUMENT TYPE: Patent CA Section: 42 (Coatings, Inks, and Related Products) Section cross-reference(s): 39 Moisture-curable, storage-stable sealing compns. contain polysulfide (mol. wt. 100-200,000) 100, moisture-activated peroxide 3-30, and ester of H3PO4 or dibasic fatty acid 5-100 parts. Thus, Thiokol LP 12 [31942-94-6] [mol. wt. 4000, viscosity 450 P (25°), crosslinking degree 0.2%] 100, o-C6H4(CO2Bu)2 38, CaCO3 50, TiO2 12, and tris(butoxyethyl) phosphate [78-51-3] 10 g were kneaded together and combined with Na perborate 10, KF 3, Mn naphthenate 1, and Zn(S2CNBu)2 0.5g to give a sealing compn. showing a surface tack-free time of 4 h (20°, relative humidity 50%) and complete curing in 6 days. .

Continuous alkoxidation: Continuous alkoxidation. Smith, Harry Martin; Williams, Raymond Daryl (FMC Corp. , USA). Eur. Pat. Appl. EP 91425 A2 12 Oct 1983, 13 pp. DESIGNATED STATES: R: AT, BE, CH, DE, FR, GB, IT, LI, LU, NL, SE. (English).Chemicals with cas numbers 126-73-8 and 2372-45-4 also play role. (European Patent Organization). CODEN: EPXXDW. CLASS: IC: C07C029-70; C07C031-30. APPLICATION: EP 83-890044 24 Mar 1983. PRIORITY: US 82-366262 7 Apr 1982. DOCUMENT TYPE: Patent CA Section: 45 (Industrial Organic Chemicals, Leather, Fats, and Waxes) Alkali metal alkoxides, such as BuOCH2CH2ONa (I) [52663-57-7] and BuONa [2372-45-4], are prepd. continuously by adding aq. alkali metal hydroxide to the upper part of a column reactor (contg. a nonoxidizing atm.), adding vaporized alc. (2-4 mol/mol hydroxide) to the lower part of the reactor, removing a water-alc. azeotrope from the upper part of the reactor, and recovering a substantially anhyd. alc.-alkali metal alkoxide mixt. from the lower part of the reactor. The alkoxides are used to prep. phosphate esters having a com. acceptable color. Thus, 50% aq. NaOH was fed to a column reactor (mid-column temp. 134°) along with BuOCH2CH2OH [111-76-2]. The product stream from the lower part of the reactor contained 29% I and 0.044% NaOH. (BuOCH2CH2O)3PO [78-51-3] prepd. from the I had a com. acceptable color. .

Detail of "78-51-3"

Tris(2-butoxyethyl) phosphate

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