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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-06 21:02:23 UTC
Update Date2021-09-14 15:18:10 UTC
HMDB IDHMDB0028763
Secondary Accession Numbers
  • HMDB28763
Metabolite Identification
Common NameAspartyl-Threonine
DescriptionAspartyl-Threonine is a dipeptide composed of aspartate and threonine. It is an incomplete breakdown product of protein digestion or protein catabolism. Some dipeptides are known to have physiological or cell-signaling effects although most are simply short-lived intermediates on their way to specific amino acid degradation pathways following further proteolysis. This dipeptide has not yet been identified in human tissues or biofluids and so it is classified as an 'Expected' metabolite.
Structure
Data?1582753337
Synonyms
ValueSource
Asp-THRHMDB
Aspartate threonine dipeptideHMDB
Aspartate-threonine dipeptideHMDB
AspartylthreonineHMDB
D-T DipeptideHMDB
DT DipeptideHMDB
L-Aspartyl-L-threonineHMDB
2-[(2-Amino-3-carboxy-1-hydroxypropylidene)amino]-3-hydroxybutanoateHMDB
Chemical FormulaC8H14N2O6
Average Molecular Weight234.2066
Monoisotopic Molecular Weight234.08518619
IUPAC Name2-(2-amino-3-carboxypropanamido)-3-hydroxybutanoic acid
Traditional Name2-(2-amino-3-carboxypropanamido)-3-hydroxybutanoic acid
CAS Registry NumberNot Available
SMILES
CC(O)C(NC(=O)C(N)CC(O)=O)C(O)=O
InChI Identifier
InChI=1S/C8H14N2O6/c1-3(11)6(8(15)16)10-7(14)4(9)2-5(12)13/h3-4,6,11H,2,9H2,1H3,(H,10,14)(H,12,13)(H,15,16)
InChI KeyNTQDELBZOMWXRS-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as dipeptides. These are organic compounds containing a sequence of exactly two alpha-amino acids joined by a peptide bond.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassCarboxylic acids and derivatives
Sub ClassAmino acids, peptides, and analogues
Direct ParentDipeptides
Alternative Parents
Substituents
  • Alpha-dipeptide
  • Aspartic acid or derivatives
  • N-acyl-alpha-amino acid
  • N-acyl-alpha amino acid or derivatives
  • Alpha-amino acid amide
  • Alpha-amino acid or derivatives
  • Beta-hydroxy acid
  • Short-chain hydroxy acid
  • Dicarboxylic acid or derivatives
  • Fatty amide
  • Hydroxy acid
  • N-acyl-amine
  • Fatty acid
  • Fatty acyl
  • Amino acid or derivatives
  • Secondary carboxylic acid amide
  • Amino acid
  • Secondary alcohol
  • Carboxamide group
  • Carboxylic acid
  • Organic nitrogen compound
  • Alcohol
  • Organooxygen compound
  • Organic oxygen compound
  • Carbonyl group
  • Organopnictogen compound
  • Primary amine
  • Organic oxide
  • Organonitrogen compound
  • Hydrocarbon derivative
  • Amine
  • Primary aliphatic amine
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogP-4.73Extrapolated
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility24.9 g/LALOGPS
logP-3.4ALOGPS
logP-4.9ChemAxon
logS-0.97ALOGPS
pKa (Strongest Acidic)3.01ChemAxon
pKa (Strongest Basic)8.53ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area149.95 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity49.79 m³·mol⁻¹ChemAxon
Polarizability21.35 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+153.9831661259
DarkChem[M-H]-147.27831661259
DeepCCS[M+H]+147.43930932474
DeepCCS[M-H]-144.98330932474
DeepCCS[M-2H]-180.43930932474
DeepCCS[M+Na]+155.98830932474
AllCCS[M+H]+151.332859911
AllCCS[M+H-H2O]+148.032859911
AllCCS[M+NH4]+154.432859911
AllCCS[M+Na]+155.332859911
AllCCS[M-H]-147.532859911
AllCCS[M+Na-2H]-148.232859911
AllCCS[M+HCOO]-148.932859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Aspartyl-ThreonineCC(O)C(NC(=O)C(N)CC(O)=O)C(O)=O3302.0Standard polar33892256
Aspartyl-ThreonineCC(O)C(NC(=O)C(N)CC(O)=O)C(O)=O1786.2Standard non polar33892256
Aspartyl-ThreonineCC(O)C(NC(=O)C(N)CC(O)=O)C(O)=O2189.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Aspartyl-Threonine,1TMS,isomer #1CC(O[Si](C)(C)C)C(NC(=O)C(N)CC(=O)O)C(=O)O2070.7Semi standard non polar33892256
Aspartyl-Threonine,1TMS,isomer #2CC(O)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C)C(=O)O2095.8Semi standard non polar33892256
Aspartyl-Threonine,1TMS,isomer #3CC(O)C(NC(=O)C(N)CC(=O)O)C(=O)O[Si](C)(C)C2057.2Semi standard non polar33892256
Aspartyl-Threonine,1TMS,isomer #4CC(O)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C)C(=O)O2095.2Semi standard non polar33892256
Aspartyl-Threonine,1TMS,isomer #5CC(O)C(C(=O)O)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C2102.3Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #1CC(O[Si](C)(C)C)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C)C(=O)O2098.5Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O)N[Si](C)(C)C)[Si](C)(C)C2185.3Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #11CC(O)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2287.8Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #2CC(O[Si](C)(C)C)C(NC(=O)C(N)CC(=O)O)C(=O)O[Si](C)(C)C2084.4Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #3CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C)C(=O)O2129.2Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #4CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C2151.4Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #5CC(O)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2099.7Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #6CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)C(=O)O2153.6Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #7CC(O)C(C(=O)O)N(C(=O)C(N)CC(=O)O[Si](C)(C)C)[Si](C)(C)C2082.6Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #8CC(O)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C2141.4Semi standard non polar33892256
Aspartyl-Threonine,2TMS,isomer #9CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C2101.3Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #1CC(O[Si](C)(C)C)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C)C(=O)O[Si](C)(C)C2109.4Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2161.7Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #11CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2303.2Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #12CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N[Si](C)(C)C)[Si](C)(C)C2175.3Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #13CC(O)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2303.1Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #14CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2326.4Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #2CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)C(=O)O2140.2Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #3CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(N)CC(=O)O[Si](C)(C)C)[Si](C)(C)C2117.7Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #4CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C)C(=O)O[Si](C)(C)C2129.0Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #5CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C2124.5Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #6CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O)N[Si](C)(C)C)[Si](C)(C)C2218.1Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #7CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2279.8Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #8CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C2149.1Semi standard non polar33892256
Aspartyl-Threonine,3TMS,isomer #9CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC(=O)O[Si](C)(C)C)[Si](C)(C)C2086.8Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #1CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C2152.5Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #1CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)C(=O)O[Si](C)(C)C2174.3Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2292.5Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2303.4Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #11CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2305.5Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #11CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2288.9Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #2CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC(=O)O[Si](C)(C)C)[Si](C)(C)C2138.5Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #2CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(N)CC(=O)O[Si](C)(C)C)[Si](C)(C)C2177.3Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #3CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2179.2Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #3CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2227.3Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #4CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2296.7Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #4CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O2261.2Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #5CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N[Si](C)(C)C)[Si](C)(C)C2198.3Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #5CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N[Si](C)(C)C)[Si](C)(C)C2220.7Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #6CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2290.8Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #6CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2263.0Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #7CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2349.9Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #7CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2296.4Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #8CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2151.2Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #8CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2205.8Standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #9CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2294.1Semi standard non polar33892256
Aspartyl-Threonine,4TMS,isomer #9CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2243.5Standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #1CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2193.6Semi standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #1CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N[Si](C)(C)C)[Si](C)(C)C2264.2Standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #2CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2279.0Semi standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #2CC(O[Si](C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)C(=O)O[Si](C)(C)C2302.1Standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #3CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2321.9Semi standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #3CC(O[Si](C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2351.1Standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #4CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2330.1Semi standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #4CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2343.6Standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #5CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2295.7Semi standard non polar33892256
Aspartyl-Threonine,5TMS,isomer #5CC(O)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2335.6Standard non polar33892256
Aspartyl-Threonine,6TMS,isomer #1CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2355.1Semi standard non polar33892256
Aspartyl-Threonine,6TMS,isomer #1CC(O[Si](C)(C)C)C(C(=O)O[Si](C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[Si](C)(C)C2394.1Standard non polar33892256
Aspartyl-Threonine,1TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(N)CC(=O)O)C(=O)O2295.9Semi standard non polar33892256
Aspartyl-Threonine,1TBDMS,isomer #2CC(O)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O2334.9Semi standard non polar33892256
Aspartyl-Threonine,1TBDMS,isomer #3CC(O)C(NC(=O)C(N)CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C2313.7Semi standard non polar33892256
Aspartyl-Threonine,1TBDMS,isomer #4CC(O)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)C(=O)O2332.1Semi standard non polar33892256
Aspartyl-Threonine,1TBDMS,isomer #5CC(O)C(C(=O)O)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C(C)(C)C2355.1Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O2546.9Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2627.7Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #11CC(O)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O2685.0Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #2CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(N)CC(=O)O)C(=O)O[Si](C)(C)C(C)(C)C2545.7Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #3CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)C(=O)O2567.6Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #4CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C(C)(C)C2580.9Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #5CC(O)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2558.0Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #6CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O2600.4Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #7CC(O)C(C(=O)O)N(C(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2549.3Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #8CC(O)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2586.6Semi standard non polar33892256
Aspartyl-Threonine,2TBDMS,isomer #9CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C(C)(C)C2559.8Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2757.9Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2828.9Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #11CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O2958.5Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #12CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2834.2Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #13CC(O)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2949.4Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #14CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2949.5Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #2CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O2811.5Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #3CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2787.9Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #4CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2809.7Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #5CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC(=O)O)[Si](C)(C)C(C)(C)C2790.2Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #6CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2852.2Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #7CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O2945.9Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #8CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2814.7Semi standard non polar33892256
Aspartyl-Threonine,3TBDMS,isomer #9CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2750.5Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2992.8Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2867.4Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3165.5Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #10CC(O)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2960.2Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #11CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3177.8Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #11CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2938.4Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #2CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2977.7Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #2CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(N)CC(=O)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2899.8Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #3CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3035.8Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #3CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2906.2Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #4CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O3182.8Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #4CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O2934.3Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #5CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3043.3Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #5CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2904.2Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #6CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3179.3Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #6CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2912.9Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #7CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3216.4Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #7CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2934.4Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #8CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3013.0Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #8CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C2908.6Standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #9CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3178.1Semi standard non polar33892256
Aspartyl-Threonine,4TBDMS,isomer #9CC(O)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C2925.2Standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3204.9Semi standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #1CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3109.4Standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #2CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3385.3Semi standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #2CC(O[Si](C)(C)C(C)(C)C)C(NC(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)C(=O)O[Si](C)(C)C(C)(C)C3134.1Standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #3CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3406.3Semi standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #3CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3169.0Standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #4CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3402.7Semi standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #4CC(O[Si](C)(C)C(C)(C)C)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3155.7Standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #5CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3353.3Semi standard non polar33892256
Aspartyl-Threonine,5TBDMS,isomer #5CC(O)C(C(=O)O[Si](C)(C)C(C)(C)C)N(C(=O)C(CC(=O)O[Si](C)(C)C(C)(C)C)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C3176.4Standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Aspartyl-Threonine GC-MS (Non-derivatized) - 70eV, Positivesplash10-000i-9300000000-c53354a73e3f405fe79c2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspartyl-Threonine GC-MS (3 TMS) - 70eV, Positivesplash10-000i-9201000000-e72ab9f1e6ae877ca0fc2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspartyl-Threonine GC-MS (TMS_3_14) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspartyl-Threonine GC-MS (TBDMS_3_14) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspartyl-Threonine GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspartyl-Threonine GC-MS ("Aspartyl-Threonine,3TMS,#14" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 10V, Positive-QTOFsplash10-014j-1690000000-90eeb27bcb808cdd83472017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 20V, Positive-QTOFsplash10-0fki-8920000000-352eacdb0a8803bcdcb42017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 40V, Positive-QTOFsplash10-006x-9100000000-a8fad084f95f87d7d7452017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 10V, Negative-QTOFsplash10-00li-0960000000-002a4d62ca94c379582d2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 20V, Negative-QTOFsplash10-00yr-0910000000-6790996438db9c4f03902017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 40V, Negative-QTOFsplash10-00di-9800000000-f3972ba1ee961afb5dce2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 10V, Positive-QTOFsplash10-00kr-0690000000-c09349aeade2ddc29a092021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 20V, Positive-QTOFsplash10-01b9-4900000000-566f080870e5aea2ea652021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 40V, Positive-QTOFsplash10-0g4i-9500000000-b23c30273a3a53391b252021-10-11Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 10V, Negative-QTOFsplash10-001i-0490000000-0e7e93187da1aed077122021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 20V, Negative-QTOFsplash10-0g7i-4900000000-951315ebd6d4def7dd852021-10-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspartyl-Threonine 40V, Negative-QTOFsplash10-0006-9200000000-e6232c882576ad216bea2021-10-12Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB111816
KNApSAcK IDNot Available
Chemspider ID14986881
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound64896714
PDB IDNot Available
ChEBI ID174200
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available