m-Anisaldehyde

Modify Date: 2024-01-01 17:40:05

m-Anisaldehyde Structure
m-Anisaldehyde structure
Common Name m-Anisaldehyde
CAS Number 591-31-1 Molecular Weight 136.148
Density 1.1±0.1 g/cm3 Boiling Point 230.8±13.0 °C at 760 mmHg
Molecular Formula C8H8O2 Melting Point N/A
MSDS Chinese USA Flash Point 100.2±13.4 °C

 Use of m-Anisaldehyde


m-Anisaldehyde is an endogenous metabolite.

 Names

Name 3-Methoxybenzaldehyde
Synonym More Synonyms

 m-Anisaldehyde Biological Activity

Description m-Anisaldehyde is an endogenous metabolite.
Related Catalog

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 230.8±13.0 °C at 760 mmHg
Molecular Formula C8H8O2
Molecular Weight 136.148
Flash Point 100.2±13.4 °C
Exact Mass 136.052429
PSA 26.30000
LogP 1.65
Vapour Pressure 0.1±0.5 mmHg at 25°C
Index of Refraction 1.547
Water Solubility insoluble

 Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
BZ2605000
CHEMICAL NAME :
m-Anisaldehyde
CAS REGISTRY NUMBER :
591-31-1
BEILSTEIN REFERENCE NO. :
0606013
LAST UPDATED :
199701
DATA ITEMS CITED :
2
MOLECULAR FORMULA :
C8-H8-O2
MOLECULAR WEIGHT :
136.16

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

MUTATION DATA

TYPE OF TEST :
Sister chromatid exchange
TEST SYSTEM :
Human Lymphocyte
DOSE/DURATION :
1 mmol/L
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 206,17,1988

 Safety Information

Personal Protective Equipment Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xi:Irritant
Risk Phrases R36/38
Safety Phrases S26-S36-S37/39
RIDADR NONH for all modes of transport
WGK Germany 3
RTECS BZ2605000
HS Code 29124900

 Synthetic Route

 Customs

HS Code 2912499000
Summary 2912499000. other aldehyde-ethers, aldehyde-phenols and aldehydes with other oxygen function. VAT:17.0%. Tax rebate rate:9.0%. . MFN tariff:5.5%. General tariff:30.0%

 Articles4

More Articles
3D-QSAR and molecular docking studies of benzaldehyde thiosemicarbazone, benzaldehyde, benzoic acid, and their derivatives as phenoloxidase inhibitors.

Bioorg. Med. Chem. 15 , 2006-15, (2007)

Phenoloxidase (PO), also known as tyrosinase, is a key enzyme in insect development, responsible for catalyzing the hydroxylation of tyrosine into o-diphenols and the oxidation of o-diphenols into o-q...

Evidence of13C non-covalent isotope effects obtained by quantitative13C nuclear magnetic resonance spectroscopy at natural abundance during normal phase liquid chromatography

J. Chromatogr. A. 1216(42) , 7043-8, (2009)

Quantitative isotopic 13C NMR at natural abundance has been used to determine the site-by-site 13C/ 12C ratios in vanillin and a number of related compounds eluted from silica gel chromatography colum...

Interesting anticandidal effects of anisic aldehydes on growth and proton-pumping-ATPase-targeted activity.

Microb. Pathog. 51(4) , 277-84, (2011)

Attention has been drawn to evaluate the antifungal activity of p-anisaldehyde (1), o-anisaldehyde (2) and m-anisaldehyde (3). To put forward this approach, antifungal activity has been assessed in th...

 Synonyms

VHR CO1
3-Anisaldehyde
Metamethoxybenzaldehyde
EINECS 209-712-8
3-Methoxybenzaldehyde
3-Methoxy-benzaldehyde
3-Methoxybezaldehyde
m-Methoxybenzaldehyde
MFCD00003361
Benzaldehyde, 3-methoxy-
3-monomethoxybenzaldehyde
META-ANISALDEHYDE
Benzaldehyde,3-methoxy
m-Anisaldehyde
m-OMe benzaldehyde
3-MeO benzaldehyde
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