Name | Laurocapram |
Synonyms | n0252 Azone tranzone Lauocapram Laurocapram acecloguanosine Azone, Laurocapram n-lauryl caprolactam 1-dodecylazepan-2-one 1-tridecylpiperidin-2-one DODECYLAZACYCLOHEPTAN-2-ONE 1-dodecylazacycloheptan-2-one 1-n-Dodecylazacycloneptan-2-one hexahydro-n-lauryl-2h-azepin-2-on 1-dodecylhexahydro-2h-azepin-2-one 1-Dodecylhexahydro-1H-azepine-2-one N-Dodecyl Nitrogen Heterocyclic Heptane-2-Ketone |
CAS | 59227-89-3 |
EINECS | 261-668-9 |
InChI | InChI=1/C18H35NO/c1-2-3-4-5-6-7-8-9-10-11-13-16-19-17-14-12-15-18(19)20/h2-17H2,1H3 |
Molecular Formula | C18H35NO |
Molar Mass | 281.48 |
Density | 0.906-0.926 |
Melting Point | -7° |
Boling Point | bp50m 160° |
Flash Point | 164.62°C |
Solubility | Insoluble in water, forms an emulsion with water, and is easily soluble in various organic solvents. |
Vapor Presure | 0mmHg at 25°C |
Appearance | Colorless or yellowish transparent liquid |
Color | Colourless |
Merck | 14,5385 |
pKa | -0.43±0.20(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.470-1.473 |
MDL | MFCD00190580 |
Physical and Chemical Properties | colorless to yellowish liquid, odorless and tasteless |
Use | Used as osmotic agent, used for all kinds of cream and hair supplies in cosmetics; Used as a penetration enhancer for topical application and massage; Used for pesticides, as a plant growth regulator and a penetration enhancer for sterilization and insecticide; In addition, it can also be used as a coloring accelerator in the fields of leather and printing and dyeing. |
Safety Description | 24/25 - Avoid contact with skin and eyes. |
RTECS | CM3995000 |
HS Code | 29339900 |
Toxicity | LD50 rats, mice (g/kg): 8 i.v., i.p. (Stoughton) |
Raw Materials | epsilon-Caprolactam |
Reference Show more | 1. Liang Jun, Wu Huichao, du Shouying, et al. Study on percutaneous permeability of main components of baimai ointment in vitro [J]. Chinese Journal of Traditional Chinese Materia Medica, 2019, 26 (12). |
This product is 1-dodecyl-hexahydro-2h-nitrogen weed -2-one. Ci8H3SNO shall be 97.0%-102.0%.
The relative density of this product (General 0601) is 0. 906~926.
The refractive index of this product (General 0622) is 1. 470~473.
The kinematic viscosity of this product (General rule 0633 first method% capillary inner diameter 1-2mm ± 0. 05mm), 32~34 mm2/ s at 25°C.
take 5 m l of this product, add 5ml neutral ethanol, warm to dissolve, let cool, the solution should be neutral reaction when it meets litmus test paper.
caprolactam and related substances
take about 0.5g of this product, put it in a 10ml measuring flask, add an appropriate amount of methanol, shake to dissolve and dilute to the scale, shake well, as a test solution. In addition, an appropriate amount of caprolactam was accurately weighed, dissolved and diluted with methanol to prepare a solution containing 0.05mg per 1m l as a reference solution. According to the test for determination of residual solvents (General 0861 second method), a capillary column with 100% dimethylpolysiloxane (or similar polarity) as stationary liquid, starting at 1 0 0 1, maintained for 1 min at 15X per minute: the temperature was raised to 2 4 0 1, and the retention time of the main peak was 2 times; The detector temperature was 3 0 0 "C; The sample inlet temperature was 2 5 0 1. Take the reference solution 1m injection human gas chromatograph, adjust the detection sensitivity, so that the peak height of the main component chromatographic peak is about 25% of the full scale, the sample solution and the reference solution are respectively injected into the human gas chromatograph to record the chromatogram. If there are impurity peaks in the chromatogram of the sample solution, the Peak area of the impurity peak consistent with the retention time of caprolactam should not be greater than the main peak area of the control solution (0. 1% ), other impurity peaks are calculated by area normalization method, and a single impurity shall not exceed 1 .5%, total impurities should not be over 3 .0%.
take this product l .O g, add 1 0 m l of water, fully shake, add 3 drops of hydrochloric acid and three gas methane lm l, add 2% gas amine T solution Dropwise while shaking (new preparation is needed) 3 drops, three gas methane layer such as color, with the standard potassium bromide solution (precision weighing at 1051C dry to constant weight of potassium bromide 0. 1489G, add water to dissolve into 1 0 M l, shake well) 1.0, compared with the control solution made by the same method, not deeper (0. 1%).
take 0841g of this product and check it according to law (general rule). The remaining residue shall not exceed.
The residue left under the item of taking the ignition residue shall not contain more than 10 parts per million of heavy metal when examined by law (General Principles 0821, Law II).
measured by gas chromatography (General 0521).
use 100% dimethyl polysiloxane (or polar similar) as the stationary liquid capillary column, the initial temperature is 100X:, maintain 1 min, 1 5 1 per minute to 2 4 0 1, maintain 45 minutes; The detector temperature is 300t;; The sample inlet temperature is 25 0 t. The number of theoretical plates shall be calculated according to the peak of azone, and shall not be less than 10 000. The degree of separation between the peak of azone and the peak of internal standard substance shall meet the requirements.
an appropriate amount of eicosane was taken, dissolved with n-hexane and diluted to a solution containing 2mg per 1 μl as an internal standard solution. Take another 20 m g of the reference compound of laurocapram ketone, weigh it accurately, put it in a 10ml measuring flask, dissolve it with internal standard solution, dilute it to the standard, and shake it well, l f I l was injected into the gas chromatograph and the correction factor was calculated.
take about 20 m g of this product, accurately weigh it, put it in a 10ml measuring flask, dissolve it with internal standard solution and dilute it to the scale, shake it well, and inject 1 /il into the gas chromatograph. Determination, calculated according to the internal standard method, that is.
pharmaceutical excipients, penetration enhancers.
light shielding, sealed storage.
EPA chemical substance information | information provided by: ofmpeb.epa.gov (external link) |
Introduction | laurocapram is a new skin penetrant first reported by Stoughton, its chemical name is 1-n-dodecylazacycloheptan-2-one. Short for azone. At room temperature, azone is a colorless, tasteless, non-toxic and non-irritating oily transparent liquid with lubricity, easy coating and strong permeability. It is also a widely used organic chemicals, as well as its efficient penetration, non-toxic safety and other characteristics have attracted more and more attention, hydrophobic compounds all have the effect of enhancing penetration. |
Application | It is mainly used in the fields of medicine, pesticide, cosmetics, printing and dyeing, leather making, petroleum and chemical fiber, china has done a lot of fruitful work on its production and application, and its application areas are gradually expanding. The consumption of azone now is increasing at a rate of 50%, the industrialization of azone has broad prospects. as an efficient skin penetration enhancer and a new type of non-ionic surfactant, laurocapram has been widely used in the pharmaceutical, chemical, pesticide, printing and dyeing, chemical fiber, leather and other industries, the use of the effect is very significant, more new applications are still expanding. |
preparation | solid-liquid phase transfer catalysis method: This method uses KOH-K2CO3 double alkali instead of potassium hydroxide or sodium hydroxide as the proton removal agent, tetrabutyl sodium bromide or polyethylene glycol is the phase transfer catalyst. Caprolactam and bromododecane were reacted in toluene or ethane solvent to form azone in one step, and the yield was over 93%. The reaction conditions are mild, without N 2 protection, easy to operate, but to be carried out in a non-aqueous solvent, is currently widely used in the domestic production of azone production process. |
penetration enhancers | , azone, chemical name for 1-N-dodecyl Nitrogen heterocycle heptan-2-one, is a new type of efficient and safe penetration enhancers, colorless and odorless transparent liquid at room temperature, slightly viscous, odorless. It forms an emulsion with water, is soluble in various organic solvents, has good lubricity, and can promote the activity of hydrophilic and lipophilic pharmaceutical products or the penetration of nutrients in cosmetics into the skin, greatly shorten the retention time of drugs in the stratum corneum, significantly enhance the efficacy of drugs and the use of cosmetics, so it can reduce the amount of main drugs, reduce costs. The transdermal absorption of azone was delayed.|
safe | it is proved to be non-toxic and non-irritating by sub-acute toxicity, skin and damaged skin irritation, sensitization, teratogenicity and other experiments, no side effects, no irritation to the domestic eye experiment. |
Use | is used as an osmotic agent for various creams and hair supplies in cosmetics, as a penetration enhancer for topical application and massage; it can be used as a pesticide, as a plant growth regulator and a penetration enhancer for sterilization and pesticides. In addition, it can also be used as a coloring promoter in the field of leather and printing and dyeing. colorless to yellowish clear oily liquid azone is a new type of efficient, safe and non-toxic transdermal absorption enhancer, which has obvious transdermal penetration effect on hydrophilic and lipophilic drugs. Can be widely used in medicine, cosmetics, pesticides, aerosol, printing and dyeing and oil exploration and other industries, this product has strong penetration, colorless, tasteless, non-toxic, non-irritating and other advantages. used as a highly effective skin penetration enhancer, for external use, cosmetics and as a surfactant |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |