1-(3-(Dimethylamino)propyl)-3-ethylcarbodiimide methiodide

HCID 122242

노트 반응

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부분 구조 검색 유사 구조 찾기

기본 정보

CAS: 22572-40-3
표준 SMILES: CCN=C=NCCC[N+](C)(C)C.[I-]
InChIKey: AGSKWMRPXWHSPF-UHFFFAOYSA-M
분자식: C9H20IN3
평균 분자량: 297.18 g/mol

이름 및 식별자

우선 이름: 1-(3-(Dimethylamino)propyl)-3-ethylcarbodiimide methiodide
IUPAC: 3-(ethyliminomethylideneamino)propyl-trimethylazanium iodide

이름 및 동의어

22572-40-3EDC methiodide1-ethyl-3-(3-(dimethylamino)propyl)carbodiimide methiodide1-[3-(Dimethylamino)propyl]-3-ethylcarbodiimide methiodide73U5123RNTNSC-2827621-ethyl-3-(3-dimethylaminopropyl)carbodiimide methiodide1-Propanaminium, 3-(ethylcarbonimidoylamino)-N,N,N-trimethyl-, iodide1-(3-(dimethylamino)propyl)-3-ethylcarbodiimide methiodideETC carbodiimideRefChem:75737245-095-1

이름 더 보기

1-(3-DIMETHYLAMINOPROPYL)-3-ETHYLCARBODIIMIDE METHIODIDEMFCD00011833UNII-73U5123RNTEINECS 245-095-1NSC 282762(3-((Ethylimidocarbonyl)amino)propyl)trimethylammonium iodide3-(((Ethylimino)methylene)amino)-N,N,N-trimethylpropan-1-aminium iodide3-[[(Ethylimino)methylene]amino]-N,N,N-trimethylpropan-1-aminium Iodide

데이터베이스 식별자

CAS: 22572-40-3
PubChem CID: 122242
DTXSID: DTXSID20945227
UNII: 73U5123RNT
EC Number: 245-095-1

물성

구조 계산 물성보충 중

극성 표면적: 24.7 Å²
수소 결합 공여자 수: 0
수소 결합 수용자 수: 3
회전 가능 결합 수: 5
무거운 원자 수: 13
형식 전하: 0
복잡도: 161

안전 및 규제

GHS 분류

GHS Classification · 4건

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 45 reports by companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Hazard Classes and CategoriesAcute Tox. 4 (100%)

화학 및 산업

약리 정보

MeSH Pharmacological Classification · 1건

Reagents with two reactive groups, usually at opposite ends of the molecule, that are capable of reacting with and thereby forming bridges between side chains of amino acids in proteins; the locations of naturally reactive areas within proteins can thereby be identified; may also be used for other macromolecules, like glycoproteins, nucleic acids, or other.