アフラトキシン B1
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アフラトキシン B1 物理性質(zhì)
- 融點(diǎn) :
- 268-269 °C
- 比旋光度 :
- D -558° (c = 0.1 in CHCl3); D -480° (c = 0.1 in DMF)
- 沸點(diǎn) :
- 372.21°C (rough estimate)
- 比重(密度) :
- 1.2810 (rough estimate)
- 屈折率 :
- 1.4800 (estimate)
- 閃點(diǎn) :
- 2 °C
- 貯蔵溫度 :
- 2-8°C
- 溶解性:
- DMF: 20 mg/ml; DMF:PBS(pH 7.2)(1:1): 0.5 mg/ml; DMSO: 12 mg/ml
- 外見(jiàn) :
- 白色から黃色の粉末。
- 色:
- White to yellow
- 水溶解度 :
- 15mg/L(溫度表記なし)
- Merck :
- 13,180
- BRN :
- 1269174
- 安定性::
- 安定。強(qiáng)力な酸化剤とは相容れない。光や空気に敏感な場(chǎng)合があります。
- InChIKey:
- OQIQSTLJSLGHID-WNWIJWBNSA-N
- LogP:
- 2.039 (est)
- EPAの化學(xué)物質(zhì)情報(bào):
- Aflatoxin B1 (1162-65-8)
安全性情報(bào)
- リスクと安全性に関する聲明
- 危険有害性情報(bào)のコード(GHS)
主な危険性 | T+,T,Xn,F | ||
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Rフレーズ | 45-46-26/27/28-36-20/21/22-11-65-48/23/24/25-36/38-39/23/24/25-23/24/25 | ||
Sフレーズ | 53-45-36-26-16-24-7-62-36/37-28 | ||
RIDADR | UN 3462 6.1/PG 1 | ||
WGK Germany | 3 | ||
RTECS 番號(hào) | GY1925000 | ||
F | 10 | ||
國(guó)連危険物分類(lèi) | 6.1(a) | ||
容器等級(jí) | I | ||
HSコード | 29322090 | ||
有毒物質(zhì)データの | 1162-65-8(Hazardous Substances Data) | ||
毒性 | LD50 orally in day old duckling: 18.2 mg/50 gm body wt (Carnaghan); i.p. in newborn mice: 9.50 mg/kg body wt (Büchi) | ||
消防法 | 危-4-1-S-II | ||
安衛(wèi)法 | 57-2 | ||
PRTR法 | 1-13 | ||
毒劇物取締法 | II |
絵表示(GHS) | |||||||||||||||||||||||||||||
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注意喚起語(yǔ) | 危険 | ||||||||||||||||||||||||||||
危険有害性情報(bào) |
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注意書(shū)き |
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アフラトキシン B1 価格 もっと(26)
メーカー | 製品番號(hào) | 製品説明 | CAS番號(hào) | 包裝 | 価格 | 更新時(shí)間 | 購(gòu)入 |
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富士フイルム和光純薬株式會(huì)社(wako) | W01LKTA2044 | アフラトキシンB1 Aflatoxin B1 |
1162-65-8 | 1mg | ¥15500 | 2024-03-01 | 購(gòu)入 |
富士フイルム和光純薬株式會(huì)社(wako) | W01W0101-2430 | アフラトキシンB1標(biāo)準(zhǔn)液 (25μg/mlアセトニトリル溶液) Aflatoxin B1 Standard Solution(25μg/ml Acetonitrile Solution) |
1162-65-8 | 1mL×5A | ¥30800 | 2024-03-01 | 購(gòu)入 |
富士フイルム和光純薬株式會(huì)社(wako) | W01LKTA2044 | Aflatoxin B1 |
1162-65-8 | 10mg | ¥100400 | 2024-03-01 | 購(gòu)入 |
富士フイルム和光純薬株式會(huì)社(wako) | W01CHDASB-00001480 | アフラトキシンB1 Aflatoxin B1 |
1162-65-8 | 10mg | ¥304200 | 2024-03-01 | 購(gòu)入 |
富士フイルム和光純薬株式會(huì)社(wako) | 49161-37 | Aflatoxin B1 standard solution |
1162-65-8 | 1mL | ¥54000 | 2024-07-01 | 購(gòu)入 |
アフラトキシン B1 化學(xué)特性,用途語(yǔ),生産方法
外観
無(wú)色澄明の液體解説
アフラトキシン B1,アスペルギルス屬が生産するかび毒の一種.1960年にイギリスで発生した,10萬(wàn)羽以上の七面鳥(niǎo)が死亡した事件をきっかけに発見(jiàn)された."アフラトキシン B1 のほか,B2,G1,G2,M1 なども知られているが,毒性,発がん性は B1 がもっとも強(qiáng)力である.無(wú)色の結(jié)晶.分解點(diǎn)268~269 ℃.[α]D"-562°(クロロホルム).ピーナツ,トウモロコシ,ナツメグなどさまざまな食品から微量であるが検出されることがある.強(qiáng)い発がん性がある.
森北出版「化學(xué)辭典(第2版)
効能
致死毒性;発がん性化學(xué)的特性
The aflatoxins are a group of molds produced by the fungus Aspergillus flavus. They are natural contaminants of fruits, vegetables, and grains. They are also described as a series of condensed ring heterocyclic compounds. They form colorless to pale yellow crystals. Practically insoluble in water.使用
Aflatoxin B1 is the major analogue of a family of bisfuranocoumarin mycotoxins produced by Aspergillus flavus and related species. Aflatoxin B1 exhibits a distinctive UV spectrum and blue fluorescence. Aflatoxins are among the most potent mycotoxins known but are in fact "pre-toxins", requiring metabolic activation to the toxic principle. Aflatoxins are found widely in nature in trace amounts, particularly in grains and nuts. The toxicity of these metabolites was first recognised in the 1950s and their structures elucidated in 1963. Aflatoxins have been extensively reviewed.定義
ChEBI: An aflatoxin having a tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h]chromene skeleton with oxygen functionality at positions 1, 4 and 11.一般的な説明
Colorless to pale yellow crystals or white powder. Exhibits blue fluorescence.空気と水の反応
Sensitive to exposure to air and light. Water insoluble.反応プロフィール
AFLATOXIN B1 is incompatible with strong oxidizing agents, strong acids and strong bases.火災(zāi)危険
Flash point data for AFLATOXIN B1 are not available; however, AFLATOXIN B1 is probably combustible.安全性プロファイル
Confirmed human carcinogen with experimental tumorigenic, neoplas tigenic, and carcinogenic data. Acute poison by ingestion, intraperitoneal, and possibly other routes. Experimental teratogenic and reproductive effects. Mutation data reported. When heated to decomposition it emits acrid smoke. See also various aflatoxins.職業(yè)ばく露
Aflatoxins are a group of toxic metabolites produced by certain types of fungi. Aflatoxins are not commercially manufactured; they are naturally occurring contaminants that are formed by fungi on food during conditions of high temperatures and high humidity. Most human exposure to aflatoxins occurs through ingestion of contaminated food. The estimated amount of aflatoxins that Americans consume daily is estimated to be 0.15 0.50 μg. Grains, peanuts, tree nuts, and cottonseed meal are among the more common foods on which these fungi grow. Meat, eggs, milk, and other edible products from animals that consume aflatoxincontaminated feed may also contain aflatoxins. Aflatoxins can also be breathed in代謝経路
Aflatoxin B1 can be activated via the monooxygenase reaction which then reacts with the N7 atom of B-DNA guanine. Conjugation of aflatoxin B1 8,9-epoxide is an important detoxification route. Although aflatoxin B1 8,9-epoxide can be hydrolyzed to the diol by epoxide hydrolase, the diol product is toxic, since it reacts readily with proteins by Schiff base formation or binds to DNA. Glutathione conjugation prevents toxicity of both the epoxide and its hydrolysis product. The aflatoxin glutathione conjugate is subsequently excreted from the hepatocyte into bile as a major biliary metabolite.輸送方法
UN3172 Toxins, extracted from living sources, solid or liquid, Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required. UN2811 Toxic solids, organic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.不和合性
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
Consult with environmental regulatory agencies for guidance on acceptable disposal practices. Generators of waste containing this contaminant (≥100 kg/mo) must conform with EPA regulations governing storage, transportation, treatment, and waste disposal. Use of oxidizing agents, such as hydrogen peroxide or 5% sodium hypochlorite bleach. Acids and bases may also be used.アフラトキシン B1 上流と下流の製品情報(bào)
原材料
2-ヘキサノイル-1,3,6,8-テトラヒドロキシ-9,10-アントラキノン
3aβ,12cβ-ジヒドロ-8-ヒドロキシ-6-メトキシ-7H-フロ[3',2':4,5]フロ[2,3-c]キサンテン-7-オン
準(zhǔn)備製品
アフラトキシン B1 生産企業(yè)
Global( 197)Suppliers
名前 | 電話番號(hào) | 電子メール | 國(guó)籍 | 製品カタログ | 優(yōu)位度 |
---|---|---|---|---|---|
Shaanxi Dideu Medichem Co. Ltd | +86-29-81148696 +86-15536356810 |
1022@dideu.com | China | 3882 | 58 |
Hebei Mojin Biotechnology Co., Ltd | +86 13288715578 +8613288715578 |
sales@hbmojin.com | China | 12840 | 58 |
Henan Fengda Chemical Co., Ltd | +86-371-86557731 +86-13613820652 |
info@fdachem.com | China | 20285 | 58 |
Hangzhou FandaChem Co.,Ltd. | +8615858145714 |
FandaChem@Gmail.com | China | 9206 | 55 |
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 |
ivan@atkchemical.com | China | 32957 | 60 |
Shanghai Zheyan Biotech Co., Ltd. | 18017610038 |
zheyansh@163.com | CHINA | 3619 | 58 |
Chengdu GLP biotechnology Co Ltd | 028-87075086 13350802083 |
scglp@glp-china.com | CHINA | 1824 | 58 |
Hubei Jusheng Technology Co.,Ltd. | 18871490254 |
linda@hubeijusheng.com | CHINA | 28172 | 58 |
Shaanxi Pioneer Biotech Co., Ltd . | +8613259417953 |
sales@pioneerbiotech.com | China | 3000 | 58 |
career henan chemical co | +86-0371-86658258 +8613203830695 |
factory@coreychem.com | China | 29811 | 58 |
1162-65-8(アフラトキシン B1)キーワード:
アフラトキシン類(lèi)
アフラトキシン B1
2,3-ジヒドロフラン
5,7-ジメトキシクマリン
ジメクロト酸
1-シクロペンテンカルボン酸
4-メチル-5,7-ジヒドロキシ-2H-1-ベンゾピラン-2-オン
6-(4-ヒドロキシフェニル)ヘキサン酸
trans-2,3-ジメトキシけい皮酸
cis-2-メトキシけい皮酸
3-メチル-2-シクロペンテノン
3,4,7aα,9,10,10aα-ヘキサヒドロ-5-メトキシ-1H,12H-フロ[3',2':4,5]フロ[2,3-h]ピラノ[3,4-c][1]ベンゾピラン-1,12-ジオン
5-メトキシ-3,4,7aα,10aα-テトラヒドロ-1H,12H-フロ[3',2':4,5]フロ[2,3-h]ピラノ[3,4-c][1]ベンゾピラン-1,12-ジオン
(6aR)-4-メトキシ-1,2,3,6aα,8,9,9aα,11-オクタヒドロシクロペンタ[c]フロ[3',2':4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
2,3,6aα,9aα-テトラヒドロ-9a-ヒドロキシ-4-メトキシシクロペンタ[c]フロ[3',2':4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
(3S)-2,3,6aα,9aα-テトラヒドロ-3-ヒドロキシ-4-メトキシシクロペンタ[c]フロ[3',2':4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
4-エチル-7-ヒドロキシ-8-メチル-2H-クロメン-2-オン
5,7-ジヒドロキシ-4-プロピル-2H-クロメン-2-オン
- 1162-65-8
- (6ar-cis)-ahydro-4-methoxy
- )(1)benzopyran-1,11-dione
- 1-Cyclopentene-1-carboxylic acid, 2-(3a,8a-dihydro-4-hydroxy-6-methoxyfuro[2,3-b]benzofuran-5-yl)-5-oxo-, delta-lactone
- 2,3,6aalpha,9aalpha-tetrahydro-4-methoxycyclopenta(c)furo(3’,2’:4,5)furo(2,3-h
- 4-Methoxy-2,3,6a,9a-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-H]chromene-1,11-dione
- 2,3,6aalpha,9aalpha-tetrahydro-4-methoxycyclopenta[c]furo[2',3':4,5]furo[2,3-h]chromene-1,11-dione
- AFLATOXIN B1 FROM ASPERGILLUS FLAVUS
- AFLATOXIN B(1) FROM ASPERGILLUS FLAVUS, VIAL WITH 10 MG
- Aflatoxin B1, crystalline
- (6aR)-4-Methoxy-2,3,6aα,9aα-tetrahydrocyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione
- 2,3,6aα,9aα-Tetrahydro-4-methoxycyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione
- (6aR,9aS)-2,3,6a,9a-Tetrahydro-4-Methoxy-1H,11H-cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione
- NSC 529592
- Aflaloxin B1
- aflatoxin b1 solution
- AFLATOXIN B1(RG)
- Aflatoxin FB1, Aflatoxin B
- cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-1,11-dione,2,3,6a,9a-tet
- cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-1,11-dione,2,3,6a,9a-tetr
- cyclopenta(c)furo(3’,2’:4,5)furo(2,3-h)(1)benzopyran-1,11-dione,2,3,6aalpha,9a
- Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione, 2,3,6a,9a-tetrahydro-4-methoxy-, (6aR-cis)-
- Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione, 2,3,6aalpha,9aalpha-tetrahydro-4-methoxy-
- rahydro-4-methoxy-
- AFLATOXIN B1
- AFLATOXIN B1, ASPERGILLUS FLAVUS
- 1H,11H-Cyclopenta[c]furo[3',2':4,5]furo[2,3-h][1]benzopyran-1,11-dione,2,3,6a,9a-tetrahydro-4-Methoxy-, (6aR,9aS)-
- 6-methoxydifurocoumarone
- ahydro-4-methoxy-
- alflatoxin
- alflatoxinb1
- 2,3,6aα,9aα-テトラヒドロ-4-メトキシシクロペンタ[c]フロ[3',2':4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
- (6aR)-4-メトキシ-2,3,6aα,9aα-テトラヒドロシクロペンタ[c]フロ[3',2':4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
- アフラトキシンB1
- アフラトキシン
- アフラトキシンB1(結(jié)晶)
- アフラトキシンB1標(biāo)準(zhǔn)品
- アフラトキシンB1標(biāo)準(zhǔn)液
- アフラトキシン B1
- アフラトキシン B1 2ΜG/ML
- アフラトキシンB1標(biāo)準(zhǔn)液 (25ΜG/MLアセトニトリル溶液)
- アフラトキシンB1 FROM ASPERGILLUS FLAVUS
- アフラトキシンB1 溶液
- (6aR)-4-メトキシ-2,3,6aα,9aα-テトラヒドロシクロペンタ[c]フロ[3′,2′:4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
- (6aR)-4-メトキシ-1,2,3,6aα,9aα,11-ヘキサヒドロシクロペンタ[c]フロ[3′,2′:4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
- (3S,7R)-11-メトキシ-6,8,19-トリオキサペンタシクロ[10.7.0.02,9.03,7.013,17]ノナデカ-1,4,9,11,13(17)-ペンタエン-16,18-ジオン
- 2,3,6aα,9aα-テトラヒドロ-4-メトキシシクロペンタ[c]フロ[3′,2′:4,5]フロ[2,3-h][1]ベンゾピラン-1,11-ジオン
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