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2461-18-9

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2461-18-9 Usage

General Description

Clear colorless viscous liquid.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

LAURYL GLYCIDYL ETHER is a ether-alcohol derivative. The ether being relatively unreactive. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert alcohols to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.

Fire Hazard

Flash point data for LAURYL GLYCIDYL ETHER are not available but LAURYL GLYCIDYL ETHER is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 2461-18-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,6 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2461-18:
(6*2)+(5*4)+(4*6)+(3*1)+(2*1)+(1*8)=69
69 % 10 = 9
So 2461-18-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O2/c1-2-3-4-5-6-7-8-9-10-11-12-16-13-15-14-17-15/h15H,2-14H2,1H3/t15-/m0/s1

2461-18-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dodecoxymethyl)oxirane

1.2 Other means of identification

Product number -
Other names dodecylglycidyl ether

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:2461-18-9 SDS

2461-18-9Synthetic route

1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

1,2-Epoxy-3-bromopropane
3132-64-7

1,2-Epoxy-3-bromopropane

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran at 20℃; for 16h;85%
With sodium carbonate In hexane; water at 60℃; for 4h;75%
1-chloro-3-dodecyloxy-propan-2-ol
17677-15-5

1-chloro-3-dodecyloxy-propan-2-ol

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

Conditions
ConditionsYield
With sodium hydride In hexane; toluene at 20℃; for 0.0833333h; Cyclization;266 mg
With sodium hydroxide In water at 60 - 70℃; for 6h;
(+-)-1-chloro-2-dodecyloxy-propan-3-ol

(+-)-1-chloro-2-dodecyloxy-propan-3-ol

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

Conditions
ConditionsYield
With sodium hydroxide; dibutyl ether
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

epichlorohydrin
106-89-8

epichlorohydrin

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

Conditions
ConditionsYield
With tetrabutylammomium bromide; sodium hydroxide In hexane
Stage #1: 1-dodecyl alcohol With tetrabutylammomium bromide; sodium hydroxide In hexane; water at 20℃;
Stage #2: epichlorohydrin In hexane; water at 50℃; for 4h;
With tetrabutyl ammonium fluoride; sodium hydroxide at 60℃;
1-dodecyl alcohol
112-53-8

1-dodecyl alcohol

dibutyl tin-dimethylate

dibutyl tin-dimethylate

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: SnCl4 / toluene; heptane / 3 h / 90 - 93 °C
2: 266 mg / NaH / toluene; hexane / 0.08 h / 20 °C
View Scheme
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

3-dodecyloxypropane-1,2-diol
100165-14-8

3-dodecyloxypropane-1,2-diol

Conditions
ConditionsYield
With formic acid; sodium hydroxide In diethylene glycol dimethyl ether at 130℃; for 12h;96.3%
Multi-step reaction with 2 steps
1: 16 h / 100 °C
2: NaH / hexane / 2 h / 20 °C
View Scheme
Multi-step reaction with 2 steps
1.1: boron trifluoride diethyl etherate / tetrahydrofuran / 20 °C / Inert atmosphere; Large scale
1.2: 5 h / 50 °C / Large scale
2.1: sulfuric acid / water; methanol / 5 h / 70 °C
View Scheme
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

N,N-dimethylaminododecane
112-18-5

N,N-dimethylaminododecane

dodecyldimethyl ammonium chloride
2016-48-0

dodecyldimethyl ammonium chloride

C29H62NO2(1+)*Cl(1-)
32818-31-8

C29H62NO2(1+)*Cl(1-)

Conditions
ConditionsYield
In isopropyl alcohol for 24h; Reflux;90%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

N,N-dimethyl-n-tetradecylamine
112-75-4

N,N-dimethyl-n-tetradecylamine

IPL 30 hydrochloride

IPL 30 hydrochloride

C31H66NO2(1+)*Cl(1-)
1159680-58-6

C31H66NO2(1+)*Cl(1-)

Conditions
ConditionsYield
In isopropyl alcohol for 24h; Reflux;90%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

N,N-dimethylhexadecylamine
112-69-6

N,N-dimethylhexadecylamine

N,N-dimethylhexadecylamine hydrochloride
2016-45-7

N,N-dimethylhexadecylamine hydrochloride

C31H66NO2(1+)*Cl(1-)

C31H66NO2(1+)*Cl(1-)

Conditions
ConditionsYield
In isopropyl alcohol for 24h; Reflux;90%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

bis(3-methylphenyl) diselenide
69468-42-4

bis(3-methylphenyl) diselenide

1-dodecyloxy-3-m-tolylselanyl-propan-2-ol

1-dodecyloxy-3-m-tolylselanyl-propan-2-ol

Conditions
ConditionsYield
Stage #1: bis(3-methylphenyl) diselenide With sodium hydroxide; sodium tetrahydroborate In ethanol for 0.1h; Irradiation;
Stage #2: dodecyl glycidyl ether In ethanol for 0.116667h; Irradiation;
87%
ammonium thiocyanate

ammonium thiocyanate

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

C16H31NO2S
1395922-37-8

C16H31NO2S

Conditions
ConditionsYield
With 2-chloro-1-methyl-pyridinium iodide at 20℃; for 0.0833333h;78%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

4-amino-2,2,6,6-tetramethyl-1-piperidine-1-oxyl
14691-88-4

4-amino-2,2,6,6-tetramethyl-1-piperidine-1-oxyl

A

C24H49N2O3
1116450-33-9

C24H49N2O3

B

C39H79N2O5
1116450-60-2

C39H79N2O5

Conditions
ConditionsYield
With calcium(II) trifluoromethanesulfonate In 1,4-dioxane at 140℃; under 1500.15 - 2250.23 Torr; for 0.333333h; Microwave irradiation;A 69%
B 18%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

2-(N,N-dimethylamino)ethanol
108-01-0

2-(N,N-dimethylamino)ethanol

(3-dodecyloxy-2-hydroxy-propyl)-(2-hydroxy-ethyl)-dimethyl-ammonium; chloride

(3-dodecyloxy-2-hydroxy-propyl)-(2-hydroxy-ethyl)-dimethyl-ammonium; chloride

Conditions
ConditionsYield
With 2-(N,N-dimethylamino)ethanol hydrochloride In methanol for 16h; pH=8; Heating;53%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

dimethyl amine
124-40-3

dimethyl amine

1-(N,N-dimethylamino)-3-(dodecyloxy)propan-2-ol
13393-70-9

1-(N,N-dimethylamino)-3-(dodecyloxy)propan-2-ol

Conditions
ConditionsYield
In water at 65℃; for 6h;50.6%
In ethanol; isopropyl alcohol at 39.9℃;
In ethanol; water at 50℃; for 4h;
In ethanol; water at 40 - 45℃; for 4h;
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

36-% hydrochloric acid

36-% hydrochloric acid

L-arginine
74-79-3

L-arginine

N-(2-hydroxy-3-dodecyloxypropyl)-L-arginine hydrochloride

N-(2-hydroxy-3-dodecyloxypropyl)-L-arginine hydrochloride

Conditions
ConditionsYield
With acetic acid In methanol; propan-1-ol; chloroform; water36%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

L-Lysine hydrochloride
657-27-2, 10098-89-2

L-Lysine hydrochloride

N-ε-(2-hydroxy-3-dodecyloxypropyl)-L-lysine hydrochloride
205486-72-2

N-ε-(2-hydroxy-3-dodecyloxypropyl)-L-lysine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; sodium hydroxide; acetic acid In methanol; propan-1-ol; chloroform; water23.7%
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

36-% hydrochloric acid

36-% hydrochloric acid

L-arginine
74-79-3

L-arginine

isopropyl alcohol
67-63-0

isopropyl alcohol

N,N-bis(2-hydroxy-3-dodecyloxypropyl)-L-arginine hydrochloride
205486-70-0

N,N-bis(2-hydroxy-3-dodecyloxypropyl)-L-arginine hydrochloride

Conditions
ConditionsYield
With acetic acid In methanol; chloroform; water17.2%
2-methyl-4,5-dihydro-thiazole
2346-00-1

2-methyl-4,5-dihydro-thiazole

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

5-dodecyloxymethyl-2-methyl-4,5-dihydro-oxazole
14225-45-7

5-dodecyloxymethyl-2-methyl-4,5-dihydro-oxazole

Conditions
ConditionsYield
at 140 - 150℃;
2-ethyl-4,5-dihydrooxazole
10431-98-8

2-ethyl-4,5-dihydrooxazole

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

2-dodecyloxymethyl-7a-ethyl-tetrahydro-oxazolo[2,3-b]oxazole
13488-75-0

2-dodecyloxymethyl-7a-ethyl-tetrahydro-oxazolo[2,3-b]oxazole

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

ethanolamine
141-43-5

ethanolamine

1-(dodecyloxy)-3-[(2-hydroxyethyl)amino]propan-2-ol
18448-68-5

1-(dodecyloxy)-3-[(2-hydroxyethyl)amino]propan-2-ol

Conditions
ConditionsYield
In ethanol
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

ethanolamine
141-43-5

ethanolamine

1-Dodecyloxy-3-[(3-dodecyloxy-2-hydroxy-propyl)-(2-hydroxy-ethyl)-amino]-propan-2-ol
65212-54-6

1-Dodecyloxy-3-[(3-dodecyloxy-2-hydroxy-propyl)-(2-hydroxy-ethyl)-amino]-propan-2-ol

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

1-[bis-(2-hydroxy-ethyl)-amino]-3-dodecyloxy-propan-2-ol
18448-70-9

1-[bis-(2-hydroxy-ethyl)-amino]-3-dodecyloxy-propan-2-ol

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

2-ethyl-1-phenyl-4,5-dihydro-1H-imidazole
13670-24-1

2-ethyl-1-phenyl-4,5-dihydro-1H-imidazole

2-dodecyloxymethyl-7a-ethyl-7-phenyl-hexahydro-imidazo[2,1-b]oxazole
14339-45-8

2-dodecyloxymethyl-7a-ethyl-7-phenyl-hexahydro-imidazo[2,1-b]oxazole

Conditions
ConditionsYield
at 150℃;
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

ethylamine
75-04-7

ethylamine

1-Dodecyloxy-3-ethylamino-propan-2-ol

1-Dodecyloxy-3-ethylamino-propan-2-ol

Conditions
ConditionsYield
In ethanol at 39.9℃;
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

diethylamine
109-89-7

diethylamine

1-diethylamino-3-dodecyloxy-propan-2-ol
76145-07-8

1-diethylamino-3-dodecyloxy-propan-2-ol

Conditions
ConditionsYield
In ethanol; isopropyl alcohol at 49.9℃;
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

methylamine
74-89-5

methylamine

1-Dodecyloxy-3-methylamino-propan-2-ol

1-Dodecyloxy-3-methylamino-propan-2-ol

Conditions
ConditionsYield
In ethanol
dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

acetic anhydride
108-24-7

acetic anhydride

acetic acid
64-19-7

acetic acid

acetic acid 2-acetoxy-1-dodecyloxymethyl-ethyl ester
117088-99-0

acetic acid 2-acetoxy-1-dodecyloxymethyl-ethyl ester

Conditions
ConditionsYield
at 100℃; for 16h; Acetoxylation; acetylation; ring cleavage;
3-(dodecyloxy)-1-propylamine
7617-74-5

3-(dodecyloxy)-1-propylamine

dodecyl glycidyl ether
2461-18-9

dodecyl glycidyl ether

C45H93NO5

C45H93NO5

2461-18-9Relevant articles and documents

Synthesis of a novel betaine-type asphalt emulsifier and its investigation by online FTIR spectrophotometry

Huai, Chunlei,Shi, Laishun,Li, Na

, p. 597 - 614 (2013)

A novel betaine-type asphalt emulsifier, 3-(dodecyloxy)-2-hydroxypropan-N- carboxymethyl-N,N-dimethylammonium chloride, has been synthesized in a three-step reaction from lauryl alcohol, epichlorohydrin, dimethylamine, and chloroacetic acid. The optimum reaction conditions were obtained for synthesis of 2-(dodecyloxymethyl)oxirane in the first step. The yield reaches 75.7 % under the optimum conditions of reaction temperature 50 C, reaction time 5 h, feedstock mole ratio of epichlorohydrin to lauryl alcohol 1.4, basicity 33.3 %. The structures of the three products were identified by FTIR. Synthesis of 2-(dodecyloxymethyl)oxirane in the first step was monitored by online FTIR, and an intermediate was detected. On the basis of the experimental data, a plausible reaction mechanism was proposed for the reaction. The critical micelle concentration (CMC) of the final product is low, 8.8 × 10-5 mol/L. The surface tension at the CMC is 21.2 mN/m. This product is an excellent emulsifier for asphalt. The prepared bituminous emulsion had high storage stability. The emulsifier is a rapid-set asphalt emulsifier.

DETERGENT FOR SKIN OR HAIR

-

Paragraph 0030, (2019/08/27)

PROBLEM TO BE SOLVED: To provide a skin detergent and a hair detergent having excellent foam quality, low skin irritation, and excellent stability at a low temperature. SOLUTION: A detergent for skin or hair contains a compound represented by general formula (1) (A), an anionic surfactant (B), and an ampholytic surfactant (C). R1OCH2CH-[O(AO)mH]-CH2O(AO)nH (1) [where R1 is a C4-18 monovalent hydrocarbon group; m+n AO independently represent an ethyleneoxy group or a propyleneoxy group; m and n independently represent an integer of 0 or greater; m+n is an integer of 1-50]. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT

ANTIMICROBIAL AGENT CONTAINING POLYALKYLENEIMINE DERIVATIVE

-

, (2017/09/23)

The present invention is an antimicrobial agent containing a polyalkyleneimine derivative formed by adding a substituent group having a structure of a following Formula (1) to a nitrogen atom of polyalkyleneimine. [in-line-formulae]—CH2CH(OH)CH2—O—R1??(1)[/in-line-formulae] In the formula, R1 represents an alkyl group with 6 to 20 carbon atoms, an alkenyl group with 6 to 20 carbon atoms, an aryl group with 6 to 20 carbon atoms, or —(CH2CH2O)n—R2. R2 represents an alkyl group with 6 to 20 carbon atoms, an alkenyl group with 6 to 20 carbon atoms, or an aryl group with 6 to 20 carbon atoms. n represents an integer of 1 to 50.

Synthesis, Surface and Antimicrobial Activities of Novel Cationic Gemini Surfactants

Ding, Zhaoyun,Fang, Shimin

, p. 1051 - 1057 (2015/11/18)

A series of novel cationic gemini surfactants [C n H2n+1-O-CH2-CH(OH)-CH2-N+(CH3)2-(CH2)2]2·2Br- [3a (n = 12), 3b (n = 14) and 3c (n = 16)] having a 2-hydroxy-1,3-oxypropylene group [-CH2-CH(OH)-CH2-O-] in the hydrophobic chain have been synthesized and characterized. Their water solubility, surface activity, foaming properties, and antibacterial activity have been examined. The critical micelle concentration (CMC) values of the novel cationic gemini surfactants are one to two orders of magnitude smaller than those of the corresponding monomeric surfactants. Furthermore, the novel cationic gemini surfactants have better water solubility and surface activity than the comparable [C n H2n+1-N+(CH3)2-(CH2)2]2·2Br- (n-4-n) geminis. The novel cationic gemini surfactants 3a and 3b also exhibit good foaming properties and show good antibacterial and antifungal activities.

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