アンピシリン三水和物

アンピシリン三水和物 化学構造式
7177-48-2
CAS番号.
7177-48-2
化学名:
アンピシリン三水和物
别名:
アンピシリン三水和物;アンピシリン三水和物標準品;D-(-)-α-アミノベンジルペニシリン三水和物;アンピシリン 三水和物;アンピシリン三水和物, RESEARCH GRADE, PH. EUR.;アンピシリン水和物;アンピシリン水和物 (JP17);アンピシリン・3水和物;アンピシリン・三水和物
英語名:
Ampicillin
英語别名:
AMPICILLIN TRIHYDRATE;amcill;trafarbiot;amcap;cymbi;amplin;pensyn;amperil;morepen;ro-ampen
CBNumber:
CB5247347
化学式:
C16H25N3O7S
分子量:
403.45
MOL File:
7177-48-2.mol
MSDS File:
SDS

アンピシリン三水和物 物理性質

融点 :
208 °C (dec.)(lit.)
沸点 :
684℃
屈折率 :
265 ° (C=0.1, H2O)
闪点 :
87 °C
貯蔵温度 :
Sealed in dry,2-8°C
溶解性:
NH4OH 1 M: 50 mg/mL、無色透明
外見 :
個体
色:
ホワイトからオフホワイト
酸解離定数(Pka):
2.5 (COOH)(at 25℃)
水溶解度 :
21℃で0.1~1g/100mL
Merck :
14,586
BRN :
5399534
安定性::
Hygroscopic
InChIKey:
RXDALBZNGVATNY-CWLIKTDRSA-N
CAS データベース:
7177-48-2(CAS DataBase Reference)
EPAの化学物質情報:
Ampicillin trihydrate (7177-48-2)
安全性情報
  • リスクと安全性に関する声明
  • 危険有害性情報のコード(GHS)
主な危険性  Xn,Xi
Rフレーズ  36/37/38-42/43
Sフレーズ  22-26-36/37-36-45-23
WGK Germany  2
RTECS 番号 XH8425000
3-10
HSコード  29411020
毒性 LD50 orl-rat: 10 g/kg ANTBAL 20,653,75
絵表示(GHS) GHS hazard pictograms
注意喚起語 危険
危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード
H317 アレルギー性皮膚反応を起こすおそれ 感作性、皮膚 1 警告 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H334 吸入するとアレルギー、喘息または、呼吸困難 を起こすおそれ 感作性、呼吸器 1 危険 GHS hazard pictograms P261, P285, P304+P341, P342+P311,P501
注意書き
P261 粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。
P272 汚染された作業衣は作業場から出さないこと。
P280 保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。
P284 呼吸用保護具を着用すること。
P302+P352 皮膚に付着した場合:多量の水と石鹸で洗うこと。
P333+P313 皮膚刺激または発疹が生じた場合:医師の診断/手当てを 受けること。

アンピシリン三水和物 価格 もっと(22)

メーカー 製品番号 製品説明 CAS番号 包装 価格 更新時間 購入
富士フイルム和光純薬株式会社(wako) W01LKTA5160 アンピシリン三水和物
Ampicillin Trihydrate
7177-48-2 5g ¥13400 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01MPB02190147
Ampicillin trihydrate
7177-48-2 100g ¥40600 2024-03-01 購入
富士フイルム和光純薬株式会社(wako) W01LKTA5160 アンピシリン三水和物
Ampicillin Trihydrate
7177-48-2 25g ¥34800 2024-03-01 購入
東京化成工業 A2092 アンピシリン三水和物 >98.0%(HPLC)(T)
Ampicillin Trihydrate >98.0%(HPLC)(T)
7177-48-2 5g ¥4100 2024-03-01 購入
東京化成工業 A2092 アンピシリン三水和物 >98.0%(HPLC)(T)
Ampicillin Trihydrate >98.0%(HPLC)(T)
7177-48-2 25g ¥13800 2024-03-01 購入

アンピシリン三水和物 MSDS


Ampicillin

アンピシリン三水和物 化学特性,用途語,生産方法

外観

白色~黄赤色~緑色粉末~結晶

効能

抗生物質, 細胞壁合成阻害薬

商品名

ビクシリン (Meiji Seikaファルマ); ビクシリン (Meiji Seikaファルマ)

化学的特性

Ampicillin in anhydrous form occurs as crystals.

使用

Commonly used to select for ampicillin resistance in mutated and transformed cells

適応症

Ampicillin may also be helpful in certain patients, particularly pregnant women with acne, for whom the use of tetracycline, erythromycin, and minocycline should be avoided. In resistant acne patients, culture may reveal a gram-negative bacteria responsive to ampicillin.

抗菌性

Ampicillin is slightly less active than benzylpenicillin against most Gram-positive bacteria but is more active against E. faecalis. MRSA and strains of Str. pneumoniae with reduced susceptibility to benzylpenicillin are resistant. Most group D streptococci, anaerobic Gram-positive cocci and bacilli, including L. monocytogenes, Actinomyces spp. and Arachnia spp., are susceptible. Mycobacteria and nocardia are resistant.
Ampicillin has similar activity to benzylpenicillin against N. gonorrhoeae, N. meningitidis and Mor. catarrhalis. It is 2–8 times more active than benzylpenicillin against H. influenzae and many Enterobacteriaceae, but β-lactamase-producing strains are resistant. Pseudomonas spp. are resistant, but Bordetella, Brucella, Legionella and Campylobacter spp. are often susceptible. Certain Gram-negative anaerobes such as Prevotella melaninogenica and Fusobacterium spp. are susceptible, but B. fragilis is resistant, as are mycoplasmas and rickettsiae.
Activity against molecular class A β-lactamase-producing strains of staphylococci, gonococci, H. influenzae, Mor. catarrhalis, certain Enterobacteriaceae and B. fragilis is enhanced by the presence of β-lactamase inhibitors, specifically clavulanic acid.
Its bactericidal activity resembles that of benzylpenicillin. Bactericidal synergy occurs with aminoglycosides against E. faecalis and many enterobacteria, and with mecillinam against a number of ampicillin-resistant enterobacteria.

獲得抵抗性

β-Lactamase-producing pathogens, including most clinical isolates of Staph. aureus, are resistant. Strains of pneumococci, enterococci, gonococci and H. influenzae with altered PBPs have reduced susceptibility to ampicillin. Isolates of N. gonorrhoeae and H. influenzae with a TEM plasmid- mediated β-lactamase (which are more common) are fully resistant. Resistance among H. influenzae is often linked with resistance to chloramphenicol, erythromycin or tetracycline, due to plasmid-encoded resistance markers that are co-transferred with the gene for the TEM enzyme. However, at least 70% of current H. influenzae isolates remain susceptible to ampicillin worldwide.
The widespread use of ampicillin and other aminopenicillins has led to resistance becoming common in formerly susceptible species of enteric pathogens as a result of the widespread dissemination of plasmid-mediated β-lactamases. Surveillance data from North America and Europe indicate less than 50% susceptibility to ampicillin in Esch. coli. At least 90% of current isolates of Mor. catarrhalis are β-lactamaseproducing strains. Ampicillin-resistant strains of salmonellae, notably S. enterica serotypes Typhi and Typhimurium (many of which are also resistant to chloramphenicol, sulfonamides and tetracyclines) present a serious problem in Africa, Asia and South America. Multiresistant strains of shigellae also predominate in many parts of the world.

一般的な説明

Odorless white microcrystalline powder with a bitter taste. A 0.25% solution in water has a pH of 3.5 to 5.5.

空気と水の反応

Slightly soluble in water.

反応プロフィール

Ampicillin absorbs insignificant amounts of moisture at 77° F and relative humidities up to approximately 80%, but under damper conditions Ampicillin absorbs significant amounts. A pH-rate profile reveals specific-acid- and specific-base- catalyzed hydrolysis. The pH of maximum stability is 5.8.

火災危険

Flash point data for Ampicillin are not available; however, Ampicillin is probably combustible.

接触アレルゲン

Ampicillin caused contact dermatitis in a nurse also sensitized to amoxicillin (with tolerance to oral phenoxymethylpenicillin) and in a pharmaceutical factory worker. Systemic drug reactions are common. Crossreactivity is regular with ampicillin and can occur with other penicillins.

臨床応用

Isolates should be tested for susceptibility before use, especially for serious infections. For oral therapy, amoxicillin is preferable to ampicillin.
Urinary tract infections
Bacterial meningitis
Respiratory tract infections
Gastrointestinal infections, including typhoid fever and bacillary dysentery Enterococcal endocarditis and septicemia (in combination with an aminoglycoside)
Listeriosis (in combination with an aminoglycoside)

安全性プロファイル

Mildly toxic by ingestion. An experimental teratogen. Other experimental reproductive effects. When heated to decomposition it emits toxic fumes of SO,xand NOx.

職業ばく露

Used as an antibiotic.

輸送方法

UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

不和合性

May be incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

廃棄物の処理

It is inappropriate and possibly dangerous to the environment to dispose of expired or waste pharmaceuticals by flushing them down the toilet or discarding them to the trash. Household quantities of expired or waste pharmaceuticals may be mixed with wet cat litter or coffee grounds, double-bagged in plastic, discard in trash. Larger quantities shall carefully take into consideration applicable DEA, EPA, and FDA regulations. If possible return the pharmaceutical to the manufacturer for proper disposal being careful to properly label and securely package the material. Alternatively, the waste pharmaceutical shall be labeled, securely packaged and transported by a state licensed medical waste contractor to dispose by burial in a licensed hazardous or toxic waste landfill or incinerator.

アンピシリン三水和物 上流と下流の製品情報

原材料

準備製品


アンピシリン三水和物 生産企業

Global( 561)Suppliers
名前 電話番号 電子メール 国籍 製品カタログ 優位度
Capot Chemical Co.,Ltd.
571-85586718 +8613336195806
sales@capotchem.com China 29797 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845
sales@amoychem.com China 6387 58
HubeiwidelychemicaltechnologyCo.,Ltd
18627774460
faith@widelychemical.com CHINA 742 58
Chongqing Chemdad Co., Ltd
+86-023-61398051 +8613650506873
sales@chemdad.com China 39916 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427
sales@conier.com China 49390 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-81138252 +86-18789408387
1057@dideu.com China 3487 58
ENBRIDGE PHARMTECH CO., LTD.
+8613812269233
tinayang@enbridgepharm.com China 303 58
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12456 58

アンピシリン三水和物  スペクトルデータ(IR1、IR2、MS、Raman)


7177-48-2(アンピシリン三水和物)キーワード:


  • 7177-48-2
  • amcap
  • aminobenzylpenicillintrihydrate
  • amperil
  • ampichel
  • ampinova
  • ro-ampen
  • trihydrate,d-(-)-do)-3-dimethyl-7-oxo-
  • AMP TABS(TM)
  • ALPHA-AMINOBENZYLPENICILLIN, TRIHYDRATE
  • (2s,5r,6r)-6-[(r)-2-amino-2-phenylacetamido]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
  • (2S,5R,6R)-6-((R)-2-AMINO-2-PHENYL-ACETYLAMINO)-3,3-DIMETHYL-7-OXO-4-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYLIC ACID
  • 6-[D-ALPHA-AMINOPHENYLACETAMIDO]PENICILLANIC ACID TRIHYDRATE
  • d-(-)-6-(2-amino-2-phenylacetamido)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid trihydrate
  • D(-)-ALPHA-AMINOBENZYLPENICILLIN TRIHYDRATE
  • ampicillin,cilleral,principen
  • AMPICILLIN TRIHYDRATE VETRANAL, 250
  • 4-Thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid, 6-(2-amino-2-phenylacetamido)- 3,3-dimethyl-7-oxo-, trihydrate, D- (-)
  • Ampicillin trihydrate,D-()-α-Aminobenzylpenicillin
  • Ampicillin Trihydrate (200 mg)
  • AMPICILLIN CRYST.RESEARCH GRADE
  • AMpicillin Trihydrate CoMpacted / Powder
  • 4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 6-[[(2R)-2-amino-2-phenylacetyl]amino]-3,3-dimethyl-7-oxo-, hydrate (1:3), (2S,5R,6R)-
  • 6-{[Amino(phenyl)acetyl]amino}-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxyl
  • amplin
  • cymbi
  • divercillin
  • lifeampil
  • morepen
  • nci-c56086
  • pensyn
  • アンピシリン三水和物
  • アンピシリン三水和物標準品
  • D-(-)-α-アミノベンジルペニシリン三水和物
  • アンピシリン 三水和物
  • アンピシリン三水和物, RESEARCH GRADE, PH. EUR.
  • アンピシリン水和物
  • アンピシリン水和物 (JP17)
  • アンピシリン・3水和物
  • アンピシリン・三水和物
  • 抗生物質
  • 生化学
  • 試験研究用抗菌剤
  • β-ラクタム系 (試験研究用抗生物質)
  • 生活関係標準物質
  • 食料品
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