DTDM
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DTDM
structure -
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CAS No:
103-34-4
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Formula:
C8H16N2O2S2
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Chemical Name:
DTDM
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Synonyms:
Morpholine,4,4′-dithiobis-;Morpholine,4,4′-dithiodi-;4,4′-Dithiobis[morpholine];4,4′-Dithiodimorpholine;Morpholine disulfide;Sulfasan R;Sulfasan;N,N′-Dithiodimorpholine;N,N′-Bismorpholine disulfide;Bismorpholino disulfide;Accel R;Morpholinodisulfide;N,N′-Dimorpholinyl disulfide;Sanfel R;Vanax A;Bismorpholine disulfide;N,N′-Dithiobis[morpholine];Deovulc M;Di(4-morpholinyl) disulfide;Rhenocure M/G;Vulnoc R;Sulfasan DTDM;DTDM;Actor R;NSC 65239;Rhenocure M;Nocmaster R 80E;DTDM 80;Rhenogran DTDM 80;Sulphasan R;TT 106;39393-19-6;186983-49-3;1081512-50-6
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CAS No:
DTDM Basic Attributes
236.35500
236.35
203-103-0
M786P489YF
65239
DTXSID8026698
CRYSTALS|GRAY TO TAN POWDER
Characteristics
75.54000
0.73800
DryPowder; DryPowder, PelletsLargeCrystals; PelletsLargeCrystals
1.36 g/cm3 @ Temp: 25 °C
125 °C
371.7ºC at 760 mmHg
154ºC
1.6300 (estimate)
Refrigerator
THE PRODUCT FROM CHLORINATION OF 4,4'-DITHIODIMORPHOLINE EXPLODED VIOLENTLY AFTER VACUUM STRIPPING OF THE SOLVENT CARBON TETRACHLORIDE.
Safety Information
R36/37/38
S26; S36/37/39
QE3325000
Stable at normal temperatures and pressures.
P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P391, P403+P233, P405, P501
H315
|Warning|H315 (10.67%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P391, P403+P233, P405, and P501|Aggregated GHS information provided by 178 companies from 10 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
THE PRODUCT FROM CHLORINATION OF 4,4'-DITHIODIMORPHOLINE EXPLODED VIOLENTLY AFTER VACUUM STRIPPING OF THE SOLVENT CARBON TETRACHLORIDE.
Drug Information
4,4'-DITHIODIMORPHOLINE INDUCED DERMATITIS OF VARIOUS DEGREES OF SPREADING ACCORDING TO THE MODE OF EXPOSURE.
4,4'-dithiodimorpholine
DTDM Use and Manufacturing
BLAKE, J AM CHEM SOC 65, 1267 (1943); BLAKE, US PATENT 2,343,524 (1944 TO MONSANTO); HARMAN, US PATENT 2,766,236 AND BRITISH PATENT 774,570 (1956, 1957, BOTH TO MONSANTO). LAMBRECH ET AL, US PATENT 2,902,402 (1959 TO PFIZER). ... AS FUNGICIDE: LADD, US PATENT 2,429,097 (1949 TO US RUBBER).|OXIDATIVE COUPLING OF 4-THIOMORPHOLINE WITH MOLECULAR OXYGEN IN THE PRESENCE OF AN AQUEOUS CAUSTIC AGENT & CATALYST
Vulcanizing agent and vulcanization accelerator for natural rubber and synthetic rubber. Active sulfur can be released at the vulcanization temperature, and the effective sulfur content is 27%. The operation is safe. The vulcanization speed is slow when used alone. Combined with thiazoles, thiurams and dithiocarbamates can increase the vulcanization speed. This product is non-frosting, non-polluting, non-discoloring, and easily dispersed. Especially suitable for butyl rubber. Mainly used to manufacture tires, butyl inner tubes, adhesive tapes and heat-resistant rubber products.
This product can be used as a vulcanizing agent and accelerator for natural rubber and synthetic rubber. The use of this product into the rubber material does not spray frost, pollution, color, and easy to disperse. When used in effective and half-effect vulcanization systems, the resulting vulcanizates have good heat resistance and aging resistance. Active sulfur can be released at the vulcanization temperature. The effective sulfur content is 27%. The operation is safe. The vulcanization speed is slow when used alone. Combined with thiazoles, thiurams and dithiocarbamate, it can increase the vulcanization speed. This product is especially suitable for butyl rubber, which is used to manufacture tires, butyl inner tubes, adhesive tapes and heat-resistant rubber products, as well as asphalt stabilizers for Lisu highways.
Accelerator
Plastic and rubber products not covered elsewhere
1,000,000 - 10,000,000 lb|(1979) PROBABLY GREATER THAN 4.54X10+5 GRAMS|(1981) PROBABLY GREATER THAN 4.54X10+5 GRAMS
Rubber product manufacturing|Morpholine, 4,4'-dithiobis-: ACTIVE
Computed Properties
Molecular Weight:236.4
XLogP3:0.6
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:3
Exact Mass:236.06532010
Monoisotopic Mass:236.06532010
Topological Polar Surface Area:75.5
Heavy Atom Count:14
Complexity:143
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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