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Molecule
ID:134931
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₁₄BrNO
Molecular Mass
184.07476
Exact Mass
183.02587607
Charge
0
InChI
InChI=1S/C5H14NO.BrH/c1-6(2,3)4-5-7;/h7H,4-5H2,1-3H3;1H/q+1;/p-1
InChIKey
JJCWKVUUIFLXNZ-UHFFFAOYSA-M
Canonic Smiles
OCC[N+](C)(C)C.[Br-]
Isomeric Smiles
C[N+](CCO)(C)C.[Br-]
Calculated Properties
JChem
Acid pKa
13.968714
H Acceptors
1
H Donor
1
LogD (pH = 5.5)
-4.662269
LogD (pH = 7.4)
-4.6622667
Log P
-4.662269
Molar Refractivity
42.194
Polarizability
12.021414
Polar Surface Area
20.23
Rotatable Bonds
2
Lipinski's Rule of Five
true
Data Source
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Registration numbers
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Properties
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Related Proteins
No Data Available
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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
•
IUPAC Traditional name
•
IUPAC name
•
Synonyms
Registration numbers
•
CAS Number
•
MDL Number
•
PubChem SID
•
PubChem CID
Properties
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Safety Information
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Physical Property
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Product Information
Related Proteins
Molecular Spectra
Molecule Details
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Sigma Aldrich
References
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PubChem Literature
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From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Commercial Catalog
Sigma Aldrich
615528
Academic Data
PubChem
71308987
Names and Identifiers
IUPAC Traditional name
(2-hydroxyethyl)tris(
2
H
3
)methylazanium bromide
IUPAC name
(2-hydroxyethyl)tris(
2
H
3
)methylazanium bromide
Synonyms
溴化胆碱-三甲基-d9
Choline bromide-(trimethyl-d9)
Registration numbers
CAS Number
285979-71-7
MDL Number
MFCD00190406
PubChem SID
162229206
PubChem CID
71308987
Properties
Safety Information
GHS Hazard statements
H315
-
H319
-
H335
Source
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Source
Risk Statements
36/37/38
Source
Safety Statements
26
-
36
Source
GHS Signal Word
Warning
Source
GHS Precautionary statements
P261
-
P305+P351+P338
Source
European Hazard Symbols
Irritant (Xi)
Source
German water hazard class
3
Source
MSDS Link
Download link
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
Physical Property
Mass Shift
M+9
Source
Product Information
Isotopic Purity
98 atom % D
Source
Linear Formula
HOCH2CH2N(CD3)3Br
Source
Mol. Weight
mol wt 192.95 by atom % calculation
Source
Molecule Details
Sigma Aldrich
615528
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
References
PubChem Literature
No Data Available
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Bioactivity
PubChem BioAssay