Weight | 280.452 g/mol |
---|---|
Formula | C18H32O2 |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 14 |
linoleic acid
Linoleate · Linolelaidic Acid · Linoleic Acid, Sodium Salt, (Z,Z)-Isomer
8024-22-4, 60-33-3, 80969-37-5, 2197-37-7
Score:
#107 in Biochemistry
,
#461 in Biology
,
#483 in Chemistry
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- Sigma-Aldrich - linoleic acid21.50 - 683.00 USD
- Fisher Scientific - Search for linoleic acid
- TCI - linoleic acid38.00 - 569.00 USD
- Dietary sources of conjugated dienoic isomers of linoleic acid, a newly recognized class of anticarcinogens (Journal of Food Composition and Analysis, 1992)
- Effect of conjugated linoleic acid on body composition in mice. (Lipids, 1997)
- Conjugated linoleic acid and atherosclerosis in rabbits (Atherosclerosis, 1994)
- The biologically active isomers of conjugated linoleic acid. (Progress in Lipid Research, 2001)
- Conjugated Linoleic Acid Is Synthesized Endogenously in Lactating Dairy Cows by 9-Desaturase (Journal of Nutrition, 2000)
- Anticarcinogens from fried ground beef: heat-altered derivatives of linoleic acid (Carcinogenesis, 1987)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Linoleate
- Linolelaidic Acid
- Linoleic Acid, Sodium Salt, (Z,Z)-Isomer
- Linoelaidic Acid
- 9 trans,12 trans Octadecadienoic Acid
- Linoleic Acid, (Z,Z)-Isomer
- cis,cis-9,12-Octadecadienoic Acid
- Linoleic Acid, (E,E)-Isomer
- trans,trans-9,12-Octadecadienoic Acid
- Linoleic Acid, Ammonium Salt, (Z,Z)-Isomer
- 9-trans,12-trans-Octadecadienoic Acid
- Linoelaidic Acid, (E,Z)-Isomer
- 9,12-Octadecadienoic Acid
- Linoleic Acid, Calcium Salt, (Z,Z)-Isomer
- Linoleic Acid, Potassium Salt, (Z,Z)-Isomer
- Linoleic Acid, Sodium Salt, (E,E)-Isomer
- Linoleic Acid, (Z,E)-Isomer
- Linoleic Acid, (Z,Z)-Isomer, 14C-Labeled
- 9,12 Octadecadienoic Acid
-
SMILESCCCCCC=CCC=CCCCCCCCC(=O)O
-
InChIKeyOYHQOLUKZRVURQ-UHFFFAOYSA-N
- Pubchem - linoleic acid
- Wikipedia - linolelaidic acid
Linolelaidic acid is an omega-6 trans fatty acid (TFA) and is a geometric isomer of linoleic acid. It is found in partially hydrogenated vegetable oils. It also comprises 12.39% of the fats from the fruit of the durian species Durio graveolens.
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Synthesis
Hexanal
+
Reactant
(Wittig)
Reactant
+
1-CHLOROPENTANE
(Heck terminal vinyl)
Similar Compounds
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UNDECANEDIOIC ACID
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PENTADECANOIC ACID
(1002-84-2)
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(7617-31-4, 660-60-6)
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(4617-33-8)
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(1679-53-4)
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(593-47-5, 143-28-2)
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(124-04-9, 25666-61-9)
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6-Hydroxyhexanoic acid
(1191-25-9)
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(6085-36-5, 24909-72-6)
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(35194-38-8)
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(26403-17-8, 5963-14-4)
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(25103-52-0, 929-10-2)
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(14112-98-2)
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(3128-07-2)
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cis-6-Nonenal
(2277-19-2)
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8-Aminooctanoic acid
(1002-57-9)
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(929-17-9)
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12-Aminododecanoic acid
(693-57-2)
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(17696-11-6)
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(13099-35-9)
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16-Bromohexadecanoic acid
(2536-35-8)
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11-BROMOUNDECANOIC ACID
(2834-05-1)
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15-Bromopentadecanoic acid
(56523-59-2)
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9-Bromononanoic acid
(41059-02-3)
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(30515-28-7)
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10-Bromodecanoic acid
(50530-12-6)
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(25118-23-4)
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5-METHYLHEXANOIC ACID
(1330-19-4, 628-46-6)
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6-Methoxyhexanoic acid
(41639-61-6)
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7-Oxononanoic acid
(20356-92-7)
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6-oxoundecanoic Acid
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