6-아미노 카프로산

6-아미노 카프로산
6-아미노 카프로산 구조식 이미지
카스 번호:
60-32-2
한글명:
6-아미노 카프로산
동의어(한글):
6-아미노카프로산;아미노캅프로산;ε-아미노카프로산;아미노캅프로산;6-아미노카프로익애씨드;아미노카프로익애씨드;아미노카프로익애씨드및그염류;6-아미노캅프로 산;6-아미노-헥사오익 산;6-아미노헥산오익 산;6-아밈노-N-헥산오익 산;아미노캅프로 산;아미카르;엡실론-노르루신;엡실론-루신;엡실론-아미노-N-캅프로 산;엡실론-아미노캅프로 산;엡실론-아미노헥산오익 산;엡실카프라민;오메가-아미노캅프로 산
상품명:
6-Aminocaproic acid
동의어(영문):
6-AMINOHEXANOIC ACID;ACS;Aminocaproic;6-aminohexanoate;EACA;Amicar;H-ACP-OH;Hepin;177 J.D;aminocaproic acid,EACA
CBNumber:
CB5223888
분자식:
C6H13NO2
포뮬러 무게:
131.17
MOL 파일:
60-32-2.mol
MSDS 파일:
SDS

6-아미노 카프로산 속성

녹는점
207-209 °C (dec.) (lit.)
끓는 점
242.49°C (rough estimate)
밀도
1.042 g/cm3
증기압
<0.1 hPa (20 °C)
굴절률
1.4870 (estimate)
인화점
207-209°C
저장 조건
Store below +30°C.
용해도
H2O: 50 mg/mL
물리적 상태
가루
산도 계수 (pKa)
4.373(at 25℃)
색상
하얀색
냄새
냄새 없는
수소이온지수(pH)
7.0-7.5 (50g/l, H2O, 20℃)
수용성
녹는
Merck
14,432
BRN
906872
InChIKey
SLXKOJJOQWFEFD-UHFFFAOYSA-N
LogP
0.027 (est)
CAS 데이터베이스
60-32-2(CAS DataBase Reference)
NIST
Hexanoic acid, 6-amino-(60-32-2)
EPA
Hexanoic acid, 6-amino- (60-32-2)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 36/37/38
안전지침서 26-36
WGK 독일 2
RTECS 번호 MO6300000
TSCA Yes
HS 번호 29224995
유해 물질 데이터 60-32-2(Hazardous Substances Data)
독성 LD50 in rats (g/kg): 7.0 i.p.; ~3.3 i.v. (Hallesy)
기존화학 물질 KE-01382
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
H320 눈에 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2B 경고 P264, P305+P351+P338,P337+P313
H335 호흡 자극성을 일으킬 수 있음 특정 표적장기 독성 - 1회 노출;호흡기계 자극 구분 3 경고 GHS hazard pictograms
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P304+P340 흡입하면 신선한 공기가 있는 곳으로 옮기고 호흡하기 쉬운 자세로 안정을 취하시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P405 밀봉하여 저장하시오.
NFPA 704
1
2 0

6-아미노 카프로산 MSDS


6-Aminohexanoic acid

6-아미노 카프로산 C화학적 특성, 용도, 생산

화학적 성질

white crystalline powder. Leaf crystals were obtained from ether. Odorless, bitter taste. Melting point 202 ~ 207 ℃ (decomposition). Soluble in water, slightly soluble in methanol, insoluble in ethanol, ether and chloroform.

제조 방법

6-aminocaproic acid is obtained by hydrolysis of 6-(N-benzoylamino)capronitrile in the presence of hydrochloric acid, or by hydrolysis of caprolactam in the presence of hydrochloric acid, and then treated with ammonium hydroxide.

정의

ChEBI: 6-aminohexanoic acid is an epsilon-amino acid comprising hexanoic acid carrying an amino substituent at position C-6. Used to control postoperative bleeding, and to treat overdose effects of the thrombolytic agents streptokinase and tissue plasminogen activator. It has a role as an antifibrinolytic drug, a hematologic agent and a metabolite. It is an epsilon-amino acid and an omega-amino fatty acid. It derives from a hexanoic acid. It is a conjugate acid of a 6-aminohexanoate. It is a tautomer of a 6-aminohexanoic acid zwitterion.

주요 응용

6-Aminohexanoic acid was used as a biochemical reagent. It is also used as a hemostatic agent. 6-aminocaproic acid has a significant effect on some severe bleeding caused by increased fibrinolytic activity. It is suitable for oozing or local bleeding during various surgical operations. 6-aminocaproic acid is used for hemoptysis, gastrointestinal bleeding and bleeding disorders in obstetrics and gynecology.
6-Aminocaproic acid is an anti-fibrinolytic drug with a similar chemical structure to lysine. It can qualitatively inhibit the binding of plasminogen to fibrin and prevent its activation, thereby inhibiting fibrinolysis and achieving hemostasis. Aminocaproic acid is a monoaminocarboxylic acid, which can inhibit the conversion of plasminogen into plasmin and its binding to fibrin. For severe bleeding caused by hyperfibrinolysis caused by increased activation of plasminogen, can have therapeutic effect.

일반 설명

6-Aminocaproic acid is a synthetic inhibitor of fibrinolysis and is utilized for the control of excessive bleeding in patients with amegakaryocytic thrombocytopenia. It also is a protease inhibitor that displays anticancer activity but is limited by cytotoxicity.

Mechanism of action

Because binding of plasminogen or plasmin to fibrinogen or fibrin is mediated by lysine groups that are part of the structures of fibrin and fibrinogen, aminocaproic acid, which is a structural analog of lysine that only differs in that it has one less amino group, acts as a competitive inhibitor for binding of plasmin(ogen) to fibrin. Aminocaproic acid shifts the homeostatic balance on the side of coagulation, thus restoring fibrinolytic mechanism activity. Aminocaproic acid, which is not a procoagulant, such as those used during surgical intervention and various pathological conditions, is accompanied by an elevation in fibrinolytic activity of blood and tissue. It is used to stop bleeding.

Safety Profile

Moderately toxic by intravenous route. Human systemic effects by ingestion: changes in tubules (includmg acute renal failure, acute tubular necrosis), hematuria, and increased body temperature. Experimental reproductive effects. An eye irritant. When heated to decomposition it emits toxic fumes such as NOx,.

6-아미노 카프로산 준비 용품 및 원자재

원자재

준비 용품


6-아미노 카프로산 공급 업체

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