Results for:
PubChem ID: 1146

N,N-dimethylmethanamine

Mass-Spectra

Compound Details

Synonymous names
Dimethylaminomethylidyneradical
tridimethylaminomethane
Dimethylmethaneamine
trimethylamine
Trimethylamine anhydrous
Trimethylamine solution
trimethylamino
Trimethylamin
Trimethylamine aqueous solution
GETQZCLCWQTVFV-UHFFFAOYSA-N
N-Trimethylamine
tri-methylamine
TRIMETHYL AMINE
trimethyl-amine
Trimethylamine, anhydrous
N,N-dimethylmethanamine
KEN
AC1L1ATW
AC1Q3VWI
N,N-Dimethylmethanamine #
NMe3
Trimethylamine, in aqueous solution
N,N-dimethyl-Methanamine
N,N,N-trimethylamine
GTPL5521
KSC181G2F
Trimethylamine, anhydrous, >=99%
UN1083
UN1297
CTK0I1322
HMDB00906
HSDB 808
LHH7G8O305
Trimethylamine, 1M solution in THF
CHEMBL439723
RL04874
bmse000224
C00565
CCRIS 6283
LTBB001214
Methanamine, N,N-dimethyl-
Methylamine, N,N-dimethyl-
Trimethylamine 2.0M in THF
Trimethylamine, >=99.0%
Trimethylamine, >=99.5%
UNII-LHH7G8O305
(CH3)3N
DTXSID2026238
FEMA Number 3241
LS-1667
METHYL, (DIMETHYLAMINO)-
N(CH3)3
NSC101179
OR034134
OR255230
OR337794
OR337795
STL264242
UN 1083
UN 1297
CHEBI:18139
DSSTox_CID_6238
Trimethylamine, 45% w/w aqueous solution
ZINC8216125
AN-23859
DSSTox_GSID_26238
KB-62087
SC-46821
Trimethylamine solution, 34-36%
Trimethylamine, aqueous solutions not >50% trimethylamine, by mass
BDBM50416499
DSSTox_RID_78071
MFCD00008327
Trimethylamine solution (30% or less)
AI3-15639
NCIOpen2_007868
NSC-101179
RTR-031873
TR-031873
Trimethylamine, 33% w/w in ethanol
AKOS000119986
ZINC112948558
FEMA No. 3241
FT-0660006
75-50-3
Tox21_302355
Trimethylamine solution, 25 wt. % in propylene glycol
F1908-0091
CAS-75-50-3
4558-12-7
MCULE-7903544426
NCGC00255170-01
EINECS 200-875-0
19530-21-3
Trimethylamine solution, 25 wt. % in H2O
Trimethylamine, 45% w/w aqueous solution 500ml
593-81-7 (hydrochloride)
Trimethylamine, anhydrous [UN1083] [Flammable gas]
MolPort-000-883-876
2840-24-6 (hydrobromide)
Hydrogen undecahydrodicarbaundecaborate(1-), compd. with trimethylamine (1:1)
11062-EP2269610A2
11062-EP2269977A2
11062-EP2269989A1
11062-EP2269990A1
11062-EP2269999A1
11062-EP2270011A1
11062-EP2270014A1
11062-EP2270505A1
11062-EP2272491A1
11062-EP2272822A1
11062-EP2272832A1
11062-EP2272834A1
11062-EP2272841A1
11062-EP2275398A1
11062-EP2275411A2
11062-EP2275412A1
11062-EP2275427A1
11062-EP2277848A1
11062-EP2277867A2
11062-EP2280001A1
11062-EP2280003A2
11062-EP2280010A2
11062-EP2281817A1
11062-EP2281821A1
11062-EP2281823A2
11062-EP2284149A1
11062-EP2284160A1
11062-EP2284169A1
11062-EP2284171A1
11062-EP2287147A2
11062-EP2287152A2
11062-EP2287153A1
11062-EP2287155A1
11062-EP2287160A1
11062-EP2287161A1
11062-EP2287162A1
11062-EP2287163A1
11062-EP2289510A1
11062-EP2289891A2
11062-EP2289965A1
11062-EP2292228A1
11062-EP2292576A2
11062-EP2292597A1
11062-EP2292615A1
11062-EP2295402A2
11062-EP2295406A1
11062-EP2295409A1
11062-EP2295414A1
11062-EP2295415A1
11062-EP2295433A2
11062-EP2295437A1
11062-EP2298731A1
11062-EP2298734A2
11062-EP2298742A1
11062-EP2298750A1
11062-EP2298761A1
11062-EP2298772A1
11062-EP2298775A1
11062-EP2298779A1
11062-EP2298828A1
11062-EP2301923A1
11062-EP2301928A1
11062-EP2301929A1
11062-EP2301931A1
11062-EP2301933A1
11062-EP2301935A1
11062-EP2301936A1
11062-EP2302015A1
11062-EP2305219A1
11062-EP2305257A1
11062-EP2305625A1
11062-EP2305636A1
11062-EP2305651A1
11062-EP2305672A1
11062-EP2305673A1
11062-EP2305674A1
11062-EP2305677A1
11062-EP2305678A1
11062-EP2305679A1
11062-EP2305682A1
11062-EP2308839A1
11062-EP2308840A1
11062-EP2308851A1
11062-EP2308854A1
11062-EP2308857A1
11062-EP2308873A1
11062-EP2308875A1
11062-EP2308879A1
11062-EP2311804A2
11062-EP2311808A1
11062-EP2311811A1
11062-EP2311815A1
11062-EP2311827A1
11062-EP2311829A1
11062-EP2311831A1
11062-EP2311834A1
11062-EP2311842A2
11062-EP2314586A1
11062-EP2314590A1
11062-EP2314593A1
11062-EP2316457A1
11062-EP2316458A1
11062-EP2316825A1
11062-EP2316826A1
11062-EP2316827A1
11062-EP2316828A1
11062-EP2316831A1
11062-EP2316836A1
11062-EP2377813A1
11062-EP2380869A1
11062-EP2380870A1
11062-EP2380874A2
28042-EP2301937A1
28042-EP2314588A1
37851-EP2292227A2
37851-EP2298732A1
37851-EP2301913A1
37851-EP2301914A1
37851-EP2311796A1
37851-EP2311797A1
37851-EP2311798A1
37851-EP2311799A1
59622-EP2272846A1
59622-EP2277868A1
59622-EP2277869A1
59622-EP2277870A1
59622-EP2292608A1
59622-EP2308852A1
Trimethylamine, anhydrous [UN1083] [Flammable gas]
Trimethylamine, anhydrous, cylinder, with 316SS needle valve, 99%
148083-EP2280005A1
148083-EP2289884A1
20230-89-1 (hydriodide)
Trimethylamine solution, 25 wt. % in H2O, FG
Trimethylamine solution, 45 wt. % in H2O, FG
Trimethylamine solution, ~45 wt. % in H2O (T)
InChI=1/C3H9N/c1-4(2)3/h1-3H
Trimethylamine, aqueous solutions not >50% trimethylamine, by mass [UN1297] [Flammable liquid]
METHAN-D3-AMINE,N,N-DI(METHYL-D3)- (9CI)
Trimethylamine, aqueous solutions not >50% trimethylamine, by mass [UN1297] [Flammable liquid]
Trimethylamine solution, 31-35 wt. % in ethanol, 4.2 M, contains toluene as stabilizer
Microorganism:

Yes

IUPAC nameN,N-dimethylmethanamine
SMILESCN(C)C
InchiInChI=1S/C3H9N/c1-4(2)3/h1-3H3
Formula(CH3)3N
PubChem ID1146
Molweight59.112
LogP0.19
Atoms13
Bonds12
H-bond Acceptor1
H-bond Donor0
Chemical ClassificationAmines nitrogen compounds

mVOC Specific Details

Volatilization
The Henry's Law constant for trimethylamine is 1.0X10-4 atm-cu m/mole(1). This Henry's Law constant indicates that trimethylamine is expected to volatilize from water surfaces(2). However, trimethylamine is a base with pKa of 9.8(3) and will exist primarily as a cation under environmental conditions (pH 5-9)(SRC). Thus, volatilization of trimethylamine from moist soil and water surfaces will not be an important fate process because cations do not volatilize(SRC). The potential for volatilization of trimethylamine from dry soil surfaces may exist(SRC) based upon a vapor pressure of 1,610 mm Hg(4).
Literature: (1) Christie AO, Crisp DJ; J Appl Chem 17: 11-4 (1967) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Perinn DD; Dissociation Constants of Organic Bases in Aqueous Solution. IUPAC Chem Data Ser: Suppl 1972. London, England: Buttersworth (1972) (4) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng, NY, NY: Hemisphere Pub Corp, 5 Vol (1989)
Soil Adsorption
The Koc of trimethylamine is estimated as 29(SRC), using a log Kow of 0.16(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that trimethylamine is expected to have very high mobility in soil(SRC). However, trimethylamine has a pKa of 9.8(4) and should exist primarily as a cation under environmental conditions (pH 5-9)(SRC). As a result, trimethylamine may have greater adsorption and less mobility than its estimated Koc value indicates since cations generally adsorb more strongly to soils containing organic carbon and clay than neutral species(5). Sorption coefficients for trimethylamine adsorption on montmorillonite, kaolinite and Flax Pond sediment (7% clay, 2.8% OM; Long Island, NY) were 15, 2 and 7 ml/g, respectively(6). The trimethylamine cation adsorbed strongest to the negatively-charged montmorillonite via electrostatic interactions(6).
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 9 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17- 28 (1983) (4) Perrin DD; Dissociation Constants of Organic Bases in Aqueous Solution. IUPAC Chem Data Ser: Suppl 1972. Buttersworth, London (1972) (5) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000) (6) Wang XC, Lee C; Mar Chem 44: 1-23 (1993)
Vapor Pressure
PressureReference
1610 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

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaStaphylococcus AureusRobacker and Flath 1995
BacteriaStreptomycesinduces exploratory growthJones et al. eLife 2017;6:e21738.
FungiTilletia Cariesn/aStotzky and Schenk, 1976
FungiTilletia Controversan/aStotzky and Schenk, 1976
FungiTilletia Foetidan/aStotzky and Schenk, 1976
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaStaphylococcus Aureusno
BacteriaStreptomycesYPD agarGCxGC-TOFMSyes
FungiTilletia Cariesn/an/a
FungiTilletia Controversan/an/a
FungiTilletia Foetidan/an/a