Sign In to View Organizational & Contract Pricing
Select a Size
About This Item
Linear Formula:
(CH3)2CHCH2CH(NH2)CH2OH
CAS Number:
Molecular Weight:
117.19
Beilstein:
1719241
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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
SMILES string
CC(C)C[C@@H](N)CO
InChI
1S/C6H15NO/c1-5(2)3-6(7)4-8/h5-6,8H,3-4,7H2,1-2H3/t6-/m1/s1
InChI key
VPSSPAXIFBTOHY-ZCFIWIBFSA-N
Looking for similar products? Visit Product Comparison Guide
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
194.0 °F - closed cup
Flash Point(C)
90 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service