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Assay
96%
form
solid
SMILES string
OCCCCCCCCCCC(O)=O
InChI
1S/C11H22O3/c12-10-8-6-4-2-1-3-5-7-9-11(13)14/h12H,1-10H2,(H,13,14)
InChI key
KNRCBASNXNXUQQ-UHFFFAOYSA-N
Related Categories
Application
11-Hydroxyundecanoic acid can be prepared by employing the following starting reagents:
- 10-undecenoic acid
- undecylenic acid and hydrobromic acid
- methyl 11-bromoundecanoate
- ricinoleic acid (12-hydroxyoleic acid)
11-Hydroxyundecanoic acid may be employed for the preparation of higher molecular weight polyesters.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Preparation of Macrocyclic Lactones by Depolymerization1.
Journal of the Chemical Society, 58(4), 654-656 (1936)
Studies on ω-Oxidation of Fatty Acids in vitro.
Journal of Biochemistry, 56(1), 72- 76 (1964)
Chemo-enzymatic synthesis of 11-hydroxyundecanoic acid and 1, 11-undecanedioic acid from ricinoleic acid.
Green Chemistry, 18(4), 1089-1095 (2016)
Bis-3-methyl-2-butylborane as a selective reagent for the reduction of representative functional groups.
Journal of the American Chemical Society, 83(2), 486-486 (1982)
Enzyme-catalysed condensation polymerization of 11-hydroxyundecanoic acid with lipase from Candida cylindracea.
Polymer, 35(14), 3576-3578 (1994)
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