| Identification | Back Directory | [Name]
2-C-Methyl-D-erythritol | [CAS]
58698-37-6 | [Synonyms]
2-C-Methyl-D-erythritol (2S,3R)-2-Methylbutane-1,2,3,4-tetrol (2S,3R)-2-Methyl-1,2,3,4-butanetetrol 1,2,3,4-Butanetetrol, 2-methyl-, (2S,3R)- (2S,3R)-2-Methyl-1,2,3,4-tetrahydroxybutane | [Molecular Formula]
C5H12O4 | [MDL Number]
MFCD17215928 | [MOL File]
58698-37-6.mol | [Molecular Weight]
136.15 |
| Chemical Properties | Back Directory | [Boiling point ]
368.1±37.0 °C(Predicted) | [density ]
1.341±0.06 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Methanol (Slightly), Water (Slightly) | [form ]
Oil to Gel | [pka]
13?+-.0.29(Predicted) | [color ]
White to Brown | [biological source]
(Carum ajowan fruit) | [BRN ]
5916602 | [Stability:]
Hygroscopic | [InChI]
1S/C5H12O4/c1-5(9,3-7)4(8)2-6/h4,6-9H,2-3H2,1H3/t4-,5+/m1/s1 | [InChIKey]
HGVJFBSSLICXEM-UHNVWZDZSA-N | [SMILES]
C[C@](O)(CO)[C@H](O)CO |
| Hazard Information | Back Directory | [Uses]
(2S,?3R)?-2-?Methyl-1,?2,?3,?4-?butanetetrol is a secondary organic aerosol formed through photooxidation of isoprene. It was identified as a glucide in methanol extracts of Carum ajowan fruit. | [General Description]
(2S,3R)-2-methylbutane-1,2,3,4-tetrol was identified as a glucide in methanol extracts of Carum ajowan fruit. | [Biochem/physiol Actions]
Metabolite of the non-mevalonate MEP pathway, generally found in prokaryotes, as precursor to isoprenoids as well as non-isoprenoids like vitamins. As this pathway is not present in humans, it is of interest for the development of bacterium-specific drugs in the search for treatments of infectious diseases. |
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