1...101112...14

Code Name Synonym
AA-147 H-Phe(4-N3).HCl 4-Azido-L-phenylalanine hydrochloride // 3-(p-Azidophenyl)-L-alanine Hydrochloride // 4-Azidophenylalanine Hydrochloride // p-Azido-L-phenylalanine Hydrochloride // p-Azidophenylalanine Hydrochloride // H-4-Azido-Phe.HCl // Phe(pN3).HCl // para-azido-Phe.HCl
CAS 34670-43-4 , 33173-53-4 net /upload/small/small_aa-147.svg
Formula C9H11ClN4O2
MW 242.7
Purity >98%
Storage -15 ... -25°C
Note H-Phe(4-N3) is used in protein biosynthesis as unnatural amino acid for genetic code expansion. The azido-funcionality can be further utilized to cross-link various functionalities to proteins utilizing click-chemistry. DOI:10.1126/science.1084772; DOI:10.1038/nature08817; DOI:10.1038/nature14095;
The azido-functionality is IR-active and can be used in protein active site electrostatic environment studies. DOI:10.1038/nchembio.167;
The azide-handle can also be used for protein PEGylation or attachment to antibodies using click-chemistry. DOI:10.1021/acssynbio.7b00316; U.S. (2
Code Name Synonym
BO-153 Boc-Phe(4-N3) N-Boc-4-azido-L-phenylalanine // Boc-4-azido-Phe-OH // Boc-p-azido-Phe-OH
CAS 33173-55-6 /upload/more_svg/small/small_bo-153.svg
Formula C14H18N4O4
MW 306.3
Purity >98%
Storage -15 ... -25 °C
Note Boc-Phe(4-N3) can be incorporated into peptides for attachment of functionalities using click-chemistry. DOI:10.1002/anie.200705456; DOI:10.1039/C6TB02848A; This material can also be used to modify graphene sheets by covalent bonding.Chem. Comm. (2010), 46(23), 4097-4099. DOI:10.1039/c001488e.
Code Name Synonym
BO-154 Boc-D-Phe(4-N3) N-Boc-4-azido-D-phenylalanine // Boc-4-azido-D-Phe-OH // Boc-p-azido-D-Phe-OH
CAS 214630-05-4 /upload/more_svg/small/small_bo-154.svg
Formula C14H18N4O4
MW 306.3
Purity >98%
Storage -15 ... -25 °C
Note Boc-D-Phe(4-N3)  can be incorporated into peptides for attachment of functionalities using click-chemistry. Sarkar, Sourav; Libby, Elizabeth A.; Pidgeon, Sean E.; Dworkin, Jonathan; Pires, Marcos M. Angewandte Chemie, International Edition (2016), 55(29), 8401-8404. DOI:10.1002/anie.201603441.
Code Name Synonym
FM-252 Fmoc-Phe(4-CH2-N3) Fmoc-L-Phe(4-CH2-N3)-OH // Fmoc-p-azidomethyl-L-phenylalanine // Fmoc-para-methylazido-L-phenylalanine // Fmoc-para-azidomethyl-L-phenylalanine // Fmoc-pN3CH2Phe // Fmoc-pAMF // Fmoc-4-(Azidomethyl)-L-phenylalanine
CAS 2375587-79-2 /upload/small/small_fm-252.svg
Formula C25H22N4O4
MW 442.5
Purity >98%
Storage +2 ... +8 °C
Note This material is used in antibody drug conjugates as a superior SPAAC reaction partner in comparison to H-Phe(4-N3). Bioconjugate Chem. (2014), 25(2), 351-361. DOI:10.1021/bc400490z. It can serve as a vibrational reporter of local protein environments after genetic incorporation into proteins.  J. Phys. Chem. B (2013), 117(30), 8987-8993. DOI:10.1021/jp4052598; Molina, Arturo PCT Int. Appl. (2019), WO 2019023316 A1.
Code Name Synonym
FM-238 Fmoc-D-Phe(4-N3) Fmoc-D-4-azidophenylalanine // Fmoc-4-azido-D-phenylalanine // Fmoc-p-azido-D-Phe-OH // Fmoc-D-Phe(N3)-OH // Fmoc-D-p-azidophenylalanine // Fmoc-D-phenylalanine-azide // (2R)-3-(4-azidophenyl)-2-{[(9H-fluoren-9- ylmethoxy)carbonyl]amino}propanoic acid
CAS 1391586-30-3 /upload/more_svg/small/small_fm-238.svg
Formula C24H20N4O4
MW 428.4
Purity >98%
Storage -15 ... -25 °C
Note Fmoc-D-Phe(4-N3) can be incorporated into peptides for attachment of functionalities using click-chemistry. Sarkar, Sourav; Libby, Elizabeth A.; Pidgeon, Sean E.; Dworkin, Jonathan; Pires, Marcos M. Angewandte Chemie, International Edition (2016), 55(29), 8401-8404. DOI:10.1002/anie.201603441.
Code Name Synonym
ET-144 N3-Phe.DCHA (S)-2-Azido-3-phenylpropionic acid (dicyclohexylammonium) salt // (S)-2-Azido-3-phenylpropionic acid (dicyclohexylammonium) salt
CAS 79410-36-9 , 79410-35-8 net /upload/more_svg/small/small_et-144.svg
Formula C21H32N4O2
MW 372.5
Purity >99%
Storage +2 ... +8 °C
Code Name Synonym
FM-220 Fmoc-Phe(4-N3) Fmoc-4-azidophenylalanine // Fmoc-4-azido-L-phenylalanine // Fmoc-p-azido-Phe-OH // Fmoc-Phe(N3)-OH // Fmoc-p-azidophenylalanine // Fmoc-phenylalanine-azide
CAS 163217-43-4 /upload/more_svg/small/small_fm-220.svg
Formula C24H20N4O4
MW 428.4
Purity >98%
Storage -15 ... -25 °C
Note Used in solid-phase peptide synthesis. The azido-funcionality can be further utilized to cross-link various functionalities to peptides or proteins utilizing Staudinger ligation or click-chemistry. Nano Letters (2015), 15(1), 603-609. DOI:10.1021/nl504079q; Angew. Chem. Int. Ed. (2013), 52(45), 11920-11924. DOI:10.1002/anie.201303467; J. Am. Chem. Soc. (2017), 139(17), 6152-6159. DOI:10.1021/jacs.7b01072.
Code Name Synonym
ET-151 4-Azidobenzyl alcohol (4-azidophenyl)methanol
CAS 31499-54-4 /upload/small/small_ET-151.svg
Formula C7H7N3O
MW 149.2
Purity >99%
Storage +2 ... +8 °C
Note 4-azidobenzyl alcohol is used as a linker for further modification using Staudinger ligation or Click-chemistry. The azide can be transformed into amine under mild and neutral conditions. Nature Chem. (2011), 3(2), 146-153. DOI:10.1038/nchem.932; Analytical Chem. (2018), 90(15), 9418-9425. DOI:10.1021/acs.analchem.8b02068;  Bioconjugate Chem. (2018), 29(2), 324-334. DOI:10.1021/acs.bioconjchem.7b00665.
Code Name Synonym
DI-117 N3-Cystamine.HCl azido-cystamine hydrochloride // 2-[(2-azidoethyl)disulfanyl]ethanaminium chloride
CAS 1807512-40-8 net /upload/more_svg/small/small_di-117.svg
Formula C4H11ClN4S2
MW 214.7
Purity >98%
Storage +2 ... +8 °C
Note N3-Cystamine can be used as a linker for various applications. The azido-group can be modified using Staudinger ligation or Click-chemistry.
Code Name Synonym
DI-102 N1-Azido-spermine.3HCl Spermine N3HHH.3HCl // 1-azido-4,9,13-triazatridecane // (3-aminopropyl)({4-[(3-azidopropyl)amino]butyl})amine trihydrochloride
CAS 1823475-98-4, 1190203-77-0 net /upload/more_svg/small/small_DI-102.svg
Formula C10H27Cl3N6
MW 337.7
Purity >98%
Storage +2 ... +8 °C
Note Spermine N3HHH can be attached to other molecules using Staudinger ligation or Click-chemistry. J. Org. Chem. (2011), 76(5), 1198-1211. DOI:10.1021/jo101761g;  Chem. Comm. (2013), 49(2), 184-186. CAPLUS, DOI:10.1039/C2CC36811K.

1...101112...14