Octanal supplier | CasNO.124-13-0

Name
Octanal
EINECS 204-683-8
CAS No. 124-13-0
Article Data514
CAS DataBase
Density 0.821 g/cm³
Solubility Slightly soluble in water
Melting Point 12-15 °C(lit.)
Formula C₈H₁₆O
Boiling Point 194.665 °C at 760 mmHg
Molecular Weight 128.214
Flash Point 81.111 °C
Transport Information UN 1191 3/PG 3
Appearance liquid
Safety 16
Risk Codes 10
Molecular Structure
Hazard Symbols R10:;
Synonyms AldehydeC 8;Antifoam LF;Caprylaldehyde;Caprylic aldehyde;NSC 1508;NSC 8969;Octaldehyde;Octanaldehyde;Octanoic aldehyde;Octylaldehyde;n-Caprylaldehyde;n-Octaldehyde;n-Octanal;n-Octyl aldehyde;n-Octylal;
PSA 17.07000
LogP 2.54580

Synthetic route

: 111-64-8
n-octanoic acid chloride

: 124-13-0
Octanal

Conditions

Conditions	Yield
With methanesulfonic acid; tributylphosphine; copper; zinc In acetonitrile for 1h; Product distribution; Ambient temperature; reactions of other acid chlorides; solvent-effect; effect of var. metals;	100%
With tri-n-butyl-tin hydride In 1-methyl-pyrrolidin-2-one at 20℃; Inert atmosphere;	96%
With pumice stone; platinum at 195℃; under 80 - 90 Torr; Hydrogenation;

: 155127-38-1
((E)-4-Oct-1-enyl)-morpholine

: 124-13-0
Octanal

Conditions

Conditions	Yield
With aq. acid for 1h; Ambient temperature;	100%

: 59092-72-7
2-heptyl-[1,3]dithiane

: 124-13-0
Octanal

Conditions

Conditions	Yield
With silica gel; ferric nitrate In hexane at 50℃; for 0.166667h;	100%
With silica gel; copper(II) nitrate In tetrachloromethane for 0.416667h; Ambient temperature;	98%
With dihydrogen peroxide; tantalum pentachloride; sodium iodide In water; ethyl acetate at 20℃; for 68h;	85%

: 111-87-5
octanol

: 124-13-0
Octanal

Conditions

Conditions	Yield
With chromium (VI) oxide In toluene for 0.416667h; microwave irradiation;	99%
With N-chloro-succinimide; N-(phenylthio)-N-(tert-butyl)amine; potassium carbonate; 4 A molecular sieve In dichloromethane at 20℃; for 3h;	99%
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; oxygen; copper(I) bromide dimethylsulfide complex In chlorobenzene at 80℃; for 8h;	99%

: 111-87-5
octanol

: 33524-31-1
2,5-dimethoxybenzyl alcohol

A: 124-13-0
Octanal

B: 93-02-7
2,5-dimethoxybenzaldehyde

Conditions

Conditions	Yield
With air; potassium carbonate at 20℃; for 16h;	A 2% B 99%

...Expand

: 93215-67-9
octanal 1,3-dithiolane

: 124-13-0
Octanal

Conditions

Conditions	Yield
With silica gel; copper(II) nitrate In tetrachloromethane for 0.25h; Ambient temperature;	98%
With silica gel; ferric nitrate In hexane at 50℃; for 0.166667h;	96%
With bismuth(III) nitrate; water In benzene at 20℃; for 4h;	98 % Chromat.

: 111-66-0
oct-1-ene

: 201230-82-2
carbon monoxide

: 124-13-0
Octanal

Conditions

Conditions	Yield
With (acetylacetonato)dicarbonylrhodium (l); C43H53O8P; hydrogen In toluene under 37503.8 Torr; for 12h; Catalytic behavior; regioselective reaction;	97.1%
With Ca8(PO4)3.5(HPO4)2.5(OH)0.5; hydrogen; Rh2(μ-S-t-Bu)2(CO)2(P(C6H4SO3Na)3)2 In toluene at 80℃; under 3750.38 Torr; for 3h; Product distribution; Further Variations:; Reagents; hydration rate of reagent;	93%

: 929-55-5
octanal oxime

: 124-13-0
Octanal

Conditions

Conditions	Yield
With silica gel; copper(II) nitrate In tetrachloromethane for 1.66667h; Heating;	97%
With ammonium peroxydisulfate; Montmorillonite K10; silver nitrate In hexane at 50℃; for 2.5h;	94%
With water; Dess-Martin periodane In dichloromethane at 5℃; for 0.5h;	92%

: 69873-64-9
4-methyl-N'-octylidenebenzene-1-sulfonohydrazide

: 124-13-0
Octanal

Conditions

Conditions	Yield
With silica gel; copper(II) nitrate In tetrachloromethane for 2h; Heating;	97%

: 111-87-5
octanol

A: 124-13-0
Octanal

B: 2306-88-9
octyl octylate

Conditions

Conditions	Yield
With 5-ethyl-2-methyl-pyridine; 4-acetylamino-2,2,6,6-tetramethylpiperidine-N-oxyl; iodine; sodium hydrogencarbonate In dichloromethane for 1h; Reagent/catalyst;	A 96.6% B 3.4%
With 2,2,6,6-tetramethyl-piperidine-N-oxyl; tert.-butylnitrite; oxygen In 1,2-dichloro-ethane under 1500.15 Torr; for 6h; Autoclave; Heating;	A 94% B 1%
With water; oxygen at 100℃; under 3750.38 Torr; for 18h; Autoclave;	A 9% B 91%

: 629-05-0
n-octyne

: 124-13-0
Octanal

Conditions

Conditions	Yield
With sodium dodecyl-sulfate; [Ru(η5-C9H7(Cl(PPh3)2] In water at 60℃; for 24h;	95%
With chloro(cyclopentadienyl)[bis(diphenylphosphino)methane]ruthenium; water In isopropyl alcohol at 100℃; for 12h;	93%
With borane N,N-diethylaniline complex; dihydrogen peroxide; sodium acetate; benzo[1,3,2]dioxaborole 1.) benzene, 25 deg C, 24 h; Yield given. Multistep reaction;

: 14246-16-3
trimethyl(oct-1-yloxy)silane

: 124-13-0
Octanal

Conditions

Conditions	Yield
With n-butyltriphenylphosphonium peroxodisulfate In acetonitrile for 0.5h; Heating;	95%
With chromium(VI) oxide; HZSM-5 zeolite for 0.025h; microwave irradiation;	93%
With chromium(VI) oxide; Hexamethyldisiloxane; silica gel In dichloromethane for 0.333333h; Ambient temperature;	89%

: 111-86-4
n-Octylamine

: 124-13-0
Octanal

Conditions

Conditions	Yield
Stage #1: n-Octylamine With tungsten(IV) sulfide at 46℃; for 3h; Stage #2: With isobutyl formate for 1.83333h; Temperature; Reflux;	94%
With potassium hydroxide In ethyl acetate at -78℃; Product distribution;	39%
Multi-step reaction with 3 steps 1: 98 percent / Et3N / CH2Cl2 / 1 h / 0 °C 2: N-tert-butylphenylsulfinimidoyl chloride; DBU / CH2Cl2 / 1 h / -78 °C 3: HCl; H2O / diethyl ether; CH2Cl2 / 2 h / 50 °C View Scheme

: 2548-87-0
(E)-2-Octenal

A: 111-87-5
octanol

B: 124-13-0
Octanal

Conditions

Conditions	Yield
With phosphate buffer; D-glucose; Synechococcus sp. PCC 7942; Triton X-100 In water at 25℃; for 72h; pH=7.0; Irradiation;	A 94% B 5%

: 122744-71-2
trans-Dihydro-3-phenyl-5-(phenylmethyl)-6-heptyl-1,2,4,5-trioxazine

A: 124-13-0
Octanal

B: 72552-76-2
α-Heptyl-N-benzylnitrone

C: 65-85-0
benzoic acid

D: 932-90-1
Benzaldoxime

Conditions

Conditions	Yield
With sodium ethanolate In ethanol for 24h; Ambient temperature; other base;	A 18% B 49% C 93% D 20%

...Expand

: 23162-72-3
octylidene diacetate

: 124-13-0
Octanal

Conditions

Conditions	Yield
With H6P2W18O62 In toluene at 100℃; for 0.0833333h;	93%
With sodium tetrahydroborate; nickel(II) chloride hexahydrate In methanol at 20℃; for 3.5h; chemoselective reaction;	86%

: 2548-87-0, 20664-46-4, 2363-89-5
2-octen-1-al

: 124-13-0
Octanal

Conditions

Conditions	Yield
With acetylacetonatodicarbonylrhodium(l); trifluorormethanesulfonic acid; carbon monoxide; N-(5-diphenylphosphanylpyrrole-2-carbonyl)guanidine; hydrogen In dichloromethane at 40℃; under 15001.5 Torr; for 3h; Autoclave; chemoselective reaction;	93%
With hydrogen; tetra-(n-butyl)ammonium iodide In water at 110℃; under 15001.5 Torr; for 24h; chemoselective reaction;	82%
With dibenzylammonium trifluoroacetate salt In dichloromethane at 20℃; for 24h;	82 %Chromat.
With hydrogen; sodium dodecyl-sulfate; palladium diacetate In tetrahydrofuran; water at 20℃; under 750.075 Torr; for 1h; Reagent/catalyst; chemoselective reaction;

: 111-87-5
octanol

A: 124-13-0
Octanal

B: 124-07-2
Octanoic acid

Conditions

Conditions	Yield
With hydrogenchloride; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; sodium nitrite In dichloromethane; water at 20℃; under 760.051 Torr; for 12h; in air;	A 92% B 5.2%
With Succinimide; sodium hypochlorite solution; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; potassium carbonate In ethyl acetate at 0 - 10℃; for 2h;	A 86% B 7%
With potassium chromate; copolyesteramide (from N,N'-bis(4-methoxycarbonylbenzoyl)hexamethylenediamine, 1,6-hexanediol, poly(ethylene glycol)); sulfuric acid In dichloromethane at -5℃; for 0.25h;	A 83% B 2.1%

: 10022-28-3
1,1-dimethoxyoctane

: 124-13-0
Octanal

Conditions

Conditions	Yield
indium(III) chloride In methanol; water for 1.16667h; Heating;	92%
1,3-di(NCS)-tetrabutyldistannoxane In diethylene glycol dimethyl ether; water at 100℃; for 2h; Deprotection of acetal;	85%
With titanium tetrachloride; lithium iodide In diethyl ether for 3h; Product distribution; Ambient temperature;	85%
Tetrabutyl-1,3-diisothiocyanato-distannoxane In diethylene glycol dimethyl ether; water at 100℃; for 2h;	85%

: 35066-22-9
2-bromooctanal

: 124-13-0
Octanal

Conditions

Conditions	Yield
With DMBI In tetrahydrofuran for 5h; Heating;	92%

: 13175-44-5
oct-7-en-1-ol

: 124-13-0
Octanal

Conditions

Conditions	Yield
With potassium hydroxide; PS-resin; potassium hexacyanoferrate(III); 4-(benzyloxycarbonyl)-2,2,6,6-tetramethylpiperidine-1-oxyl In water; toluene at 20℃; for 24h;	92%

: 99178-22-0
N'-octylidene-N,N-dimethyl-hydrazine

: 124-13-0
Octanal

Conditions

Conditions	Yield
With Glyoxilic acid In water at 20℃; for 4h;	91%
tin(ll) chloride; palladium dichloride In water for 0.025h; microwave irradiation;	88%

: 4359-57-3
2-heptyl-1,3-dioxolane

: 124-13-0
Octanal

Conditions

Conditions	Yield
indium(III) chloride In methanol; water for 1.33333h; Heating;	90%
1,3-di(NCS)-tetrabutyldistannoxane In diethylene glycol dimethyl ether; water at 100℃; for 2h; Deprotection of acetal;	87%
Tetrabutyl-1,3-diisothiocyanato-distannoxane In diethylene glycol dimethyl ether; water at 100℃; for 2h;	87%

: 20308-70-7
1-(pyrrolidin-1-yl)nonan-1-one

A: 111-87-5
octanol

B: 124-13-0
Octanal

Conditions

Conditions	Yield
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane for 1h; Ambient temperature; Yield given;	A n/a B 90%
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane for 1h; Ambient temperature; Yields of byproduct given;	A n/a B 90%

: 996-97-4
N,N-diethyloctanamide

A: 111-87-5
octanol

B: 124-13-0
Octanal

Conditions

Conditions	Yield
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane for 1h; Ambient temperature; Yields of byproduct given;	A n/a B 90%
With Li(1+)*C12H28AlO3(1-) In tetrahydrofuran; hexane for 0.5h; Ambient temperature; Yield given. Yields of byproduct given. Title compound not separated from byproducts;

: 3240-34-4
[bis(acetoxy)iodo]benzene

: 63318-32-1
3-methylthio-5-octyl-1,4-diphenyl-1,2,4-triazolium iodide

A: 591-50-4
iodobenzene

B: 124-13-0
Octanal

C: 13136-15-7
1,4-Diphenyl-3-methylmercapto-1,2,4-triazolium iodide

Conditions

Conditions	Yield
With sulfuric acid; iodine; sodium methylate; potassium iodide 1.) CHCl3, 2.) MeOH, room temp, 15 min; Yield given. Multistep reaction;	A 90% B n/a C 31%

...Expand

: 111-83-1
1-bromo-octane

: 124-13-0
Octanal

Conditions

Conditions	Yield
With dimethyl sulfoxide for 0.0638889h; Kornblum oxidation; Microwave irradiation;	89%
With sodium periodate In N,N-dimethyl-formamide at 150℃; for 0.75h;	85%
With sodium hydrogencarbonate; dimethyl sulfoxide; sodium iodide at 115℃; for 2h;	60%
With silver(I) 4-methylbenzenesulfonate; acetonitrile Erhitzen mit Dimethylsulfoxyd und Natriumhydrogencarbonat auf 150grad;
With 4-(dimethylamino)pyridine N-oxide; 1,8-diazabicyclo[5.4.0]undec-7-ene 1.) CH3CN, reflux, 15 min, 2.) CH3CN, reflux, 40 min; Yield given. Multistep reaction;

: 122744-71-2
trans-Dihydro-3-phenyl-5-(phenylmethyl)-6-heptyl-1,2,4,5-trioxazine

A: 124-13-0
Octanal

B: 72552-76-2
α-Heptyl-N-benzylnitrone

C: 100-52-7
benzaldehyde

Conditions

Conditions	Yield
With titanium tetrachloride In dichloromethane for 0.5h; Product distribution; Ambient temperature;	A 44% B 28% C 89%

...Expand

: 54852-64-1
((octyloxy)methyl)benzene

: 124-13-0
Octanal

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; chromium-pillared montmorillonite In 2,2,4-trimethylpentane; dichloromethane for 18h; Ambient temperature;	88%

: 75-52-5
nitromethane

: 124-13-0
Octanal

: 4013-87-0
2-hydroxy-1-nitrononane

Conditions

Conditions	Yield
With potassium tert-butylate In tetrahydrofuran; butan-1-ol at 23℃; Inert atmosphere;	100%
With silica gel; triethylamine at 20℃; for 3h; Henry Nitro Aldol Condensation;	95%
With potassium tert-butylate In tetrahydrofuran; tert-butyl alcohol at 20℃; for 18.5h; Henry reaction;	94%

: 124-13-0
Octanal

: 149-73-5
trimethyl orthoformate

: 10022-28-3
1,1-dimethoxyoctane

Conditions

Conditions	Yield
With lithium tetrafluoroborate In methanol for 0.5h; Heating;	100%
With cerium triflate In methanol at 20℃; for 0.0166667h;	95%
With Pd(PhCN)2(OTf)2 at 20℃; for 0.333333h; Inert atmosphere;	90%

: 867-13-0
diethoxyphosphoryl-acetic acid ethyl ester

: 124-13-0
Octanal

: 7367-88-6
ethyl (E)-2-decenate

Conditions

Conditions	Yield
With n-butyllithium In 1,2-dimethoxyethane; hexane 1.) 0 deg C, 10 min, 2.) 30 min;	100%
Stage #1: diethoxyphosphoryl-acetic acid ethyl ester With sodium hydride In diethyl ether at 0℃; for 0.0833333h; Stage #2: Octanal In diethyl ether for 0.25h;	96%
Stage #1: diethoxyphosphoryl-acetic acid ethyl ester With sodium hydride In diethyl ether; mineral oil at 0℃; Stage #2: Octanal In diethyl ether; mineral oil at 0℃;	96%

: 124-13-0
Octanal

: 59983-39-0
(S)-1-amino-2-(methoxymethyl)pyrrolidine

: 72170-92-4
((S)-2-Methoxymethyl-pyrrolidin-1-yl)-oct-(E)-ylidene-amine

Conditions

Conditions	Yield
at 20℃; for 16h;	100%
Yield given;

: 124-13-0
Octanal

: 7393-43-3
tetraallyl tin

: 13891-96-8
1-undecen-4-ol

Conditions

Conditions	Yield
With hydrogenchloride In tetrahydrofuran at 20℃; for 1h;	100%
With C20H23BBiF4N In methanol; water at 20℃; for 1h;	95%
With C17H18BiF3O5S In methanol at 20℃; for 1h;	92%

: 124-13-0
Octanal

: 593-51-1
methylamine hydrochloride

: 151-50-8
potassium cyanide

: 112101-12-9
2-Methylamino-nonanenitrile

Conditions

Conditions	Yield
With aluminum oxide In acetonitrile at 50℃; for 22h; ultrasound;	100%

...Expand

: 124-13-0
Octanal

: 111-87-5
octanol

Conditions

Conditions	Yield
With hydrogen; Et4N In 1,2-dimethoxyethane at 100℃; under 38000 Torr; for 13h;	100%
With zirconium(IV) tetraisopropoxide 2-propanol; 4 Angstroem MS; 1,1'-bi-2-naphthol In isopropyl alcohol; toluene at 20℃; for 18h;	100%
With zirconium(IV) tetraisopropoxide 2-propanol; 1,1'-bi-2-naphthol In toluene at 20℃; for 1h;	100%

: 930-30-3
cyclopent-2-enone

: 124-13-0
Octanal

: 2-(1-hydroxy-octyl)-cyclopent-2-enone

Conditions

Conditions	Yield
With tributylphosphine; 1,1'-bi-2-naphthol In tetrahydrofuran at 20℃; for 3h; Baylis-Hillman addition;	100%

: 124-13-0
Octanal

: 119-26-6
(2,4-dinitro-phenyl)-hydrazine

: C14H20N4O4

Conditions

Conditions	Yield
	100%

: 124-13-0
Octanal

: 141-05-9
Diethyl maleate

: 73642-72-5
2-Octanoylbutandisaeure-diethylester

Conditions

Conditions	Yield
With 4-cyanobenzaldehyde In Petroleum ether at 20℃; for 16h; Reagent/catalyst; Sealed tube; Irradiation;	100%
With dibenzoyl peroxide
With dibenzoyl peroxide

: 18971-59-0
1-pentylisonitrile

: 124-13-0
Octanal

: 1032198-35-8
C22H43NO3

Conditions

Conditions	Yield
With water; sodium sulfate at 20℃; for 7h; Passerini Condensation;	100%
With air; water at 40℃; for 3h;	71%

: 627-27-0
homoalylic alcohol

: 124-13-0
Octanal

: cis-2-heptyl-4-fluorotetrahydro-2H-pyran

Conditions

Conditions	Yield
With Et4NF*5HF at 20℃; for 0.166667h; Prins reaction; stereoselective reaction;	100%
With Et4NF*5HF at 20℃; for 0.166667h; Prins cyclization; stereoselective reaction;

: 124-13-0
Octanal

: 13891-96-8
1-undecen-4-ol

: 1070331-37-1
cis-4-fluoro-2,6-diheptyltetrahydropyran

Conditions

Conditions	Yield
With Et4NF*5HF at 20℃; for 0.166667h; Prins reaction; stereoselective reaction;	100%
With Et4NF*5HF at 20℃; for 0.166667h; Prins cyclization; stereoselective reaction;

: 124-13-0
Octanal

: 2Br(1-)*C26H32NO2P(2+)

: 7367-88-6
ethyl (E)-2-decenate

Conditions

Conditions	Yield
With potassium carbonate In dichloromethane at 40℃; for 24h; Wittig reaction; Inert atmosphere; optical yield given as %de; diastereoselective reaction;	100%

: 124-13-0
Octanal

: 77-86-1
2-amino-2-hydroxymethyl-1,3-propanediol

: 944882-97-7
C20H39NO3

Conditions

Conditions	Yield
In methanol for 3h; Reflux;	100%

: 124-13-0
Octanal

: ethyl isocyano formate

: 1032198-30-3
C21H39NO5

Conditions

Conditions	Yield
With water; sodium sulfate at 20℃; for 7h; Passerini Condensation;	100%

: 59-48-3
2-oxoindole

: 124-13-0
Octanal

: C16H21NO

Conditions

Conditions	Yield
Reagent/catalyst; Aldol Condensation; Inert atmosphere;	100%

: 124-13-0
Octanal

acetylated chitosan, degree of acetylation 5%: acetylated chitosan, degree of acetylation 5%

methylated acetylated chitosan, degree of acetylation 5%, alkylation 5%: methylated acetylated chitosan, degree of acetylation 5%, alkylation 5%

Conditions

Conditions	Yield
With sodium cyanoborohydride In ethanol; water; acetic acid at 40℃; for 1h; Microwave irradiation;	100%

: 124-13-0
Octanal

acetylated chitosan, degree of acetylation 5%: acetylated chitosan, degree of acetylation 5%

methylated acetylated chitosan, degree of acetylation 5%, alkylation 10%: methylated acetylated chitosan, degree of acetylation 5%, alkylation 10%

Conditions

Conditions	Yield
With sodium cyanoborohydride In ethanol; water; acetic acid at 40℃; for 1h; Temperature; Time; Microwave irradiation;	100%

: 124-13-0
Octanal

acetylated chitosan, degree of acetylation 5%: acetylated chitosan, degree of acetylation 5%

methylated acetylated chitosan, degree of acetylation 5%, alkylation 20%: methylated acetylated chitosan, degree of acetylation 5%, alkylation 20%

Conditions

Conditions	Yield
With sodium cyanoborohydride In ethanol; water; acetic acid at 40℃; for 1h; Temperature; Time; Microwave irradiation;	100%

: 124-13-0
Octanal

acetylated chitosan, degree of acetylation 25%: acetylated chitosan, degree of acetylation 25%

methylated acetylated chitosan, degree of acetylation 25%, alkylation 5%: methylated acetylated chitosan, degree of acetylation 25%, alkylation 5%

Conditions

Conditions	Yield
With sodium cyanoborohydride In ethanol; water; acetic acid at 40℃; for 1h; Microwave irradiation;	100%

: 124-13-0
Octanal

acetylated chitosan, degree of acetylation 25%: acetylated chitosan, degree of acetylation 25%

methylated acetylated chitosan, degree of acetylation 25%, alkylation 10%: methylated acetylated chitosan, degree of acetylation 25%, alkylation 10%

Conditions

Conditions	Yield
With sodium cyanoborohydride In ethanol; water; acetic acid at 40℃; for 1h; Temperature; Time; Microwave irradiation;	100%

: 124-13-0
Octanal

acetylated chitosan, degree of acetylation 25%: acetylated chitosan, degree of acetylation 25%

methylated acetylated chitosan, degree of acetylation 25%, alkylation 20%: methylated acetylated chitosan, degree of acetylation 25%, alkylation 20%

Conditions

Conditions	Yield
With sodium cyanoborohydride In ethanol; water; acetic acid at 40℃; for 1h; Temperature; Time; Microwave irradiation;	100%

: 124-13-0
Octanal

: 1354483-32-1
(1R)-1-C-allyl-2,3,4-tri-O-benzyl-1,5-dideoxy-1,5-imino-D-xylitol

: C37H49NO3

Conditions

Conditions	Yield
With sodium cyanoborohydride; acetic acid In ethanol at 20℃; for 6h;	100%

: 75-75-2
methanesulfonic acid

: 124-13-0
Octanal

: C9H17O3S(1-)*Na(1+)

Conditions

Conditions	Yield
With sodium butanolate In butan-1-ol Reflux;	100%

: 124-13-0
Octanal

: 13086-95-8
1,1-diacetoxy-1-(2-chlorophenyl)methane

: 1-(2-chlorophenyl)-2-oxononyl acetate

Conditions

Conditions	Yield
With 2-(4-methoxyphenyl)-6,7-dihydro-5H-pyrrolo[2,1-c][1,2,4]triazol-2-ium tetrafluoroborate; potassium carbonate In tetrahydrofuran for 24h; Inert atmosphere; Reflux;	100%

: 124-13-0
Octanal

: 944883-07-2
[2-methyl-2-phenyl-1,3-oxazolidin-4-yl]methanol

: 1-aza-3,7-dioxa-2-phenylacetyl-8-octylbicyclo[3.3.0]octane

Conditions

Conditions	Yield
	99.9%

Octanal Chemical Properties

MF: C₈H₁₆O
MW: 128.21
EINECS: 204-683-8
mp： 12-15 °C(lit.)
bp： 171 °C(lit.)
density： 0.822 g/mL at 20 °C
vapor pressure： 2 mm Hg ( 20 °C)
refractive index： n20/D 1.421(lit.)
FEMA： 2797
Fp： 125 °F
storage temp： 0-6°C
Water Solubility ： slightly soluble
Merck： 14,1766
The structure of Octanal is:

Octanal Uses

Octanal is used commercially as a component in perfumes and in flavor production for the food industry.

Octanal Toxicity Data With Reference

1.	skn-rbt 500 mg/24H MLD	FCTXAV Food and Cosmetics Toxicology. 11 (1973),1079.
2.	eye-rbt 100 mg MLD	FCTXAV Food and Cosmetics Toxicology. 11 (1973),1079.
3.	orl-rat LD50:5630 mg/kg	FCTXAV Food and Cosmetics Toxicology. 11 (1973),95.
4.	skn-rbt LD50:6350 mg/kg	FCTXAV Food and Cosmetics Toxicology. 11 (1973),95.

Octanal Consensus Reports

1-OCTANAL is reported in EPA TSCA Inventory.

Octanal Safety Profile

Risk Statements： 10
Safety Statements： 16
RIDADR： UN 1191 3/PG 3
WGK Germany： 2
RTECS： RG7780000
F： 10
HazardClass： 3
PackingGroup： III
Mildly toxic by ingestion and skin contact. A skin and eye irritant. Flammable liquid when exposed to heat, sparks, or flame. Can react with oxidizing materials. To fight fire, use foam, CO₂, dry chemical.

Octanal Specification

1、Fire Fighting Measures
General Information: As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. Will burn if involved in a fire. Flammable liquid and vapor.
Extinguishing Media: In case of fire, use water, dry chemical, chemical foam, or alcohol-resistant foam. Use agent most appropriate to extinguish fire.
2、Handling and Storage
Handling: Use spark-proof tools and explosion proof equipment. Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes. Empty containers retain product residue, (liquid and/or vapor), and can be dangerous. Keep away from heat, sparks and flame.
Storage: Keep away from heat, sparks, and flame. Keep away from sources of ignition. Store in a tightly closed container. Keep refrigerated. (Store below 4°C/39°F.)

Product Name

Octanal

Synthetic route

Octanal Chemical Properties

Octanal Uses

Octanal Toxicity Data With Reference

Octanal Consensus Reports

Octanal Safety Profile

Octanal Specification

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