| Identification | More | [Name]
PENTAERYTHRITOL TETRAACETATE | [CAS]
597-71-7 | [Synonyms]
2,2-BIS[(ACETYLOXY)METHYL]-1,3-PROPANEDIOL
2,2-BIS[(ACETYLOXY)METHYL]-1,3-PROPANEDIOL DIACETATE
2,2-BIS(HYDROXYMETHYL)-1 3-PROPANEDIOL TETRAACETATE
PENTAERYTHRITOL TETRAACETATE
PENTAERYTHRITYL TETRAACETATE
TETRAHYDROXYMETHYLMETHANE TETRAACETATE
TETRAKIS(HYDROXYMETHYL)METHANEETRAACETATE
TETRAMETHYLOLMETHANE TETRAACETATE
1,3-Propanediol, 2,2-bis[(acetyloxy)methyl]-, diacetate
1,3-Propanediol,2,2-bis[(acetyloxy)methyl]-,diacetate
3-(Acetyloxy)-2,2-bis[(acetyloxy)methyl]propyl acetate
3-propanediol,2,2-bis((acetyloxy)methyl)-diacetate
3-propanediol,2,2-bis[(acetyloxy)methyl]-diacetate
Normo-level
Normosterol
PAG
Pentaerythrityl tetracetate
T. A. P. E.
t.a.p.e.
Tetraacetil pentoetriol | [EINECS(EC#)]
209-907-8 | [Molecular Formula]
C13H20O8 | [MDL Number]
MFCD00026206 | [Molecular Weight]
304.29 | [MOL File]
597-71-7.mol |
| Safety Data | Back Directory | [Hazard Codes ]
F,C | [Risk Statements ]
R11:Highly Flammable.
R34:Causes burns. | [Safety Statements ]
S24/25:Avoid contact with skin and eyes .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S16:Keep away from sources of ignition-No smoking . | [RTECS ]
RZ2600000 | [HS Code ]
29153900 | [Toxicity]
LD50 oral in mouse: 3500mg/kg |
| Hazard Information | Back Directory | [Chemical Properties]
white to off-white powder | [Safety Profile]
Moderately toxic by ingestion.Slightly toxic by intraperitoneal route. When heated todecomposition it emits acrid smoke and irritating vapors | [Purification Methods]
Crystallise pentaerythritol tetraacetate from hot water, then leach it with cold water until the odour of acetic acid is no longer detectable. It also crystallises from 95% EtOH after dissolving in CHCl3, washing with saturated NaHCO3, then H2O, drying over anhydrous CaCl2 and evaporating. It has been prepared by acetolysis of the tetranitrate in 95% yield [Wolfrom et al. J Am Chem Soc 73 874 1951]. [Breusch & Oguzer Chem Ber 88 1511 1955, LeFèvre et.al. J Chem Soc 16 1958, Beilstein 1 IV 1812, 2 IV 264.] |
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