Butyraldehyde Property

Melting point:

-96 °C

Boiling point:

75 °C(lit.)

Density 

0.817

vapor density 

2.5 (vs air)

vapor pressure 

90 mm Hg ( 20 °C)

refractive index 

n20/D 1.380(lit.)

FEMA 

2219 | BUTYRALDEHYDE

Flash point:

12 °F

storage temp. 

2-8°C

solubility 

water: soluble50g/L at 20°C

form 

Liquid

color 

Clear colorless

PH

6-7 (71g/l, H2O, 20℃)

Odor

Pungent aldehyde; pungent and intense.

PH Range

6-7

Odor Threshold

0.00067ppm

Odor Type

chocolate

explosive limit

1.7-11.1%(V)

Water Solubility 

7.1 g/100 mL (25 ºC)

Sensitive 

Air Sensitive

JECFA Number

86

Merck 

14,1591

BRN 

506061

Exposure limits

No exposure limit is set for n-butyraldehyde.

Dielectric constant

13.4（26℃）

Stability:

Stable. Incompatible with oxidizing agents, strong bases, strong reducing agents, strong acids. Highly flammable.

LogP

1.3 at 20℃ and pH4.4-4.7

Surface tension

70mN/m at 1g/L and 20℃

CAS DataBase Reference

123-72-8(CAS DataBase Reference)

NIST Chemistry Reference

Butanal(123-72-8)

EPA Substance Registry System

Butyraldehyde (123-72-8)

Safety

Hazard Codes 

F

Risk Statements 

11-R11

Safety Statements 

9-29-33-S9-S33-S29-16

RIDADR 

UN 1129 3/PG 2

WGK Germany 

1

RTECS 

ES2275000

F 

13-23

Autoignition Temperature

390 °F

TSCA 

Yes

HS Code 

2912 19 00

HazardClass 

3

PackingGroup 

II

Hazardous Substances Data

123-72-8(Hazardous Substances Data)

Toxicity

Single-dose LD50 orally in rats: 5.89 g/kg (Smyth)

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H225Highly Flammable liquid and vapour

H319Causes serious eye irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

P337+P313IF eye irritation persists: Get medical advice/attention.

P370+P378In case of fire: Use … for extinction.

Butyraldehyde Chemical Properties,Usage,Production

Description

Butanal (N-butyraldehyde) is an organic compound which is the aldehyde derivative of butane. It appeases as a clear liquid. Butyraldehye is used mainly as an intermediate in the production of synthetic resins, rubber vulcanization accelerators, solvents, and plasticizers. It is also an intermediate for the manufacture of pharmaceuticals, crop protection products, pesticides, antioxidants, tanning auxiliaries, and perfumes. Butyraldehyde has a characteristic pungent odor and it is used as a food additive.

References

[1] George A. Burdock, Encyclopedia of Food and Color Additives, Volume 1, 2000
[2] Sunggye Lee, Methane and Its Derivatives, 1997
[3] http://www.solvents.basf.com

Description

Butyraldehyde (butanal, IUPAC) is a water-white liquid with a pungent aldehyde odor. Butyraldehyde is a dangerous fire risk, with a flammable range of 2.5%–12.5% in air. Boiling point is 168°F (75°C), flash point is 10°F (?12°C), and ignition temperature is 446°F (230°C). It is slightly soluble in water, with a specific gravity of 0.8, which is lighter than water. Vapor density is 0.804, which is lighter than air. In addition to flammability, butyraldehyde is corrosive and causes severe eye and skin burns. It may be harmful if inhaled. The four-digit UN identification number is 1129. The NFPA 704 designation is health 3, flammability 3, and reactivity 2. The primary uses of butyraldehyde are in plastics and rubber and as a solvent.

Chemical Properties

Butyraldehyde is a highly flammable, colorless liquid with a pungent odor.

Chemical Properties

colourless liquid with a very unpleasant smell

Chemical Properties

Butyraldehyde has a characteristic pungent odor.

Occurrence

Reported found in the essential oils from flowers, fruits, leaves or bark of Monarda fistulosa L., Litsea cubeba, Bulgarian clary sage, cajeput, Eucalyptus cinerea, E. globules, and others, as well as in apple and strawberry aromas. Also reported found in fresh apple, pears, carrots, peas, soybean, butter, milk, black tea, roast chicken, peanuts, loganberry, honey, white wine and hog plums (Spondias mombins L.).

Uses

n-Butyraldehyde is used to make rubberaccelerators, synthetic resins, and plasticizers;and as a solvent.

Uses

1. Butyraldehyde is an important intermediate. n-Butanol can be prepared by hydrogenation of n-butyraldehyde; 2-ethylhexanol can be prepared by condensation dehydration and then hydrogenation, and n-butanol and 2-ethylhexanol are the main raw materials of plasticizer. Oxidation of n-butyraldehyde can produce n-butyric acid; condensation with formaldehyde can produce trimethylolpropane, which is a plasticizer for synthesizing alkyd resin and raw material for air drying oil; condensation with phenol to produce oil-soluble resin; and urea Condensation can produce alcohol-soluble resin; the products condensed with polyvinyl alcohol; butylamine; The condensate is used as celluloid; resin; solvent for rubber and pharmaceutical products; pharmaceutical industry is used to make "Mianertong"; "pyrimethamine"; methamphetamine, etc. Plasticizers, synthetic resins, rubber accelerators, pesticides and other important intermediate raw materials.
2. Butyraldehyde is an important chemical raw material. It is also used in the preparation of flavors and fragrances. It is contained in various essential oils such as flowers, leaves, fruits, grasses, dairy products, and alcohol in nature. [Food additive usage limit (mg/kg): soft drink 0.71; cold drink 4.8; Candy 2.9; baked goods 5.4; alcohol 0.50; sugar 0.25. ]. It is usually diluted before adding the essence, which has a certain effect on coordinating and increasing the elegance of the top fragrance.
3. Can be used as anesthetic and stimulant.

Uses

Butanal is used in the manufacture of rubber accelerators, synthetic resins, solvents, and plasticizers. n-Butyraldehyde is used as an intermediate in the manufacturing of plasticizers, alcohols, solvents, and polymers (such as 2-ethylhexanol, n-butanol, trimethylolpropane, n-butyric acid, polyvinyl butyral, and methyl amyl ketone). It is also used as an intermediate to make pharmaceuticals, agrochemicals, antioxidants, rubber accelerators, textile auxiliaries, perfumery, and flavors. It has no therapeutic use at the present time.

Uses

Chiefly in the manufacture of rubber accelerators, synthetic resins, solvents, plasticizers.

Preparation

By dry distillation of calcium butyrate and calcium formate.

Definition

ChEBI: A member of the class of butanals that consists of propane bearing a formyl substituent at the 1-position. The parent of the class of butanals.

Aroma threshold values

Detection: 19 to 37 ppb; recognition: 11 to 27 ppb

Taste threshold values

Taste characteristics at 5 ppm: musty, fusel, fermented, bready and yeasty with a malty nuance.

General Description

A clear liquid with a pungent odor. Flash point 20°F. Boiling point 75.7°F (Hawley's). Less dense than water and insoluble in water. Vapors heavier than air.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

A colorless liquid, Butyraldehyde can react with oxidizing materials. In contact with strong acids or bases Butyraldehyde will undergo an exothermic condensation reaction. The dry aldehyde may undergo some polymerization reaction. Reacts vigorously with chlorosulfonic acid, nitric acid, sulfuric acid (oleum). [Sax, 9th ed., 1996, p. 607].

Hazard

Flammable, dangerous fire risk.

Health Hazard

Inhalation will cause irritation and possibly nausea, vomiting, headache, and loss of consciousness. Contact with eyes causes burns. Skin contact may be irritating.

Health Hazard

n-Butyraldehyde is a mild skin and eye irritant.The liquid in 100% pure form producedmoderate irritation on guinea pig skin. Theirritation resulting from 20 mg in 24 hours on rabbit eye was moderate. A higher dosecould produce severe irritation.
Toxicity of n-butyraldehyde is very low.The effect is primarily narcotic. No toxiceffect, however, was observed in mice from 2-hour exposure at a concentration of 44.6 g/m³.At a higher concentration, 174 g/m³ for30 minutes, it exhibited a general anestheticeffect on rats. Subcutaneous administrationof a high dose, >3 g/kg, produced the sameeffect, affecting the kidney and bladder.

Fire Hazard

Behavior in Fire: Vapors are heavier than air and may travel considerable distance to a source of ignition and flash back. Fires are difficult to control due to ease of reignition.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: May occur in the presence of heat, acids or alkalis; Inhibitor of Polymerization: Not pertinent.

Biochem/physiol Actions

Taste at 10 ppm

Safety Profile

Moderately toxic by ingestion, inhalation, skin contact, intraperitoneal, and subcutaneous routes. Severe skin and eye irritant. Human immunologcal effects by inhalation: delayed hypersensitivity. See also ALDEHYDES. Highly flammable liquid. To fight fire, use foam, CO2, dry chemical. Incompatible with oxidzing materials. Reacts vigorously with chlorosulfonic acid, HNO3, oleum, H2SO4. When heated to decomposition it emits acrid smoke and fumes

Potential Exposure

Mutagen,Human Data; Primary Irritant. Used in making syntheticresins, solvents, and plasticizers

First aid

If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR ifheart action has stopped. Transfer promptly to a medicalfacility. When this chemical has been swallowed, get medical attention. Give large quantities of water and inducevomiting. Do not make an unconscious person vomit.Medical observation is recommended for 24
48 h afterbreathing overexposure, as pulmonary edema may bedelayed. As first aid for pulmonary edema, a doctor orauthorized paramedic may consider administering a corticosteroid spray

Carcinogenicity

Although butyraldehyde interacts with DNA, no experimental studies of its carcinogenic potency were found.

Environmental Fate

Butanal does not possess high acute toxicity but is a potent irritant of the skin, eyes, and upper respiratory tract. The mechanism of toxicity probably involves direct reaction between the active aldehyde group and cellular components.

storage

Color Code—Red: Flammability Hazard: Store ina flammable liquid storage area or approved cabinet awayfrom ignition sources and corrosive and reactive materials.Protect against physical damage. Before entering confinedspace where this chemical may be present, check to makesure that an explosive concentration does not exist. Outsideor detached storage is preferred. Prior to working withButyraldehyde you should be trained on its proper handlingand storage. Store in tightly closed containers in a cool,well-ventilated area away from incompatible materialslisted above. Metal containers involving the transfer of thischemical should be grounded and bonded. Drums must beequipped with self-closing valves, pressure vacuum bungs,and flame arresters. Use only nonsparking tools and equipment, especially when opening and closing containers ofthis chemical. Sources of ignition, such as smoking andopen flames, are prohibited where this chemical is used,handled, or stored in a manner that could create a potentialfire or explosion hazard.

Shipping

UN1129 Butyraldehyde, Hazard Class: 3; Labels: 3—Flammable liquid

Toxicity evaluation

The primary degradation process in soil is expected to be biodegradation. A number of biological screening studies have demonstrated that butyraldehyde is readily biodegradable.
The major environmental fate processes for butyraldehyde in water are biodegradation and volatilization. A number of biological screening studies have demonstrated that butyraldehyde is readily biodegradable. Volatilization half-lives of 9 h and 4.1 days have been estimated for a model river (1-m deep) and a model pond, respectively. Aquatic hydrolysis, adsorption to sediment, and bioconcentration are not expected to be important fate processes.

Incompatibilities

May form explosive mixture with air. Butyraldehyde can presumably form explosive peroxides, and may polymerize due to heat or contact with acids or alkalis. Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides, caustics, ammonia, aliphatic amines; alkanolamines, aromatic amines. May accumulate static electrical charges, and may cause ignition of its vapors. Possible self-reaction in air; undergoes rapid oxidation to

Waste Disposal

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.