Conditions | Yield |
---|---|
With hydrogen; Rh/Al2O3; molybdenum hexacarbonyl In 1,2-dimethoxyethane at 150℃; under 76000 Torr; for 16h; | 97% |
tridecan-1-ol
Conditions | Yield |
---|---|
With lithium borohydride; sodium hydroxide In isopropyl alcohol Temperature; Jocic Reaction; Heating; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
Stage #1: methyl tridecanoate With bis(acetylacetonato)dioxidomolybdenum(VI); 1,1,3,3-Tetramethyldisiloxane; Triphenylphosphine oxide In toluene at 100℃; for 20h; Inert atmosphere; Sealed tube; Stage #2: With tetrabutyl ammonium fluoride In tetrahydrofuran; toluene for 2h; Inert atmosphere; | 94% |
C18H36O2
tridecan-1-ol
Conditions | Yield |
---|---|
With methanol; toluene-4-sulfonic acid at 20℃; for 2h; | 90% |
(E)-tridec-2-enoic acid
tridecan-1-ol
Conditions | Yield |
---|---|
With hydrogen; Rh/Al2O3; molybdenum hexacarbonyl In 1,2-dimethoxyethane at 150℃; under 76000 Torr; for 16h; | 89% |
1-Methyl-4-(1-methylsulfanyl-tridecane-1-sulfinyl)-benzene
tridecan-1-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In 1,4-dioxane; water Irradiation; | 80% |
ethyl tridecanoate
tridecan-1-ol
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride In diethyl ether at 0 - 20℃; | 79% |
With ethanol; sodium |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
pentadecanol
B
tridecan-1-ol
C
1-Hexadecanol
D
20-hydroxyeicosanoic acid
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 2.8% B 3.5% C 12.6% D 65% |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
tridecan-1-ol
B
1-Tetradecanol
C
1-Hexadecanol
D
20-hydroxyeicosanoic acid
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 3.5% B 6% C 12.6% D 65% |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
tridecan-1-ol
B
1-Tetradecanol
C
tridecyl hexanoate
D
20-hydroxyeicosanoic acid
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 3.5% B 6% C 0.5% D 65% |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
tridecan-1-ol
B
1-Tetradecanol
C
tetradecyl hexanoate
D
20-hydroxyeicosanoic acid
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 3.5% B 6% C 0.6% D 65% |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
tridecan-1-ol
B
1-Tetradecanol
C
20-hydroxyeicosanoic acid
D
n-hexanoic acid 1-hexadecyl
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 3.5% B 6% C 65% D 0.1% |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
tridecan-1-ol
B
1-Tetradecanol
C
20-hydroxyeicosanoic acid
D
hexadecyl hexanoate
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 3.5% B 6% C 65% D 0.25% |
2-(3-carboxypropyl)-5-(12-hydroxydodecyl)thiophene
A
tridecan-1-ol
B
1-Tetradecanol
C
20-hydroxyeicosanoic acid
D
tetradecyl heptanoate
Conditions | Yield |
---|---|
With Raney nickel W-2 In ethanol for 2h; Heating; Further byproducts given; | A 3.5% B 6% C 65% D 0.4% |
C27H40OS2
tridecan-1-ol
Conditions | Yield |
---|---|
With sodium tetrahydroborate In 1,4-dioxane; water Irradiation; | 61% |
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; sodium cyanoborohydride In tert-butyl alcohol; benzene at 90℃; under 60800 Torr; for 3h; | 60% |
Conditions | Yield |
---|---|
With dodecacarbonyl-triangulo-triruthenium; sodium formate; lithium chloride at 150℃; for 24h; Autoclave; Ionic liquid; | A 8.5% B 42% |
formaldehyd
dodecylmagnesium chloride
A
formaldehyde ditridecylacetal
B
tridecan-1-ol
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
With diethyl ether |
Conditions | Yield |
---|---|
at 150℃; und Erwaermen des Reaktionsprodukts mit aethanol.Kalilauge; |
Conditions | Yield |
---|---|
With ethanol; platinum Hydrogenation; |
formaldehyd
diethyl ether
1-chlorododecane
A
formaldehyde ditridecylacetal
B
tridecan-1-ol
Conditions | Yield |
---|---|
Reaktion der Magnesiumverbindung; |
methyl 12-tridecenoate
tridecan-1-ol
Conditions | Yield |
---|---|
(i) H2, Raney-Ni, (ii) LiAlH4, Et2O; Multistep reaction; |
Conditions | Yield |
---|---|
(i) Mg, Et2O, (ii) /BRN= 1209228/; Multistep reaction; |
Conditions | Yield |
---|---|
With water Multistep reaction; |
1,13-tridecanediol
tridecan-1-ol
Conditions | Yield |
---|---|
With lithium triethylborohydride In various solvent(s) for 0.416667h; Thermodynamic data; ΔH; |
Conditions | Yield |
---|---|
With lithium triethylborohydride In various solvent(s) for 0.416667h; Thermodynamic data; ΔH; |
tridecan-1-ol
Conditions | Yield |
---|---|
With hydrogen; platinum(IV) oxide In ethanol for 1h; |
tridecanal
tridecan-1-ol
Conditions | Yield |
---|---|
With ruthenium trichloride; trisodium tris(3-sulfophenyl)phosphine; heptakis(2,6-di-O-methyl)cyclomaltoheptaose; hydrogen; sodium iodide In water; toluene at 80℃; under 22501.8 Torr; for 2.5h; |
tridecan-1-ol
tridecanal
Conditions | Yield |
---|---|
Stage #1: tridecan-1-ol With oxalyl dichloride; dimethyl sulfoxide In dichloromethane at -60℃; for 1.5h; Stage #2: With triethylamine In dichloromethane at -60℃; for 0.5h; | 100% |
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; trichloroisocyanuric acid In diethyl ether at -30℃; for 0.5h; | 95% |
With N-chloro-succinimide; N-(phenylthio)-N-(tert-butyl)amine; potassium carbonate; 4 A molecular sieve In dichloromethane at 20℃; for 1h; | 91% |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In pyridine at 0 - 20℃; for 48h; | 100% |
tridecan-1-ol
1-iodotridecane
Conditions | Yield |
---|---|
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 0.5h; | 98% |
With iodine; triphenylphosphine In dichloromethane at 23℃; for 3h; | 96.3% |
With iodine; 1,2-bis-(diphenylphosphino)ethane In dichloromethane at 25℃; for 2h; | 87% |
With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 0 - 20℃; for 3h; | 84% |
With phosphorus; iodine at 180℃; |
tridecan-1-ol
tridecyl tridecanoate
Conditions | Yield |
---|---|
With iodine; potassium carbonate In tert-butyl alcohol at 20℃; for 41h; | 98% |
Conditions | Yield |
---|---|
Stage #1: carbon disulfide; tridecan-1-ol With triphenylphosphine; diethylazodicarboxylate In dimethyl sulfoxide at 20℃; Stage #2: octanol In dimethyl sulfoxide at 20℃; for 4h; | 98% |
Conditions | Yield |
---|---|
With triphenylphosphine; diethylazodicarboxylate In dimethyl sulfoxide for 4h; | 98% |
sulphomaleic anhydride
tridecan-1-ol
Conditions | Yield |
---|---|
at 70℃; for 1h; | 96% |
5,5-bis-bromomethyl-2,2-dimethyl-[1,3]dioxane
tridecan-1-ol
Conditions | Yield |
---|---|
Stage #1: tridecan-1-ol With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 0.25h; Inert atmosphere; Stage #2: 5,5-bis-bromomethyl-2,2-dimethyl-[1,3]dioxane In N,N-dimethyl-formamide at 120℃; for 15h; Inert atmosphere; | 95% |
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 0 - 20℃; for 18h; Inert atmosphere; | 93% |
Conditions | Yield |
---|---|
Stage #1: tridecan-1-ol With hydrogen at 180 - 200℃; under 6000.6 - 11251.1 Torr; for 1h; Large scale; Stage #2: 6-methylheptylamine With hydrogen at 210 - 220℃; under 6000.6 - 7500.75 Torr; Temperature; Pressure; Large scale; | 92% |
Conditions | Yield |
---|---|
With ammonium hydroxide; iodine at 60℃; for 8h; | 91% |
With ammonium hydroxide; iodine at 60℃; for 8h; | 91% |
Conditions | Yield |
---|---|
With silphos at 20℃; for 0.0833333h; Neat (no solvent); | 90% |
Conditions | Yield |
---|---|
With sodium hydrogencarbonate In toluene at 110℃; for 20h; Inert atmosphere; | 89% |
Conditions | Yield |
---|---|
With carbon tetrabromide In dichloromethane at -30 - 20℃; | 88% |
With hydrogen bromide at 100℃; | |
With hydrogen bromide |
Conditions | Yield |
---|---|
With LACTIC ACID; triethylamine 1.) 4 deg C, 5 d, CH2Cl2; 2.) 4 deg C, 1 d; | 87% |
BOC-glycine
tridecan-1-ol
tridecyl 2-((tert-butoxycarbonyl)amino)acetate
Conditions | Yield |
---|---|
With dmap; 2-chloro-1-methyl-pyridinium iodide In dichloromethane at 0℃; for 0.5h; | 86% |
Conditions | Yield |
---|---|
With iodine; potassium carbonate In tert-butyl alcohol at 20℃; for 24h; | 84% |
Conditions | Yield |
---|---|
With di-isopropyl azodicarboxylate; triphenylphosphine In diethyl ether at 20℃; Mitsunobu reaction; | 84% |
Conditions | Yield |
---|---|
With toluene-4-sulfonic acid In toluene Reflux; | 83.15% |
tridecan-1-ol
3β-chlorocarbonylmercaptocholest-5-ene
Conditions | Yield |
---|---|
With pyridine In diethyl ether; benzene for 4h; Heating; | 80% |
tridecan-1-ol
3-(tert-butyloxycarbonylamino)propionic acid
tridecyl 3-((tert-butoxycarbonyl)amino)propanoate
Conditions | Yield |
---|---|
With dmap; 2-chloro-1-methyl-pyridinium iodide In dichloromethane at 0℃; for 0.5h; | 79% |
ethanol
tridecan-1-ol
acetonitrile
A
diethyl-tridecyl-amine
B
triethylamine
Conditions | Yield |
---|---|
With hydrogen; copper at 240℃; under 7600 Torr; | A 78% B n/a |
Conditions | Yield |
---|---|
With dicyclohexyl-carbodiimide In tetrahydrofuran for 20h; | 77% |
With dicyclohexyl-carbodiimide In tetrahydrofuran for 20h; | 77% |
IUPAC Name: Tridecan-1-ol
Synonyms : N-Tridecanol ; N-Tridecyl alcohol ; Rarechem al bd 0158 ; Tridecanol ; Tridecyl alcohol ; 1-Hydroxytridecane ; C13 linear primary alcohol ; N-Tridecan-1-ol
Product Categories: 1-Alkanols;Biochemistry;Higher Fatty Acids & Higher Alcohols;Monofunctional & alpha,omega-Bifunctional Alkanes;Monofunctional Alkanes;Saturated Higher Alcohols
CAS NO: 112-70-9
Molecular Formula: C13H28O
Molecular Weight: 200.36
Molecular Structure:
EINECS: 203-998-8
BRN : 1739991
Mol File: 112-70-9.mol
Index of Refraction: 1.443
Surface Tension: 30.6 dyne/cm
Density: 0.832 g/cm3
Flash Point: 121.1 °C
Enthalpy of Vaporization: 59.25 kJ/mol
Boiling Point: 272.1 °C at 760 mmHg
Vapour Pressure: 0.000807 mmHg at 25°C
Melting point: 29-34 °C(lit.)
Appearance: 1-Tridecanol (CAS NO.112-70-9) is white low melting solid.
Solubility: 1-Tridecanol (CAS NO.112-70-9) is soluble in alcohol and ether, insoluble in water.
1-Tridecanol (CAS NO.112-70-9) is used raw materials in production of lubricants, surfactants, pesticides, and ink solvents.
1. | skn-rbt 410 mg open MLD | UCDS** Union Carbide Data Sheet. (Industrial Medicine and Toxicology Dept., Union Carbide Corp., 270 Park Ave., New York, NY 10017) 10/14 ,1964. | ||
2. | orl-rat LD50:17,200 mg/kg | NPIRI* Raw Material Data Handbook, Vol.1: Organic Solvents, 1974. 1 (1974),114. | ||
3. | skn-rbt LD50:5600 mg/kg | NPIRI* Raw Material Data Handbook, Vol.1: Organic Solvents, 1974. 1 (1974),114. |
Reported in EPA TSCA Inventory.
Hazard Codes Xi
Risk Statements 36/37/38
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements 26-36
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36:Wear suitable protective clothing.
WGK Germany 3
RTECS YD4200000
1.General Information: As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. During a fire, irritating and highly toxic gases may be generated by thermal decomposition or combustion.
Extinguishing Media: In case of fire, use water, dry chemical, chemical foam, or alcohol-resistant foam.
2.Handling: Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Avoid contact with eyes, skin, and clothing. Avoid ingestion and inhalation.
Storage: Store 1-Tridecanol (CAS NO.112-70-9) in a cool, dry place. Keep container closed when not in use.
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