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ChemicalBook--->CAS DataBase List--->5910-85-0

5910-85-0

5910-85-0 Structure

5910-85-0 Structure
IdentificationMore
[Name]

TRANS,TRANS-2,4-HEPTADIENAL
[CAS]

5910-85-0
[Synonyms]

2,4-HEPTADIEN-1-AL
2,4-HEPTADIENAL
FEMA 3164
T2 T4 HEPTADIENAL
TRANS-2,TRANS-4-HEPTADIEN-1-AL
TRANS-2-TRANS-4-HEPTADIENAL
TRANS,TRANS-2,4-HEPTADIEN-1-AL
TRANS,TRANS-2,4-HEPTADIENAL
(E)-2,(Z)-4-heptadienal
(E, Z)-2,4-heptadienal
(E,Z)-Hepta-2,4-dienal
2,4-Heptadienal, (E,Z)-
2,4-Heptadienal, (Z,Z)-
hepta-2,4-dienal
trans,trans-2,4-tIeotadienal
[EINECS(EC#)]

224-328-0
[Molecular Formula]

C7H10O
[MDL Number]

MFCD00007005
[Molecular Weight]

110.15
[MOL File]

5910-85-0.mol
Chemical PropertiesBack Directory
[Boiling point ]

84-84.5 °C(lit.)
[density ]

0.881 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.534(lit.)
[Fp ]

150 °F
[Odor]

Citrus flavors, especially orange and tangerine. Can also be used for mouth feel in a variety of dairy type flavors.green pungent fruity spicy
[Odor Type]

green
[LogP]

1.891 (est)
[CAS DataBase Reference]

5910-85-0(CAS DataBase Reference)
[EPA Substance Registry System]

2,4-Heptadienal (5910-85-0)
Safety DataBack Directory
[Hazard Codes ]

T
[Risk Statements ]

R22:Harmful if swallowed.
R24:Toxic in contact with skin.
R38:Irritating to the skin.
[Safety Statements ]

S36/37:Wear suitable protective clothing and gloves .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

UN 2810 6.1/PG 3
[WGK Germany ]

3
[F ]

10-23
Raw materials And Preparation ProductsBack Directory
[Raw materials]

heptadienoic acid
Hazard InformationBack Directory
[Chemical Properties]

Yellowish liquid. It has a grassy, fat, fruit and spice-like aroma. Flash point 60 ℃. Soluble in ethanol and most non-volatile oils, insoluble in water.
[Uses]

2,4-Heptadienal is mainly used for the preparation of blueberry, raspberry and miscellaneous fruit flavors.
[Definition]

ChEBI: (E,E)-hepta-2,4-dienal is a heptadienal in which the two double bonds are located at positions 2 and 4 (the E,E-geoisomer). It has a role as a flavouring agent.
[Synthesis]

2,4-Heptadienal is synthesized by reducing heptadienoic acid to heptadienol with LiAlH4 and then oxidizing it with MnO2.
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