O-ALLYLHYDROXYLAMINE HYDROCHLORIDE

O-ALLYLHYDROXYLAMINE HYDROCHLORIDE 구조식 이미지
카스 번호:
38945-21-0
상품명:
O-ALLYLHYDROXYLAMINE HYDROCHLORIDE
동의어(영문):
(Allyloxy)amine hydrochloride;O-ALLYHYDROXYAMINE HYDROCHLORIDE);O-ALLYLHYDROXYLAMINE HYDROCHLORIDE;3-(Aminooxy)prop-1-ene hydrochloride;O-Allylhydroxylamine Hydrochloride >O-prop-2-enylhydroxylamine hydrochloride;O-(2-PROPENYL)HYDROXYLAMINE HYDROCHLORIDE;O-Allylhydroxylamine Hydrochloride;HydroxylaMine, O-2-propenyl-, hydrochloride;O-Allylhydroxylamine hydrochloride >=98.0% (AT)
CBNumber:
CB7738618
분자식:
C3H8ClNO
포뮬러 무게:
109.55
MOL 파일:
38945-21-0.mol
MSDS 파일:
SDS

O-ALLYLHYDROXYLAMINE HYDROCHLORIDE 속성

녹는점
~170 °C (dec.)
저장 조건
under inert gas (nitrogen or Argon) at 2-8°C
물리적 상태
powder to crystal
색상
흰색에서 거의 흰색
BRN
3552394
InChIKey
XIQUJVRFXPBMHS-UHFFFAOYSA-N
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36
WGK 독일 3
F 고인화성물질 3-9
HS 번호 2928009090
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
NFPA 704
0
2 0

O-ALLYLHYDROXYLAMINE HYDROCHLORIDE C화학적 특성, 용도, 생산

제조 방법

To a solution of 86.8 gm (1.55 moles) of potassium hydroxide in 330 ml of absolute ethanol is added a solution of 159 gm (1.52 moles) of ethyl N-hydroxycarbamate in 330 ml of absolute ethanol. With external cooling to maintain an internal temperature of 25°C to this mixture is added 195.5 gm (1.62 moles) of allyl bromide. After the addition has been com­pleted, the mixture is heated under reflux for 2 hr. After separating the potassium bromide formed during the reaction and washing it with abso­lute alcohol, the alcoholic solution is evaporated under reduced pressure. The residue is dissolved in ether and then the ether solution is extracted repeatedly with 10% aqueous sodium hydroxide solution. [From the ether solution, on evaporation 25.5 gm (18%) of ethyl N,O-diallylhydroxycar-bamate, b.p. 91-92°C (8.55 mm Hg) may be isolated.] The aqueous ex­tract is acidified with 10% aqueous sulfuric acid and the ethyl O-allylhy-droxycarbamate is extracted with ether. Upon evaporating the ether off, 134.2 gm (61%) of the intermediate product, b.p. 107°C (12.5 mm Hg), is isolated.
In a steam distillation apparatus, 134 gm of ethyl O-allylhydroxy-carbamate is treated with a solution of 120 gm of potassium hydroxide in 280 ml of water. The product is steam-distilled into a receiver containing dilute hydrochloric acid.
The steam distillate is evaporated under reduced pressure. The residue is taken up twice in absolute ethanol and dried by evaporation under re­duced pressure. The yield is 91 gm (55%, overall), m.p. 169-170°C. Upon recrystallization from absolute alcohol and dry ether, the melting point is raised to 170.6-170.8°C (172-174°C). Free O-allylhydrox-ylamine has the following reported properties: b.p. 98-99°C, n25D 1.4300.
The problems connected with the preparation of O-arylhydroxylamines by this method have been attributed to the instability of the aryl- substituted aminooxy group to the hydrolytic system used in its prepara­tion. This problem has recently been circumvented by substituting for ethyl N-hydroxycarbamate, t-butyl N-hydroxycarbamate.
Preparation of O-Allylhydroxylamine Hydrochloride

O-ALLYLHYDROXYLAMINE HYDROCHLORIDE 준비 용품 및 원자재

원자재

준비 용품


O-ALLYLHYDROXYLAMINE HYDROCHLORIDE 공급 업체

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