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59227-89-3

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59227-89-3 Usage

Chemical properties

Colorless or slightly yellow transparent liquid, insoluble in water, it can form emulsion with water, soluble in various organic solvents.

Penetration enhancer

Laurocapram, also known as azone, lauric Lun, N-lauryl caprolactam, quinacridone, nitrogen ketone. Its chemical name is 1-n-dodecyl azetidin-2-one, which is a new high security penetration enhancer. It is colorless transparent liquid at room temperature, slightly viscous, odorless. It can form emulsion with water, soluble in various organic solvents, and it has good lubricity, which promote the hydrophilic and lipophilic drug product activity or cosmetics nutrients to penetrate into the skin, greatly reducing the drug remain time in the stratum corneum, significantly enhancing drug efficacy and cosmetic results. Thus, we can reduce the amount of primary medical and reduce costs. Azone transdermal absorption enhancing effect lags behind. Laurocapram on hydrophilic and lipophilic drugs have significantly transdermal Aided role.? It has good aided effect on many kinds of plant extracts in emulsion state or colloidal state, and alkaloids effect is particularly evident. Transdermal penetration is stronger than dimethyl sulfoxide. 8-bromo cyclic nucleotide containing 1% azone permeability effect is equivalent to 12 times the 50% dimethyl sulfoxide. Often in combination with propylene glycol, synergy, the best use of transdermal concentration of 0.1% to 5%, safe and low toxic, non-irritating. The chemical property is stable, and it is kept up to four years at the room temperature. It can be considered a decyl methyl sulfoxide with pyrrolidone composite for good novel penetration enhancers, skin irritation. It can promote the drug through the skin barrier corticosteroids, indomethacin, fluorouracil, hydroquinone and many other drugs transdermal absorption, improving local and systemic blood concentration, and improving the bioavailability of the drug. Lipophilic, they have transdermal effect for hydrophilic drugs. It can soften the skin and enhance its permeability. They have anti-inflammatory, analgesic and anti-itching effect. Low toxicity, oral LD50> 7g/kg, it is not compatible with strong acids or Vaseline to avoid reduce the effect.

Application

Laurocapram is used as the penetration enhancer in cosmetic preparations and personal-care products. Laurocapram is combined as an excipient (an inert substance) not an active ingredient. Excipients are added to ensure that the shelf-life of the active ingredients can be long enough to be active until internal use. It can be used as a topical smear, massage penetration enhancers; pesticides, as a pro-absorbing agent and sterilization plant growth regulators, pesticides pro penetration; in addition, can be used for coloring and dyeing leather and other areas of accelerator.

References

http://www.chemicalland21.com/lifescience/foco/LAUROCAPRAM.htm

Uses

Different sources of media describe the Uses of 59227-89-3 differently. You can refer to the following data:
1. antifungal lipopeptide
2. Pharmaceutic aid (excipient).
3. Laurocapram is a useful intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 59227-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,2,2 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59227-89:
(7*5)+(6*9)+(5*2)+(4*2)+(3*7)+(2*8)+(1*9)=153
153 % 10 = 3
So 59227-89-3 is a valid CAS Registry Number.
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

59227-89-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Laurocapram

1.2 Other means of identification

Product number -
Other names 1 dodecylperhydroazepin 2 one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:59227-89-3 SDS

59227-89-3Synthetic route

caprolactam
105-60-2

caprolactam

1-dodecylbromide
143-15-7

1-dodecylbromide

Conditions
ConditionsYield
With sodium hydroxide In water; toluene99.6%
With sodium hydroxide In toluene95%
With sodium hydroxide; tetrabutylammomium bromide; potassium carbonate In cyclohexane92.8%
1-chlorododecane
112-52-7

1-chlorododecane

Conditions
ConditionsYield
95.2%
caprolactam
105-60-2

caprolactam

Conditions
ConditionsYield
With sodium; xylene anschliessend mit Dodecylbromid;
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 91 percent / 48percent aq. HBr / dodecylpyridinium bromide / 1.5 h / Irradiation
2: 87 percent / NaOH / n-C12H25N(CH3)3Br / 9 h / 70 - 75 °C
View Scheme
caprolactam
105-60-2

caprolactam

tert-butyl methyl ether
1634-04-4

tert-butyl methyl ether

1-dodecylbromide
143-15-7

1-dodecylbromide

Conditions
ConditionsYield
With sodium hydroxide; tetrabutylammomium bromide
sodium oxide (Na2 O)

sodium oxide (Na2 O)

1-dodecylbromide
143-15-7

1-dodecylbromide

1-trimethylsilanyl-azepan-2-one
3553-94-4

1-trimethylsilanyl-azepan-2-one

Conditions
ConditionsYield
In 1,2-dimethoxyethane
caprolactam
105-60-2

caprolactam

pet

pet

1-dodecylbromide
143-15-7

1-dodecylbromide

Conditions
ConditionsYield
In toluene; mineral oil
1-dodecylbromide
143-15-7

1-dodecylbromide

Conditions
ConditionsYield
With sodium hydroxide; Aliquat 336 In toluene
caprolactam
105-60-2

caprolactam

sodium hydride-mineral oil

sodium hydride-mineral oil

1-dodecylbromide
143-15-7

1-dodecylbromide

Conditions
ConditionsYield
60 g (80%)
4-toluenesulfonyl azide
941-55-9

4-toluenesulfonyl azide

C25H42N2O2S

C25H42N2O2S

Conditions
ConditionsYield
Stage #1: Azone With bis(triphenylphosphine)carbonyliridium(I) chloride; 1,1,3,3-Tetramethyldisiloxane In dichloromethane at 20℃; for 0.5h;
Stage #2: 4-toluenesulfonyl azide In dichloromethane at 20℃; for 3h; chemoselective reaction;
70%
6-dodecylamino-hexanoic acid
58157-72-5

6-dodecylamino-hexanoic acid

Conditions
ConditionsYield
With hydrogenchloride
(5-carboxy-pentyl)-dodecyl-dimethyl-ammonium; iodide

(5-carboxy-pentyl)-dodecyl-dimethyl-ammonium; iodide

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: concentrated HCl
2: Na2CO3; methanol
View Scheme
3-bromo-1-dodecylazacycloheptan-2-one
114919-82-3

3-bromo-1-dodecylazacycloheptan-2-one

Conditions
ConditionsYield
With phosphorus pentachloride; bromine In dichloromethane; chloroform
uranyl nirate hexahydrate

uranyl nirate hexahydrate

UO2(NO3)2(CH2(CH2)4CONC12H25)2
147186-51-4

UO2(NO3)2(CH2(CH2)4CONC12H25)2

Conditions
ConditionsYield
In nitric acid aq. HNO3; addn. of soln. of uranyl nitrate in aq. HNO3 to ligand in petroleum ether, shaking (several hours), pptn.; filtration, washing (water, petroleum ether), recrystn. (toluene), washing (petroleum ether), filtration, drying (vac.); elem. anal.;

59227-89-3Downstream Products

59227-89-3Relevant articles and documents

Process for the preparation of N-substituted lactams

-

, (2008/06/13)

The invention relates to a process for the preparation of N-substituted lactams by reaction of a lactam, which is unsubstituted on the nitrogen, with an organic halide in the presence of at least one solid-liquid phase transfer catalyst, such as a quaternary ammonium salt, and of at least one solid inorganic base, such as an alkali metal hydroxide, and in the absence of solvent. By this process, N-substituted lactams are obtained with good yields and high purity. The absence of solvent makes possible a considerable gain in productivity and an improvement in safety and in regard for the environment.

N-allyl-lactams as crystallization inhibitors

-

, (2008/06/13)

Crystallization of active material in spraying of an aqueous solution of certain specified fungicides is retarded by incorporation therein of an N-alkyl-lactam of the formula STR1 in which R represents alkyl having 6 to 18 carbon atoms and n represents the numbers 3, 4 or 5.

Solid formulations

-

, (2008/06/13)

New solid formulations of A) at least one agrochemical active compound, B) at least one additive from the groups mentioned in the description, C) at least one dispersant, D) at least one carrier and E) if appropriate, further active compounds and/or additives, a process for preparing the solid formulations and their use for treating plants. A new device for preparing new granules.

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