Chemistry:Isopropylmalic acid

Isopropylmalic acid

2-Isopropylmalic acid
3-Isopropylmalic acid
Names
IUPAC names 3-Isopropylmalic acid 2-Hydroxy-3-isopropylsuccinic acid
Other names Isopropylmalate
Identifiers
CAS Number	(2): 3237-44-3 N (3): 16048-89-8 N
3D model (JSmol)	(2): Interactive image (3): Interactive image
ChEBI	(2): CHEBI:28635 (3): CHEBI:35114
ChemSpider	(2): 76 (3): 35
DrugBank	(3): DB04279
EC Number	(2): 630-924-5
PubChem CID	(2): 77 (3): 36
UNII	(3): 29405QVM5W
CompTox Dashboard (EPA)	(3): DTXSID30274257
InChI (2): InChI=1S/C7H12O5/c1-4(2)7(12,6(10)11)3-5(8)9/h4,12H,3H2,1-2H3,(H,8,9)(H,10,11) Key: BITYXLXUCSKTJS-UHFFFAOYSA-N (3): InChI=1/C7H12O5/c1-3(2)4(6(9)10)5(8)7(11)12/h3-5,8H,1-2H3,(H,9,10)(H,11,12) Key: RNQHMTFBUSSBJQ-UHFFFAOYAR InChI=1S/C7H12O5/c1-3(2)4(6(9)10)5(8)7(11)12/h3-5,8H,1-2H3,(H,9,10)(H,11,12) Key: RNQHMTFBUSSBJQ-UHFFFAOYSA-N
SMILES (2): O=C(O)C(O)(CC(=O)O)C(C)C (3): O=C(O)C(O)C(C(=O)O)C(C)C
Properties
Chemical formula	C7H12O5
Molar mass	176.168 g·mol−1
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H315, H319, H335
GHS precautionary statements	P261, P264, P271, P280, P302+352, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P403+233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Tracking categories (test):

• SizeSet

Isopropylmalic acid (isopropylmalate) is an intermediate in the biosynthesis of leucine, synthesized from oxoisovalerate by 2-isopropylmalate synthase and converted into isopropyl-3-oxosuccinate by 3-isopropylmalate dehydrogenase. Two isomers are important, the 2- and 3-isopropyl derivatives, and these are interconverted by isopropylmalate dehydratase.