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Molecule
ID:90073
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₄H₁₁NO
Molecular Mass
89.13624
Exact Mass
89.08406398
Charge
0
InChI
InChI=1S/C4H11NO/c1-2-4(5)3-6/h4,6H,2-3,5H2,1H3/t4-/m1/s1
InChIKey
JCBPETKZIGVZRE-SCSAIBSYSA-N
Canonic Smiles
CC[C@H](CO)N
Isomeric Smiles
OC[C@@H](CC)N
Calculated Properties
JChem
Acid pKa
15.12831
H Acceptors
2
H Donor
2
LogD (pH = 5.5)
-3.3887622
LogD (pH = 7.4)
-2.720577
Log P
-0.37646344
Molar Refractivity
25.1539
Polarizability
10.242338
Polar Surface Area
46.25
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
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Molecule Details
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References
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Bioactivity
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General Information
Calculated Properties
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RDKit
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JChem
Data Source
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Commercial Catalog
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Academic Data
Names and Identifiers
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Synonyms
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IUPAC Traditional name
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IUPAC name
Registration numbers
Properties
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Physical Property
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Safety Information
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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MP Biomedicals
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Sigma Aldrich
References
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PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Apollo Scientific
OR5871
MP Biomedicals
05225887
Sigma Aldrich
307084
07180
Enamine
EN300-125884
Bide Pharmatech
BD21614
Alfa Aesar
B25212
Academic Data
PubChem
2723856
Names and Identifiers
Synonyms
(R)-(-)-2-Aminobutan-1-ol
(R)-(-)-2-Amino-1-butanol
(R)-(-)-2-氨基-1-丁醇
D-2-AMINO-1-BUTANOL
(2R)-2-aminobutan-1-ol
(R)-2-Aminobutan-1-ol
IUPAC Traditional name
(2R)-2-aminobutan-1-ol
IUPAC name
(2R)-2-aminobutan-1-ol
Registration numbers
CAS Number
5856-63-3
5856-62-2
MDL Number
MFCD00064419
EC Number
227-476-4
Beilstein Number
1718929
PubChem SID
24858559
24846023
162076928
PubChem CID
2723856
Molecule Details
MP Biomedicals
05225887
MP Biomedicals Rare Chemical collection
Sigma Aldrich
307084
Packaging
5 g in glass bottle
07180
Other Notes
N-Protection and O-tosylation1; Preparation of chiral thiazolidine-2-thiones and oxazolidine-2-thiones, which are auxiliaries2,3
References
PubChem Literature
From Data Sources
•
For an extensive review of the use of 1,2-amino alcohols as chiral auxiliaries in asymmetric synthesis, see:
Chem. Rev.
,
96
, 835 (1996).
Bioactivity
PubChem BioAssay
Registration numbers
•
CAS Number
•
MDL Number
•
EC Number
•
Beilstein Number
•
PubChem SID
•
PubChem CID
Properties
Physical Property
Boiling Point
172-174°C
Source
172-174 °C(lit.)
Source
176-178°C
Source
Melting Point
-2°C
Source
-2 °C(lit.)
Source
Refractive Index
n20/D 1.452
Source
1.4525
Source
95 °C
Source
203 °F
Source
89°C(192°F)
Source
[α]19/D -10°, neat
Source
[α]20/D -8.5±1°, c = 2% in ethanol
Source
-10 (neat)
Source
0.943 g/mL at 20 °C(lit.)
Source
0.947
Source
-0.457
Source
Safety Information
Corrosive
Source
Air Sensitive & Hygroscopic
Source
Download link
Source
Download link
Source
Download link
Source
Product Information
Download link
Source
ee: 96% (GLC)
Source
enantiomeric ratio: ≥90:10 (GC)
Source
C2H5CH(NH2)CH2OH
Source
98%
Source
≥90% (sum of enantiomers, GC)
European Hazard Symbols
Corrosive (C)
Source
Harmful (X)
Safety Statements
26
-
36/37/39
-
45
Source
Packing Group
3
Source
III
Source
German water hazard class
3
Source
GHS Precautionary statements
P280
-
P305+P351+P338
-
P310
Source
P280
-
P305+P351+P338
-
P309
-
P310
Source
RID/ADR
UN 2735 8/PG 3
Source
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Risk Statements
22
-
34
-
37
Source
22
-
34
Source
GHS Hazard statements
H302
-
H314
Source
H314
-
H318
-
H302
-
H227
Source
Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
GHS Signal Word
Danger
Source
Hazard Class
8
Source
UN Number
2735
Source
UN2735
Source
TSCA Listed
是
Source
Source
95%
Source
Impurities
~2% water
Source
Grade
technical
Source
Flash Point
Optical Rotation
Density
Hydrophobicity(logP)
Storage Warning
MSDS Link
Certificate of Analysis
Optical Purity
Linear Formula
Purity
Source
Source