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Molecule
ID:103187
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₁₂H₂₃N
Molecular Mass
181.31772
Exact Mass
181.18304974
Charge
0
InChI
InChI=1S/C12H23N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h11-13H,1-10H2
InChIKey
XBPCUCUWBYBCDP-UHFFFAOYSA-N
Canonic Smiles
C1CCC(CC1)NC1CCCCC1
Isomeric Smiles
C1CCC(CC1)NC1CCCCC1
Calculated Properties
JChem
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
0.16547571
LogD (pH = 7.4)
0.28951243
Log P
3.4056625
Molar Refractivity
56.7218
Polarizability
22.937813
Polar Surface Area
12.03
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
•
RDKit
•
JChem
Data Source
•
Commercial Catalog
•
Academic Data
Names and Identifiers
•
Synonyms
•
IUPAC name
•
IUPAC Traditional name
Registration numbers
Properties
•
Safety Information
•
Product Information
•
Physical Property
Related Proteins
Molecular Spectra
Molecule Details
•
MP Biomedicals
•
Sigma Aldrich
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
MP Biomedicals
02150877
05211894
Sigma Aldrich
185841
36630
36620
442564
Alfa Aesar
A15671
A&J Pharmtech
AJA-O11773
Academic Data
PubChem
7582
Names and Identifiers
Synonyms
DICYCLOHEXYLAMINE
N-Cyclohexylcyclohexanamine
Di-CHA
N,N-Dicyclohexylamine
Dodecahydrodiphenylamine
DCHA
Dicyclohexylamine
二环己胺
IUPAC name
N-cyclohexylcyclohexanamine
IUPAC Traditional name
dicha
Registration numbers
EC Number
202-980-7
CAS Number
101-83-7
PubChem CID
7582
PubChem SID
162090327
24851183
24862627
24867910
24862638
MDL Number
MFCD00011658
Beilstein Number
605923
Merck Index
143095
Molecule Details
MP Biomedicals
02150877
Purity: >99%
Reagent for preparation of crystalline amino acid salts.
1 ml = approx. 0.91 g
05211894
MP Biomedicals Rare Chemical collection
Sigma Aldrich
185841
Packaging
2, 3 kg in glass bottle
5, 100, 500 g in glass bottle
References
PubChem Literature
From Data Sources
•
Forms highly crystalline salts with N-protected amino acids:
Liebigs Ann. Chem.
,
640
, 157 (1961).
•
Reacts with n-BuLi to give a hindered strong base; cf LDA (see
Diisopropylamine, A10280
), which has been used to promote, e.g. the ɑ -carboethoxylation of ketones; see
Diethyl dicarbonate, B22753
.
Bioactivity
PubChem BioAssay
Registration numbers
•
EC Number
•
CAS Number
•
PubChem CID
•
PubChem SID
•
MDL Number
•
Beilstein Number
•
Merck Index
Properties
Safety Information
Emergency Response Guidebook(ERG) Number
153
Source
Risk Statements
R:
22
-
34
-
50/53
Source
22
-
34
-
50/53
Source
S:
26
-
45
-
60
-
61
-
36/37/39
Source
26
-
36/37/39
-
45
-
60
-
61
Room Temperature (15-30°C)
Source
8
Source
Nature polluting (N)
3X
Source
C9
Source
2565
Source
UN2565
Source
8B
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
Download link
Source
HY4025000
Source
III
Source
3
Source
P273
-
P280
-
P305+P351+P338
-
P310
-
P501
Source
P260
-
P303+P361+P353
-
P305+P351+P338
-
P301+P330+P331
-
P405
-P501A
UN 2565 8/PG 3
Source
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
3
Source
H302
-
H314
-
H410
Source
H314
-
H400
-
H410
-
H302
Source
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Source
Danger
Source
是
Source
Air Sensitive
Source
Product Information
Download link
Source
Download link
Source
>99%
Source
99%
Source
≥98.0% (GC)
Source
≥99.5% (GC)
Source
98%
Physical Property
.91 g/cm
3
at 25 °C
Source
0.91 g/ml
Source
0.912 g/mL at 20 °C(lit.)
Source
0.913
Source
106 °C (closed cup)
Source
96 °C
Source
204.8 °F
Source
Source
1/2
-
26
-
36/37/39
-
45
-
60
-
61
Source
Source
Corrosive (C)
Source
Harmful (X)
Source
Download link
Source
Source
Source
Hazardous to the aquatic environment
Acute hazard, category1
Chronic hazard, categories 1,2
Source
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
Source
Linear Formula
(C6H11)2NH
Source
Grade
purum
Source
analytical standard
Source
Quality
for titrimetric determination of isocyanates
Source
Packaging
ampule of 1000 mg
Source
99°C(210°F)
Source
Vapor Pressure
1 hPa at 65 °C
Source
12 mmHg ( 37.7 °C)
Source
Boiling Point
255.8 °C at 1013 hPa
Source
255.8°C
Source
117-120 °C/10 mmHg
Source
256 °C(lit.)
Source
256°C
Source
Melting Point
-.1 °C
Source
-1°C
Source
-2 °C(lit.)
Source
-2°C
Source
Refractive Index
n20/D 1.484(lit.)
Source
n20/D 1.484
Source
1.4842
Source
Vapor Density
6 (vs air)
Source
Safety Statements
Storage Condition
Hazard Class
European Hazard Symbols
Australian Hazchem
EU Classification
UN Number
EU Hazard Identification Number
MSDS Link
RTECS
Packing Group
GHS Precautionary statements
RID/ADR
GHS Pictograms
German water hazard class
GHS Hazard statements
Personal Protective Equipment
GHS Signal Word
TSCA Listed
Storage Warning
Certificate of Analysis
Purity
Density
Flash Point