Products for Research Use Only

N3-TEMPO

CAT: 0013-GTR19233346-02Size: 10 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19233346-02Size:10 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
N3-TEMPO is a versatile click chemistry reagent containing an azide group, enabling efficient and specific conjugation of biomolecules like proteins, lipids, and nucleic acids. Its high yield and specificity facilitate applications in proteomics, bioconjugation, and cellular labeling for both in vitro and in vivo studies.
CAS Number
63697-61-0
Purity
98.62% (May vary between batches)
Smiles
CC1 (C) CC (N=[N+]=[N-]) CC (C) (C) N1[O]
Molecular Formula
C9H17N4O*
Molecular Weight
197.26
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

1-Piperidinyloxy, 4-azido-2,2,6,6-tetramethyl-
CAS Number63697-61-0
PubChem CID149016
Molecular FormulaC9H17N4O
Molecular Weight197.26
XLogP2.4
Topological Polar Surface Area18.6
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Heavy Atom Count14
Formal Charge0
Complexity250
SMILES
CC1(CC(CC(N1[O])(C)C)N=[N+]=[N-])C
InChI
InChI=1S/C9H17N4O/c1-8(2)5-7(11-12-10)6-9(3,4)13(8)14/h7H,5-6H2,1-4H3
InChIKey
HFUMVJSTAKNMEX-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of 1-Piperidinyloxy, 4-azido-2,2,6,6-tetramethyl-
CAS: 63697-61-0
CID: 149016
Formula: C9H17N4O
MW: 197.26
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight197.26
XLogP32.4
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count1
Exact Mass197.14023618
Monoisotopic Mass197.14023618
Topological Polar Surface Area18.6 Ų
Heavy Atom Count14
Formal Charge0
Complexity250
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes