1...11121314

Code Name Synonym
DI-118 Spermine(N3HHN3).2TsOH Spermine N3HHN3.2TsOH // 1,12-diazido-4,9-diazadodecane // (3-azidopropyl)({4-[(3-azidopropyl)amino]butyl})amine di-tosylate
CAS 2250433-79-3 net /upload/more_svg/small/small_di-118.svg
Formula C24H38N8O6S2
MW 598.7
Purity >98%
Storage +2 ... +8 °C
Note Spermine N3HHN3 can be attached to other molecules using Staudinger ligation or Click-chemistry. It can be used as a polyamine linker and to produce dendrimer-like structures using Click-chemistry.
Code Name Synonym
DI-110 Fmoc-EDA-N3 9H-fluoren-9-ylmethyl N-(2-azidoethyl)carbamate
CAS 432507-62-5 /upload/more_svg/small/small_di-110.svg
Formula C17H16N4O2
MW 308.3
Purity >99%
Storage +2 ... +8 °C
Code Name Synonym
DI-115 Z-EDA-N3 benzyl N-(2-azidoethyl)carbamate
CAS 146552-66-1 /upload/more_svg/small/small_di-115.svg
Formula C10H12N4O2
MW 220.2
Purity >95%
Storage +2 ... +8 °C
Code Name Synonym
DI-116 Fmoc-DAP-N3 Fmoc-propylenediamine-azido // 9H-fluoren-9-ylmethyl N-(3-azidopropyl)carbamate
CAS 1021422-85-4 /upload/more_svg/small/small_di-116.svg
Formula C18H18N4O2
MW 322.4
Purity >98%
Storage +2 ... +8 °C
Code Name Synonym
ET-123 N3-DOOA-Suc-OH 3-({2-[2-(2-azidoethoxy)ethoxy]ethyl}carbamoyl)propanoic acid
CAS 1189096-56-7 /upload/more_svg/small/small_et-123.svg
Formula C10H18N4O5
MW 274.3
Purity >95%
Storage +2 ... +8 °C
Code Name Synonym
ET-167 N3-C11H22-COOH 12-Azidododecanoic acid // 12-ADA // 12AZ // 12-Azido-dodecanoic acid
CAS 80667-36-3 /upload/small/small_et-167.svg
Formula C12H23N3O2
MW 241.3
Purity >98%
Storage +2 ... +8 °C
Note Used as a hydrophobic bioconjugation linker (using N-Myristoyltransferase) that can be further modified at the azido-position using Staudinger ligation or Click-chemistry. Kinzer-Ursem, T. L. Bioconjugation, 2019, 149, DOI:10.1007/978-1-4939-9654-4_11; Tirrell, D. A. J. Am. Chem. Soc. 2016, 15098, DOI:10.1021/jacs.6b07067.
Code Name Synonym
ET-169 N3-C11H22-COOSu 12-Azidododecanoic acid NHS ester // 12-Azidododecanoic acid N-hydroxysuccinimide ester // 12-ADA-NHS// 12AZ-NHS// 12-Azido-dodecanoic acid NHS ester // 2,5‐dioxopyrrolidin‐1‐yl 12‐azidododecanoate
CAS n/a /upload/small/small_et-169.svg
Formula C16H26N4O4
MW 338.4
Purity >98%
Storage +2 ... +8 °C
Note Used as a hydrophobic bioconjugation linker that can be further modified at the azido-position using Staudinger ligation or Click-chemistry.
Code Name Synonym
DI-106 1-(Boc-amino)-3,6-dioxa-8-octaneazide tert-butyl {2-[2-(2-azidoethoxy)ethoxy]ethyl}carbamate // Boc-N-Amido-PEG2-N3 // BocNH-PEG2-CH2CH2N3
CAS 950683-55-3 /upload/more_svg/small/small_DI-106.svg
Formula C11H22N4O4
MW 274.3
Purity >98%
Storage +2 ... +8 °C
Code Name Synonym
DI-107 1-Amino-8-azido-3,6-dioxaoctane.TosOH 2-[2-(2-azidoethoxy)ethoxy]ethanaminium 4-methylbenzenesulfonate // 2-(2-(2-azidoethoxy)ethoxy)ethanamine TosOH salt // Azido-PEG2-Amine
CAS 2173092-98-1, 166388-57-4 net /upload/more_svg/small/small_DI-107.svg
Formula C13H22N4O5S
MW 346.4
Purity >98%
Storage +2 ... +8 °C
Note N3-PEG2-Amine is used as a Click-chemistry linker in various applications. JACS (2010), 132(12), 4490-4499. DOI:10.1021/ja100455c; ACIEE (2014), 53(44), 11822-11827. DOI:10.1002/anie.201406764; JACS (2012), 134(45), 18809-18815. DOI:10.1021/ja309000s; Nature Communications (2014), 5, 5378. DOI:10.1038/ncomms6378; ACIEE (2018), 57(18), 5029-5032. DOI:10.1002/anie.201801081.
Code Name Synonym
DI-127 N3-PEG(4)-NH-Boc tert‐butyl N‐(2‐{2‐[2‐(2‐ azidoethoxy)ethoxy]ethoxy}ethyl)carbamate // 11-azido-3,6,9-trioxaundecan-1-Boc-amine // BocNH-PEG3-CH2CH2N3 // t-Boc-N-Amido-PEG3-azide // 1-azido-3,6,9-trioxaundecan-11-Boc-amine
CAS 642091-68-7 /upload/small/small_di-127.svg
Formula C13H26N4O5
MW 318.4
Purity >98%
Storage -15 ... -25 °C
Note Used as a Click-chemistry linker in various applications. For example, in the construction of HyT5 linker. Crews, C. M. et. al. Nature Chem. Biol. 2011, 538, DOI:10.1038/nchembio.597; Schaaf P. et. al. J. Am. Chem. Soc. 2012, 83, DOI:10.1021/ja208970b; Huc I. et. al. Bioconj. Chem. 2019, 54, DOI:10.1021/acs.bioconjchem.8b00710; WO2019060693A1; Ojida A. et. al. Bull. Chem. Soc. Jap. 2019, 995, DOI:10.1246/bcsj.20190034.

1...11121314