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9,12-OCTADECADIYNOIC ACID

CAS No.
2012-14-8
Chemical Name:
9,12-OCTADECADIYNOIC ACID
Synonyms
RO 3-1314;9,12-ODYA;ODYA, Ro 3-1314;9,12-OCTADECADIYNOIC ACID;9a-12a-octadecadiynoic acid;KDYILQLPKVZDGB-UHFFFAOYSA-N;9,12-Octadecadiynoic acid >=98%
CBNumber:
CB7311228
Molecular Formula:
C18H28O2
Molecular Weight:
276.41
MDL Number:
MFCD00797685
MOL File:
2012-14-8.mol
MSDS File:
SDS
Last updated:2023-05-18 11:31:03

9,12-OCTADECADIYNOIC ACID Properties

Melting point 42-43 °C(Solv: ligroine (8032-32-4))
Boiling point 143-154 °C(Press: 0.005-0.01 Torr)
Density 0.963±0.06 g/cm3(Predicted)
storage temp. -20°C
solubility ≤10mg/ml in ethanol;10mg/ml in DMSO;10mg/ml in methanol;10mg/ml in acetone;10mg/ml in acetonitrile
form crystalline solid
pka 4.77±0.10(Predicted)

SAFETY

Risk and Safety Statements

WGK Germany  3

9,12-OCTADECADIYNOIC ACID price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich O5636 9,12-Octadecadiynoic acid ≥98% 2012-14-8 1mg $216 2024-03-01 Buy
Cayman Chemical 90400 9,12-Octadecadiynoic Acid ≥98% 2012-14-8 1mg $76 2024-03-01 Buy
Cayman Chemical 90400 9,12-Octadecadiynoic Acid ≥98% 2012-14-8 5mg $335 2024-03-01 Buy
Cayman Chemical 90400 9,12-Octadecadiynoic Acid ≥98% 2012-14-8 10mg $593 2024-03-01 Buy
American Custom Chemicals Corporation CHM0115121 9,12-OCTADECADIYNOIC ACID 95.00% 2012-14-8 1MG $618.5 2021-12-16 Buy
Product number Packaging Price Buy
O5636 1mg $216 Buy
90400 1mg $76 Buy
90400 5mg $335 Buy
90400 10mg $593 Buy
CHM0115121 1MG $618.5 Buy

9,12-OCTADECADIYNOIC ACID Chemical Properties,Uses,Production

Definition

ChEBI: Octadeca-9,12-diynoic acid is an octadecadiynoic acid having its triple bonds at positions 9 and 12.

Biological Activity

ki: 0.6 μm for ram seminal vesicle cox9,12-octadecadiynoic acid is a cox and lipoxygenase inhibitor.cyclooxygenase (cox) is an enzyme responsible for the formation of prostanoids, such as thromboxane and prostaglandins. pharmaceutical inhibition of cox can lead to relief from the symptoms of inflammation and pain. nonsteroidal anti-inflammatory drugs, including aspirin and ibuprofen, display their effects via inhibition of cox.

Biochem/physiol Actions

Potent cyclooxygenase and lipoxygenase inhibitor.

in vitro

9,12-octadecadiynoic acid was identified as an inhibitor of both cox and lipoxygenase, which could inhibit ram seminal vesicle cox. 9,12-octadecadiynoic acid was found to be a more effective inhibitor of cox-1 than of 15-lo when used at a concentration of 48 μm [1,2]. in another study, fatty acids from natural sources including 9,12-octadecadiynoic acid were isolated and assayed for their effect on the bioconversion of arachidonic acid into prostaglandin e2. two very active cyclooxygenase inhibitors were discovered, namely jacarandic acid and the synthetic 8z, 10e, 12e-octadecatrienoic acid. earlier described potent inhibitors showed the following ic50 values: 1.3 μm for indomethacin; 1.3 μm for 9,12-octadecadiynoic acid, 2.7 μm for 8z, 12e, 14z-eicosatrienoic acid; 4.4 μm for 5,8,11,14-eicosatetraynoic acid [3].

References

[1] vanderhoek, j. y. and lands, w.e.m. acetylenic inhibitors of sheep vesicular gland oxygenase. biochimica et biophysica acta 296, 374-381 (1973).
[2] downing, d. t.,barve, j.a.,gunstone, f.d., et al. structural requirements of acetylenic fatty acids for inhibition of soybean lipoxygenase and prostaglandin synthase. biochimica et biophysica acta 280, 343-347 (1972).
[3] nugteren dh, christ-hazelhof e. naturally occurring conjugated octadecatrienoic acids are strong inhibitors of prostaglandin biosynthesis. prostaglandins. 1987 mar;33(3):403-17.

9,12-OCTADECADIYNOIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

9,12-OCTADECADIYNOIC ACID Suppliers

Global( 27)Suppliers
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RO 3-1314 9,12-OCTADECADIYNOIC ACID 9,12-ODYA 9a-12a-octadecadiynoic acid ODYA, Ro 3-1314 KDYILQLPKVZDGB-UHFFFAOYSA-N 9,12-Octadecadiynoic acid >=98% 2012-14-8 BioChemical Biochemicals and Reagents A to C Cyclooxygenase Enzymes, Inhibitors, and Substrates Enzyme Inhibitors Enzyme Inhibitors by Enzyme