Results for:
PubChem ID: 178

Acetamide

Mass-Spectra

Compound Details

Synonymous names
acetamide
60-35-5
Ethanamide
Acetic acid amide
Methanecarboxamide
Acetimidic acid
Ethanimidic acid
Amide C2
Amid kyseliny octove
Caswell No. 003H
Acetimidic acid (VAN)
CCRIS 2
NCI-C02108
HSDB 4006
CH3CONH2
AI3-02060
8XOE1JSO29
DTXSID7020005
CHEBI:27856
MFCD00008023
NSC-25945
acetamid
acetoamide
Amid kyseliny octove [Czech]
EINECS 200-473-5
NSC 25945
UNII-8XOE1JSO29
acetylamine
BRN 1071207
Essigsaeureamid
Ethanamid
imidoacetic acid
N-Methylformamde
Acetamide, >=98%
ACETAMIDE [MI]
ACETAMIDE [FHFI]
ACETAMIDE [HSDB]
ACETAMIDE [IARC]
Lopac-A-0500
bmse000825
bmse000895
DTXCID505
EC 200-473-5
ACETAMIDE [WHO-DD]
Acetamide, sublimed, 99%
WLN: ZV1
Acetic acid amide;Ethanamide
Acetamide, ~99% (GC)
Lopac0_000003
4-02-00-00399 (Beilstein Handbook Reference)
MLS002153504
Acetamide, analytical standard
BIDD:ER0566
CHEMBL16081
GTPL4661
FEMA NO. 4251
Acetamide, crystalline, >=99%
CHEBI:49028
Acetamide, >=98.0% (GC)
Acetamide, >=99.0% (GC)
HMS3260A07
Acetamide (6CI,7CI,8CI,9CI)
BCP26153
HY-Y0946
NSC25945
STR01066
Tox21_300776
Tox21_500003
s6011
STL283915
AKOS000118788
AKOS015917387
CCG-204099
DB02736
LP00003
MCULE-9280264861
SDCCGSBI-0049992.P002
99.8% pound notpurified by sublimation
CAS-60-35-5
Benzeneacetic?acid,?|A-amino-4-methyl-
NCGC00015030-01
NCGC00015030-02
NCGC00015030-03
NCGC00015030-04
NCGC00015030-05
NCGC00015030-06
NCGC00093530-01
NCGC00093530-02
NCGC00254680-01
NCGC00260688-01
SMR000326670
DB-342147
A0007
CS-0015934
EU-0100003
NS00006888
EN300-15608
A 0500
C06244
A832706
Q421721
SR-01000076247
J-523678
SR-01000076247-1
Acetamide, zone-refined, purified by sublimation, 99%
InChI=1/C2H5NO/c1-2(3)4/h1H3,(H2,3,4
Z33546370
F1908-0077
02U
74330-92-0
Microorganism:

Yes

IUPAC nameacetamide
SMILESCC(=O)N
InchiInChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4)
FormulaC2H5NO
PubChem ID178
Molweight59.07
LogP-0.9
Atoms4
Bonds0
H-bond Acceptor1
H-bond Donor1
Chemical Classificationamides nitrogen compounds
CHEBI-ID27856
Supernatural-IDSN0068759

mVOC Specific Details

Boiling Point
DegreeReference
222 °C peer reviewed
Volatilization
The Henry's Law constant for acetamide is estimated as 2.0X10-9 atm-cu m/mole(SRC) derived from its vapor pressure, 0.018 mm Hg(1), and water solubility, 7.05E10+5 mg/L(2). This Henry's Law constant indicates that acetamide is expected to be essentially nonvolatile from water surfaces(3). Acetamide's estimated Henry's Law constant indicates that volatilization from moist soil surfaces is not expected to occur(SRC). Acetamide is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure. Evaporation of acetamide at 20 deg C is reported to be negligible(4).
Literature: (1) ECHA; Search for Chemicals. Acetamide (CAS 60-35-5) Registered Substances Dossier. European Chemical Agency. Available from, as of August 8, 2016: http://echa.europa.eu/ (2) Yalkowsky SH et al; Handbook of Aqueous Solubility Data Second Edition. CRC Press, Boca Raton, FL, p. 35 (2010) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) CDC; International Chemical Safety Cards (ICSC) 2012. Atlanta, GA: Centers for Disease Prevention & Control. National Institute for Occupational Safety & Health (NIOSH). Ed Info Div. Available from, as of August 9, 2016: http://www.cdc.gov/niosh/ipcs/default.html
Soil Adsorption
An experimental Koc of 5 has been reported for acetamide(1). According to a classification scheme(2), this Koc value suggests that acetamide is expected to have very high mobility in soil.
Literature: (1) Schuurmann G et al; Environ Sci Technol 40: 7005-7011 (2006), Supporting Information. Available at, as of August 9, 2016: http://pubs.acs.org/doi/suppl/10.1021/es060152f (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.0182 mm Hg at 25 deg C /OECD Guideline 104 (Vapor Pressure Curve)/ECHA; Search for Chemicals. Acetamide (CAS 60-35-5) Registered Substances Dossier. European Chemical Agency. Available from, as of August 8, 2016: http://echa.europa.eu/
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus Sp.Inhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaStenotrophomonas MaltophiliaInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaAlcaligenes FaecalisInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaArthrobacter NitroguajacolicusInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaLysobacter GummosusInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
ProkaryotaSporosarcina GinsengisoliInhibition of Mycelium growth of Paecilomyces lilacinus and Pochonia chlamydosporia.NAZou et al. 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus Sp.n/an/ano
ProkaryotaStenotrophomonas Maltophilian/an/ano
ProkaryotaAlcaligenes Faecalisn/an/ano
ProkaryotaArthrobacter Nitroguajacolicusn/an/ano
ProkaryotaLysobacter Gummosusn/an/ano
ProkaryotaSporosarcina Ginsengisolin/an/ano