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Home CSSS00015251744

3-methyl-2-(methylamino)butanoic acid hydrochloride


Structure Info


Chemspace ID
CSSS00015251744 (In-Stock Screening Compounds)
CAS
2566-32-7
MFCD
MFCD00038969
IUPAC Name
3-methyl-2-(methylamino)butanoic acid hydrochloride
Mol formula
C6H14ClNO2
Mol weight
168 Da
Catalog Number(s)
04461, 2566-32-7, ACM2566327, AG00BH6K, AGN-PC-0WAENL, AKOS025404686, ALBB-021453, BAT-003618, CP26894, CSC015251744, D764475, EN300-7360854, F79583, HY-W142140, HY-W142140A, M338623, NA-0932, P39309, R136861, R648512, SAB-094210, SAB-094821, Z5785

Properties

LogP
-1.73
Heavy atoms count
10
Rotatable bond count
3
Number of rings
0
Carbon bond saturation, Fsp3
0.83333333333333
Polar surface area (Å)
49
Hydrogen bond acceptors count
3
Hydrogen bond donors count
2

SDS

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Items Overall 4 items from 2 suppliers

SupplierLead timeShips fromPurityPackPrice, $Qty
MedChemExpress10 daysUnited States
To:
9850 mg50.00
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MedChemExpress10 daysUnited States
To:
98100 mg70.00
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Description: Names: N-Methyl-DL-valine (hydrochloride); N-Methylvaline (hydrochloride); Product Description: N-Methyl-DL-valine (N-Methylvaline) hydrochloride is a valine derivant, is metabolized to cysteine, alanine, tyrosine, tryptophan, citric acid, and succinic acid in the sprout. N-Methyl-DL-valine hydrochloride involves in the modification of monomethyl auristatin F (MMAF), an anti-tubulin agent, makes it hydrophobic functionalization and increases cell permeability; Target: Amino Acid Derivatives
MedChemExpress EU10 daysSweden
To:
9850 mg50.00
Go to cartEnquire
MedChemExpress EU10 daysSweden
To:
98100 mg70.00
Go to cartEnquire
Description: Names: N-Methyl-DL-valine (hydrochloride); N-Methylvaline (hydrochloride); Product Description: N-Methyl-DL-valine (N-Methylvaline) hydrochloride is a valine derivant, is metabolized to cysteine, alanine, tyrosine, tryptophan, citric acid, and succinic acid in the sprout. N-Methyl-DL-valine hydrochloride involves in the modification of monomethyl auristatin F (MMAF), an anti-tubulin agent, makes it hydrophobic functionalization and increases cell permeability; Target: Amino Acid Derivatives
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