Substance
ID:364405
Names and Identifiers
Synonyms
EDC hydrochlorideEDC 盐酸盐N-乙基-N′-(3-二甲基氨丙基)碳二亚胺 盐酸盐1-(3-二甲氨基丙基)-3-乙基碳二亚胺 盐酸盐WSC 盐酸盐N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochlorideEDACN-Ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochlorideWSC hydrochloride
IUPAC name
(3-{[(ethylimino)methylidene]amino}propyl)dimethylamine hydrochloride
IUPAC Traditional name
(3-{[(ethylimino)methylidene]amino}propyl)dimethylamine hydrochloride
Registration numbers
CAS Number
Beilstein Number
EC Number
MDL Number
Properties
Product Information
Grade
purum
Purity
≥98.0% (AT)
Empirical Formula (Hill Notation)
C8H17N3 · HCl
Safety Information
RTECS
FF2200000
German water hazard class
3
Storage Temperature
-20°C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Safety Statements
26-36/37/39
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Hazard statements
H315-H318-H335
Risk Statements
37/38-41
European Hazard Symbols
Irritant (Xi)GHS Precautionary statements
P261-P280-P305+P351+P338
GHS Signal Word
Danger
MSDS Link
Physical Property
Melting Point
110-115 °C(lit.)
110-115 °C
Molecule Details
Biochem/physiol Actions
Water soluble condensing reagent. EDAC is generally utilized as a carboxyl activating agent for amide bonding with primary amines. In addition, it will react with phosphate groups. EDAC has been used in peptide synthesis; crosslinking proteins to nucleic acids; and preparation of immunoconjugates as examples. Typically, EDAC is utilized in the pH range 4.0-6.0 without buffers. In particular, amine and carboxylate buffers should be avoided.
Water soluble condensing reagent. EDAC is generally utilized as a carboxyl activating agent for amide bonding with primary amines. In addition, it will react with phosphate groups. EDAC has been used in peptide synthesis; crosslinking proteins to nucleic acids; and preparation of immunoconjugates as examples. Typically, EDAC is utilized in the pH range 4.0-6.0 without buffers. In particular, amine and carboxylate buffers should be avoided.
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data