1589-49-7

Basic information

• Product Name: 3-Methoxy-1-propanol
• Synonyms: 3-METHOXY-1-PROPANOL;3-METHOXYPROPAN-1-OL;3-METHOXYPROPANE-1-OL;3-METHOXYPROPANOL;3-METHOXYPROPANOL-1;1,3-PROPANEDIOL MONOMETHYL ETHER;MPOL;1-Propanol, 3-methoxy-
• CAS NO: 1589-49-7
• Molecular Formula: C₄H₁₀O₂
• Molecular Weight: 90.12
• EINECS: 433-230-9
• Product Categories: PHARMACEUTICAL INTERMEDIATES;Alcohols;C2 to C6;Oxygen Compounds;Rabeprazole
• Mol File: 1589-49-7.mol
• Article Data: 36

Chemical Properties

• Melting Point: -84.2°C (estimate)
• Boiling Point: 150-152 °C
• Flash Point: 38°C
• Appearance: Clear colorless/Liquid
• Density: 0.942 g/mL at 20 °C(lit.)
• Vapor Pressure: 0.952mmHg at 25°C
• Refractive Index: n20/D 1.413
• Storage Temp.: Store below +30°C.
• PKA: 14.89±0.10(Predicted)
• Water Solubility: Completely miscible in water
• BRN: 1731204
• CAS DataBase Reference: 3-Methoxy-1-propanol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Methoxy-1-propanol(1589-49-7)
• EPA Substance Registry System: 3-Methoxy-1-propanol(1589-49-7)

Safety Data

• Hazard Codes: Xi,F
• Statements: 10-38-36/38
• Safety Statements: 16-37-26
• RIDADR: UN 1987 3/PG 3
• WGK Germany: 1
• RTECS: UB7650000
• HazardClass: FLAMMABLE
• PackingGroup: III
• Hazardous Substances Data: 1589-49-7(Hazardous Substances Data)

Usage

Chemical Properties

Colorless liqui

General Description

3-Methoxy-1-propanol is a primary alcohol. Kinetics of the reactions of 3-methoxy-1-propanol with phenyl isocyanate in the presence of metal catalysts has been reported. Selective synthesis of 3-methoxy-1-propanol from methanol and allyl alcohol with metal oxides and zeolites catalysts in the liquid phase has been studied.

InChI:InChI=1/C4H10O2/c1-6-4-2-3-5/h5H,2-4H2,1H3

Synthetic route

methylallylether (627-40-7) → methoxypropanol (1589-49-7)

Conditions	Yield
Stage #1: methylallylether With diborane In dimethyl sulfoxide Inert atmosphere; Stage #2: With dihydrogen peroxide; sodium hydroxide In dimethyl sulfoxide Reagent/catalyst; Solvent;	91.2%

methyl iodide (74-88-4) + trimethyleneglycol (504-63-2) → methoxypropanol (1589-49-7)

Conditions	Yield
With mercury(II) oxide In dichloromethane at 20℃; for 28h;	72%
With sodium In octane
With potassium carbonate Multistep reaction;

1,3-dioxane (505-22-6) → methoxypropanol (1589-49-7)

Conditions	Yield
With diisobutylaluminium hydride In benzene for 1h; Heating; further reagents: triethylaluminum, triisobutylaluminum with Pd(acac)2;	65%
With lithium aluminium tetrahydride; boron trichloride 1.) CH2Cl2, 0.2 h, 2.) Et2O, 30 min; Yield given. Multistep reaction;

methyl 3-methoxypropionate (3852-09-3) → methoxypropanol (1589-49-7)

Conditions	Yield
Stage #1: methyl 3-methoxypropionate With lithium aluminium tetrahydride In diethyl ether for 4.5h; Inert atmosphere; Stage #2: With water; sodium hydroxide In diethyl ether at 0 - 20℃;	60%
Stage #1: methyl 3-methoxypropionate With lithium aluminium tetrahydride In diethyl ether for 4.5h; Stage #2: With sodium hydroxide; water In diethyl ether at 0℃;	60%
With hydrogen In methanol at 170℃; under 150015 Torr;	51%

methanol (67-56-1) + 1-bromo-3-propanol (627-18-9) → methoxypropanol (1589-49-7)

Conditions	Yield
With sodium In methanol 1.) 20 deg. C, 1 h, 2.) reflux, 1 h;	20%

trimethylene oxide (503-30-0) + methanol (67-56-1) → methoxypropanol (1589-49-7)

Conditions	Yield
With sulfuric acid

trimethylene oxide (503-30-0) + sodium methylate (124-41-4) → methoxypropanol (1589-49-7)

Conditions	Yield
With methanol at 175℃;

3-methoxy-1-propanal (2806-84-0) → methoxypropanol (1589-49-7)

Conditions	Yield
With methanol; pumice stone; nickel at 45 - 100℃; Hydrogenation;
With sodium metaborate In water
With hydrogen; nickel at 80℃; under 37503.8 Torr; for 3h;
With hydrogen; Ru/C under 37503.8 Torr; for 3h;

methanol (67-56-1) + acrolein (107-02-8) → methoxypropanol (1589-49-7)

Conditions	Yield
With sodium hydroxide; hydroquinone beim Ansaeuern mit Essigsaeure und anschliessenden Hydrieren an Raney-Nickel bei 93grad/70 at;

3-Methoxypropionitrile (110-67-8) → methoxypropanol (1589-49-7)

Conditions	Yield
(i) EtOH, H2SO4, (ii) LiAlH4; Multistep reaction;

sodium methylate (124-41-4) + 1-chloro-3-hydroxypropane (627-30-5) → methoxypropanol (1589-49-7)

Conditions	Yield
In methanol

tetrahydrofuran (109-99-9) → trimethylene oxide (503-30-0) + methoxypropanol (1589-49-7)

Conditions	Yield
With methane; water; oxygen Irradiation;

1,3-dioxane (505-22-6) → methoxypropanol (1589-49-7) + trimethyleneglycol (504-63-2)

Conditions	Yield
With lithium aluminium tetrahydride; boron tribromide 1.) CH2Cl2, 0 deg C, 0.03 h, 2.) Et2O, 30 min; Yield given. Multistep reaction. Yields of byproduct given. Title compound not separated from byproducts;

3-bromopropanol methyl ether (36865-41-5) → methoxypropanol (1589-49-7)

Conditions	Yield
With water; triethylamine In ethanol at 124.8℃; Kinetics; further temperatures, further solvent, activation enthalpy and entropy;

methylallylether (627-40-7) → propan-1-ol (71-23-8) + 1-methoxy-2-propanol (107-98-2) + methoxypropanol (1589-49-7)

Conditions	Yield
With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; dihydrogen peroxide Product distribution; 1) THF, 25 deg C, 2 h;	A 1.5 % Chromat. B n/a C 94 % Chromat.

methylallylether (627-40-7) → 1-methoxy-2-propanol (107-98-2) + methoxypropanol (1589-49-7)

Conditions	Yield
With sodium hydroxide; sodium tetrahydroborate; mercury(II) diacetate 1) water, THF, 30 min, 2) ca. 0.5 h; Yield given. Multistep reaction. Yields of byproduct given;
With sodium hydroxide; mercury(II) diacetate In tetrahydrofuran; water Product distribution; 1) 30 min, 2) ca. 0.5 h;

((3-methoxypropoxy)methyl)benzene (96516-91-5) → methoxypropanol (1589-49-7) + (diethoxymethyl)benzene (774-48-1) + [Ethoxy-(3-methoxy-propoxy)-methyl]-benzene (100189-72-8) + benzaldehyde (100-52-7)

Conditions	Yield
With hydrogen; palladium hydroxide - carbon In ethanol Heating;

trimethylene glycol monosodium salt (37480-93-6, 54481-30-0, 59571-05-0) + methyl iodide (74-88-4) → methoxypropanol (1589-49-7)

Conditions	Yield
In various solvent(s)

1,3-dioxane (505-22-6) → methoxypropanol (1589-49-7) + 3-methoxy-1-propanal (2806-84-0) + alkoxyalkyl substd. 1,3-dioxanes, H2, CO, CO2

Conditions	Yield
Mechanism; Product distribution; Quantum yield; Irradiation; 185 nm vacuum-ultraviolet photolysis;

methyl iodide (74-88-4) + monosodium compound of trimethylene glycol → methoxypropanol (1589-49-7)

1-methoxy-3-vinyloxy-propane (3046-32-0) + ethylene glycol (107-21-1) → methoxypropanol (1589-49-7) + acetaldehyde ethylenacetal

Conditions	Yield
With hydrogenchloride

hydrogenchloride (7647-01-0) + 1-methoxy-3-vinyloxy-propane (3046-32-0) + ethylene glycol (107-21-1) → methoxypropanol (1589-49-7) + acetaldehyde ethylenacetal

methanol (67-56-1) + propene (187737-37-7) → propylene glycol (57-55-6) + methoxypropanol (1589-49-7) + methyloxirane (75-56-9, 16033-71-9)

Conditions	Yield
With dihydrogen peroxide; Nb-hexagonal mesoporous silica In water at 49.85℃; under 6000.48 Torr; for 4h; Product distribution; Further Variations:; Catalysts; Reagents;

1,1,3-trimethoxypropane (14315-97-0) + 3-methoxy-1-propanal (2806-84-0) → methoxypropanol (1589-49-7)

Conditions	Yield
With hydrogen; nickel at 80℃; under 37503.8 Torr; for 3 - 4h;

1,1,3-trimethoxypropane (14315-97-0) → methoxypropanol (1589-49-7) + propionic acid-(3-methoxy-propyl ester) + propionic acid (802294-64-0)

Conditions	Yield
With hydrogen; Ru/C at 80℃; under 37503.8 Torr; for 3h;

1,1,3-trimethoxypropane (14315-97-0) → methoxypropanol (1589-49-7)

Conditions	Yield
With hydrogen; nickel at 80℃; under 37503.8 Torr; for 3h;
In trifluoroacetic acid

methanol (67-56-1) + allyl alcohol (107-18-6) → methoxypropanol (1589-49-7) + 3-allyloxy-1-propanol (6180-67-2)

Conditions	Yield
activated carbon-supported lantahanium oxide at 200℃; for 6h; Product distribution / selectivity;
magnesium oxide In water at 200℃; for 6h; Product distribution / selectivity;
magnesium oxide at 200℃; for 6h; Product distribution / selectivity;

3-methoxy-1-propanal (2806-84-0) + pyrographite (7440-44-0) + ruthenium (7440-18-8) → methoxypropanol (1589-49-7)

methylene chloride (74-87-3) + C3H7O2(1-) → methoxypropanol (1589-49-7)

Conditions	Yield
at 76.84℃; under 3E-07 - 5E-06 Torr; Kinetics;

methoxypropanol (1589-49-7) + methyl 6-(2,6-difluoro-4-hydroxyphenyl)-5-fluoropyridine-2-carboxylate (1355011-30-1) → methyl 6-(2,6-difluoro-4-(3-methoxypropoxy)phenyl)-5-fluoropicolinate (1395283-97-2)

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃;	100%
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 20℃;	100%

methoxypropanol (1589-49-7) → trimethyleneglycol (504-63-2)

Conditions	Yield
With Strong acid resin at 100℃; for 1h; Temperature; Reagent/catalyst;	99.2%
With phosphoric acid; hydrogen iodide; sodium iodide at 105℃; Reagent/catalyst; Autoclave;	88%
With water; sulfuric acid at 190℃; for 10h; Product distribution / selectivity;

methoxypropanol (1589-49-7) + methanesulfonyl chloride (124-63-0) → 3-Methoxy-1-propanol methanesulphonate (127686-58-2)

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 18h;	97%
With triethylamine In dichloromethane at 0 - 20℃; for 18h;	97%
With triethylamine In dichloromethane at 0 - 20℃; for 2h;	96%

4-chloro-2,3-dimethylpyridine-N-oxide (59886-90-7) + methoxypropanol (1589-49-7) → 2,3-dimethyl-4-(3-methoxypropoxy)pyridine nitroxide (117977-18-1)

Conditions	Yield
Stage #1: methoxypropanol With sodium hydroxide In dimethyl sulfoxide at 20 - 60℃; Stage #2: 4-chloro-2,3-dimethylpyridine-N-oxide In dimethyl sulfoxide at 75℃; for 5h;	95%
With methyl tributylammonium chloride; sodium hydroxide In water; toluene at 100℃; for 8h; Large scale reaction;	94%
With sodium hydroxide; N-methyl-tri-n-butyl-ammonium bromide In water at 100℃; for 8h;	84.6%

methoxypropanol (1589-49-7) + (6S,9S)-N-benzyl-6-(4-hydroxybenzyl)-2,9-dimethyl-4,7-dioxo-8-(quinolin-8-ylmethyl)octahydro-1H-pyrazino[2,1-c][1,2,4]triazine-1-carboxamide (1198780-43-6) → (6S,9S)-N-benzyl-6-(4-(3-methoxypropoxy)benzyl)-2,9-dimethyl-4,7-dioxo-8-(quinolin-8-ylmethyl)octahydro-1H-pyrazino[2,1-c][1,2,4]triazine-1-carboxamide (1394313-73-5)

Conditions	Yield
With tributylphosphine; 1,1'-azodicarbonyl-dipiperidine In tetrahydrofuran at 20℃;	95%

methoxypropanol (1589-49-7) + cyclohexene-1-carboxylic acid (636-82-8) → 3-methoxypropyl cyclohex-1-enecarboxylate (1449522-67-1)

Conditions	Yield
With dmap; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide In dichloromethane at 0 - 20℃; Inert atmosphere;	95%

norborn-2-ene (498-66-8) + methoxypropanol (1589-49-7) → exo-2-(3-methoxypropoxy)bicyclo[2.2.1]heptane

Conditions	Yield
With (triphenylphosphine)gold(I) chloride; silver trifluoromethanesulfonate; triphenylphosphine In Tridecane; toluene at 85℃; for 24h;	92%

4-nitro-phenol (100-02-7) + methoxypropanol (1589-49-7) → 1-(3-methoxypropoxy)-4-nitrobenzene (102015-09-8)

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 2h;	91%
With di-isopropyl azodicarboxylate; triphenylphosphine at 0 - 20℃; for 2.5h;	89%

methoxypropanol (1589-49-7) + p-toluenesulfonyl chloride (98-59-9) → 3-methoxypropyl p-toluenesulfonate (54646-36-5)

Conditions	Yield
With pyridine at 0 - 10℃; for 3h;	89%
	84%
With pyridine; dmap In dichloromethane at 20℃; for 72h;	76%

5-chloro-1,3-benzodioxole (7228-38-8) + methoxypropanol (1589-49-7) → 5-(3-methoxypropoxy)benzo[d][1,3]dioxole

Conditions	Yield
With C12H10N(1-)*CH3O3S(1-)*Pd(2+)*C39H57O2P; sodium t-butanolate In 1,4-dioxane at 60℃; for 18h; Reagent/catalyst; Sealed tube; Schlenk technique; Inert atmosphere;	87%

2-chloro-4-picoline (3678-62-4) + methoxypropanol (1589-49-7) → 2-(3-methoxypropoxy)-4-methylpyridine

Conditions	Yield
With C12H10N(1-)*Pd(2+)*CH3O3S(1-)*C31H49O2P; sodium t-butanolate In 1,4-dioxane at 20℃; for 6h; Sealed tube; Schlenk technique; Inert atmosphere;	86%

methoxypropanol (1589-49-7) → 3-methoxy-1-propanal (2806-84-0)

Conditions	Yield
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione In ethyl acetate Reflux;	85%
With pyridinium chlorochromate In dichloromethane at 20℃; for 12h; Inert atmosphere;	65%
With PyCrO3*HCl In dichloromethane at 20℃; for 2h;	36.8%

{Cu(2,2,6,6-tetramethylheptane-3,5-dionate)(isopropoxy)}2 + methoxypropanol (1589-49-7) → {Cu(2,2,6,6-tetramethylheptane-3,5-dionate)(OCH2CH2CH2OCH3)}2

Conditions	Yield
In tetrahydrofuran (dry N2), dry solvents; addn. of Cu-compd. to mixt. of 3-methoxypropanol and THF, react. time 2 h; evapn. to dryness, recrystn. (hexane) at -30°C; elem. anal.;	85%

methoxypropanol (1589-49-7) + 6-(6-fluoro-1H-indol-1-yl)-2-(3-(5-hydroxypyrimidin-2-yl)benzyl)pyridazin-3(2H)-one → 6-(6-fluoro-1H-indol-1-yl)-2-(3-(5-(3-methoxypropoxy)pyrimidin-2-yl)benzyl)pyridazin-3(2H)-one

Conditions	Yield
With di-isopropyl azodicarboxylate; triphenylphosphine In tetrahydrofuran at 0 - 20℃; for 12h; Mitsunobu Displacement;	84%

7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid chloride (929904-81-4) + methoxypropanol (1589-49-7) → 3-methoxypropyl 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

Conditions	Yield
With triethylamine In dichloromethane at 0 - 20℃; for 4h;	84%

methoxypropanol (1589-49-7) + 7-bromo-5-chloro-3-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[4,3-b]pyridine → 5-chloro-3-iodo-7-(3-methoxypropoxy)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[4,3-b]pyridine

Conditions	Yield
Stage #1: methoxypropanol With sodium hydride In 1,4-dioxane; mineral oil for 0.5h; Stage #2: 7-bromo-5-chloro-3-iodo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazolo[4,3-b]pyridine In 1,4-dioxane; mineral oil at 100℃; for 2h;	81%

methoxypropanol (1589-49-7) + 2-chloro-5-methylphenol (615-74-7) → 1-chloro-2-(3-methoxy-propoxy)-4-methyl-benzene (1000045-32-8)

Conditions	Yield
With triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine In dichloromethane at 20℃; for 16h;	80%
With triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine In dichloromethane at 20℃; for 16h; Mitsunobu reaction;	80%

3-chlorothiophene (17249-80-8) + methoxypropanol (1589-49-7) → C8H12O2S

Conditions	Yield
With N1,N2-bis(naphthalen-1-ylmethyl)oxalamide; potassium tert-butylate; copper diacetate In 1,4-dioxane at 100℃; for 24h; Schlenk technique; Inert atmosphere; Molecular sieve;	78%

methoxypropanol (1589-49-7) + 2-bromo-6-iodo-3-methoxypyridine (321535-37-9) → 6-iodo-3-methoxy-2-(3-methoxypropoxy)pyridine

Conditions	Yield
Stage #1: methoxypropanol With sodium hydride In N,N-dimethyl-formamide for 0.666667h; Stage #2: 2-bromo-6-iodo-3-methoxypyridine In N,N-dimethyl-formamide at 100℃; for 3h;	77%

methoxypropanol (1589-49-7) + C66H4O3 (273214-08-7) → C70H14O5

Conditions	Yield
In toluene at 60℃; for 5h; Esterification;	76%

methoxypropanol (1589-49-7) + methyl 4-bromo-3-hydroxybenzoate (106291-80-9) → 4-bromo-3-(3-methoxy-propoxy)-benzoic acid methyl ester (895240-78-5)

Conditions	Yield
With triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine In dichloromethane at 20℃;	75%
With triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine In dichloromethane at 20℃; Mitsunobu reaction;	75%
With triphenylphosphine; 1,1'-azodicarbonyl-dipiperidine In dichloromethane at 20℃;

methoxypropanol (1589-49-7) + ethyl 1-(6-chloropyrimidin-4-yl)cyclopropane-1-carboxylate → ethyl 1-(6-(3-methoxypropoxy)pyrimidin-4-yl)cyclopropane-1-carboxylate

Conditions	Yield
With sodium hydride In ethanol for 5h; Reflux;	74.8%

methoxypropanol (1589-49-7) + pivaloyl chloride (3282-30-2) → 3-methoxypropyl pivalate

Conditions	Yield
With pyridine In dichloromethane at 20℃;	74%

methoxypropanol (1589-49-7) → 1-Chloro-3-methoxypropane (36215-07-3)

Conditions	Yield
With pyridine; thionyl chloride at 10 - 65℃; for 3h;	72%
With pyridine; thionyl chloride at 10 - 65℃;	72%
With pyridine; thionyl chloride at 10 - 70℃; for 8h; Inert atmosphere;	71%

methoxypropanol (1589-49-7) + tetrakis(chlorodimethylsilyl)silane (17082-82-5) → tetrakis(dimethyl(3-methoxypropoxy)silyl)silane (1293370-37-2)

Conditions	Yield
With triethylamine In hexane at 20℃; Inert atmosphere; Cooling with ice;	71%

methoxypropanol (1589-49-7) + benzylamine (100-46-9) → N-benzylpropanamide (10264-12-7)

Conditions	Yield
With dichloro(benzene)ruthenium(II) dimer; N,N-diisopropylimidazolium bromide; sodium hydride In toluene; acetonitrile for 24h; Inert atmosphere; Reflux;	71%

methoxypropanol (1589-49-7) + rac-Pro-OH (609-36-9) → 1-(3-methoxypropyl)pyrrolidine

Conditions	Yield
With bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]; sodium hydrogencarbonate In toluene at 110℃; for 72h; Inert atmosphere;	69%

methoxypropanol (1589-49-7) + 4-amino-2-chloro-6-(trifluoromethyl)pyridine (34486-22-1) → 2-(3-methoxypropoxy)-6-(trifluoromethyl)pyridin-4-amine

Conditions	Yield
Stage #1: methoxypropanol With sodium hydride In 1,4-dioxane at 20℃; for 1h; Stage #2: 2-chloro-6-(trifluoromethyl)pyridin-4-amine In 1,4-dioxane at 110℃;	68%

Upstream product

• 505-22-6 1,3-dioxane 
• 3046-32-0 1-methoxy-3-vinyloxy-propane 
• 107-21-1 ethylene glycol 
• 7647-01-0 hydrogenchloride 
• 67-56-1 methanol 
• 187737-37-7 propene 
• 2806-84-0 3-methoxy-1-propanal 
• 7440-44-0 pyrographite 
• 7440-18-8 ruthenium 
• 627-40-7 methylallylether 
• 74-87-3 methylene chloride 
• 107-18-6 allyl alcohol 
• 14315-97-0 1,1,3-trimethoxypropane 
• 74-88-4 methyl iodide 

Downstream Products

• 54646-36-5 3-methoxypropyl p-toluenesulfonate 
• 141100-26-7 3-(2,6-dioxaheptyl)-3-methyloxetane 
• 96516-91-5 ((3-methoxypropoxy)methyl)benzene 
• 1122567-79-6 1-iodo-2-(3-methoxy-propoxy)-benzene 
• 897956-21-7 4-bromo-2-(3-methoxypropoxy)-1-trifluoromethylbenzene 
• 1190423-51-8 4-[4-(6-fluoro-1H-benzimidazol-2-yl)-9H-carbazol-9-yl]-2-(3-methoxypropoxy)benzonitrile 
• 96-18-4 1,2,3-trichloropropane 
• 133649-66-8 1-Methoxy-3-(diphenylmethoxy)propan 
• 112-28-7 di-(1,3-propylene) glycol monomethyl ether 
• 141100-13-2 2-Bromomethyl-1,3-bis-(3-methoxy-propoxy)-2-methyl-propane 
• 141100-17-6 8-methoxymethyl-8-methyl-2,6,10,14-tetraoxapentadecane 
• 141100-11-0 8-(2,6-dioxaheptyl)-8-methyl-2,6,10,14-tetraoxapentadecane 
• 141100-15-4 2-Bromomethyl-1-methoxy-3-(3-methoxy-propoxy)-2-methyl-propane 
• 141100-16-5 4-methoxymethyl-4-methyl-2,6,10-trioxaundecane 

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