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Merck
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Key Documents

524395

Sigma-Aldrich

11-羟基十一烷酸

96%

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About This Item

線性公式:
HO(CH2)10CO2H
CAS號碼:
分子量::
202.29
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

96%

形狀

solid

官能基

carboxylic acid
hydroxyl

SMILES 字串

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 密鑰

KNRCBASNXNXUQQ-UHFFFAOYSA-N

應用

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.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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Enzyme-catalysed condensation polymerization of 11-hydroxyundecanoic acid with lipase from Candida cylindracea.
O'Hagan D and Zaidi NA.
Polymer, 35(14), 3576-3578 (1994)
Bis-3-methyl-2-butylborane as a selective reagent for the reduction of representative functional groups.
Brown HC and Bigley DB.
Journal of the American Chemical Society, 83(2), 486-486 (1982)
Studies on ω-Oxidation of Fatty Acids in vitro.
Kamei S, et al.
Journal of Biochemistry, 56(1), 72- 76 (1964)
Preparation of Macrocyclic Lactones by Depolymerization1.
Spanagel EW and Carothers WH.
Journal of the Chemical Society, 58(4), 654-656 (1936)
Chemo-enzymatic synthesis of 11-hydroxyundecanoic acid and 1, 11-undecanedioic acid from ricinoleic acid.
Jang HY, et al.
Green Chemistry, 18(4), 1089-1095 (2016)

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