| Identification | More | [Name]
5-Hydroxyvanillin | [CAS]
3934-87-0 | [Synonyms]
3,4-DIHYDROXY-5-METHOXYBENZALDEHYDE
5-hydroxyvanillin
5-METHOXY-3,4-DIHYDROXYBENZALDEHYDE
AKOS BBS-00007007
3,4-dihydroxy-5-methoxy-benzaldehyd
5-methoxy-protocatechualdehyd
5-Methoxyprotocatechualdehyde
Benzaldehyde, 3,4-dihydroxy-5-methoxy-
Protocatechualdehyde, 5-methoxy-
3,4-Dihydroxy-5-methoxybenzaldehdye
3-METHOXY-4,5-DIHYDROXYBENZALDEHYDE
4,5-Dihydroxy-3-methoxybenzaldehyde | [EINECS(EC#)]
223-513-3 | [Molecular Formula]
C8H8O4 | [MDL Number]
MFCD00016610 | [Molecular Weight]
168.15 | [MOL File]
3934-87-0.mol |
| Chemical Properties | Back Directory | [Melting point ]
131-134°C | [Boiling point ]
339.9±37.0 °C(Predicted) | [density ]
1.378±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [form ]
solid | [pka]
7.63±0.23(Predicted) | [color ]
Light grey/ brown | [Cosmetics Ingredients Functions]
HAIR DYEING | [InChI]
InChI=1S/C8H8O4/c1-12-7-3-5(4-9)2-6(10)8(7)11/h2-4,10-11H,1H3 | [InChIKey]
RRKMWVISRMWBAL-UHFFFAOYSA-N | [SMILES]
C(=O)C1=CC(OC)=C(O)C(O)=C1 | [LogP]
1.050 (est) | [CAS DataBase Reference]
3934-87-0(CAS DataBase Reference) | [NIST Chemistry Reference]
3,4-Dihydroxy-5-methoxybenzaldehyde(3934-87-0) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3 | [RTECS ]
CU5620000 | [HS Code ]
2912490090 |
| Hazard Information | Back Directory | [Chemical Properties]
Crystallized. Melting point 130-131°C (132.5-134°C). | [Uses]
3,4-Dihydroxy-5-methoxybenzaldehyde may be used for the preparation of 3,4-dihydroxy-6-methoxy-β-nitrostyrene and 5-hydroxyconiferyl alcohol. | [Synthesis Reference(s)]
Synthetic Communications, 18, p. 507, 1988 DOI: 10.1080/00397918808060744 | [General Description]
3,4-Dihydroxy-5-methoxybenzaldehyde can be obtained by reactting 5-iodovaniliin with sodium hydroxide and copper sulfate solution. | [Synthesis]
The bromination reaction of vanillal and bromine generate 5-bromovanillal, which is then reacted with sodium hydroxide solution under the participation of copper powder to give 5-Hydroxyvanillin. |
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