ChemicalBook > CAS DataBase List > Phenylpropyl aldehyde

Phenylpropyl aldehyde

Product Name
Phenylpropyl aldehyde
CAS No.
104-53-0
Chemical Name
Phenylpropyl aldehyde
Synonyms
3-PHENYLPROPANAL;HYDROCINNAMALDEHYDE;Benzenepropanal;3-PHENYLPROPIONALDEHYDE;HYDROZIMTALDEHYD;3-PHENYL-1-PROPANAL;Dihydrocinnamaldehyde;NSC 9271;FEMA 2887;Hydrocinnamide
CBNumber
CB3143311
Molecular Formula
C9H10O
Formula Weight
134.18
MOL File
104-53-0.mol
More
Less

Phenylpropyl aldehyde Property

Melting point:
-42 °C
Boiling point:
97-98 °C/12 mmHg (lit.)
Density 
1.019 g/mL at 25 °C (lit.)
vapor pressure 
15 hPa (98 °C)
FEMA 
2887 | 3-PHENYLPROPIONALDEHYDE
refractive index 
n20/D 1.523(lit.)
Flash point:
203 °F
storage temp. 
Store below +30°C.
solubility 
0.74mg/l
form 
Liquid
color 
Clear colorless to light yellow
Odor
at 10.00 % in dipropylene glycol. fresh cortex green leaf foliage balsam storax
Odor Type
green
biological source
synthetic
Water Solubility 
Miscible with chloroform, dichloromethane, ethyl acetate, alcohol and ether. Immiscible with water.
Sensitive 
Air Sensitive
JECFA Number
645
BRN 
1071910
InChIKey
YGCZTXZTJXYWCO-UHFFFAOYSA-N
LogP
2.04
CAS DataBase Reference
104-53-0(CAS DataBase Reference)
NIST Chemistry Reference
3-Phenylpropanal(104-53-0)
EPA Substance Registry System
Benzenepropanal (104-53-0)
More
Less

Safety

Hazard Codes 
Xi
Risk Statements 
36/38-36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
2
RTECS 
MW4890000
10-23
Autoignition Temperature
245 °C DIN 51794
TSCA 
Yes
HS Code 
29122900
Toxicity
LD50 orally in Rabbit: > 5000 mg/kg LD50 dermal Rabbit > 5000 mg/kg
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P405Store locked up.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.04542
Product name
3-Phenylpropionaldehyde
Purity
for synthesis
Packaging
100mL
Price
$86.8
Updated
2025/07/31
Sigma-Aldrich
Product number
393193
Product name
Hydrocinnamaldehyde
Purity
technical grade, 90%
Packaging
100ml
Price
$116.85
Updated
2025/07/31
TCI Chemical
Product number
P0217
Product name
3-Phenylpropionaldehyde
Purity
>93.0%(GC)
Packaging
25g
Price
$55
Updated
2025/07/31
TCI Chemical
Product number
P0217
Product name
3-Phenylpropionaldehyde
Purity
>93.0%(GC)
Packaging
100g
Price
$183
Updated
2025/07/31
TRC
Product number
P336050
Product name
3-Phenylpropanal
Packaging
5g
Price
$175
Updated
2021/12/16
More
Less

Phenylpropyl aldehyde Chemical Properties,Usage,Production

Chemical Properties

Pale Yellow Oil

Chemical Properties

Phenylpropyl aldehyde occurs in Sri Lanka cinnamon bark oil, among others. The aldehyde is a colorless liquid with a strong, floral, slightly balsamic, heavy hyacinth-like odor. It tends to undergo self-condensation. Dihydrocinnamaldehyde can be obtained with scarcely any byproducts by selective hydrogenation of cinnamaldehyde. It is used in perfumery for hyacinth and lilac compositions.

Chemical Properties

3-Phenylpropionaldehyde has a strong, pungent, floral odor reminiscent of hyacinth with a balsamic, green, warm (almost burning) flavor.

Occurrence

Reported found in the essential oil of Ceylon cinnamon and in strawberry. Also reported found in tomato, cinnamon, cassia leaf, Gruyere de Comte cheese, beer, cooked trassi, origanum (Spanish) and strawberry.

Uses

3-Phenylpropanal (cas# 104-53-0) is a compound useful in organic synthesis.

Definition

ChEBI: 3-phenylpropanal is a benzene which is substituted by a 3-oxopropyl group at position 1. It has a role as a flavouring agent and a plant metabolite. It is an aldehyde and a member of benzenes. It is functionally related to a benzene.

Production Methods

Henylpropyl aldehyde is most commonly prepared by the partial hydrogenation of cinnamaldehyde. The 3-phenylpropanal that is formed during the hydroformylation of styrene can be separated from the isomeric 2-phenylpropanal as the bisulfite adduct. The Rosenmund reduction of dihydrocinnamoyl chloride in the presence of Pd/BaSO4 gives good yields of the aldehyde. The reaction of 2-propen-1-ol and phenylmercury chloride with CuCl2 and LiPdCl4 catalysts in methanol, and the reaction of phenyl bromide and allyl alcohol in the presence of PdCl2 and NaHCO3 in nonpolar solvents also lead to the formation of 3-phenylpropanal.

Preparation

From phenyl propionitrile; also from cinnamic aldehyde diethylacetal.

Taste threshold values

Taste characteristics at 20 ppm: green, melon, fruity and citrus.

Synthesis Reference(s)

Chemical and Pharmaceutical Bulletin, 42, p. 1041, 1994 DOI: 10.1248/cpb.42.1041
Tetrahedron Letters, 35, p. 1275, 1994 DOI: 10.1016/0040-4039(94)88042-5

General Description

Hydrocinnamaldehyde is C=C double bond hydrogenated cinnamaldehyde. It has been synthesized by the selective hydrogenation of C=C double bond of cinnamaldehyde by various methods. Hydrocinnamaldehyde and nitromethane undergoes Henry reaction to form nitroaldols. The C1 and C3 position labelled with 13C of hydrocinnamaldehyde was subjected to mass spectrometry and the fragmentation pattern was elucidated.

Biological Activity

Taste at 20 ppm

Phenylpropyl aldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Phenylpropyl aldehyde Suppliers

HBCChem, Inc.
Tel
+1-510-219-6317
Fax
+1-650-486-1361
Email
sales@hbcchem.com
Country
United States
ProdList
10648
Advantage
60
AbaChemScene
Tel
732-484-9848
Fax
888-484-5008
Email
sales@chemscene.com
Country
United States
ProdList
3982
Advantage
60
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
Advantage
58
Alchem Pharmtech,Inc.
Tel
8485655694
Email
sales@alchempharmtech.com
Country
United States
ProdList
63687
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
52923
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Aceschem Inc.
Tel
+1-817863-6948 +1-(817)863-6948
Email
sales@aceschem.com
Country
United States
ProdList
19632
Advantage
58
Frontier Scientific Services, Inc.
Tel
--
Fax
--
Email
customerservice@frontierssi.com
Country
United States
ProdList
1575
Advantage
0
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Penta Manufacturing Company (a division of Penta International Corporation)
Tel
--
Fax
--
Email
@pentamfg.com
Country
United States
ProdList
901
Advantage
58
Lluch Essence S.L.
Tel
--
Fax
--
Email
web@lluche.com
Country
United States
ProdList
2352
Advantage
58
Augustus Oils Ltd
Tel
--
Fax
--
Email
essentials@augustus-oils.ltd.uk
Country
United States
ProdList
1404
Advantage
58
VWR International, LLC.
Tel
--
Fax
--
Email
@sargentwelch.com
Country
United States
ProdList
6262
Advantage
58
Oakwood Products, Inc.
Tel
--
Fax
--
Email
sales@oakwoodchemical.com
Country
United States
ProdList
6193
Advantage
74
Vigon International, Inc.
Tel
--
Fax
--
Email
jpassamonte@vigoninternational.com
Country
United States
ProdList
1268
Advantage
64
Ernesto Ventós S.A.
Tel
--
Fax
--
Email
info@ventos.com
Country
United States
ProdList
2257
Advantage
58
Excellentia International
Tel
--
Fax
--
Email
info@excellentiaint.com
Country
United States
ProdList
567
Advantage
58
PerfumersWorld Ltd.
Tel
--
Fax
--
Email
pwenquiries@perfumersworld.com
Country
United States
ProdList
723
Advantage
58
Pell Wall Perfumes
Tel
--
Fax
--
Email
//pellwall.com/contact-us/
Country
United States
ProdList
559
Advantage
58
Berje Inc.
Tel
--
Fax
--
Email
tlauzurica@berjeinc.com
Country
United States
ProdList
958
Advantage
58
M&U International LLC
Tel
--
Fax
--
Email
sales@mu-intel.com
Country
United States
ProdList
2011
Advantage
58
Penta International Corporation
Tel
--
Fax
--
Email
lisaa@pentamfg.com
Country
United States
ProdList
5042
Advantage
58
Alfrebro LLC/ Archer Daniels Midland Company
Tel
--
Fax
--
Email
sforbis@alfrebro.com
Country
United States
ProdList
768
Advantage
58
Vigon International
Tel
--
Fax
--
Email
sales@vigon.com
Country
United States
ProdList
1776
Advantage
58
R C Treatt and Co Ltd
Tel
--
Fax
--
Email
enquiries@treatt.com
Country
United States
ProdList
1690
Advantage
58
Beijing Lys Chemicals Co, LTD.
Tel
--
Fax
--
Email
jiayanyong@lyschem.com
Country
United States
ProdList
710
Advantage
58
WholeChem, LLC
Tel
--
Fax
--
Email
info@wholechem.com
Country
United States
ProdList
814
Advantage
58
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Matrix Scientific
Tel
--
Fax
--
Email
sales@matrixscientific.com
Country
United States
ProdList
6632
Advantage
80
HBCChem Inc.
Tel
--
Fax
--
Email
sales@hbcchem-inc.com
Country
United States
ProdList
4569
Advantage
30
BroadPharm. Inc.
Tel
--
Fax
--
Email
sales@broadpharm.com
Country
United States
ProdList
891
Advantage
50
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
AlliChem, LLC
Tel
--
Fax
--
Email
sales@allichemllc.com
Country
United States
ProdList
6516
Advantage
60
ChemService Inc.
Tel
--
Fax
--
Country
United States
ProdList
6379
Advantage
68
Medical Isotopes
Tel
--
Fax
--
Email
stohler@medicalisotopes.com
Country
United States
ProdList
6181
Advantage
68
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Leonid Chemicals Private Limited
Tel
--
Fax
--
Email
careers@leonidchemicals.com
Country
United States
ProdList
1700
Advantage
43
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
APAC Pharmaceutical, LLC
Tel
--
Fax
--
Email
sales@apacpharma.com
Country
United States
ProdList
6322
Advantage
38
MP Biomedicals, Inc.
Tel
--
Fax
--
Country
United States
ProdList
6561
Advantage
81
American Custom Chemicals Corporation
Tel
--
Fax
--
Email
sales@acccorporation.com
Country
United States
ProdList
6820
Advantage
51
ASDI Incorporated
Tel
--
Fax
--
Email
customerservice@asdi.net
Country
United States
ProdList
6922
Advantage
67
Beta Pharma, Inc.
Tel
--
Fax
--
Email
sales@betapharma.com
Country
United States
ProdList
6226
Advantage
60
Alfa Aesar
Tel
--
Fax
--
Email
tech@alfa.com
Country
United States
ProdList
6814
Advantage
81
ChemPacific Corporation
Tel
--
Fax
--
Email
sales@chempacific.com
Country
United States
ProdList
6891
Advantage
51
Eastern Chemical Corp.
Tel
--
Fax
--
Email
eastern@u-g.com
Country
United States
ProdList
2786
Advantage
34
More
Less

View Lastest Price from Phenylpropyl aldehyde manufacturers

Hebei Chuanghai Biotechnology Co., Ltd
Product
Phenylpropyl aldehyde 104-53-0
Price
US $10.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
100 mt
Release date
2024-11-15
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Phenylpropyl aldehyde 104-53-0
Price
US $45.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 tons
Release date
2024-12-02
Hebei Chuanghai Biotechnology Co,.LTD
Product
Phenylpropyl aldehyde 104-53-0
Price
US $9.00/KG
Min. Order
1KG
Purity
99.8%
Supply Ability
100tons
Release date
2024-08-23

104-53-0, Phenylpropyl aldehydeRelated Search:


  • TIMTEC-BB SBB006730
  • PHENYLPROPYL ALDEHYDE
  • 3-Phenylpropanaldehyde
  • NSC 9271
  • PHENYLPROPYL ALDEHYDE ( 3-PHENYLPROPIONALDEHYDE )
  • 3-Phenylprpanal
  • Hydrocinnamaldehyde,3-Phenylpropionaldehyde
  • 3-Phenylpropionaldehyde, 95% 5GR
  • 3-PHENYLPROPIONALDEHYDE FOR SYNTHESIS
  • 3-Phenylpropionaldehyde,97%
  • 3-Phenylpropionaldehyde,95%
  • Hydrocinnamaldehyde technical grade, 90%
  • 2-acetamido-3-(5-bromo-1H-indol-3-yl)propanoic acid
  • 3-Phenylpropan-1-al
  • Benzenepropanal
  • Dihydrocinnamaldehyde
  • Phenylpropionaldehyde
  • Propionaidehyde, 3-phenyl-
  • 3-PHENYL-1-PROPANAL
  • 3-PHENYLPROPANAL
  • 3-PHENYLPROPYL ALDEHYDE
  • 3-PHENYLPROPIONALDEHYDE
  • BETA-PHENYLPROPIONALDEHYDE
  • BENZYLACETALDEHYDE
  • DIHYDRO CINNAMIC ALDEHYDE
  • HYDROCINNAMALDEHYDE
  • HYDROCINNAMIC ALDEHYDE
  • FEMA 2887
  • HYDROCINNAMALDEHYDE, TECH., 90%
  • HYDROCINNAMALDEHYDE 90+% FCC
  • 3-Phenylpropionaldehyd
  • HYDROZIMTALDEHYD
  • Hydrocinnamide
  • 3-Phenylpropionaldehyde&gt
  • Phenylpropyl aldehyde USP/EP/BP
  • Benzenepropanal (9CI, ACI)
  • Phenyl Propionic Aldehyde 1600003
  • Phenyl Propanal
  • Imidafenacin Impurity 23
  • p-tert-Butylphenylpropionaldehyde
  • 3-Phenylpropioldehyde
  • 104-53-0
  • 9032-75-3
  • C6H5CH22CHO
  • CH3CHC6H5CHO
  • C6H5CH2CH2CHO
  • ALDEHYDE
  • Building Blocks
  • Carbonyl Compounds
  • C9
  • Aldehydes
  • Organic Building Blocks
  • Aromatics
  • Aromatics Compounds
  • Aroma Chemicals