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Butyraldehyde

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Name

Butyraldehyde

EINECS 204-646-6
CAS No. 123-72-8 Density 0.784 g/cm3
PSA 17.07000 LogP 0.98540
Solubility water: 7.1 g/100 mL (25 °C) Melting Point -96 °C
Formula C4H8O Boiling Point 77.6 °C at 760 mmHg
Molecular Weight 72.1069 Flash Point 12°F
Transport Information UN 1129 3/PG 2 Appearance colourless liquid with a very unpleasant smell
Safety 9-29-33 Risk Codes 11
Molecular Structure Molecular Structure of 123-72-8 (Butyraldehyde) Hazard Symbols FlammableF
Synonyms

Butyraldehyde(8CI);Butal;Butaldehyde;Butanaldehyde;Butyl aldehyde;Butyral;Butyricaldehyde;Butyrylaldehyde;NSC 62779;n-Butanal;n-Butyl aldehyde;n-Butyraldehyde;n-Butyric aldehyde;Butanal;

Article Data 1035

Butyraldehyde Synthetic route

71-36-3

butan-1-ol

123-72-8

butyraldehyde

Conditions
ConditionsYield
With oxidase In water at 40℃; for 1.5h; Reformatsky Reaction; Enzymatic reaction;100%
With tetramethylammonium monofluorochromate(VI) In dichloromethane at 20℃; for 2h;98%
With DIQCC In dichloromethane at 20℃; for 0.5h;98%
123-73-9

trans-Crotonaldehyde

123-72-8

butyraldehyde

Conditions
ConditionsYield
palladium on charcoal In hexane100%
With sodium tetrahydroborate; nickel dichloride In methanol; water at 20℃; for 0.25h;75%
With hydrogen; aluminum oxide; titanium-palladium at 100℃;
109-74-0

propyl cyanide

123-72-8

butyraldehyde

Conditions
ConditionsYield
With potassium carbonate In water; dimethyl sulfoxide at 60℃; for 8h; High pressure; Green chemistry;99.9%
Stage #1: propyl cyanide With diisobutylaluminium hydride In toluene at -20℃; for 0.222222h; Flow reactor;
Stage #2: With water; sodium L-tartrate In toluene at 0℃; chemoselective reaction;
64%
With Diisobutylaluminium hydride(1 M solution in tetrahydrofuran, 4.9 mL, 4.9 mmol) In dichloromethane at -78℃; for 1h;
123-73-9

crotonaldehyde

123-72-8

butyraldehyde

Conditions
ConditionsYield
With hydrogen In 1,4-dioxane at 20℃; for 12h;99%
With hydrogen; potassium carbonate In acetone at 20℃; under 760.051 Torr; for 0.25h; Concentration; Reagent/catalyst; chemoselective reaction;99%
With ammonium formate; PdMCM-41 In methanol at 69.84℃; for 1.5h;88%
201230-82-2

carbon monoxide

123-72-8

butyraldehyde

Conditions
ConditionsYield
With tributylphosphine; hydrogen; cobalt(II) acetate In methanol at 85℃; under 63755.1 Torr; for 30h; Irradiation;99%
With tributylphosphine; hydrogen; cobalt(II) acetate In methanol at 85℃; under 63755.1 Torr; for 30h; Product distribution; Irradiation; other educt and product, different catalysts, temperatures times pressures with and without irradiation;99%
With hydrogen; 2,7-bis(SO3Na)-4,5-bis(PPh2)-9,9-Me2-xanthene Rh complex at 100℃; under 9075.91 Torr; for 0.00472222h;95.6%
21303-03-7

butyric acid Li-salt

123-72-8

butyraldehyde

Conditions
ConditionsYield
With 9-borabicyclo[3.3.1]nonane dimer In tetrahydrofuran for 1h; Ambient temperature;97%
111-92-2

dibutylamine

123-72-8

butyraldehyde

Conditions
ConditionsYield
With tert.-butylhydroperoxide In methanol; decane at 60℃; for 2.75h;96%
With zinc dichromate trihydrate at 20℃; grinding; neat (no solvent); chemoselective reaction;92%
With dipotassium peroxodisulfate; sodium carbonate In water for 0.333333h; Rate constant; Irradiation; pH: 11.5, rate constant (k M-1s-1);
29949-17-5

1,1-diacetoxybutane

123-72-8

butyraldehyde

Conditions
ConditionsYield
With 2,6-dicarboxypyridinium chlorochromate In acetonitrile at 20℃; for 0.25h;95%
With N-Bromosuccinimide; water; silica gel at 20℃; for 0.0666667h; neat (no solvent); chemoselective reaction;94%
With cellulose sulfonic acid In acetonitrile at 50℃; for 0.5h;87%
10424-98-3

butanal N,N-dimethylhydrazone

123-72-8

butyraldehyde

Conditions
ConditionsYield
With iron(II) sulfate In chloroform at 20℃; for 0.75h; Hydrolysis;95%
123-73-9

trans-Crotonaldehyde

A

123-72-8

butyraldehyde

B

71-36-3

butan-1-ol

Conditions
ConditionsYield
With (acetylacetonato)dicarbonylrhodium (l); hydrogen In water; toluene at 60℃; under 37503.8 Torr; for 22h; chemoselective reaction;A 94%
B 6%
With bis(1,5-cyclooctadiene)diiridium(I) dichloride; hydrogen In water; toluene at 60℃; under 37503.8 Torr; for 22h; chemoselective reaction;

Butyraldehyde Specification

The Butanal, with the CAS registry number 123-72-8 and EINECS registry number 204-646-6, is the aldehyde derivative of butane. It is a colourless flammable liquid with an acrid smell, and miscible with most organic solvents. The molecular formula of this chemical is C4H8O.

The physical properties of Butanal are as followings: (1)ACD/LogP: 0.91; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.91; (4)ACD/LogD (pH 7.4): 0.91; (5)ACD/BCF (pH 5.5): 2.88; (6)ACD/BCF (pH 7.4): 2.88; (7)ACD/KOC (pH 5.5): 74.13; (8)ACD/KOC (pH 7.4): 74.13; (9)#H bond acceptors: 1; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 2; (12)Polar Surface Area: 17.07 Å2; (13)Index of Refraction: 1.369; (14)Molar Refractivity: 20.76 cm3; (15)Molar Volume: 91.8 cm3; (16)Polarizability: 8.23×10-24cm3; (17)Surface Tension: 22.5 dyne/cm; (18)Density: 0.784 g/cm3; (19)Enthalpy of Vaporization: 31.86 kJ/mol; (20)Boiling Point: 77.6 °C at 760 mmHg; (21)Vapour Pressure: 96 mmHg at 25°C.

Preparation of Butanal: It can be prepared by the catalytic dehydrogenation of n-butanol. And at one time, it was produced industrially by the catalytic hydrogenation of crotonaldehyde, which is derived from acetaldehyde. It is produced almost exclusively by the hydroformylation of propylene
CH3CH=CH2 + H2 + CO → CH3CH2CH2CHO

Uses of Butanal: It is an important intermediate used in plasticizers, synthetic resins, rubber accelerators and pesticides. It is also a kind of important chemical raw material which is used for the preparation of flavor & aromas.

You should be cautious while dealing with this chemical. It is a kind of highly flammable chemical. Therefore, you had better take the following instructions: Keep container in a well-ventilated place; Do not keep the container sealed; Take precautionary measures against static discharges.

You can still convert the following datas into molecular structure:
(1)SMILES: O=CCCC
(2)InChI: InChI=1/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3
(3)InChIKey: ZTQSAGDEMFDKMZ-UHFFFAOYAZ

The toxicity data is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mammal (species unspecified) LC50 inhalation 38gm/m3 (38000mg/m3)   Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(5), Pg. 61, 1986.
mouse LC50 inhalation 44610mg/m3/2H (44610mg/m3)   "Toxicometric Parameters of Industrial Toxic Chemicals Under Single Exposure," Izmerov, N.F., et al., Moscow, Centre of International Projects, GKNT, 1982Vol. -, Pg. 30, 1982.
mouse LD50 intraperitoneal 1140mg/kg (1140mg/kg)   Food and Cosmetics Toxicology. Vol. 17, Pg. 731, 1979.
mouse LD50 subcutaneous 2700mg/kg (2700mg/kg) BEHAVIORAL: GENERAL ANESTHETIC

KIDNEY, URETER, AND BLADDER: HEMATURIA
Acta Pharmacologica et Toxicologica. Vol. 6, Pg. 299, 1950.
rabbit LD50 skin 3560uL/kg (3.56mL/kg)   Union Carbide Data Sheet. Vol. 7/20/1965,
rat LCLo inhalation 8000ppm/4H (8000ppm)   National Technical Information Service. Vol. OTS0516688,
rat LD50 intraperitoneal 800mg/kg (800mg/kg)   Food and Cosmetics Toxicology. Vol. 17, Pg. 731, 1979.
rat LD50 oral 2490mg/kg (2490mg/kg)   National Technical Information Service. Vol. OTS0516688,
rat LD50 subcutaneous 10gm/kg (10000mg/kg) BEHAVIORAL: GENERAL ANESTHETIC Acta Pharmacologica et Toxicologica. Vol. 6, Pg. 299, 1950.

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