Identification | More | [Name]
3'-Methylacetanilide | [CAS]
537-92-8 | [Synonyms]
3'-METHYLACETANILIDE 3-METHYLACETANILIDE (3-METHYLPHENYL)-ACETAMIDE ACETYL-M-TOLUIDINE M-ACETOTOLUIDIDE M-ACETOTOLUIDINE M-METHYL ACETANILIDE M-TOLYL-ACETAMIDE N1-(3-METHYLPHENYL)ACETAMIDE N-ACETYL-M-TOLUIDINE 1-Acetamido-3-methylbenzene 3-Acetamidotoluene Acetamide, N-(3-methylphenyl)- Aceto-m-aminotoluene Acetotoluide m-Acetotoluide meta-Acetotoluidide n-(3-methylphenyl)-acetamid N-(3-Methylphenyl)acetamide N-(3-methylphenyl)-Acetamide | [EINECS(EC#)]
208-678-1 | [Molecular Formula]
C9H11NO | [MDL Number]
MFCD00014962 | [Molecular Weight]
149.19 | [MOL File]
537-92-8.mol |
Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed. R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [RTECS ]
AN2875000
| [HS Code ]
29242998 | [Toxicity]
LD50 orl-mus: 1450 mg/kg TXAPA9 19,20,71 |
Hazard Information | Back Directory | [General Description]
White solid. | [Reactivity Profile]
N-ACETYL-M-TOLUIDINE(537-92-8) is an amide. Flammable gases are formed by the reaction of organic amides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx). | [Air & Water Reactions]
Water insoluble. | [Health Hazard]
ACUTE/CHRONIC HAZARDS: When heated to decomposition this compound emits toxic fumes of nitrogen oxides. | [Fire Hazard]
Flash point data for this chemical are not available; however, N-ACETYL-M-TOLUIDINE is probably combustible. | [Chemical Properties]
white crystalline solid | [Safety Profile]
Moderately toxic by ingestion. Seealso p-ACETOTOLUIDIDE. When heated todecomposition it emits toxic fumes of NOx. | [Purification Methods]
Crystallise the toluidide from H2O, EtOH, aqueous EtOH or Et2O/pet ether (m 66o). UV: max 245nm (EtOH). [Beilstein 12 H 860, 12 I 400, 12 II 468, 12 III 1962, 12 IV 1823.] |
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Company Name: |
JSK Chemicals
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Tel: |
+919879767970 |
Website: |
www.jskchemicals.com |
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