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ChemicalBook--->CAS DataBase List--->764-39-6

764-39-6

764-39-6 Structure

764-39-6 Structure
IdentificationBack Directory
[Name]

TRANS-2-PENTENAL
[CAS]

764-39-6
[Synonyms]

FEMA 3218
2-Pentanal
2-pentenal
T2 PENTENAL
Pent-2-enal
PENTENE-2-AL
TRANS-2-PENTEN-1-AL
gamma-methylcrotonaldehyde
TRANS-2-PENTENAL USP/EP/BP
[EINECS(EC#)]

212-120-2
[Molecular Formula]

C5H8O
[MDL Number]

MFCD00009615
[MOL File]

764-39-6.mol
[Molecular Weight]

84.12
Chemical PropertiesBack Directory
[Melting point ]

-101.15°C (estimate)
[Boiling point ]

80-81 °C160 mm Hg(lit.)
[density ]

0.86 g/mL at 25 °C(lit.)
[FEMA ]

3218 | 2-PENTENAL
[refractive index ]

n20/D 1.440-1.446(lit.)
[Fp ]

73 °F
[Odor]

at 1.00 % in dipropylene glycol. pungent green apple orange tomato
[Odor Type]

green
[JECFA Number]

1364
[LogP]

1.281 (est)
[EPA Substance Registry System]

2-Pentenal (764-39-6)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

10-36/37/38
[Safety Statements ]

29
[RIDADR ]

UN 1989 3/PG 2
[WGK Germany ]

3
[RTECS ]

SB1560000
[F ]

10
[Toxicity]

msc-ham:lng 300 mmol/L MUREAV 244,153,90
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Acrolein-->Allyl phenyl ether
Hazard InformationBack Directory
[Chemical Properties]

2-Pentenal has a pungent, green, apple, orange, tomato odor.
[Occurrence]

Reported found in aqueous orange essence (trans-form); as a flavor component in cognac oil, in Chrysocoris stolli, in tomato aroma, in the autooxidation of cod liver oil, in peas, as a flavoring component of reverted soybean oil, in salmon oil, in potato chips during storage, in butterfat fishy flavor. Also reported found in strawberry, cooked potato, wheat bread, parmesan cheese, butter, caviar, fatty fish, cooked beef, tea, peanuts, peas, trassi, mango, raspberry, pumpkin, Bourbon vanilla, oysters and loganberry.
[Definition]

ChEBI: An enal consisting of pent-2-ene having an oxo group at the 1-position
[Preparation]

By treating β-phenoxyacrolein with secondary amines, Grignard reagent and active methylene compounds; by heating 1-ethoxy-1,3-pentadiene with H3PO4 at 80°C; from cis- and trans-but-2-ene-1,4-diol and SOCl2, followed by treatment of the chloroalcohol with methyl magnesium bromide and final oxidation with MnO2.
[Safety Profile]

Poison by intraperitoneal route. Mutation data reported. Whenheated to decomposition it emits acrid smoke and irritating fumes.
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