3-Methoxy-1-propanol supplier

Name
3-Methoxy-1-propanol
EINECS 433-230-9
CAS No. 1589-49-7
Article Data46
CAS DataBase
Density 0.915 g/cm³
Solubility Completely miscible in water
Melting Point -96.7ºC
Formula C₄H₁₀O₂
Boiling Point 158.1 °C at 760 mmHg
Molecular Weight 90.1222
Flash Point 52.8 °C
Transport Information UN 1987 3/PG 3
Appearance Colorless liquid
Safety 16-37
Risk Codes 10-38
Molecular Structure
Hazard Symbols Xi,F
Synonyms 1-Methoxy-3-hydroxypropane;3-(Methyloxy)propan-1-ol;3-Methoxypropanol;Trimethyleneglycol monomethyl ether;b-Propylene glycol monomethyl ether;
PSA 29.46000
LogP 0.01520

Synthetic route

: 627-40-7
methylallylether

: 1589-49-7
methoxypropanol

Conditions

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%

: 74-88-4
methyl iodide

: 504-63-2
trimethyleneglycol

: 1589-49-7
methoxypropanol

Conditions

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

: 505-22-6
1,3-dioxane

: 1589-49-7
methoxypropanol

Conditions

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;

: 3852-09-3
methyl 3-methoxypropionate

: 1589-49-7
methoxypropanol

Conditions

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%

: 67-56-1
methanol

: 627-18-9
1-bromo-3-propanol

: 1589-49-7
methoxypropanol

Conditions

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

: 503-30-0
trimethylene oxide

: 67-56-1
methanol

: 1589-49-7
methoxypropanol

Conditions

Conditions	Yield
With sulfuric acid

: 503-30-0
trimethylene oxide

: 124-41-4
sodium methylate

: 1589-49-7
methoxypropanol

Conditions

Conditions	Yield
With methanol at 175℃;

: 2806-84-0
3-methoxy-1-propanal

: 1589-49-7
methoxypropanol

Conditions

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;

: 67-56-1
methanol

: 107-02-8
acrolein

: 1589-49-7
methoxypropanol

Conditions

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

: 110-67-8
3-Methoxypropionitrile

: 1589-49-7
methoxypropanol

Conditions

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

: 124-41-4
sodium methylate

: 627-30-5
1-chloro-3-hydroxypropane

: 1589-49-7
methoxypropanol

Conditions

Conditions	Yield
In methanol

: 109-99-9
tetrahydrofuran

A: 503-30-0
trimethylene oxide

B: 1589-49-7
methoxypropanol

Conditions

Conditions	Yield
With methane; water; oxygen Irradiation;

: 505-22-6
1,3-dioxane

A: 1589-49-7
methoxypropanol

B: 504-63-2
trimethyleneglycol

Conditions

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;

: 36865-41-5
3-bromopropanol methyl ether

: 1589-49-7
methoxypropanol

Conditions

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

: 627-40-7
methylallylether

A: 71-23-8
propan-1-ol

B: 107-98-2
1-methoxy-2-propanol

C: 1589-49-7
methoxypropanol

Conditions

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.

...Expand

: 627-40-7
methylallylether

A: 107-98-2
1-methoxy-2-propanol

B: 1589-49-7
methoxypropanol

Conditions

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;

: 96516-91-5
((3-methoxypropoxy)methyl)benzene

A: 1589-49-7
methoxypropanol

B: 774-48-1
(diethoxymethyl)benzene

C: 100189-72-8
[Ethoxy-(3-methoxy-propoxy)-methyl]-benzene

D: 100-52-7
benzaldehyde

Conditions

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

...Expand

: 37480-93-6, 54481-30-0, 59571-05-0
trimethylene glycol monosodium salt

: 74-88-4
methyl iodide

: 1589-49-7
methoxypropanol

Conditions

Conditions	Yield
In various solvent(s)

: 505-22-6
1,3-dioxane

A: 1589-49-7
methoxypropanol

B: 2806-84-0
3-methoxy-1-propanal

C alkoxyalkyl substd. 1,3-dioxanes, H2, CO, CO2: alkoxyalkyl substd. 1,3-dioxanes, H2, CO, CO2

Conditions

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

...Expand

: 74-88-4
methyl iodide

monosodium compound of trimethylene glycol: monosodium compound of trimethylene glycol

: 1589-49-7
methoxypropanol

: 3046-32-0
1-methoxy-3-vinyloxy-propane

: 107-21-1
ethylene glycol

A: 1589-49-7
methoxypropanol

B acetaldehyde ethylenacetal: acetaldehyde ethylenacetal

Conditions

Conditions	Yield
With hydrogenchloride

...Expand

: 7647-01-0
hydrogenchloride

: 3046-32-0
1-methoxy-3-vinyloxy-propane

: 107-21-1
ethylene glycol

A: 1589-49-7
methoxypropanol

B acetaldehyde ethylenacetal: acetaldehyde ethylenacetal

...Expand

: 67-56-1
methanol

: 187737-37-7
propene

A: 57-55-6
propylene glycol

B: 1589-49-7
methoxypropanol

C: 75-56-9, 16033-71-9
methyloxirane

Conditions

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;

...Expand

: 14315-97-0
1,1,3-trimethoxypropane

: 2806-84-0
3-methoxy-1-propanal

: 1589-49-7
methoxypropanol

Conditions

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

: 14315-97-0
1,1,3-trimethoxypropane

A: 1589-49-7
methoxypropanol

B: propionic acid-(3-methoxy-propyl ester)

C: 802294-64-0
propionic acid

Conditions

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

...Expand

: 14315-97-0
1,1,3-trimethoxypropane

: 1589-49-7
methoxypropanol

Conditions

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

: 67-56-1
methanol

: 107-18-6
allyl alcohol

A: 1589-49-7
methoxypropanol

B: 6180-67-2
3-allyloxy-1-propanol

Conditions

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;

...Expand

: 2806-84-0
3-methoxy-1-propanal

: 7440-44-0
pyrographite

: 7440-18-8
ruthenium

: 1589-49-7
methoxypropanol

...Expand

: 74-87-3
methylene chloride

: C3H7O2(1-)

: 1589-49-7
methoxypropanol

Conditions

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

: 1589-49-7
methoxypropanol

: 1355011-30-1
methyl 6-(2,6-difluoro-4-hydroxyphenyl)-5-fluoropyridine-2-carboxylate

: 1395283-97-2
methyl 6-(2,6-difluoro-4-(3-methoxypropoxy)phenyl)-5-fluoropicolinate

Conditions

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

: 1589-49-7
methoxypropanol

: 504-63-2
trimethyleneglycol

Conditions

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;

: 1589-49-7
methoxypropanol

: 124-63-0
methanesulfonyl chloride

: 127686-58-2
3-Methoxy-1-propanol methanesulphonate

Conditions

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%

: 59886-90-7
4-chloro-2,3-dimethylpyridine-N-oxide

: 1589-49-7
methoxypropanol

: 117977-18-1
2,3-dimethyl-4-(3-methoxypropoxy)pyridine nitroxide

Conditions

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%

: 1589-49-7
methoxypropanol

: 1198780-43-6
(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

: 1394313-73-5
(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

Conditions

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

: 1589-49-7
methoxypropanol

: 636-82-8
cyclohexene-1-carboxylic acid

: 1449522-67-1
3-methoxypropyl cyclohex-1-enecarboxylate

Conditions

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

: 498-66-8
norborn-2-ene

: 1589-49-7
methoxypropanol

: exo-2-(3-methoxypropoxy)bicyclo[2.2.1]heptane

Conditions

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

: 100-02-7
4-nitro-phenol

: 1589-49-7
methoxypropanol

: 102015-09-8
1-(3-methoxypropoxy)-4-nitrobenzene

Conditions

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%

: 1589-49-7
methoxypropanol

: 98-59-9
p-toluenesulfonyl chloride

: 54646-36-5
3-methoxypropyl p-toluenesulfonate

Conditions

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

: 7228-38-8
5-chloro-1,3-benzodioxole

: 1589-49-7
methoxypropanol

: 5-(3-methoxypropoxy)benzo[d][1,3]dioxole

Conditions

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%

: 3678-62-4
2-chloro-4-picoline

: 1589-49-7
methoxypropanol

: 2-(3-methoxypropoxy)-4-methylpyridine

Conditions

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%

: 1589-49-7
methoxypropanol

: 2806-84-0
3-methoxy-1-propanal

Conditions

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

: 1589-49-7
methoxypropanol

: {Cu(2,2,6,6-tetramethylheptane-3,5-dionate)(OCH2CH2CH2OCH3)}2

Conditions

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%

: 1589-49-7
methoxypropanol

: 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

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

: 929904-81-4
7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid chloride

: 1589-49-7
methoxypropanol

: 3-methoxypropyl 7-chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

Conditions

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

: 1589-49-7
methoxypropanol

: 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

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%

: 1589-49-7
methoxypropanol

: 615-74-7
2-chloro-5-methylphenol

: 1000045-32-8
1-chloro-2-(3-methoxy-propoxy)-4-methyl-benzene

Conditions

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%

: 17249-80-8
3-chlorothiophene

: 1589-49-7
methoxypropanol

: C8H12O2S

Conditions

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%

: 1589-49-7
methoxypropanol

: 321535-37-9
2-bromo-6-iodo-3-methoxypyridine

: 6-iodo-3-methoxy-2-(3-methoxypropoxy)pyridine

Conditions

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%

: 1589-49-7
methoxypropanol

: 273214-08-7
C66H4O3

: C70H14O5

Conditions

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

: 1589-49-7
methoxypropanol

: 106291-80-9
methyl 4-bromo-3-hydroxybenzoate

: 895240-78-5
4-bromo-3-(3-methoxy-propoxy)-benzoic acid methyl ester

Conditions

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℃;

: 1589-49-7
methoxypropanol

: ethyl 1-(6-chloropyrimidin-4-yl)cyclopropane-1-carboxylate

: ethyl 1-(6-(3-methoxypropoxy)pyrimidin-4-yl)cyclopropane-1-carboxylate

Conditions

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

: 1589-49-7
methoxypropanol

: 3282-30-2
pivaloyl chloride

: 3-methoxypropyl pivalate

Conditions

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

: 1589-49-7
methoxypropanol

: 36215-07-3
1-Chloro-3-methoxypropane

Conditions

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%

: 1589-49-7
methoxypropanol

: 17082-82-5
tetrakis(chlorodimethylsilyl)silane

: 1293370-37-2
tetrakis(dimethyl(3-methoxypropoxy)silyl)silane

Conditions

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

: 1589-49-7
methoxypropanol

: 100-46-9
benzylamine

: 10264-12-7
N-benzylpropanamide

Conditions

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

: 1589-49-7
methoxypropanol

: 609-36-9
rac-Pro-OH

: 1-(3-methoxypropyl)pyrrolidine

Conditions

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

: 1589-49-7
methoxypropanol

: 34486-22-1
4-amino-2-chloro-6-(trifluoromethyl)pyridine

: 2-(3-methoxypropoxy)-6-(trifluoromethyl)pyridin-4-amine

Conditions

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%

3-Methoxy-1-propanol Specification

The 3-Methoxy-1-propanol, with the CAS registry number 1589-49-7, is also known as 1-Propanol, 3-methoxy-. It belongs to the product categories of Pharmaceutical Intermediates; Alcohols; C2 to C6; Oxygen Compounds. This chemical's molecular formula is C₄H₁₀O₂ and molecular weight is 90.12. Its IUPAC name is called 3-methoxypropan-1-ol. What's more, this chemical can be used as solvent and also used as coupling and dispersant.

Physical properties of 3-Methoxy-1-propanol: (1)ACD/LogP: -0.37; (2)ACD/LogD (pH 5.5): -0.37; (3)ACD/LogD (pH 7.4): -0.37; (4)ACD/BCF (pH 5.5): 1; (5)ACD/BCF (pH 7.4): 1; (6)ACD/KOC (pH 5.5): 14.98; (7)ACD/KOC (pH 7.4): 14.98; (8)#H bond acceptors: 2; (9)#H bond donors: 1; (10)#Freely Rotating Bonds: 4; (11)Index of Refraction: 1.399; (12)Molar Refractivity: 23.86 cm³; (13)Molar Volume: 98.4 cm³; (14)Surface Tension: 28.6 dyne/cm; (15)Density: 0.915 g/cm³; (16)Flash Point: 52.8 °C; (17)Enthalpy of Vaporization: 45.97 kJ/mol; (18)Boiling Point: 158.1 °C at 760 mmHg; (19)Vapour Pressure: 0.952 mmHg at 25°C.

Preparation of 3-Methoxy-1-propanol: this chemical can be prepared by [1,3]dioxane. This reaction will need reagent diisobutylaluminum hydride and solvent benzene. The reaction time is 1 hour. The yield is about 65%.

3-Methoxy-1-propanol can be prepared by [1,3]dioxane

Uses of 3-Methoxy-1-propanol: it can be used to produce 1-bromo-3-methoxy-propane at temperature of 60 °C. This reaction will need reagent PBr₃.

3-Methoxy-1-propanol can be used to produce 1-bromo-3-methoxy-propane

When you are using this chemical, please be cautious about it as the following:
This chemical may cause inflammation to the skin or other mucous membranes. It is highly flammable. In addition, it is irritating to skin. You should keep it away from sources of ignition - No smoking. Whenever you will contact it, please wear suitable gloves.

You can still convert the following datas into molecular structure:
(1)Canonical SMILES: COCCCO
(2)InChI: InChI=1S/C4H10O2/c1-6-4-2-3-5/h5H,2-4H2,1H3
(3)InChIKey: JDFDHBSESGTDAL-UHFFFAOYSA-N

The toxicity data is as follows:

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
rabbit	LD50	skin	5660uL/kg (5.66mL/kg)		American Industrial Hygiene Association Journal. Vol. 30, Pg. 470, 1969.
rat	LD50	oral	5710mg/kg (5710mg/kg)	BEHAVIORAL: GENERAL ANESTHETIC GASTROINTESTINAL: OTHER CHANGES KIDNEY, URETER, AND BLADDER: OTHER CHANGES	Journal of Industrial Hygiene and Toxicology. Vol. 23, Pg. 259, 1941.

Product Name

3-Methoxy-1-propanol

Synthetic route

3-Methoxy-1-propanol Specification

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