Basic information
- CAS
36875-25-9- Standard SMILES
COC(=N)CCCCCC(=N)OC- InChIKey
LRPQMNYCTSPGCX-UHFFFAOYSA-N- Molecular formula
- C9H18N2O2
- Average molar mass
- 186.25 g/mol
- Monoisotopic mass
- 186.13682782
Names & identifiers
- Preferred name
- Dimethyl pimelimidate
- IUPAC
- dimethyl heptanediimidate
- English name
- dimethyl pimelimidate
- Molecular formula
- C9H18N2O2
- Molecular weight
- 186.25
Names & synonyms
Dimethyl pimelimidate36875-25-9L9U23Y3EV3Heptanediimidic acid, dimethyl esterDTXSID80905140RefChem:134266DTXCID401334244dimethyl heptanediimidateDimethyl heptanebis(imidate)1,7-dimethyl heptanediimidateDimethyl heptane-1,7-diimidate dihydrochlorideUNII-L9U23Y3EV3
Show more names
Heptanediimidic acid dimethyl esterdimethyl (1Z,7Z)-heptanebis(imidoate)Heptanediimidic acid, 1,7-dimethyl ester
SCHEMBL43895Dimethyl pimelimidate, 2HCl saltEINECS 261-320-6NSC 341945BP-46746LS-13703Q5277319
Database identifiers
- CAS
36875-25-9、58537-94-3- PubChem CID
- 65403
- DTXSID
DTXSID80905140- UNII
- L9U23Y3EV3
- EC Number
- 261-320-6
- Nikkaji
- J257.521C
Properties
Computed structural properties
- XLogP
- 1.3
- Topological polar surface area
- 66.2 Ų
- Hydrogen bond donors
- 2
- Hydrogen bond acceptors
- 4
- Rotatable bonds
- 8
- Heavy atoms
- 13
- Formal charge
- 0
- Complexity
- 151
Physicochemical properties
- FDA UNII
- 9 U23Y3EV3 · L9U23Y3EV3
Safety & regulation
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
GHS classification
GHS Classification
Warning
H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
P264, P280, P302+P352, P321, P332+P317, and P362+P364 (click each P-code to see the statement)
Aggregated GHS information provided per 157 reports by companies from 2 notifications to the ECHA C&L Inventory.
Hazard information
Hazard Classes and CategoriesSkin Irrit. 2 (100%)
Chemistry & industry
Applications
DescriptionDimethyl pimelimidate is a mid-length crosslinking reagent that features imidoester reactive groups at both ends, which are specifically reactive towards primary amines. It is one of three similar imidoester crosslinkers, alongside DMA and DMP. This water-soluble reagent reacts with amines at alkaline pH values (between 8 and 10) to form amidine bonds. Notably, the amidine bonds created retain the net charge character of the protein's primary amine to which they react. These bonds are reversible at high pH values, making dimethyl pimelimidate a valuable tool for studying the quaternary structure of proteins.
Suppliers1 total
DAYANG CHEM (HANGZHOU) CO.,LTD+86-88938639 +86-17705817739 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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