Results for:
PubChem ID: 7344

Ethyl 2-hydroxypropanoate

Mass-Spectra

Compound Details

Synonymous names
ETHYL LACTATE
97-64-3
Ethyl 2-hydroxypropanoate
Solactol
Actylol
Acytol
Lactic acid, ethyl ester
Ethyl 2-hydroxypropionate
Propanoic acid, 2-hydroxy-, ethyl ester
Lactate d'ethyle
2-Hydroxypropanoic acid ethyl ester
Lactic Acid Ethyl Ester
Ethyl alpha-hydroxypropionate
FEMA No. 2440
Eusolvan
Ethylester kyseliny mlecne
NSC 8850
DL-Ethyl Lactate
2-Hydroxypropionic Acid Ethyl Ester
Ethyl ester of lactic acid
Ethyl L(-)-lactate
F3P750VW8I
Ethyl .alpha.-hydroxypropionate
DTXSID6029127
CHEBI:78321
NSC-8850
ethyl d-lactate
Ethyl lactate (natural)
Ethyl lactate,C5H10O3,97-64-3
Lactate d'ethyle [French]
HSDB 412
EthylL-(-)-Lactate
Ethylester kyseliny mlecne [Czech]
EINECS 202-598-0
UN1192
BRN 1209448
UNII-F3P750VW8I
ethyl-lactate
AI3-00395
ethyl DL-lactate
Milchsaureathylester
MFCD00065359
Ethyl racemic-lactate
lactic acid ethylester
(S)-(-)-2-Hydroxypropionic acid ethyl ester
PURASOLV ELS
VERTECBIO EL
Lactic acid-ethyl ester
Propanoic acid, 2-hydroxy-, ethyl ester, (S)-
Mono-Ethyl mono-lactate
ETHYL LACTATE [MI]
(.+/-.)-Ethyl lactate
Ethyl 2-hydroxypropanoate #
ETHYL LACTATE [FCC]
SCHEMBL22598
ETHYL LACTATE [FHFI]
ETHYL LACTATE [HSDB]
ETHYL LACTATE [INCI]
4-03-00-00643 (Beilstein Handbook Reference)
ETHYL LACTATE [MART.]
DTXCID509127
WLN: QVY1 & O2
ETHYL LACTATE [WHO-DD]
CHEMBL3186323
(+-)-Ethyl 2-hydroxypropanoate
(+-)-Ethyl 2-hydroxypropionate
FEMA 2440
NSC8850
Tox21_200889
2-hydroxy-propionic acid ethyl ester
Ethyl lactate, >=98%, FCC, FG
AKOS009157222
MCULE-8057202883
UN 1192
(+/-)-LACTIC ACID ETHYL ESTER
CAS-97-64-3
NCGC00248866-01
NCGC00258443-01
(+/-)-ETHYL 2-HYDROXYPROPIONATE
AS-13500
SY030456
DB-057680
A9137
Ethyl lactate, natural, >=98%, FCC, FG
Ethyl lactate, SAJ first grade, >=97.5%
L0003
NS00001187
Ethyl lactate [UN1192] [Flammable liquid]
EN300-115258
A845735
Q415418
J-521263
2-[(4-benzylpiperazin-1-yl)methyl]isoindoline-1,3-dione
(R)-Ethyl D-lactate;(2R)-2-Hydroxypropionic acid ethyl ester
(R)-Ethyl D-lactate ; (2R)-2-Hydroxypropionic acid ethyl ester
Microorganism:

Yes

IUPAC nameethyl 2-hydroxypropanoate
SMILESCCOC(=O)C(C)O
InchiInChI=1S/C5H10O3/c1-3-8-5(7)4(2)6/h4,6H,3H2,1-2H3
FormulaC5H10O3
PubChem ID7344
Molweight118.13
LogP0.2
Atoms8
Bonds3
H-bond Acceptor3
H-bond Donor1
Chemical Classificationalcohols esters
CHEBI-ID78321
Supernatural-IDSN0219329

mVOC Specific Details

Boiling Point
DegreeReference
154 °C peer reviewed
Volatilization
The Henry's Law constant for ethyl lactate is estimated as 5.8X10-7 atm-cu m/mole(SRC) derived from its vapor pressure, 3.75 mm Hg(1), and an assigned value for water solubility of 1X10+6 mg/L (miscible)(2). This Henry's Law constant indicates that ethyl lactate is expected to be essentially nonvolatile from moist soil and water surfaces(3). The potential for volatilization of ethyl lactate from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng., New York, NY: Hemisphere Pub Corp, Vol 4 (1989) (2) Yalkowsky SH, Dannenfelser RM; The AQUASOL DataBase of Aqueous Solubility. Ver 5. Tucson, AZ: Univ AZ, College of Pharmacy (1992) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of ethyl lactate can be estimated to be 1(SRC). According to a classification scheme(2), this estimated Koc value suggests that ethyl lactate is expected to have very high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Aug 24, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
3.75 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaLactobacillus Casein/an/ano
ProkaryotaLactobacillus Plantarumn/an/ano
ProkaryotaPediococcus Damnosusn/an/ano
ProkaryotaLeuconostoc Cremorisn/an/ano
ProkaryotaLeuconostoc Dextranicumn/an/ano
ProkaryotaLactococcus Lactisn/an/ano
ProkaryotaLeuconostoc Mesenteroidesn/an/ano
ProkaryotaLeuconostoc Oenosn/an/ano
ProkaryotaOenococcus Oenin/an/ano
ProkaryotaLentilactobacillus Buchnerimaize silageHS-SPME coupled with GC-TOF MSno
ProkaryotaLacticaseibacillus Paracaseimaize silageHS-SPME coupled with GC-TOF MSno
EukaryotaSaccharomyces Cerevisiaegrape juiceLC-15C HPLCno
Saccharomyces Cerevisiaefermentation of mulberry wineHS-SPME-GC-MSno