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2452-01-9

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2452-01-9 Usage

Chemical Properties

White powder. Almost insoluble in water and alcohol. Combustible.

Uses

Paints, varnishes, rubber compounding (softener and activator).

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 2452-01-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,5 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2452-01:
(6*2)+(5*4)+(4*5)+(3*2)+(2*0)+(1*1)=59
59 % 10 = 9
So 2452-01-9 is a valid CAS Registry Number.
InChI:InChI=1/2C12H24O2.Zn/c2*1-2-3-4-5-6-7-8-9-10-11-12(13)14;/h2*2-11H2,1H3,(H,13,14);/q;;+2/p-2

2452-01-9Synthetic route

lauric acid
143-07-7

lauric acid

zinc(II) oxide

zinc(II) oxide

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
In ethanol prepn. by refluxing ZnO with excess of carboxylic acid in EtOH for about2 h; cooled; ppt. filtered off; washed (EtOH) repeatedly; collected; kept over silica gel in vac. desiccator; elem. anal.;85%
With dihydrogen peroxide In water at 135℃; for 1.5h;
lauric acid
143-07-7

lauric acid

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
With H2O2; electrogalvanized steel In water Kinetics; carboxylation in bath of water/3-methoxy-3-methyl-1-butanol (50:50 v/v) at 45 °C in presence of H2O2; detd. by XRD;
With zinc diacetate In ethanol
zinc(II) nitrate
10196-18-6

zinc(II) nitrate

Sodium laurate
629-25-4

Sodium laurate

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
In ethanol; water water-alcoholic solns. of Zn(NO3)2 and Na laurate combined; according toA. A. Sanchez, M. V. Garcia, M. I. Redondo, J. A. R. Cheda, Liq. Cryst. , 1995, 18, 431 and I. Konkoly-Thege, I. Ruff, S. O. Adeosun, S. J. Sime, Thermochim. Acta, 1978, 24, 1, 89; recrystd. from hot toluene; vac. dried at 80°C for 48 h;
Sodium laurate
629-25-4

Sodium laurate

zinc(II) chloride
7646-85-7

zinc(II) chloride

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
In ethanol; water stoich. amt. of aq. soln. of ZnCl2 added to alcoholic soln. of org. compd.; ppt. filtered and washed with EtOH and water, characterized by powder XRD patterns;
lauric acid
143-07-7

lauric acid

zinc(II) hydroxide

zinc(II) hydroxide

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
In octane byproducts: H2O; Zn(OH)2 refluxed with 50% excess of C12H23OOH in octane; cooled slow, filtered off, washed with octane, elem. anal.;
lauric acid
143-07-7

lauric acid

zinc(II) chloride
7646-85-7

zinc(II) chloride

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
With sodium hydroxide at 40℃;
zinc diacrylate

zinc diacrylate

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

zinc(II) oxide

zinc(II) oxide

4Zn(2+)*O(2-)*5.5C3H3O2(1-)*0.5C12H23O2(1-)

4Zn(2+)*O(2-)*5.5C3H3O2(1-)*0.5C12H23O2(1-)

Conditions
ConditionsYield
In chloroform at 64℃; for 3h; Inert atmosphere;98%
zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

4Zn(2+)*O(2-)*6C12H23O2(1-) = Zn4O(C12H23O2)6

4Zn(2+)*O(2-)*6C12H23O2(1-) = Zn4O(C12H23O2)6

Conditions
ConditionsYield
With water In octane byproducts: (C12H23COOH)2; H2O added to a hot soln. of Zn-compd.; detected by IR;
zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

Conditions
ConditionsYield
With CH3(CH2)13N(CH3)2O or CH3(CH2)15N(CH3)2O In water Electrolysis; electrochem. deposition Zn nanoparticles on In-doped tin oxide at 70 °C;
diethylzinc
557-20-0

diethylzinc

zinc(II) dodecanoate
2452-01-9

zinc(II) dodecanoate

[Zn5(dodecanoato)6(Et)4]
1191422-23-7

[Zn5(dodecanoato)6(Et)4]

Conditions
ConditionsYield
In benzene-d6 (N2); a soln. of Zn(C2H5)2 dild. with benzene-d6, added to Zn salt, equilibrated for 16 h, warmed gently; not isolated, detected by NMR;

2452-01-9Downstream Products

2452-01-9Relevant articles and documents

Environment-friendly metal carboxylate and preparation method thereof

-

Paragraph 0047-0048, (2017/01/23)

The invention discloses an environment-friendly metal carboxylate and a preparation method thereof. The metal carboxylate has the following structure: CH3(CH2)nCOO-M-OOC(CH2)nCH3, wherein M is Zn and Mg, and n is equal to 10 to 16. Straight-chain saturated monocarboxylic acid and oxide powder or hydroxide powder of zinc and magnesium are subjected to salt-forming reaction under the action of catalyst, the metal carboxylate is a meltable solid, and after grinding, a powdery environment-friendly metal carboxylate product can be prepared. The preparation process is simple, operability is high, energy is saved, the product purity is high, and the environment-friendly metal carboxylate is environment-friendly, and meets the requirement of ROHS directive, EU (European Union) REACH regulation and EN71-3 standard.

Compact metal-organic frameworks for anti-corrosion applications: New binary linear saturated carboxylates of zinc

Mesbah, Adel,Jacques, Sophie,Rocca, Emmanuel,Francois, Michel,Steinmetz, Jean

, p. 1315 - 1321 (2011/06/10)

Zinc-based metal-organic frameworks (MOFs), binary zinc carboxylates ZnCnCn′ with Cn and Cn′ = CH3(CH2)n - 2COO-, have been synthesised and characterised for anti-corrosion applications. The crystallographic structures of ZnC10C14 and ZnC 10C16 were determied from synchrotron powder diffraction data and refined by the Rietveld method. Protective coatings on electrogalvanised steel composed of ZnC12C16 have been developed by formulating a particular "carboxylating" bath. The ZnC12C16 coating exhibits better anti-corrosion behaviour than the pure Zn(C16)2 and Zn(C12)2 coatings, according to electrochemical and non-electrochemical measurements. The crystallographic results and corrosion measurements demonstrate the great flexibility of the zinc carboxylate lamellar structures in modifying the insolubility and hydrophobicity of the protective coatings. In addition, the conditions for the ZnC12C16 coating process fulfil the specifications for the surface treatment of zinc. Finally, these new compounds, which can be easily synthesised in water, provide a new and environmentally friendly anti-corrosion treatment for metals. New zinc-based metal-organic frameworks (MOFs), binary zinc carboxylates ZnCnCn′ with Cn and Cn′ = CH3(CH2)n - 2COO-, have been synthesised and characterised for anti-corrosion applications on zinc. The crystallographic structures demonstrate the great flexibility of these MOFs in modifying the insolubility and hydrophobicity of the protective coatings on metals in an aqueous solvent process. Copyright

Melting of saturated fatty acid zinc soaps

Barman,Vasudevan

, p. 22407 - 22414 (2008/10/09)

The melting of alkyl chains in the saturated fatty acid zinc soaps of different chain lengths, Zn(CnH2n-1COO)2; n = 11, 13, 15, and 17, have been investigated by powder X-ray diffraction, differential scanning calorimetry, and vibrational spectroscopy. These compounds have a layer structure with the alkyl chains arranged as tilted bilayers and with all methylene chains adopting a planar, all-trans conformation at room temperature. The saturated fatty acid zinc soaps exhibit a single reversible melting transition with the associated enthalpy change varying linearly with alkyl chain length, but surprisingly, the melting temperature remaining constant. Melting is associated with changes in the conformation of the alkyl chains and in the nature of coordination of the fatty acid to zinc. By monitoring features in the infrared spectra that are characteristic of the global conformation of the alkyl chains, a quantitative relation between conformational disorder and melting is established. It is found that, irrespective of the alkyl chain length, melting occurs when 30% of the chains in the soap are disordered. These results highlight the universal nature of the melting of saturated fatty acid zinc soaps and provide a simple explanation for the observed phenomena.

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