Introduction：Basic information about CAS 881-68-5|O-Acetylvanillin, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | O-Acetylvanillin |
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| CAS Number | 881-68-5 | Molecular Weight | 194.184 |
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| Density | 1.2±0.1 g/cm3 | Boiling Point | 288.5±25.0 °C at 760 mmHg |
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| Molecular Formula | C10H10O4 | Melting Point | 77-79 °C(lit.) |
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| MSDS | ChineseUSA | Flash Point | 124.9±23.2 °C |
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Names
| Name | vanillin acetate |
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| Synonym | More Synonyms |
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O-Acetylvanillin BiologicalActivity
| Description | Vanillin acetate is easily synthesized from vanillin by treatment with acetic anhydride[1]. |
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| Related Catalog | Research Areas >>OthersSignaling Pathways >>Others >>Others |
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| References | [1]. Baru, A. R.， et al. The Discovery-Oriented Approach to Organic Chemistry. 6. Selective Reduction in Organic Chemistry: Reduction of Aldehydes in the Presence of Esters Using Sodium Borohydride. Journal of Chemical Education, 82(11), 1674. |
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Chemical & Physical Properties
| Density | 1.2±0.1 g/cm3 |
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| Boiling Point | 288.5±25.0 °C at 760 mmHg |
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| Melting Point | 77-79 °C(lit.) |
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| Molecular Formula | C10H10O4 |
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| Molecular Weight | 194.184 |
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| Flash Point | 124.9±23.2 °C |
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| Exact Mass | 194.057907 |
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| PSA | 52.60000 |
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| LogP | 1.10 |
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| Vapour Pressure | 0.0±0.6 mmHg at 25°C |
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| Index of Refraction | 1.540 |
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| InChIKey | PZSJOBKRSVRODF-UHFFFAOYSA-N |
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| SMILES | COc1cc(C=O)ccc1OC(C)=O |
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Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xi: Irritant; |
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| Risk Phrases | R36/37/38 |
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| Safety Phrases | S26-S37 |
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| RIDADR | NONH for all modes of transport |
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| WGK Germany | 3 |
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| HS Code | 2915390090 |
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Customs
| HS Code | 2915390090 |
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| Summary | 2915390090. esters of acetic acid. VAT:17.0%. Tax rebate rate:13.0%. Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward). MFN tariff:5.5%. General tariff:30.0% |
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Articles3
More Articles
| Azlactones and phenylacetic acids derived from the 2-nitro-derivatives of vanillin, isovanillin, and veratraldehyde. J. Chem. Soc. 174 , 376-8, (1948)
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| The discovery-oriented approach to organic chemistry. 6. Selective reduction in organic chemistry: Reduction of aldehydes in the presence of esters using sodium borohydride. Baru AR and Mohan RS J. Chem. Educ. 82(11) , 1674, (2005)
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| New synthesis of 2, 3-dimethoxy-5-methyl-1, 4-benzoquinone and hexahydrocoenzyme Q4 chromanol. Weinstock LM, et al. J. Chem. Eng. Data 12(1) , 154-55, (1967)
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Synonyms
| EINECS 212-920-1 |
| 4-Acetoxy-3-Methoxybenzaldehyde |
| Vanillin, acetate |
| Vanillin, acetate (8CI) |
| 3-methoxy-4-acetyloxybenzaldehyde |
| 4-ACETYLVANILLIN |
| acetic acid 4-formyl-2-methoxy-phenyl ester |
| 3-Methoxy-4-acetoxybenzaldehyde |
| MFCD00003362 |
| 4-Formyl-2-methoxyphenol acetate |
| Benzaldehyde, 4-(acetyloxy)-3-methoxy- |
| Acetovanillin |
| 4-(Acetyloxy)-3-methoxybenzaldehyde |
| acetyl vanillin |
| 4-Formyl-2-methoxyphenyl acetate |
| 4-O-Acetylvanillin |
| Benzaldehyde, 4- (acetyloxy)-3-methoxy- |
| O-Acetylvanillin |
| Vanillin Acetate |
| FEMA 3108 |
