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Merck
CN

298417

(R)-(−)-Leucinol

98%

Synonym(s):

(R)-2-Amino-4-methyl-1-pentanol, D-Leucinol

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About This Item

Linear Formula:
(CH3)2CHCH2CH(NH2)CH2OH
CAS Number:
53448-09-2
Molecular Weight:
117.19
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
24857984
MDL number:
MFCD00004734
Beilstein/REAXYS Number:
1719241

Key Documents

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Product Name

(R)-(−)-Leucinol, 98%

InChI

1S/C6H15NO/c1-5(2)3-6(7)4-8/h5-6,8H,3-4,7H2,1-2H3/t6-/m1/s1

SMILES string

CC(C)C[C@@H](N)CO

InChI key

VPSSPAXIFBTOHY-ZCFIWIBFSA-N

assay

98%

optical activity

[α]20/D −4°, c = 9 in ethanol

reaction suitability

reaction type: solution phase peptide synthesis

refractive index

n20/D 1.4496 (lit.)

bp

198-200 °C/768 mmHg (lit.)

density

0.917 g/mL at 25 °C (lit.)

application(s)

peptide synthesis

Quality Level

100

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Related Categories

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

194.0 °F - closed cup

flash_point_c

90 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBL7137
MKBC9730
10505PH
04925AH
09931JE

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Klaus Ringsborg Westphal et al.
Toxins, 11(5) (2019-05-19)
Fungal non-ribosomal peptide synthetase (NRPS) clusters are spread across the chromosomes, where several modifying enzyme-encoding genes typically flank one NRPS. However, a recent study showed that the octapeptide fusaoctaxin A is tandemly synthesized by two NRPSs in Fusarium graminearum. Here
Griet Van Zeebroeck et al.
Nature chemical biology, 5(1), 45-52 (2008-12-09)
Transporter-related nutrient sensors, called transceptors, mediate nutrient activation of signaling pathways through the plasma membrane. The mechanism of action of transporting and nontransporting transceptors is unknown. We have screened 319 amino acid analogs to identify compounds that act on Gap1

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