4-아미노살리실 산

4-아미노살리실 산
4-아미노살리실 산 구조식 이미지
카스 번호:
65-49-6
한글명:
4-아미노살리실 산
동의어(한글):
4-아미노살리실산;4-아미노살리실산;4-아미노살리실릭애씨드;4-아미노살리실릭애씨드및그염류
상품명:
4-Aminosalicylic acid
동의어(영문):
4-AMINO-2-HYDROXYBENZOIC ACID;PAS;AMINOSALICYLIC ACID;Pasa;4-Asa;P-AMINOSALICYLIC ACID;Apas;Paser;Aminox;Parasal
CBNumber:
CB9679687
분자식:
C7H7NO3
포뮬러 무게:
153.14
MOL 파일:
65-49-6.mol
MSDS 파일:
SDS

4-아미노살리실 산 속성

녹는점
135-145 °C (lit.)
끓는 점
276.03°C (rough estimate)
밀도
1.3585 (rough estimate)
굴절률
1.5500 (estimate)
저장 조건
Keep in dark place,Inert atmosphere,Room temperature
용해도
1.69g/L
물리적 상태
가루
산도 계수 (pKa)
3.25(at 25℃)
색상
무색의
수소이온지수(pH)
3.5 (1g/l, H2O, 20℃)
수용성
2g/L(20℃)
Merck
14,477
BRN
473071
BCS Class
4/2
안정성
흡습성
CAS 데이터베이스
65-49-6(CAS DataBase Reference)
NIST
Aminosalicylic acid(65-49-6)
EPA
4-Aminosalicylic acid (65-49-6)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi,T
위험 카페고리 넘버 22-36-36/37/38-45-35-61
안전지침서 26-37/39-45-53-36-36/37/39
유엔번호(UN No.) UN 1789 8/PG 3
WGK 독일 2
RTECS 번호 VO1225000
TSCA Yes
HS 번호 29225000
유해 물질 데이터 65-49-6(Hazardous Substances Data)
독성 LD50 orally in mice: 4 g/kg (Bavin)
기존화학 물질 KE-01389
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:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
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
0
2 0

4-아미노살리실 산 MSDS


PAS

4-아미노살리실 산 C화학적 특성, 용도, 생산

화학적 성질

beige powder

용도

antimycobacterial antitubercular;NF-kB inhibitor.
4-Aminosalicylic acid (p-aminosalicylic acid, PAS), an antituberculosis drug, is a model active pharmaceutical ingredient to study salt and cocrystal formation in a multiple hydrogen-bonding functionality molecule with carboxylic acid, amine, and phenol groups.
It has also been used as a second line agent to sulfasalazine in people with inflammatory bowel disease such as ulcerative colitis and Crohn's disease.It is typically taken by mouth.

주요 응용

4-Aminosalicylic acid (4-ASA) can be used in the synthesis of:
Azo derivatives of 4-ASA with anti-inflammatory effects.
Ammonium 4-aminosalicylate salt polymorphs which are used as pharmaceutical ingredients.
Salicylic acid-triazole analogs which are used as quorum sensing inhibitors against Pseudomonas aeruginosa.

Indications

p-Aminosalicylic acid is a bacteriostatic that inhibits most tuberculous mycobacteria. In terms of tuberculostatic activity it is inferior to isoniazid and streptomycin. It is nephroand hepatotoxic, and is rarely used. A synonym of this drug is apacizin.

정의

ChEBI: An aminobenzoic acid that is salicylic acid substituted by an amino group at position 4.

일반 설명

4-Aminosalicylic acid occurs as a white to yellowish white crystalline solid that darkens on exposure to light or air. It is slightly soluble in water but more soluble in alcohol. Alkali metal salts and the nitric acid salt are soluble in water, but the salts of hydrochloric acid and sulfuric acid are not. The acid undergoes decarboxylation when heated. An aqueous solution has a pH of approximately 3.2. PAS is administered orally in the form of the sodium salt, usually in tablet or capsule form. Symptoms of gastrointestinal irritation are common with both the acid and the sodium salt. Various enteric-coated dosage forms have been used in an attempt to overcome this disadvantage. Other forms that are claimed to improve gastrointestinal tolerance include the calcium salt, the phenyl ester, and a combination with an anion exchange resin (Rezi-PAS). An antacid such as aluminum hydroxide is frequently prescribed. The oral absorption of PAS is rapid and nearly complete, and it is widely distributed into most of the body fluids and tissues, with the exception of the CSF, in which levels are significantly lower.It is excreted primarily in the urine as both unchanged drug and metabolites.

생물학적 활성

4-Aminosalicylic acid is an antimetabolite of p-aminobenzoic acid (PABA) that has antibacterial activity.It is active against streptomycin-sensitive and -resistant strains of M. tuberculosis (MICs = 0.78 and 0.39 μg/ml, respectively), an effect that can be reversed by PABA. 4-Aminosalicylic acid is an alternative substrate for mycobacterial dihydropteroate synthase (FolP1) and misincorporation into the folate pathway leads to accumulation of several folate-dependent metabolites including serine, homocysteine, dUMP, and AICAR, markers of folate pathway inhibition, in a concentration-dependent manner. It reverses manganese-induced increases in rat hippocampal levels of NOD-like receptor protein 3 (NLRP3), cleaved caspase-1, and phosphorylated p65, markers of NLRP3 inflammasome-dependent pyroptosis, when administered at a dose of 300 mg/kg. 4-Aminosalycilic acid is also a building block that has been used in the synthesis of luminescent lanthanide complexes. Formulations containing 4-aminosalicylic acid have been used in the treatment of tuberculosis.

Mechanism of action

p-aminosalicylic acid is thought to act as an antimetabolite interfering with the incorporation of p-aminobenzoic acid into folic acid. When coadministered with INH, PAS is found to reduce the acetylation of INH, itself being the substrate for acetylation, thus increasing the plasma levels of INH. This action may be especially valuable in patients who are rapid acetylators.

Safety Profile

Moderately toxic ingestion andother routes. An eye irritant. Mutation data reported.When heated to decomposition it emits toxic fumes ofNOx.

신진 대사

p-aminosalicylic acid is extensively metabolized by acetylation of the amino group and by conjugation with glucuronic acid and glycine at the carboxyl group. It is used primarily in cases of resistance, retreatment, and intolerance of other agents and is available from the CDC.

Purification Methods

Crystallise the acid from EtOH. [Beilstein 14 IV 1967.]

4-아미노살리실 산 준비 용품 및 원자재

원자재

준비 용품


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