Results for:
PubChem ID: 1001

2-phenylethanamine

Mass-Spectra

Compound Details

Synonymous names
Phenethylamine
2-phenylethylamine
2-Phenylethanamine
64-04-0
Benzeneethanamine
2-Phenethylamine
phenylethylamine
beta-phenylethylamine
beta-Phenethylamine
1-Amino-2-phenylethane
beta-Aminoethylbenzene
(2-Aminoethyl)benzene
1-Phenyl-2-aminoethane
2-Amino-1-phenylethane
Ethanamine, 2-phenyl-
Ethylamine, 2-phenyl-
1-Phenyl-2-amino-athan
2-Fenylethylamin
2-Amino-fenylethan
2-Phenylethan-1-Amine
PHENETHYLAMINE, BETA
b-phenylethylamine
2-Fenylethylamin [Czech]
beta-Phenylaethylamin
2-phenyl-d5-ethylamine
2-Amino-fenylethan [Czech]
.beta.-Phenylethylamine
beta-Phenylaethylamin [German]
FEMA No. 3220
2-Aminoethylbenzene
1-Phenyl-2-amino-athan [German]
.beta.-Phenethylamine
NSC 10811
phenethyl-amine
.beta.-Aminoethylbenzene
HSDB 3526
1tnj
1utm
1uto
b-aminoethylbenzene
EINECS 200-574-4
UNII-327C7L2BXQ
MFCD00008184
BRN 0507488
327C7L2BXQ
omega-Phenylethylamine
CHEBI:18397
AI3-03117
.beta.-Phenylaethylamin
.omega.-Phenylethylamine
NSC-10811
CHEMBL610
912627-99-7
DTXSID5058773
EC 200-574-4
PHENETHYLAMINE, HYDROCHLORIDE
beta-phenylaethylamin (german)
phenethyl amine
1-Phenyl-2-amino-athan (GERMAN)
.beta.-Phenylathylaminhydrochlorid
SMR000471837
PHEA
phenethylamin
phenethylarnine
b-phenethylamine
N-phenethylamine
Phenylethyl amine
b-phenylaethylamin
benzene-ethanamine
2-penylethylamine
beta Phenethylamine
2-phenylethaneamine
2-phenylethariamine
2-phenyl-ethylamine
2-phenyl-Ethanamine
2-Phenylethyl amine
N-Benzylmethyl-amine
14C-phenylethylamine
(2-phenylethyl)amine
2-(phenyl)ethylamine
2-Phenylethanamine #
2-(aminoethyl)benzene
Phenethylamine, 99%
Phenethylamine, .beta.
2-Phenethylamine, liquid
Phenethylamine, >=99%
1-Phenyl-2-amino-aethan
SCHEMBL968
bmse000377
PHENETHYLAMINE [MI]
b-phenylaethylamin (german)
WLN: Z2R
PHENETHYLAMINE [FHFI]
MLS001066395
MLS001075768
SCHEMBL330324
GTPL2144
PHENETHYLAMINE [WHO-DD]
DTXCID3044172
BDBM10758
2-PHENYLETHYLAMINE [HSDB]
HMS2267J14
HMS3886K21
AMY39444
NSC10811
STR01455
s5347
STL264196
2-Phenethylamine, analytical standard
2-phenylethanamine (ACD/Name 4.0)
2-phenylethylamine (ACD/Name 4.0)
AKOS000119084
CCG-266078
CS-W011199
DB04325
HY-W010483
MCULE-5305816256
NCGC00163366-01
DB-002852
NS00010853
P0085
C05332
D78532
Q407411
Q-201553
Phenethylamine, purified by redistillation, >=99.5%
60BC7032-7CEC-4B97-B365-EA6E475E6E3C
InChI=1/C8H11N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6-7,9H
Microorganism:

Yes

IUPAC name2-phenylethanamine
SMILESC1=CC=C(C=C1)CCN
InchiInChI=1S/C8H11N/c9-7-6-8-4-2-1-3-5-8/h1-5H,6-7,9H2
FormulaC8H11N
PubChem ID1001
Molweight121.18
LogP1.4
Atoms9
Bonds2
H-bond Acceptor1
H-bond Donor1
Chemical Classificationamines aromatic compounds nitrogen compounds benzenoids
CHEBI-ID18397
Supernatural-IDSN0025482

mVOC Specific Details

Boiling Point
DegreeReference
197.5 °CPhysProp
194.5-195 deg CO'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. 13th Edition, Whitehouse Station, NJ: Merck and Co., Inc., 2001., p. 1296
Volatilization
The Henry's Law constant for 2-phenylethylamine is estimated as 8.1X10-7 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 2-phenylethylamine expected to volatilize slowly from water surfaces(2). Based on this estimated Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 50 days(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 365 days(SRC).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Solubility
Sol in water; freely sol in alc, ether
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. 13th Edition, Whitehouse Station, NJ: Merck and Co., Inc., 2001., p. 1296
Soil Adsorption
The soil/water distribution coefficient (Kd) for 2-phenylethylamine was experimentally determined to be 2.1 in a silty-clay loam soil with an organic carbon content of 1.7%(1), which corresponds to a Koc value of 120(SRC). According to a classification scheme(2), this Koc value suggests that 2-phenylethylamine is expected to have high mobility in soil. The pKa of 2-phenylethylamine is 9.83(3), indicating that this compound will primarily exist in cation form in the environment and cations generally adsorb to organic carbon and clay more strongly than their neutral counterparts(4); however, aliphatic cations are more weakly sorbed than those associated with aromatic ring systems(1).
Literature: (1) Nicholls PH; Organic Contaminants in the Environment. Jones KC, ed. Essex, England: Elsevier Sci Publ Ltd, Chpt 3, p. 95 (1991) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Lide DR, ed; CRC Handbook of Chemistry and Physics, 81st Ed. Boca Raton, FL: CRC Press LLC, p. 8-52 (2000) (4) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals; Boethling RS, Mackay D, eds, Boca Raton, FL: Lewis Publ (2000)
MS-Links
1D-NMR-Links
Massbank-Links
Massbank Spectrum MSBNK-Athens_Univ-AU510901
Massbank Spectrum MSBNK-Athens_Univ-AU510908
Massbank Spectrum MSBNK-Athens_Univ-AU510909
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP002932
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP005862
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP005943
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP008252
Massbank Spectrum MSBNK-Fac_Eng_Univ_Tokyo-JP009400
Massbank Spectrum MSBNK-Keio_Univ-KO003738
Massbank Spectrum MSBNK-Keio_Univ-KO003739
Massbank Spectrum MSBNK-Keio_Univ-KO003740
Massbank Spectrum MSBNK-Keio_Univ-KO003741
Massbank Spectrum MSBNK-Keio_Univ-KO003742
Massbank Spectrum MSBNK-Keio_Univ-KO003793
Massbank Spectrum MSBNK-Keio_Univ-KO003794
Massbank Spectrum MSBNK-Keio_Univ-KO003795
Massbank Spectrum MSBNK-Keio_Univ-KO003796
Massbank Spectrum MSBNK-Keio_Univ-KO003797

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaStaphylococcus Schleifericlinical isolateLemfack et al. 2016
ProkaryotaArthrobacter Globiformisn/aNASchulz and Dickschat 2007
Meyerozyma GuilliermondiiXiong et al. 2023
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaStaphylococcus Schleiferibrain heart infusion mediumPorapak / GC/MSno
ProkaryotaArthrobacter Globiformisn/an/ano
Meyerozyma GuilliermondiiYEPD, 10 g/L yeast extrac, 20 g/L peptone, 20 g dextroseGC-MS and GC-IMSno