11-HYDROXYUNDECANOIC ACID

Names

[ Name ]:
11-HYDROXYUNDECANOIC ACID

[Synonym ]:
11-Hydroxy-undecansaeure
11-hydroxy-undecanoic acid
Undecanoic acid,11-hydroxy
EINECS 222-932-9
11-Hydroxy-undecylsaeure
11-HYDROXYUNDECANOIC ACID
MFCD00041564

Chemical & Physical Properties

[ Density]:
1g/cm3

[ Boiling Point ]:
345ºC at 760mmHg

[ Melting Point ]:
65-69 °C

[ Molecular Formula ]:
C₁₁H₂₂O₃

[ Molecular Weight ]:
202.29100

[ Flash Point ]:
176.7ºC

[ Exact Mass ]:
202.15700

[ PSA ]:
57.53000

[ LogP ]:
2.57420

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2918199090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

10-Undecynoic acid
11-Bromoundecanoic acid
CIS-11-TETRADECEN-1-OL
(Z)-11-TETRADECEN-1-YL ACETATE
10-Undecenoic acid
oxacyclododecan-2-one
Br-C10-methyl ester
11-Aminoundecanoic acid
Methyl 11-hydroxyundecanoate

DownStream

11-CHLORO-UNDECANOIC ACID
Icosanedioic acid
Decan-1-ol
9-Decen-1-ol
1,20-EICOSANEDIOL
11-Bromoundecanoic acid
trans-11-tetradecenyl acetate
methyl tetradec-11-enoate
e-11-tetradecen-1-ol
oxacyclododecan-2-one

Customs

[ HS Code ]: 2918199090

[ Summary ]:
2918199090 other carboxylic acids with alcohol function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

Articles

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.

J. Am. Chem. Soc. 83(2) , 486-486, (1982)

Preparation of Macrocyclic Lactones by Depolymerization1. Spanagel EW and Carothers WH.

J. Chem. Soc. 58(4) , 654-656, (1936)

11-Hydroxyundecanoic acid,lactone
11-hydroxyundecanoic acid ethyl ester
11-hydroxyundecanoic acid methyl ester
11-bromo-10-hydroxyundecanoic acid
9-Hydroxyundecanoic acid methyl ester
5-Hydroxyundecanoic acid
2-[([1,1a(2)-Biphenyl]-2-yloxy)methyl]piperidine
3-[(3-Isopropylphenoxy)methyl]piperidine
N-(2-((6-phenylpyridazin-3-yl)oxy)ethyl)-2-(thiophen-2-yl)acetamide
3-[(2-Isopropyl-5-methylphenoxy)methyl]piperidine
2-[(2-Naphthyloxy)methyl]piperidine
2-(3,4-dimethoxyphenyl)-N-(2-((6-phenylpyridazin-3-yl)oxy)ethyl)acetamide
N-(2-((6-(4-fluorophenyl)pyridazin-3-yl)oxy)ethyl)-2-nitrobenzamide
2-chloro-N-(2-((6-(4-fluorophenyl)pyridazin-3-yl)oxy)ethyl)benzamide
3-chloro-N-(2-((6-(4-fluorophenyl)pyridazin-3-yl)oxy)ethyl)benzamide
2-bromo-N-(2-((6-(4-fluorophenyl)pyridazin-3-yl)oxy)ethyl)benzamide

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