4-Propoxybenzaldehyde

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Names

[ CAS No. ]:
5736-85-6

[ Name ]:
4-Propoxybenzaldehyde

[Synonym ]:
4-Propoxybenzaldehyde
Benzaldehyde, 4-propoxy-
MFCD00014134
p-Propoxybenzaldehyde

Chemical & Physical Properties

[ Density]:
1.0±0.1 g/cm3

[ Boiling Point ]:
263.0±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C10H12O2

[ Molecular Weight ]:
164.201

[ Flash Point ]:
118.3±13.4 °C

[ Exact Mass ]:
164.083725

[ PSA ]:
26.30000

[ LogP ]:
2.76

[ Vapour Pressure ]:
0.0±0.5 mmHg at 25°C

[ Index of Refraction ]:
1.531

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
CU7700000
CHEMICAL NAME :
Benzaldehyde, p-propoxy-
CAS REGISTRY NUMBER :
5736-85-6
BEILSTEIN REFERENCE NO. :
0743408
LAST UPDATED :
199701
DATA ITEMS CITED :
5
MOLECULAR FORMULA :
C10-H12-O2
MOLECULAR WEIGHT :
164.22
WISWESSER LINE NOTATION :
VHR DO3

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
1600 uL/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 93,26,1948
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
9 mL/kg
TOXIC EFFECTS :
Skin and Appendages - dermatitis, allergic (after systemic exposure)
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 93,26,1948
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
1800 uL/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 93,26,1948 ** OTHER MULTIPLE DOSE TOXICITY DATA **
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Administration onto the skin
SPECIES OBSERVED :
Rodent - rabbit
DOSE/DURATION :
90 mL/kg/13W-I
TOXIC EFFECTS :
Skin and Appendages - dermatitis, other (after systemic exposure) Related to Chronic Data - death
REFERENCE :
JPETAB Journal of Pharmacology and Experimental Therapeutics. (Williams & Wilkins Co., 428 E. Preston St., Baltimore, MD 21202) V.1- 1909/10- Volume(issue)/page/year: 93,26,1948

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H315-H319-H332-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn: Harmful;Xi: Irritant;

[ Risk Phrases ]:
R22

[ Safety Phrases ]:
S26-S27-S36/37/39

[ RIDADR ]:
UN3334

[ WGK Germany ]:
3

[ RTECS ]:
CU7700000

[ HS Code ]:
2912499000

Synthetic Route

Precursor & DownStream

Precursor

  • 4-allyloxybenzaldehyde
  • 4-hydroxybenzaldehyde
  • 1-Bromopropane
  • 4-Propoxylmandelic acid
  • 1-Propanol
  • 4-Fluorobenzaldehyde
  • 4-(3-bromopropoxy)benzaldehyde
  • 1-Iodopropane
  • Propoxybenzene
  • Aminoform

DownStream

  • N-(4-pentoxyphenyl)-1-(4-propoxyphenyl)methanimine
  • N,1-bis(4-propoxyphenyl)methanimine
  • 4-Propoxylmandelic acid
  • 4-Propoxycinnamic acid
  • N-(4-Propoxybenzylidene)-4-pentylaniline
  • N-(4-ethoxyphenyl)-1-(4-propoxyphenyl)methanimine
  • 1-[(E)-2-nitroethenyl]-4-propoxy-benzene
  • (4-propoxyphenyl)methanol
  • 3-(4-propoxyphenyl)prop-2-enal
  • 3-Chloro-4-propoxybenzaldehyde

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%

Articles

Competitive inhibition of mushroom tyrosinase by 4-substituted benzaldehydes.

J. Agric. Food Chem. 49(8) , 4060-3, (2001)

A kinetic study of the inhibition of mushroom tyrosinase by 4-substituted benzaldehydes showed that these compounds behave as classical competitive inhibitors, inhibiting the oxidation of L-3,4-dihydr...

C-HO and CH (arene) interactions in (2S, 4S, 5R)-(-)-2-(4-propoxyphenyl)-3, 4-dimethyl-5-phenyl-1, 3-oxazolidine. Duffy M, et al.

AZojomo 60(2) , o234-236, (2004)


More Articles


Related Compounds

  • 3-bromo-4-propoxybenzaldehyde
  • 2-Fluoro-4-propoxybenzaldehyde
  • 3-Ethoxy-4-propoxybenzaldehyde
  • 2-ethoxy-4-propoxybenzaldehyde
  • 3-methyl-4-propoxybenzaldehyde
  • 3-Chloro-4-propoxybenzaldehyde
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 4-[(4-Oxo-1-piperidinyl)methyl]benzamide
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • tert-Butyl-DL-alanine
  • 4-amino-N-[2-tert-butyl-1-(tetrahydro-2H-pyran-4-ylmethyl)-1H-benzimidazol-5-yl]-N-ethylbenzenesulfonamide