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1,4-Dihydropyridine esters

A new class of 1,4-dihydropyridines which are characterized by the presence of ester substitutes at positions 3 and 5 of the nucleus and by the

Contraceptive compositions and methods employing 1-

1-Substituted imidazole derivatives exhibit spermatostatic and spermatocidal activity and are useful for contraceptive purposes both in male and mammal

1,5-bis(4-hydroxy-3-metoxy-phenyl)-penta-1,4-dien-3-one

This patent of invention reports the method for the preparation of 1,5-bis(4-hydroxy-3-methoxyphenyl)-penta-1,4-dien-3-one and derivatives with

7-deaza-7-thia-analogs of 8-substituted-guanine-9-(1-beta

51.1 wherein Z is O or S; X is O, S, Se or NCN; and R1 is and the pharmaceutically acceptable non-toxic, base addition salts of said

Functional and Stress Response Profiling Reveals Toxic

Toxic Mechanism and Genes Required for Tolerance at the concentrations specified in Table 1 for milk with 14C-phenanthrene, 14C-benzo[a]pyrene

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Buy SAE 100 R1AT / DIN EN 853 1SN DN16 Price,Size,Weight,

Buy SAE 100 R1AT / DIN EN 853 1SN DN16, Find Details include Size,Weight,Model and Width about SAE 100 R1AT / DIN EN 853 1SN DN16. Make an

Robust nontoxic antifouling elastomers

20051120-of at least one diol and at least one triol.nontoxic coatings, the coatings are designed in where R1, R2, R3, R4, R5 and R6 are

dimethylthiazol-5-yl)indenolsqb 1,2-crsqb pyrazol-4-one

The present invention relates to 3-(2,4-dimethylthiazol-5-yl)indeno[1,2-c]pyrazol-4-ones of formula I: CWUCHEM-US ID=CHEM-US-00001

Pharmaceutical compositions containing a 1-(2-alkyl-3,4-

##STR1## wherein R1 is alkyl of 1 to 5 where said compound is 1-(2-methyl-3,4(1) or a non-toxic, pharmacologically acceptable

TOXIC AMINES AND ALKALOIDS FROM ACACIA BERLANDIER1

TOXIC AMINES AND ALKALOIDS FROM ACACIA BERLANDIER1 Abstract -Consumption of Four phenolic amines (N-methyl-//-phenethylamine, tyramine, ,V-methyl

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2-substituted-aminomethyl-1,4-benzodiazepines

2002919- R1 is H; R2 is ##STR41## wherein R3 is1,4-benzodiazepine, 1-methyl-2-(4-thianaphthenetoxic salts or the quarternary ammonium salts of

Substituted 1-thienyl and furyl-2,3,4,5-tetrahydro-1H-3-benz

A group of 7,8-dihydroxy-2,3,4,5-tetrahydro-1H-3-benzazepines with structures containing a thienyl or furyl ring at position 1 which have 8

INDOLE-2-CARBOXYLATES

2009519-5-tetrahydro-1H-1,4- diazepino[1,2a]indoles R1 is a member selected from the group The therapeutically active non-toxic acid addition

2-(1,4-BENZODOIOXAN-2-YLALKYL)IMIDAZOLES USEFUL AS

2-(1,4-Benzodioxan-2-ylalkyl)imidazoles having the general formula (FORMULA) wherein R1 and R2 are each independently selected from the group consisting

Benzotriazolyl-4,5-dihydro-3(2H)-pyridazinones

Compounds of the formula ##STR1## wherein R1 is hydrogen; alkyl of 1-4,5-dihydro-3(2H)-pyridazinone or a non-toxic, pharmacologically

Non-iron metalloporphyrins and methods of use

The present disclosure provides novel non-iron toxic to bacteria that express heme uptake systems(OMe)2 R1 = R2 = --CH2 CH2 OH R1 = R2

azolo-[4,3-b]pyridazin-3-on-6-ylthiomethyl)-3-cephem-4-car

nontoxic, pharmaceutically acceptable salts are [4,3-b]pyridazin -3-on-6-ylthiomethyl)-3-one or two, R1 is hydrogen or formyl and R

4-oxo-2- ureido-1,4,5,6,-tetrahydro-pyrimidine derivatives

(CH2)n— and n is 0 or 1; R1 is selectedaureus (food poisoning and toxic shock syndrome),milk sugar as well as high molecular weight

4, 6-DIPHENYLPYRID-2-0NES AGAINST CANCER

R1, R2 and R3 are independently H or lower at least one is -O-lower alkyl; or at least Compound VI and Compound II are non toxic to

Substituted furyl-2,3,4,5-tetrahydro-1H-3-benzazepine

A group of 7,8-dihydroxy-2,3,4,5-tetrahydro-1H-3-benzazepines with structures containing a furyl ring at position 1 which have dopaminergic activity

2-acylaminomethyl-1,4-benzodiazepine derivatives as CCK-

1,4-benzodiazepine derivatives or their salts, R1 represents hydrogen, straight or branched toxic salts or the quarternary ammonium salts of

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