ChemicalBook--->CAS DataBase List--->123-72-8

123-72-8

123-72-8 Structure

123-72-8 Structure
IdentificationMore
[Name]

Butyraldehyde
[CAS]

123-72-8
[Synonyms]

ALDEHYDE C4
BUTAL
BUTALDEHYDE
BUTANAL
BUTYL ALDEHYDE
BUTYRAL
BUTYRALDEHYDE
BUTYRIC ALDEHYDE
FEMA 2219
N-BUTANAL
N-BUTYL ALDEHYDE
N-BUTYRALDEHYDE
1-Butanal
1-propanecarbaldehyde
Aldehyde butyrique
aldehydebutyrique
aldehydebutyrique(french)
Aldeide butirrica
aldeidebutirrica
Butalyde
[EINECS(EC#)]

204-646-6
[Molecular Formula]

C4H8O
[MDL Number]

MFCD00007023
[Molecular Weight]

72.11
[MOL File]

123-72-8.mol
Chemical PropertiesBack Directory
[Appearance]

Butyraldehyde is a highly flammable, colorless liquid with a pungent odor.
[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)
[FEMA ]

2219
[refractive index ]

n20/D 1.380(lit.)
[Fp ]

12 °F
[storage temp. ]

Flammables area
[solubility ]

water: soluble50g/L at 20°C
[form ]

Liquid
[color ]

Clear colorless
[Odor]

Pungent aldehyde; pungent and intense.
[PH]

6-7 (71g/l, H2O, 20℃)
[PH Range]

6-7
[Stability:]

Stable. Incompatible with oxidizing agents, strong bases, strong reducing agents, strong acids. Highly flammable.
[explosive limit]

1.7-11.1%(V)
[Odor Threshold]

0.00067ppm
[Odor Type]

chocolate
[Water Solubility ]

7.1 g/100 mL (25 ºC)
[Sensitive ]

Air Sensitive
[JECFA Number]

86
[Merck ]

14,1591
[BRN ]

506061
[Dielectric constant]

13.4(26℃)
[Exposure limits]

No exposure limit is set for n-butyraldehyde.
[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 DataBack Directory
[Hazard Codes ]

F
[Risk Statements ]

R11:Highly Flammable.
[Safety Statements ]

S9:Keep container in a well-ventilated place .
S29:Do not empty into drains .
S33:Take precautionary measures against static discharges .
[RIDADR ]

UN 1129 3/PG 2
[WGK Germany ]

1
[RTECS ]

ES2275000
[F ]

13-23
[Autoignition Temperature]

390 °F
[TSCA ]

Yes
[HazardClass ]

3
[PackingGroup ]

II
[HS Code ]

29121900
[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
[Hazardous Substances Data]

123-72-8(Hazardous Substances Data)
[Toxicity]

Single-dose LD50 orally in rats: 5.89 g/kg (Smyth)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

PROPYLENE-->Isobutyraldehyde-->2-Amino-3-chlorobenzoic acid-->Phosphine-->Calcium formate-->Cobalt carbonyl-->CALCIUM BUTYRATE
[Preparation Products]

1-Butanol-->2-Methyl-1-propanol-->Butyric Acid-->Isobutyraldehyde-->2-Ethylhexanol-->2-Ethylhexanoic acid-->(6-ETHYL-THIENO[2,3-D]PYRIMIDIN-4-YLAMINO)-ACETIC ACID-->(6-ETHYL-4-OXO-4H-THIENO[2,3-D]PYRIMIDIN-3-YL)-ACETIC ACID-->Quinaldine-->2-(CHLOROMETHYL)-6-ETHYLTHIENO[2,3-D]PYRIMIDIN-4(3H)-ONE-->4-CHLORO-6-ETHYLTHIENO[2,3-D]PYRIMIDINE-->6-ethylthieno[2,3-d]pyrimidin-4(3H)-one-->Trimethylolpropane-->2-Ethylacrylaldehyde-->3-HEPTEN-2-ONE-->2-AMINO-5-ETHYL-THIOPHENE-3-CARBOXYLIC ACID METHYL ESTER-->ETHYL 2-AMINO-5-ETHYLTHIOPHENE-3-CARBOXYLATE-->Benzyl isobutyrate-->1,3-Butanediol-->3-Methoxy-1-butanol-->CIS-3-HEXENOIC ACID-->trans-3-Hexenoic acid-->PVB-->2-Ethyl-1,3-hexanediol-->trans-2-Hexenoic acid
Hazard InformationBack Directory
[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.
[Reactivity Profile]

A colorless liquid, BUTYRALDEHYDE(123-72-8) can react with oxidizing materials. In contact with strong acids or bases BUTYRALDEHYDE(123-72-8) 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].
[Air & Water Reactions]

Highly flammable. Insoluble in water.
[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.
[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.
[First aid]

If this chemical gets into the eyes, remove any contact lenses at once and irrigate immediately for at least 15 minutes, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts the skin, remove contaminated clothing and wash immediately with soap and water. Seek medical attention immediately. If this chemical has been inhaled, remove from exposure, begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and CPR if heart action has stopped. Transfer promptly to a medical facility. When this chemical has been swallowed, get medical attention. Give large quantities of water and induce vomiting. Do not make an unconscious person vomit. Medical observation is recommended for 24 to 48 hours after breathing overexposure, as pulmonary edema may be delayed. As
[Shipping]

UN1129 Butyraldehyde, Hazard Class: 3; Labels: 3—Flammable liquid
[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
[Chemical Properties]

Butyraldehyde has a characteristic pungent odor.
[Chemical Properties]

Butyraldehyde is a highly flammable, colorless liquid with a pungent odor.
[Chemical Properties]

colourless liquid with a very unpleasant smell
[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.
[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]

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.
[Uses]

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

By dry distillation of calcium butyrate and calcium formate.
[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.
[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
[Potential Exposure]

Mutagen,Human Data; Primary Irritant. Used in making syntheticresins, solvents, and plasticizers
[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.
[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.
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

butyraldehyde(123-72-8).msds
Questions And AnswerBack Directory
[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
Spectrum DetailBack Directory
[Spectrum Detail]

Butyraldehyde(123-72-8)MS
Butyraldehyde(123-72-8)1HNMR
Butyraldehyde(123-72-8)13CNMR
Butyraldehyde(123-72-8)IR1
Butyraldehyde(123-72-8)IR2
Butyraldehyde(123-72-8)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Butyraldehyde, contains less than 1% butyric acid, 99+%(123-72-8)
[Alfa Aesar]

Butyraldehyde, 99%(123-72-8)
[Sigma Aldrich]

123-72-8(sigmaaldrich)
[TCI AMERICA]

Butyraldehyde,>98.0%(GC)(123-72-8)
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