Phenformin Hydrochloride 盐酸苯乙双胍

CAS 834-28-6 MFCD00035039

化学结构图

834-28-6
SMILES: Cl.N=C(N)NC(=N)NCCc1ccccc1

化学属性

Mol. FormulaC10H16ClN5
Mol. Weight242
Melting Point175-178°C
Solubility>=10 g/100 mL at 21 °C
Density1.24

别名和识别编码

Chemical NamePhenformin Hydrochloride
MDL NumberMFCD00035039
CAS Number834-28-6
EC Number212-637-3
Synonym USAF VI-6 1-phenylaethylbiguanidhydrochlorid {Chem dbi-td 1-phenethylbiguanide diabis 1-Phenethylbiguanide hydrochloride azucaps 盐酸苯乙双胍 debinyl n-(2-phenylethyl)imidodicarbonimidic diamide N'-beta-Phenethylbiguanide hydrochloride Meltrol 降糖灵 盐酸盐 苯乙福明 {Chemicalb Biguanide, 1-phenethyl-, hydrochloride 1-Fenetilbiguanide cloridrato N-beta-Phenylethyl biguanide hydrochloride meltrol PHENFORMIN HYDROCHLORIDE 1-phenethyl-biguanidhydrochloride dbcomb beta-Phenethybiguanide PHENFORMIN HCL Imidodica {C 1-phenethylbiguanide hydrochloride PHENFORMINI H 苯乙双胍 PHENETHYLBIGUANIDE HYDROCHLORIDE n-beta-phenylethylbiguanideh Phenformin HCl No. 9113 1-Phenethyl 1-phenethyl-biguanid Dipar usafvi-6 降糖灵 DBI-TD PHENFORMIN Phenformine HCL 1-Phenylaethylbiguanid hydrochlorid N(sup 1)-beta-Phenethylbiguanide hydrochloride 1-苯乙胺双胍 n’-beta-phenethylbiguanidehydrochloride 1-(2 Phenoformine hydrochloride 盐酸苯乙福明 phenoforminehydrochloride db-retard beta-Phenethylbiguanide 苯乙双胍盐酸盐,降糖灵盐酸盐 聚苯并咪唑 n-(2-phenylethyl)-imidodicarbonimidicdiamidmonohydrochloride n(sup1)-beta-phenethylbiguanidehydrochloride 1-phenethyl-biguanidmonohydrochloride Phenethylbiguanide hydrochloride N-(2-Phenylethyl)imidodic
PubChem Substance ID13266
Chemical Name Translation盐酸苯乙双胍
InChIKeyYSUCWSWKRIOILX-UHFFFAOYSA-N
Wiswesser Line NotationMUYZMYUM&M2R &GH
LabNetwork Molecule IDLN00223478
InChIInChI=1S/C10H15N5.ClH/c11-9(12)15-10(13)14-7-6-8-4-2-1-3-5-8;/h1-5H,6-7H2,(H6,11,12,13,14,15);1H
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分类

  • {SNA} AMPK通路抑制剂和激活剂, Alphabetical Index of Analytical Standards, Analytical Standards, Analytical/Chromatography, P, PER - POLA, 有氧糖酵解(Warburg效应), 有氧糖酵解(Warburg效应)抑制剂, 癌症代谢, 癌症研究, 细胞生物学
  • {SNA} Alphabetical Index of Analytical Standards, Analytical Standards, Analytical/Chromatography, Cancer Metabolism, Cell Biology, Inhibitors and Activators of the AMPK pathway, Inhibitors of Aerobic Glycolysis (the Warburg Effect), P, PER - POLA, 有氧糖酵解(Warburg效应), 癌症研究
  • {SNA} Alphabetical Index of Analytical Standards, Aerobic Glycolysis (the Warburg Effect),
  • {SNA} Alphabetical Index of Analytical Standards, Analyt

相关文献及参考

  • Merck: 14,7231

安全信息

Hazard Codes Xn
WGK Germany3
GHS Symbol
Hazard statements
  • H302 Harmful if swallowed 吞食有害
RTECSDU2200000
Signal word
Safety Statements
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
Risk Statements
  • R22 Harmful if swallowed 吞咽有害
TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intravenous
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 17800 ug/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   CSLNX* U.S. Army Armament Research & Development Command, Chemical Systems
   Laboratory, NIOSH Exchange Chemicals.  (Aberdeen Proving Ground, MD 21010)
   Volume(issue)/page/year: NX#00094

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE

TYPE OF TEST            : LDLo - Lowest published lethal dose
ROUTE OF EXPOSURE       : Subcutaneous
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 200 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   JACSAT Journal of the American Chemical Society.  (American Chemical Soc.,
   Distribution Office Dept. 223, POB 57136, West End Stn., Washington, DC
   20037)  V.1-    1879-  Volume(issue)/page/year: 81,3728,1959

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Oral
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 407 mg/kg
TOXIC EFFECTS :
   Endocrine - hypoglycemia
REFERENCE :
   TXAPA9 Toxicology and Applied Pharmacology.  (Academic Press, Inc., 1 E.
   First St., Duluth, MN 55802) V.1-    1959-  Volume(issue)/page/year:
   14,393,1969

TYPE OF TEST            : LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE       : Intraperitoneal
SPECIES OBSERVED        : Rodent - mouse
DOSE/DURATION           : 150 mg/kg
TOXIC EFFECTS :
   Details of toxic effects not reported other than lethal dose value
REFERENCE :
   NTIS** National Technical Information Service.  (Springfield, VA 22161)
   Formerly U.S. Clearinghouse for Scientific & Technical Information.
   Volume(issue)/page/year: AD691-490

TYPE OF TEST            : DNA damage
TEST SYSTEM             : Rodent - rat Liver
DOSE/DURATION           : 1 mmol/L
REFERENCE :
   EMMUEG Environmental and Molecular Mutagenesis.  (Alan R. Liss, Inc., 41 E.
   11th St., New York, NY 10003)  V.10-    1987-  Volume(issue)/page/year:
   24,181,1994

Precautionary statements

其他信息

  • MSDS 信息:1-Phenethylbiguanide hydrochloride(834-28-6).msds
  • MSDS 信息:Phenformin(114-86-3).msds
  • Sigma Aldrich:834-28-6(sigmaaldrich)
  • 用途一:聚苯并咪唑可制成各种用品如玻璃布层压板、模塑料薄膜、胶粘剂、绝缘漆、泡沫塑料及纤维等。层压板可用于飞机和航天的雷达天线罩、印刷线路板等。还用于绝缘材料、隔离层、耐辐射材料等。
  • 上游原料:多聚磷酸 --> N,N-二甲基乙酰胺 --> 双氰胺 --> 预聚物 --> 间苯二甲酰氯 --> 间苯二甲酸二苯酯 --> 盐酸联苯胺 --> 高沸点溶剂
  • 方法一:聚苯并咪唑的制备一般有三种方法: 高温溶液缩聚法: 将3, 3 ' , 4, 4 ' -四氨基联苯胺盐酸盐与间苯二甲酸二苯酯。在高沸点溶剂和多磷酸存在下,于200℃反应数小时,用水沉淀聚合物,洗涤、干燥得预聚物。然后在250-300℃高温脱水环化得聚苯并咪唑。该法易制得高分子量产品。 低温溶液缩聚法: 将3, 3 ' , 4, 4 ' -四氨基联苯与间苯二甲酰氯在二甲基乙酰胺等强极性溶剂中,以吡啶为酸吸收剂,于低温(0℃以下)进行缩聚制得预聚物,加入沉淀剂,分离、洗涤、干燥预聚物,再于250-300℃高温脱水环化制得聚苯并咪唑。 熔融缩聚法: 将3, 3 ' , 4, 4 ' -四氨基联苯和间苯二甲酸二苯酯加入反应釜中,在氮气保护下,于260℃反应1-2h,脱苯酚生成聚氨基酰胺预聚物,经粉碎,再于385-400℃高真空脱水环化3-4h,可制得聚苯并咪唑。
  • 用途二:本品为降血糖药,以成年型糖尿病的疗效约为88%,适用于各类型的糖尿病。小鼠口服LD50为450mg/kg。
  • 方法二:由苯乙胺盐酸盐与双氰 胺在142℃左右加热反应,经后处理、精制而得。
  • 用途一:用作降血糖药
  • 上游原料:双氰胺
  • Sigma Aldrich:114-86-3(sigmaaldrich)
  • MOL 文件:834-28-6.mol
  • MOL 文件:114-86-3.mol

系列性分类


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