Detail of > 91-67-8
- CAS Number:
- 91-67-8
- Name:
Benzenamine,N,N-diethyl-3-methyl-
- Superlist Name:
- N,N-Diethyl-m-toluidine
- Formula:
- C11H17N
- Molecular Structure:

- Synonyms:
- m-Toluidine,N,N-diethyl- (6CI,7CI,8CI);1-(Diethylamino)-3-methylbenzene;3-(Diethylamino)-1-methylbenzene;3-(Diethylamino)toluene;3-(N,N-Diethylamino)toluene;3-Methyl-N,N-diethylaniline;N,N-Diethyl-3-methylaniline;N,N-Diethyl-m-methylaniline;NSC 96629;m-Methyl(diethylamino)benzene;m-Methyl-N,N-diethylaniline;
- Molecular Weight:
- 163.26
- EINECS:
- 202-089-3
- Density:
- 0.923 g/cm3
- Boiling Point:
- 243.6 °C at 760 mmHg
- Flash Point:
- 98.4 °C
- Appearance:
- clear pale yellow to orange-brown liquid
- Hazard Symbols:
Xn,
N,
T- Risk Codes:
- 36/37/38-20/21/22-51/53-26-24/25
- Safety:
- 24/25-61-45-36/37-28Details
- Transport Information:
- UN 1708 6.1/PG 2
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Reference
- Azo disperse dyes
- Azo disperse dyes. Baumann, Werner (Sandoz A.-G., Switz.). Ger. (East) DD 209641 A5 16 May 1984, 15 pp. (German). (German Democratic Republic). CODEN: GEXXA8. CLASS: IC: C09B029-085; C09B029-24; C09B043-40. APPLICATION: DD 83-247994 16 Feb 1983. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Red to blue disperse dyes (I; R = benzene or naphthalene coupler residue) with good fastness and color strength are described. Thus, diazotization of 5,2,4-NCS(O2N)2C6H2NH2 [53488-27-0] and coupling with m-MeC6H4NEt2 [91-67-8] gave I [R = C6H3(NEt2)Me-4,2] (II) [87855-55-8], lmax 602 nm (CH2Cl2), also prepd. by reaction of its chloro analog [87855-56-9] with KSCN. II gave fast, level blue dyeings on polyester fibers.
- Monoazo dyes for polyamides
- Monoazo dyes for polyamides. Hurter, Rudolf (Ciba-Geigy A.-G. , Switz.). Eur. Pat. Appl. EP 102325 A1 7 Mar 1984, 111 pp. DESIGNATED STATES: R: BE, CH, DE, FR, GB, IT, LI. 90492-59-4 which is the cas registry number of one of substances is just one of reagents here. (German). (European Patent Organization). CODEN: EPXXDW. CLASS: IC: C09B029-01; C09B062-008; C07C147-12. ICA: D06P001-02. APPLICATION: EP 83-810341 29 Jul 1983. PRIORITY: CH 82-4696 4 Aug 1982. DOCUMENT TYPE: Patent CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Fast yellow to red dyes (I) are prepd., where R is the radical of a benzene, naphthalene, or heterocyclic coupler, R1 = H, halogen, carboxy, C1-6 alkyl, etc., and R2 = H, halogen, C1-6 alkyl, C1-6 alkoxy, C2-6 alkanoylamino, or C1-6 alkylsulfonylamino. R may also contain a fiber-reactive substituent. Thus, diazotization of 2-C10H7SO2C6H3(NH2)SO3H-2,4 [90492-59-4] (prepn. described) and coupling with 3-MeC6H4NEt2 [91-67-8] gave II [90492-60-7]. II was applied to polyamide material from a weakly acidic bath to produce yellowish red shades with good buildup and good fastness to light, HCHO, and wet processing. Other I were similarly prepd. .
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