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Safety Information

518042

Sigma-Aldrich

4-Butylbenzaldehyde

90%

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About This Item

Linear Formula:
CH3(CH2)3C6H4CHO
CAS Number:
1200-14-2
Molecular Weight:
162.23
MDL number:
MFCD00040751
UNSPSC Code:
12352100
PubChem Substance ID:
24873996
NACRES:
NA.22

Assay

90%

refractive index

n20/D 1.522 (lit.)

bp

250-263 °C (lit.)

density

0.968 g/mL at 25 °C (lit.)

SMILES string

CCCCc1ccc(C=O)cc1

InChI

1S/C11H14O/c1-2-3-4-10-5-7-11(9-12)8-6-10/h5-9H,2-4H2,1H3

InChI key

ARIREUPIXAKDAY-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335,H412

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

518042-5G:
518042-VAR:
518042-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
MKBX8765V
MKBJ6992
66996PJ
08705DH
02402CE

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Central linkage influence upon mesomorphic and electrooptical behavior of diaryl nematics. General proton magnetic resonance method employing a lanthanide shift reagent for analysis of isomeric azoxybenzenes.
Rondeau RE, et al.
Journal of the American Chemical Society, 94(4), 1096-1102 (1972)
Francis Giraud et al.
Journal of enzyme inhibition and medicinal chemistry, 24(5), 1067-1075 (2009-06-27)
A new series of 1-benzyl-3-(imidazol-1-ylmethyl)indoles were synthesized according to a previous 3D-QSAR predictive model and assayed for their antiparasitic activity upon Leishmania mexicana promastigotes. The biological results obtained for these twelve molecules showed an IC(50) ranging from 2.3 to 32
Chao-Bin Xue et al.
Bioorganic & medicinal chemistry, 15(5), 2006-2015 (2007-01-30)
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-quinones. Inhibition of PO may provide a basis for novel environmentally friendly

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