Conditions | Yield |
---|---|
With sodium hydroxide In water at 60 - 80℃; | 91% |
With sodium hydrogencarbonate In ethanol at 77℃; | 54.4% |
With sodium hydroxide In ethanol for 12h; Heating; | |
With sodium hydrogencarbonate In ethanol; water Inert atmosphere; Reflux; Large scale reaction; | |
With sodium hydroxide In methanol at 60℃; for 0.00277778h; Time; Industrial scale; |
Conditions | Yield |
---|---|
With buffer (0.05 M H2PO4-/HPO42-); sodium chloride In 1,4-dioxane; methanol at 30℃; Rate constant; pH 8; | |
With steareth-10; sodium hydroxide In water at 25℃; Kinetics; Reagent/catalyst; |
Conditions | Yield |
---|---|
With sodium hydroxide; water In butan-1-ol at 59.84℃; Kinetics; Solvent; |
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: dichloromethane / 20 °C / Inert atmosphere 2: water; sodium hydroxide / dimethylsulfoxide-d6; n-heptyloxybenzaldehyde / 20 °C View Scheme |
N,N,N-trimethyl-2-(dodecanoyloxy)ethaneammonium bromide
Sodium laurate
Conditions | Yield |
---|---|
With water; sodium hydroxide In dimethylsulfoxide-d6; n-heptyloxybenzaldehyde at 20℃; |
Conditions | Yield |
---|---|
With hexanediyl-α,ω-bis-(N-(2-hydroxyethyl)-N-methylhexadecylammonium bromide); sodium hydroxide In water at 25℃; pH=9.2; Kinetics; Concentration; Reagent/catalyst; Micellar solution; |
Sodium laurate
Conditions | Yield |
---|---|
With cobalt(II) chloride hexahydrate In water at 65℃; for 0.833333h; Temperature; | 99.6% |
Conditions | Yield |
---|---|
In water at 70℃; for 1h; | 99.5% |
Nα-lauroyl-L-arginine ethyl ester monohydrochloride
Sodium laurate
Nα-lauroyl-L-arginine ethyl ester laurate
Conditions | Yield |
---|---|
In water at 80 - 85℃; for 0.5h; | 96.5% |
Conditions | Yield |
---|---|
In methanol at 20℃; | 96% |
Conditions | Yield |
---|---|
With 1-butyl-3-ethylimidazolinium methanesulfonate at 90℃; for 0.5h; | 95% |
With lauric acid at 170 - 180℃; |
Conditions | Yield |
---|---|
In methanol at 20℃; | 95% |
Sodium laurate
sodium butyrate
n-butylamine hydrochloride
A
N-butyl-butyramide
B
N-butyldodecanamide
Conditions | Yield |
---|---|
octyl 2-(N-(4,6-dimethoxy-1,3,5-triazin-2-yl)-N,N-dimethylammonio)acetate trifluoromethanesulfonate In water at 25℃; for 1h; pH=8; Product distribution / selectivity; Aqueous phosphate buffer; | A 0.4% B 87.3% |
Conditions | Yield |
---|---|
In ethanol; water soln. of org. salt (in 1:1 EtOH:H2O) added dropwise to soln. of rare earth compd. dissolved in same mixed solvent with stirring at ambient temp., mixt. stirred for 1 h at same temp.; ppt. filtered, washed with water, EtOH then acetone, dried for 24 h at 50°C in vac., recrystd. from 1-pentanol/EtOH (5:1), filtered, washed with EtOH, dried in vac. at 50°C for 24 h; elem. anal.; | 87% |
Sodium laurate
{Pd(H21C10OC6H3CH=NN=CHC6H4OC10H21)(μ-O2CC11H23)}2
Conditions | Yield |
---|---|
In acetone byproducts: NaCl; excess carboxylate, refluxing (14 h); evapn., extn. (CH2Cl2), filtration of NaCl, partial evapn., EtOH addn. (crystn.); mixt. of isomers not sepd.; | 75% |
Sodium laurate
{Pd(H21C10OC6H3CH=NN=CHC6H4OC10H21)(μ-O2CC11H23)}2
Conditions | Yield |
---|---|
In acetone byproducts: AgCl, NaClO4; stirring of Pd-complex and AgClO4 (molar ratio Pd:Ag = 1:1, 10 h, protection from light), filtration of AgCl, addn. of Na-carboxylate (molar ratio Pd:carboxylate = 1:2), stirring (24 h, pptn.); evapn., extn. (CH2Cl2), filtration of NaClO4, partial evapn., EtOH addn. (crystn.); mixt. of isomers not sepd.; elem. anal.; | 75% |
Conditions | Yield |
---|---|
With 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride In methanol at 20℃; for 5h; | 65% |
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine; phosphatidylcholine; N,N-dimethylglycine hexadecyl ester; Rh-PE fluorescent dye In methanol; phosphate buffer; chloroform at 20℃; for 24h; membrane fusion; |
Conditions | Yield |
---|---|
With copper(I) triflate In 1,4-dioxane; methanol at 60℃; for 50h; Schlenk technique; Inert atmosphere; | 65% |
Sodium laurate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 20℃; for 16h; | 51% |
Sodium laurate
L-ascorbic acid-2-phosphate-6-laurate
Conditions | Yield |
---|---|
50% |
Sodium laurate
Conditions | Yield |
---|---|
Stage #1: Sodium laurate In ethanol; water at 0.5℃; for 0.416667h; Sonication; Stage #2: C21H35Cl2MnN5 In ethanol; water for 2h; | 44% |
Sodium laurate
Conditions | Yield |
---|---|
In ethanol; water for 2h; | 44% |
Conditions | Yield |
---|---|
octyl 2-(N-(4,6-dimethoxy-1,3,5-triazin-2-yl)-N,N-dimethylammonio)acetate trifluoromethanesulfonate In water; acetone at 25℃; for 0.25 - 24h; Conversion of starting material; | 39% |
Sodium laurate
1-chloromethylbenzindol-2(1H)-one (CMBI)
BIM laurate
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 100℃; for 0.333333h; | 30% |
Conditions | Yield |
---|---|
at 100℃; |
Conditions | Yield |
---|---|
at 135℃; |
Conditions | Yield |
---|---|
With water |
Conditions | Yield |
---|---|
With benzene |
5-(chloromethyl)-6-propyl-1,3-benzodioxole
Sodium laurate
5-lauroyloximethyl-6-propyl-benzo[1,3]dioxole
Conditions | Yield |
---|---|
With lauric acid at 160℃; |
6-chloromethyl-1,2,3,4-tetrahydronaphthalene
Sodium laurate
Conditions | Yield |
---|---|
With methyl n-dodecanoate |
Conditions | Yield |
---|---|
With formaldehyd; water at 275℃; | |
With formaldehyd; water at 275℃; in Gegenwart eines Oxydationskatalysators; |
Sodium laurate
Conditions | Yield |
---|---|
With aluminium trichloride; water Extraktion des Niederschlags mit wasserfreiem Aceton; |
Conditions | Yield |
---|---|
at 135℃; |
Conditions | Yield |
---|---|
at 130℃; |
The Sodium laurate, with the CAS registry number 629-25-4, is also known as Dodecanoic acid, sodium salt. Its EINECS registry number is 211-082-4. This chemical's molecular formula is C12H24O2•Na and molecular weight is 223.35. This chemical's classification codes are Mutation data; Skin / Eye Irritant.
Uses of Sodium laurate: it can be used to produce BIM laurate with 1-chloromethyl-1H-benzo[cd]indol-2-one at temperature of 100°C. This reaction will need solvent dimethylformamide with reaction time of 20 min. The yield is about 30%.
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LDLo | unreported | 400mg/kg (400mg/kg) | Food and Cosmetics Toxicology. Vol. 14, Pg. 431, 1976. |
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