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Di-t-butyl iminodiacetate
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Amino PEG
Amino-PEG10-acid (Cat#: X24-03-YW0001) N-(Mal-PEG6)-N-bis(PEG3-amine) (Cat#: X24-03-YW0002) Amino-PEG23-amine (Cat#: X24-03-YW0056) Amino-PEG20-t-butyl ester (Cat#: X24-03-YW0057) Amino-PEG1-amine (Cat#: X24-03-YW0058) Gly-PEG3-amine TFA salt (Cat#: X24-03-YW0064) Amino-PEG9-amine (Cat#: X24-03-YW0068) Amino-PEG8-amine (Cat#: X24-03-YW0072) Amino-PEG8-t-butyl ester (Cat#: X24-03-YW0087)
Biotin PEG
Biotin-PEG2-azide (Cat#: X24-03-YW0091) Biotin-PEG5-azide (Cat#: X24-03-YW0113) Biotin-PEG6-t-butyl ester (Cat#: X24-03-YW0114) Dde biotin azide plus (Cat#: X24-03-YW0115) Biotin-PEG2-NH-Boc (Cat#: X24-03-YW0116) Biotin-PEG11-amine (Cat#: X24-03-YW0117) Biotin-PEG4-amide (Cat#: X24-03-YW0118) Biotin-PEG4-azide (Cat#: X24-03-YW0119) Biotin-PEG12-NHS ester (Cat#: X24-03-YW0124)
DBCO PEG
DBCO-PEG5-TFP ester (Cat#: X24-03-YW0294) DBCO-C3-alcohol (Cat#: X24-03-YW0306) Hydroxy-PEG7-DBCO (Cat#: X24-03-YW0307) DBCO-C5-acid (Cat#: X24-03-YW0308) DBCO-PEG2-amine (Cat#: X24-03-YW0310) DBCO STP ester (Cat#: X24-03-YW0311) DBCO-PEG6-DBCO (Cat#: X24-03-YW0312)
Poly PEG
m-PEG-succinic acid (Cat#: X24-10-WXX03) Lipoamide-PEG-Mal (Cat#: X24-10-WXX05) m-PEG-SPDP (Cat#: X24-10-WXX06) Lipoamide-PEG-biotin (Cat#: X24-10-WXX07) Rhodamine-PEG-Mal (Cat#: X24-10-WXX08) Cholesterol-PEG-methoxy (Cat#: X24-10-WXX10) DSPE-PEG-Ald (Cat#: X24-10-WXX12) 4-Arm PEG-OH (Cat#: X24-10-WXX13)
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Bromo PEG
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Cat. No.: X24-09-YYX123

Di-t-butyl iminodiacetate

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Synonym: 85916-13-8; Di-tert-butyl iminodiacetate; Di-tert-butyl 2,2'-azanediyldiacetate; NH-bis(C1-Boc); di-t-butyl iminodiacetate

  • CAS Number: 85916-13-8
  • PubChem CID: 4393691
Size
5 g; 10 g
Price
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Datasheet
Datasheet
MSDS
MSDS
Properties
Description
Di-t-butyl iminodiacetate consists of two tert-butyl groups attached to an iminodiacetate moiety. It is frequently used in the synthesis of peptides and other organic compounds where the protected amine groups provide controlled reactivity and protection during reactions.
Molecular Weight
245.3
Molecular Formula
C12H23NO4
Functional Group 1
t-Butyl
Functional Group 2
Amine
Functional Group 3
Ester
Reactive Group 1
Acid
Form
Solid
Identity
Confirmed by NMR.
Applications
This compound is frequently used as a reagent in peptide synthesis and as a building block in organic synthesis. Its structure allows it to participate in various reactions, including acylation and amidation, and it’s also studied for use in drug development and biological research.
Storage
Store at -20°C.
For Research Use Only. Not For Clinical Use.
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