132152
2,4,5-Trimethoxybenzaldehyde
98%
Synonym(s):
Asaronaldehyde
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About This Item
Linear Formula:
(CH3O)3C6H2CHO
CAS Number:
Molecular Weight:
196.20
Beilstein:
1951403
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
solid
mp
112-114 °C (lit.)
SMILES string
[H]C(=O)c1cc(OC)c(OC)cc1OC
InChI
1S/C10H12O4/c1-12-8-5-10(14-3)9(13-2)4-7(8)6-11/h4-6H,1-3H3
InChI key
IAJBQAYHSQIQRE-UHFFFAOYSA-N
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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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D Dillon et al.
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Several aldehydes and peroxides were tested for mutagenicity using Salmonella typhimurium tester strains TA97a, TA100, TA102 and TA104, in the presence and absence of Aroclor-induced liver S9 mix from F344 rats and B6C3F1 mice, in either preincubation or vapour phase
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Journal of agricultural and food chemistry, 61(38), 9160-9165 (2013-08-13)
The antiproliferation activity of the ethanol extract of A. cinnamomea mycelium on hepatocellular cancer cells HepG2 was found to be associated with aroma intensity of the broth during fermentation. We hypothesized that some of the volatile compounds are the precursors
J J Cypher et al.
Biochemical genetics, 20(3-4), 315-332 (1982-04-01)
The substrate specificities of aldehyde and pyridoxal oxidases in Drosophila melanogaster have been determined with a variety of aliphatic and aromatic aldehydes. This analysis has led to the discovery that 2,4,5-trimethoxybenzaldehyde is a specific substrate for pyridoxal oxidase, as based
D F Qiu et al.
Se pu = Chinese journal of chromatography, 19(5), 461-463 (2003-01-28)
The content ratio of the two isomers in the products of condensation reaction with trimethoxybenzaldehyde as raw material is the key factor to improve the productivity of trimethoprim(TMP). A quantitative method using Nova-Pak C18 column (3.9 mm i.d. x 150
Xiao-Gang Tong et al.
Journal of natural products, 73(6), 1160-1163 (2010-05-19)
A new cadinane-type sesquiterpenoid, tatarinowin A (1), two phenylpropanoids, tatarinoids A (2) and B (3), and a trinorlignan, tatarinoid C (4), along with 15 known compounds including two pairs of mixtures were isolated from the rhizome of Acorus tatarinowii. The
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