Fmoc-9-Aminononanoic acid

Catalog No.: A82129
PROTAC Linker
Fmoc-9-Aminononanoic acid functions as a PROTAC linker, featuring a terminal Fmoc-protected amine and a carboxylic acid group. This compound is instrumental in the synthesis of PROTACs and other conjugation applications. The Fmoc group is removable under basic conditions, yielding a free amine suitable for further conjugations. Additionally, the carboxylic acid can readily engage with primary amines in the presence of coupling agents such as EDC or HATU, facilitating the formation of stable amide bonds for diverse biochemical applications.
Grouped product items
Size Price Stock Qty
25mg
$20.00
In stock
50mg
$25.00
In stock
100mg
$30.00
In stock
250mg
$50.00
In stock
500mg
$80.00
In stock
1g
$130.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionFmoc-9-Aminononanoic acid functions as a PROTAC linker, featuring a terminal Fmoc-protected amine and a carboxylic acid group. This compound is instrumental in the synthesis of PROTACs and other conjugation applications. The Fmoc group is removable under basic conditions, yielding a free amine suitable for further conjugations. Additionally, the carboxylic acid can readily engage with primary amines in the presence of coupling agents such as EDC or HATU, facilitating the formation of stable amide bonds for diverse biochemical applications.
Product Information
Catalog NumA82129
FormulaC24H29NO4
Molecular Weight395.49
CAS Number212688-52-3
SMILESO=C(O)CCCCCCCCNC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O
Useful Calculator

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Mass (mg) = Concentration (mM) × Volume (mL) × Molecular Weight (g/mol)

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This equation is commonly abbreviated as: C1V1 = C2V2

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