Valinol

{{Chembox

|ImageFile = S-valinol.svg

|PIN = (2S)-2-Amino-3-methylbutan-1-ol

|OtherNames = (S)-(+)-2-Amino-3-methyl-1-butanol

|Section1={{Chembox Identifiers

|CASNo = 16369-05-4

|CASNo_Comment = (DL)

|CASNo1 = 2026-48-4

|CASNo1_Comment = (L)

|CASNo2 = 4276-09-9

|CASNo2_Comment = (D)

|PubChem = 79019

|PubChem_Comment = (DL)

|PubChem1 = 640993

|PubChem1_Comment = (L)

|PubChem2 = 6950587

|PubChem2_Comment = (D)

|ChemSpiderID = 71352

|ChemSpiderID_Comment = (DL)

|ChemSpiderID1 = 556322

|ChemSpiderID1_Comment = (L)

|ChemSpiderID2 = 5323522

|ChemSpiderID2_Comment = (D)

|SMILES = CC(C)C(CO)N

|SMILES_Comment = (DL)

|SMILES1 = CC(C)[C@@H](CO)N

|SMILES1_Comment = (L)

|SMILES2 = CC(C)[C@H](CO)N

|SMILES2_Comment = (D)

|InChI = 1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3

|InChIKey = NWYYWIJOWOLJNR-UHFFFAOYSA-N

|InChI_Comment = (DL)

|InChI1 = 1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1

|InChIKey1 = NWYYWIJOWOLJNR-RXMQYKEDSA-N

|InChI1_Comment = (L)

|InChI2 = 1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m0/s1

|InChIKey2 = NWYYWIJOWOLJNR-YFKPBYRVSA-N

|InChI2_Comment = (D)

}}

|Section2={{Chembox Properties

|C=5 | H=13 | N=1 | O=1

|Appearance = White to yellow crystalline powder

|Density = 0.926 g/mL

|MeltingPtC = 30 to 34

|BoilingPtC = 189 to 190

|Solubility = Very soluble

}}

|Section3={{Chembox Hazards

|ExternalSDS = Sigma Aldrich{{Sigma-Aldrich| id=184837 |name=2-Amino-3-methyl-1-butanol|accessdate=2014-10-22}}

|GHSSignalWord = Warning

|GHSPictograms = {{GHS07}}

|HPhrases = {{H-phrases|315|319|335|}}

|PPhrases = {{P-phrases|261|305+351+338}}

|GHS_ref =

|FlashPt = 90°C

|FlashPt_ref =

|FlashPt_notes = closed cup

}}

}}

Valinol is an organic compound named after, and commonly produced from, the amino acid valine. The compound is chiral and is produced almost exclusively as the S‑isomer (also designated as the L‑isomer), due to the abundant supply of S-valine. It is part of a broader class of amino alcohols.