Aleuritic acid: Difference between revisions

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Revision as of 16:51, 7 July 2015 editDePiep (talk \| contribs)Extended confirmed users294,285 editsm Chembox: rm/replace deprecated params. Fix unknown parameters (via AWB script)← Previous edit		Revision as of 16:31, 1 June 2020 edit undoFswitzer4 (talk \| contribs)Extended confirmed users10,578 editsm Validated CAS and added FDA UNIINext edit →
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	\| StdInChIKey_Ref = {{stdinchicite\|correct\|chemspider}}		\| StdInChIKey_Ref = {{stdinchicite\|correct\|chemspider}}
	\| StdInChIKey = MEHUJCGAYMDLEL-LSDHHAIUSA-N		\| StdInChIKey = MEHUJCGAYMDLEL-LSDHHAIUSA-N
	\| CASNo_Ref = {{cascite\|~~changed~~\|??}}		\| CASNo_Ref = {{cascite\|correct\|CAS}}
	\| CASNo=533-87-9		\| CASNo=533-87-9
			\| UNII_Ref = {{fdacite\|correct\|FDA}}
			\| UNII = 442LQ2K03A
	\| SMILES = O=C(O)CCCCCCC(O)(O)CCCCCCO		\| SMILES = O=C(O)CCCCCCC(O)(O)CCCCCCO
	\| PubChem = 222178		\| PubChem = 222178

Revision as of 16:31, 1 June 2020

Aleuritic acid
Names

IUPAC name (9R,10S)-rel-9,10,16-Trihydroxyhexadecanoic acid
Other names Aleuritolic acid
Identifiers
CAS Number	533-87-9
3D model (JSmol)	Interactive image
ChemSpider	5602481
ECHA InfoCard	100.007.800
PubChem CID	222178
UNII	442LQ2K03A
CompTox Dashboard (EPA)	DTXSID10878090
InChI InChI=1S/C16H32O5/c17-13-9-5-4-7-11-15(19)14(18)10-6-2-1-3-8-12-16(20)21/h14-15,17-19H,1-13H2,(H,20,21)/t14-,15+/m0/s1Key: MEHUJCGAYMDLEL-LSDHHAIUSA-N InChI=1/C16H32O5/c17-13-9-5-4-7-11-15(19)14(18)10-6-2-1-3-8-12-16(20)21/h14-15,17-19H,1-13H2,(H,20,21)/t14-,15+/m0/s1Key: MEHUJCGAYMDLEL-LSDHHAIUBJ
SMILES O=C(O)CCCCCCC(O)(O)CCCCCCO
Properties
Chemical formula	C₁₆H₃₂O₅
Molar mass	304.43 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references

Chemical compound

Aleuritic acid, or α-aleuritic acid, is a major ingredient in shellac, constituting about 35% of it. It is used as a starting material in the perfume industry for the preparation of musk aroma.

References

EPA Registry

v t e Lipids: fatty acids
Saturated	Propionic (C3) Butyric (C4) Valeric (C5) Caproic (C6) Enanthic (C7) Caprylic (C8) Pelargonic (C9) Capric (C10) Undecylic (C11) Lauric (C12) Tridecylic (C13) Myristic (C14) Pentadecylic (C15) Palmitic (C16) Margaric (C17) Stearic (C18) Nonadecylic (C19) Arachidic (C20) Heneicosylic (C21) Behenic (C22) Tricosylic (C23) Lignoceric (C24) Pentacosylic (C25) Cerotic (C26) Carboceric (C27) Montanic (C28) Nonacosylic (C29) Melissic (C30) Hentriacontylic (C31) Lacceroic (C32) Psyllic (C33) Geddic (C34) Ceroplastic (C35) Hexatriacontylic (C36) Heptatriacontanoic (C37) Octatriacontanoic (C38) Nonatriacontanoic (C39) Tetracontanoic (C40)
ω−3 Unsaturated	Octenoic (8:1) Decenoic (10:1) Decadienoic (10:2) Lauroleic (12:1) Laurolinoleic (12:2) Myristovaccenic (14:1) Myristolinoleic (14:2) Myristolinolenic (14:3) Palmitolinolenic (16:3) Palmitidonic (16:4) α-Linolenic (18:3) Stearidonic (18:4) α-Parinaric (18:4) Dihomo-α-linolenic (20:3) Eicosatetraenoic (20:4) Eicosapentaenoic (20:5) Clupanodonic (22:5) Docosahexaenoic (22:6) 9,12,15,18,21-Tetracosapentaenoic (24:5) 6,9,12,15,18,21-Tetracosahexaenoic (24:6)
ω−5 Unsaturated	Myristoleic (14:1) Palmitovaccenic (16:1) α-Eleostearic (18:3) β-Eleostearic (trans-18:3) Punicic (18:3) 7,10,13-Octadecatrienoic (18:3) 9,12,15-Eicosatrienoic (20:3) β-Eicosatetraenoic (20:4)
ω−6 Unsaturated	8-Tetradecenoic (14:1) 12-Octadecenoic (18:1) Linoleic (18:2) Linolelaidic (trans-18:2) γ-Linolenic (18:3) Calendic (18:3) Pinolenic (18:3) Dihomo-linoleic (20:2) Dihomo-γ-linolenic (20:3) Sciadonic (20:3) Arachidonic (20:4) Adrenic (22:4) Osbond (22:5)
ω−7 Unsaturated	Palmitoleic (16:1) Vaccenic (18:1) Rumenic (18:2) Paullinic (20:1) 7,10,13-Eicosatrienoic (20:3)
ω−9 Unsaturated	Oleic (18:1) Elaidic (trans-18:1) Gondoic (20:1) Erucic (22:1) Nervonic (24:1) 8,11-Eicosadienoic (20:2) Mead (20:3)
ω−10 Unsaturated	Sapienic (16:1)
ω−11 Unsaturated	Gadoleic (20:1)
ω−12 Unsaturated	4-Hexadecenoic (16:1) Petroselinic (18:1) 8-Eicosenoic (20:1)

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