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275-51-4

275-51-4 Structure

275-51-4 Structure
IdentificationMore
[Name]

AZULENE
[CAS]

275-51-4
[Synonyms]

AZULEN
AZULENE
BICYCLO(5.3.0)-DECA-1,3,5,7,9-PENTAENE
BICYCLO[5.3.0]DECAPENTAENE
CYCLOPENTACYCLOHEPTEN
CYCLOPENTACYCLOHEPTENE
LABOTEST-BB LT00007822
Azunamic
Azusalen [as sodium sulfonate]
Bicyclo(0.3.5)deca-1,3,5,7,9-pentaene
Bicyclo(5.3.0)-1,3,5,7,9-decapentaene
BICYCLO(5.3.0)-DECA-2,4,6,8,10-PENTAENE
bicyclo[0.3.5]deca-1,3,5,7,9-pentaene
bicyclo[5.3.0]deca-2,4,6,8,10-pentaene
Soluble azulene
AZULENE OEKANAL
AZULENE, FOR GC
AZULENE OEKANAL 100 MG
Azulene,99%
AZULENE(RG)
[EINECS(EC#)]

205-993-6
[Molecular Formula]

C10H8
[MDL Number]

MFCD00003810
[Molecular Weight]

128.17
[MOL File]

275-51-4.mol
Chemical PropertiesBack Directory
[Appearance]

Blue Crystal
[Melting point ]

98-100 °C(lit.)
[Boiling point ]

242 °C(lit.)
[density ]

1.0530
[refractive index ]

1.5736 (estimate)
[Fp ]

241-243°C
[storage temp. ]

Store at +2°C to +8°C.
[solubility ]

Soluble in organic solvents.
[form ]

Fine Crystalline Powder
[color ]

Dark blue
[Stability:]

Stable. Combustible. Incompatible with strong oxidizing agents.
[Merck ]

14,926
[BRN ]

969517
[InChIKey]

CUFNKYGDVFVPHO-UHFFFAOYSA-N
[LogP]

3.200
[Uses]

azulene is renowned as an anti-inflammatory, calming, and soothing agent. excellent for sensitive skin, azulene is a german chamomile derivative with a characteristic deep blue color. Careful, it stains!
[CAS DataBase Reference]

275-51-4(CAS DataBase Reference)
[EPA Substance Registry System]

Azulene (275-51-4)
Safety DataBack Directory
[Hazard Codes ]

N
[Risk Statements ]

R51/53:Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment .
[Safety Statements ]

S61:Avoid release to the environment. Refer to special instructions safety data sheet .
[RIDADR ]

UN 3077 9/PG 3
[WGK Germany ]

2
[RTECS ]

CO4570000
[F ]

8
[TSCA ]

Yes
[HS Code ]

29029000
[Toxicity]

LD50 orl-rat: >4 g/kg DRUGAY 6,13,82
Hazard InformationBack Directory
[Chemical Properties]

Azulene(275-51-4) is a blue crystalline compound with the chemical formula C10H8 and a melting point of 99°C. It contains afive-membered ring fused to a seven-membered ring and has aromatic properties. When heated it is converted into naphthalene.
[Definition]

ChEBI: A mancude carbobicyclic parent consisting of a cycloheptatriene and cyclopentadiene rings.
[Synthesis Reference(s)]

Journal of the American Chemical Society, 75, p. 2386, 1953 DOI: 10.1021/ja01106a030
Tetrahedron Letters, 23, p. 495, 1982 DOI: 10.1016/S0040-4039(00)86871-9
[Safety Profile]

Poison by intraperitoneal,intravenous, and subcutaneous routes. When heated todecomposition it emits acrid smoke and irritating vapors.
[Source]

Azulene is a natural product and function as pigment in living organisms like plants, fungi etc. This compound was first isolated from the German Chamomile and later from yarrow, wormwood and other plants as oily liquid.
[storage]

Store at -20°C
[Purification Methods]

Crystallise azulene from EtOH. It has UV max 270nm (log 4.72) in hexane. [Platner & Magyar Helv Chim Acta 25 581 1942, Beilstein 5 IV 1636.]
Spectrum DetailBack Directory
[Spectrum Detail]

AZULENE(275-51-4)MS
AZULENE(275-51-4)1HNMR
AZULENE(275-51-4)13CNMR
AZULENE(275-51-4)IR1
AZULENE(275-51-4)IR2
AZULENE(275-51-4)Raman
AZULENE(275-51-4)ESR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Azulene, 99%(275-51-4)
[Alfa Aesar]

Azulene, 99%(275-51-4)
[Sigma Aldrich]

275-51-4(sigmaaldrich)
[TCI AMERICA]

Azulene,>99.0%(GC)(275-51-4)
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