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O-Acetylvanillin

Names

[ CAS No. ]:
881-68-5

[ Name ]:
O-Acetylvanillin

[Synonym ]:
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

Biological Activity

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
288.5±25.0 °C at 760 mmHg

[ Melting Point ]:
77-79 °C(lit.)

[ Molecular Formula ]:
C10H10O4

[ Molecular Weight ]:
194.184

[ Flash Point ]:
124.9±23.2 °C

[ Exact Mass ]:
194.057907

[ PSA ]:
52.60000

[ LogP ]:
1.10

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.540

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S37

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2915390090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2915390090

[ 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%

Articles

Azlactones and phenylacetic acids derived from the 2-nitro-derivatives of vanillin, isovanillin, and veratraldehyde.

J. Chem. Soc. 174 , 376-8, (1948)

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)

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)


More Articles


Related Compounds

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