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186708

Sigma-Aldrich

(S)-(+)-2-Amino-3-methyl-1-butanol

96%

Synonym(s):

L-Valinol

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¥36,600

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1 G
¥3,480
5 G
¥8,860
25 G
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About This Item

Linear Formula:
(CH3)2CHCH(NH2)CH2OH
CAS Number:
2026-48-4
Molecular Weight:
103.16
Beilstein:
1719137
EC Number:
217-975-5
MDL number:
MFCD00064296
UNSPSC Code:
12352104
PubChem Substance ID:
24851236
NACRES:
NA.22

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Assay

96%

optical activity

[α]25/D +10°, c = 10 in H2O

optical purity

ee: 95% (GLC)

refractive index

n20/D 1.4548 (lit.)

bp

81 °C/8 mmHg (lit.)

mp

30-32 °C (lit.)

density

0.926 g/mL at 25 °C (lit.)

functional group

amine
hydroxyl

storage temp.

2-8°C

SMILES string

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

InChI

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

InChI key

NWYYWIJOWOLJNR-RXMQYKEDSA-N

Related Categories

Application

(S)-(+)-2-Amino-3-methyl-1-butanol can be used to prepare:
  • Imines and oxazolines by reacting with aldehydes and nitriles, respectively.[1][2]
  • Chiral oxazoline derived multidentate ligands containing cyclophosphazene moiety.[3]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

172.4 °F - closed cup

Flash Point(C)

78 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

186708-5G:
186708-VAR:
186708-25G:
186708-1G:
186708-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG4243
BCBM7112V
BCBM2839V
BCBF6325V
1390410V

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Tetrahedron Letters, 34, 2015-2015 (1993)
Journal of the Chemical Society. Perkin Transactions 1, 192-192 (1989)
Enantioselective palladium catalysed allylic substitution with thienyl oxazoline ligands
Frost CG and Williams JMJ
Tetrahedron Letters, 34(12), 2015-2018 (1993)
Asymmetric synthesis of alpha-substituted o-methoxybenzyl alcohols via stereoselective additions to kinetically resolved o-anisaldehyde (tricarbonyl) chromium
Davies SG and Goodfellow CL
Journal of the Chemical Society. Perkin Transactions 1, 1, 192-194 (1989)
Dheeraj Kumar et al.
Dalton transactions (Cambridge, England : 2003), 43(37), 13899-13912 (2014-08-12)
Chiral oxazoline based bi and hexadentate ligands built on cyclophosphazene cores have been synthesized and characterized. (NPPh2)2[NP(m-OC6H4C(O)OCH3)2] (1) was prepared by the reaction of gem-(NPPh2)2(NPCl2) with methyl-3-hydroxy benzoate in the presence of Cs2CO3. Compound 1 was converted to the dicarboxylic
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