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Purity | Size | Price | VIP Price | USA Stock *0-1 Day | Global Stock *5-7 Days | Quantity | |||||
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* Storage: {[proInfo.prStorage]}
CAS No. : | 638-03-9 | MDL No. : | MFCD00070607 |
Formula : | C7H10ClN | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | VDXZPXIEEVOGLV-UHFFFAOYSA-N |
M.W : | 143.61 | Pubchem ID : | 522105 |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P260-P264-P270-P301+P312+P330-P307+P311-P405-P501 | UN#: | 2811 |
Hazard Statements: | H302-H370-H373 | Packing Group: | Ⅲ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With 1,4-dioxane; ethanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With water |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With ethanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium bromide; calcium chloride; copper dichloride at 175 - 180℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
28% | In various solvent(s) at 160 - 170℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | With phosphorus pentoxide; triethylamine hydrochloride at 190 - 200℃; for 7h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
99% | Stage #1: 1-methyl-3-nitrobenzene With hydrogen In ethanol at 25℃; Flow reactor; Stage #2: With hydrogenchloride In ethanol Flow reactor; chemoselective reaction; | |
With hydrogenchloride; tin(ll) chloride In ethanol; water at 30℃; various concentration of HCl; | ||
550 mg | Stage #1: 1-methyl-3-nitrobenzene With phosgene; sodium tetrahydroborate; copper(II) sulfate In methanol at 20℃; Stage #2: With hydrogenchloride In methanol; diethyl ether | General Procedure for the Reduction of Aromatic Nitro Compounds General procedure: The catalyst precursor in form of a 0.04 M CuSO4 and 0.004 M CoCl2 solution (3.0 ml,3.0 mol% CuSO4, 0.3 mol% CoCl2) was added to a magnetically stirred solution ofthe nitro compound (4 mmol) in 25 ml methanol. The reaction was initiated by addingan initial portion of 210 mg (5.6 mmol) NaBH4, resulting in a color change to black(catalyst generated in situ) and vigorous gas evolution. Additional portions of NaBH4(7 × 35 mg, 7 × 0.9 mmol) NaBH4 were added in intervals of 3 min. Although thereaction was carried out at room temperature and under normal atmosphere, the generation of heat due to the exothermic character of the reaction usually heated the reaction mixture to 30-40C and cooling is generally not necessary on a small scale. However,for large scale reactions (10 mmol), a reflux condenser was attached. After 25 min,the reaction mixture was quenched by adding 30 ml of water and extracted with 3 ×40 ml of CH2Cl2. The combined organic layers were dried over MgSO4. After removal of the drying agent, 6 M HCl in ether (10 ml) was added to produce the more stable hydrochloride, which was freed from excess HCl, CH2Cl2 and Et2O under reduced pressure(10 mmHg). An aliquot of the amine was analyzed using GC-MS, 1H-NMR and 13C-NMR. The NMR data for the compounds are shown in Table 2. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
46% | With phosphorus pentoxide; N,N-dimethyl-cyclohexanamine at 200℃; for 2h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With phosphorus pentoxide; N,N-dimethyl-cyclohexanamine at 200℃; for 1h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
61% | With phosphorus pentoxide; N,N-dimethyl-cyclohexanamine at 220℃; for 2h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
71% | With phosphorus pentoxide; N,N-dimethyl-cyclohexanamine at 200℃; for 2.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
32% | With phosphorus pentoxide; <i>N</i>,<i>N</i>-dimethyl-aniline at 170 - 190℃; for 2h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
46% | With phosphorus pentoxide; <i>N</i>,<i>N</i>-dimethyl-aniline at 170 - 190℃; for 2h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
88% | at 240℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
50% | With N,N-dimethyl-cyclohexanamine; phosphorus pentoxide at 150℃; for 24h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With 1-chloro-2,4-dinitro-benzene In 1,4-dioxane; water at 45℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
40% | With phosphorus pentoxide; N,N-dimethylcyclohexylamine hydrochloride In water at 180℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
93% | In ethanol; isopropyl alcohol for 0.5h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | In butan-1-ol for 12h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
55% | With sodium hydroxide In i-Amyl alcohol for 19h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With water-d2 at 25 - 100℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
50% | Stage #1: m-toluidine hydrochloride With hydrogenchloride; sodium nitrite In water at 5℃; Stage #2: salicylic acid With sodium hydroxide In water |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In 1,2-dimethoxyethane at 160 - 175℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 1,2-dimethoxy-ethane / 160 - 175 °C 2: DIEA / dimethylformamide / 16 h / 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 2: 3.9 g / Raney nickel / benzene / 2.5 h / Heating 3: Br2, acetic acid / ethanol / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: ethanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: water 2: 124 °C / und Erwaermen des Reaktionsprodukts mit Phosphorylchlorid |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 2: methanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 2: methanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 2: aqueous NaOH |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
67% | Stage #1: m-toluidine hydrochloride With trimethylaluminum In toluene at 20℃; for 0.0833333h; Stage #2: 5-(4-chlorophenyl)furan-2-carbonitrile In toluene for 1h; Heating; Further stages.; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | With ethanol for 0.0125h; Microwave irradiation; Neat (no solvent); | |
Stage #1: m-toluidine hydrochloride With hydrogenchloride In water for 0.5h; Reflux; Stage #2: ammonium thiocyanate In water at 20℃; for 4h; Reflux; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
39% | With sodium dihydrogenphosphate In water; acetonitrile at 0 - 20℃; | |
39% | With sodium dihydrogenphosphate In water; acetonitrile at 0 - 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With tert.-butylnitrite In acetonitrile at 20℃; for 0.166667h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
64.6% | In acetonitrile at 0℃; for 1.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
96% | Stage #1: 1-naphthalenesulfonic acid; N,N-dimethyl-formamide With oxalyl dichloride In dichloromethane at 20℃; for 2h; Stage #2: m-toluidine hydrochloride With oxalyl dichloride; triethylamine In dichloromethane at 20℃; for 2h; Cooling with ice; | 20.a Preparation of N-(3-methylphenyl)-1-naphthalene carboxamide The reaction flask was added 1-naphthalenesulfonic acid 0.57 g (3. 3mmol) and the amount of dry methylene chloride, add a drop of DMF, stirring at room temperature was added dropwise oxalyl chloride 63 g (4. 95mmol), add complete, stirring was continued for 2 hours at room temperature. Evaporated under reduced pressure, dissolved in dichloromethane and dried for later use. The reaction flask was added 3-methyl aniline hydrochloride 0.43 g (3_1), stirring and dissolving with an appropriate amount of dry dichloromethane was added dry triethylamine 0.43 g (4. 3mmol), ice-cooled , the above acid chloride solution was added dropwise with stirring, and then stirring was continued for 2 hours at room temperature. The solvent was distilled off under reduced pressure, the resulting solid was washed with 10% sodium hydroxide solution and water, successively washed, dried, and recrystallized from ethanol to give 0.75 g of white crystals (yield 96%), |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
72% | Stage #1: m-toluidine hydrochloride With hydrogenchloride; sodium nitrite In water at 10℃; for 0.0777778h; Flow reactor; Stage #2: ascorbic acid In water at 20℃; for 1.43333h; Flow reactor; Stage #3: With water for 1h; | 3.2. Reactor Configuration for the Synthesis of Hydrazine Derivatives from Diazonium Salts 1-18 General procedure: Three stock solutions were prepared and connected to the flow reactor feed lines for Pumps A-C (see Figure 3 for a pictorial layout). Pump A delivered hydrochloric acid (0.84 M), Pump B a solution of aqueous sodium nitrite (0.98 M) and pump C delivered an aqueous solution of ascorbic acid (0.35 M). In addition a further pump was used to provide the solutions of aniline as their HCl salts dissolved in water (0.35 M). The entire reactor was maintained under positive internal pressure using a 75 psi back pressure regulator at the exit of the reactor. To initiate the reaction each flow channel was pumped at 0.5 mL/min. Progressing through the reactor; Channel A and B were mixed in a Uniqsis mixer chip of 0.27 mL internal volume (16 s residence time) before passing into a 2.75 mL PFA tubular residence coil (165 s residence time). The combined flow was then further united with the aniline solution mixing in a second Uniqsis mixer chip of 2 mL internal volume (80 s residence time). The reacting solution then passed into a 5 mL residence PFA foil coil (150 s residence time, the solution turns pale yellow to orange). The whole initial stage mixing unit was temperature regulated (10° C) using a Polar Bear Plus flow reactor unit. In the second stage reactor the freshly prepared diazonium mixture (combined flow rate 2 mL/min) was united at an Upchurch peek T-mixer with a solution of ascorbic acid delivered from Pump C set at 0.5 mL/min. The flow stream was then progressed into a 52 mL PFA flow coil (20.8 min residence time).The isolation of certain intermediate hydroxamic esters, namely 13-18, could be achieved by immediate extraction of the reactor output with ethyl acetate (5 volumes) and washing the organic phase with sodium hydrogen carbonate (2 M; 2). The organic solution was dried over MgSO4, filtered and concentrated in vacuo to provide a pale yellow solid which was triturated with a 1:1 mixture of hexane and acetone to furnishing the desired product. Alternatively, the output solution was collected and left to stir for 1 h to ensure complete hydrolysis to the corresponding oxamic acid, 1-12, had occurred. The products were isolated by basification of the reaction mixture pH ~9 followed by extraction with EtOAc (3 volumes). The aqueous solution was then acidified to pH ~4 and extracted with EtOAc (3 volumes), the organic phase was dried over MgSO4, the solvent evaporated to yield compounds 1-12. Note: for compounds 1-12 a proton signal sites under the residual DMSO signal. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride In lithium hydroxide monohydrate for 0.5h; Heating; | ||
With hydrogenchloride In diethyl ether at 0 - 20℃; for 3.3h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
60% | In acetonitrile at 20℃; for 18h; | 76.1 Example 76. Step 1. tert-butyl 4-(N-(m-tolyl)sulfamoyl)piperazine-1-carboxylate A solution of 1-((4-(tert-butoxycarbonyl)piperazin-1-yl)sulfonyl)-3-methyl-1H-imidazol-3-ium trifluoromethanesulfonate (4.750 g, 9.886 mmol) and m-toluidine hydrochloride (1.704 g, 11.863 mmol) in acetonitrile (50 mL) was stirred at the room temperature for 18 hr. Then, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with aqueous saturated sodium chloride solution, dried with anhydrous MgSO4, filtered, and concentrated in vacuo. The residue was chromatographed (SiO2, 12 g cartridge; ethyl acetate / hexane = 0 % to 30 %) to give tert-butyl 4-(N-(m-tolyl)sulfamoyl)piperazine-1-carboxylate as white solid (2.110 g, 60.0 %). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
43.9% | In acetonitrile for 16h; Reflux; | 66.3 Example 66. Step 3. tert-butyl (R)-2-methyl-4-(N-(m-tolyl)sulfamoyl)piperazine-1-carboxylate A mixture of (R)-1-((4-(tert-butoxycarbonyl)-3-methylpiperazin-1-yl)sulfonyl)-3-methyl-1H-imidazol-3-ium trifluoromethanesulfonate (3.350 g, 6.775 mmol) and m-toluidine hydrochloride (1.070 g, 7.452 mmol) in acetonitrile (100 mL), prepared at the ambient temperature, was heated at reflux for 16 hr, and cooled down to the ambient temperature. Then, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with aqueous saturated ammonium chloride solution, dried with anhydrous MgSO4, filtered, and concentrated in vacuo. The residue was chromatographed (SiO2, 24 g cartridge; ethyl acetate / hexane = 0 % to 30 %) to give tert-butyl (R)-2-methyl-4-(N-(m-tolyl)sulfamoyl)piperazine-1-carboxylate as yellow solid (1.100 g, 43.9 %). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
38.8% | In acetonitrile for 16h; Reflux; | 70.3 Example 70. Step 3. tert-butyl (S)-2-methyl-4-(N-(m-tolyl)sulfamoyl)piperazine-1-carboxylate A mixture of (S)-1-((4-(tert-butoxycarbonyl)-3-methylpiperazin-1-yl)sulfonyl)-3-methyl-1H-imidazol-3-ium trifluoromethanesulfonate (4.000 g, 8.089 mmol) and m-toluidine hydrochloride (1.278 g, 8.898 mmol) in acetonitrile (100 mL), prepared at the ambient temperature, was heated at reflux for 16 hr, and cooled down to the ambient temperature. Then, water was added to the reaction mixture, followed by extraction with ethyl acetate. The organic layer was washed with aqueous saturated ammonium chloride solution, dried with anhydrous MgSO4, filtered, and concentrated in vacuo. The residue was chromatographed (SiO2, 24 g cartridge; ethyl acetate / hexane = 0 % to 30 %) to give tert-butyl (S)-2-methyl-4-(N-(m-tolyl)sulfamoyl)piperazine-1-carboxylate as yellow solid (1.160 g, 38.8 %). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
50.2% | With triethylamine; In dichloromethane; at 20℃; for 18h; | A solution of <strong>[782501-25-1]tert-butyl 4-(chlorosulfonyl)piperidine-1-carboxylate</strong> (3.000 g, 10.572 mmol) in dichloromethane (50 mL) was mixed at the room temperature with mtoluidine hydrochloride (1.822 g, 12.686 mmol) and triethylamine (3.684 mL, 26.430 mmol), and stirred at the same temperature for 18 hr. Then, water was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was washed with aqueous saturated sodium chloride solution, dried with anhydrous Mg504, filtered, and concentrated in vacuo. The residue was chromatographed (5i02, 40 g cartridge; ethyl acetate / hexane = 20 % to 50 %) to give the concentrate, and then the concentrate was dissolved in ethyl acetate (10 mL) and hexane (100 mL) and stilTed. The resulting precipitates were collected by filtration, washed by hexane, and dried to give tert-butyl 4-(N-(m-tolyl)sulfamoyl)piperidine-1-carboxylate as white solid (1.880 g, 50.2 %). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85.3% | With pyridine In dichloromethane at 20℃; for 12h; | 27.1 [Step 1] N-(m-tolyl)methanesulfonamide A solution of m-toluidine hydrochloride (1.000 g, 6.963 mmol), pyridine (0.6 18 mL, 7.660 mmol) and methanesulfonyl chloride (0.651 mL, 8.356 mmol) in dichloromethane (10 mL) was stirred at the room temperature for 12 hr. Then, water was added to the reaction mixture, followed by extraction with dichloromethane. The organic layer was washed with aqueous iN-hydrochloric acid solution, dried with anhydrous Mg504, filtered, and concentrated in vacuo. The title compound was used without further purification (N-(m-tolyl)methanesulfonamide, 1.100 g, 85.3 %, white solid). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
69% | With 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical In N,N-dimethyl-formamide at 50℃; Green chemistry; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With zinc(II) chloride at 180 - 185℃; for 0.5h; | 3.1 Step 1: Synthesis of intermediate 2-amino-4-methyl-phenazine: 1.4 g (0.01 mol) of 3-methylaniline hydrochloride,1.4 g (0.01 mol) o-nitroanilineAnd 4 g (0.03 mol) of zinc chloride were placed in a reaction kettle,The reaction was stirred at 180-185 ° C for 30 min,After the end of the reaction began to cool naturally,Cooled to 100 ° C with 20ml of ethanol reflux twice for 30min,Then neutralized with saturated aqueous sodium carbonate solution,There is a solid precipitation,Filter filter cake,After treatment of crude crude brown solid 0.8g,Yield 38.3%. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
92% | With bis-triphenylphosphine-palladium(II) chloride In tetrahydrofuran at 110℃; for 24h; Autoclave; regioselective reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | In toluene at 120℃; for 3h; Green chemistry; |
Tags: 638-03-9 synthesis path| 638-03-9 SDS| 638-03-9 COA| 638-03-9 purity| 638-03-9 application| 638-03-9 NMR| 638-03-9 COA| 638-03-9 structure
[ 26346-38-3 ]
5-Methylbenzene-1,3-diamine dihydrochloride
Similarity: 0.95
[ 90642-55-0 ]
3,4,5-Trimethylaniline hydrochloride
Similarity: 0.90
[ 197571-77-0 ]
4-methylbenzene-1,2-diamine hydrochloride
Similarity: 0.90
[ 26346-38-3 ]
5-Methylbenzene-1,3-diamine dihydrochloride
Similarity: 0.95
[ 90642-55-0 ]
3,4,5-Trimethylaniline hydrochloride
Similarity: 0.90
[ 197571-77-0 ]
4-methylbenzene-1,2-diamine hydrochloride
Similarity: 0.90
Precautionary Statements-General | |
Code | Phrase |
P101 | If medical advice is needed,have product container or label at hand. |
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Prevention | |
Code | Phrase |
P201 | Obtain special instructions before use. |
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P220 | Keep/Store away from clothing/combustible materials. |
P221 | Take any precaution to avoid mixing with combustibles |
P222 | Do not allow contact with air. |
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P402 + P404 | Store in a dry place. Store in a closed container. |
P403 + P233 | Store in a well-ventilated place. Keep container tightly closed. |
P403 + P235 | Store in a well-ventilated place. Keep cool. |
P410 + P403 | Protect from sunlight. Store in a well-ventilated place. |
P410 + P412 | Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. |
P411 + P235 | Keep cool. |
Disposal | |
Code | Phrase |
P501 | Dispose of contents/container to ... |
P502 | Refer to manufacturer/supplier for information on recovery/recycling |
Physical hazards | |
Code | Phrase |
H200 | Unstable explosive |
H201 | Explosive; mass explosion hazard |
H202 | Explosive; severe projection hazard |
H203 | Explosive; fire, blast or projection hazard |
H204 | Fire or projection hazard |
H205 | May mass explode in fire |
H220 | Extremely flammable gas |
H221 | Flammable gas |
H222 | Extremely flammable aerosol |
H223 | Flammable aerosol |
H224 | Extremely flammable liquid and vapour |
H225 | Highly flammable liquid and vapour |
H226 | Flammable liquid and vapour |
H227 | Combustible liquid |
H228 | Flammable solid |
H229 | Pressurized container: may burst if heated |
H230 | May react explosively even in the absence of air |
H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
H240 | Heating may cause an explosion |
H241 | Heating may cause a fire or explosion |
H242 | Heating may cause a fire |
H250 | Catches fire spontaneously if exposed to air |
H251 | Self-heating; may catch fire |
H252 | Self-heating in large quantities; may catch fire |
H260 | In contact with water releases flammable gases which may ignite spontaneously |
H261 | In contact with water releases flammable gas |
H270 | May cause or intensify fire; oxidizer |
H271 | May cause fire or explosion; strong oxidizer |
H272 | May intensify fire; oxidizer |
H280 | Contains gas under pressure; may explode if heated |
H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
H290 | May be corrosive to metals |
Health hazards | |
Code | Phrase |
H300 | Fatal if swallowed |
H301 | Toxic if swallowed |
H302 | Harmful if swallowed |
H303 | May be harmful if swallowed |
H304 | May be fatal if swallowed and enters airways |
H305 | May be harmful if swallowed and enters airways |
H310 | Fatal in contact with skin |
H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
H317 | May cause an allergic skin reaction |
H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
H330 | Fatal if inhaled |
H331 | Toxic if inhaled |
H332 | Harmful if inhaled |
H333 | May be harmful if inhaled |
H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
H335 | May cause respiratory irritation |
H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
H341 | Suspected of causing genetic defects |
H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
H361 | Suspected of damaging fertility or the unborn child |
H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
H370 | Causes damage to organs |
H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
Sorry,this product has been discontinued.
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