IP Library Granted Patent US 7,781,504
Granted Patent B2
US 7,781,504 · App. 11/634,474 · Granted Aug 24, 2010

Alkyltin sulfanyl diester thiols

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Quick Facts
Patent No.
US 7,781,504
App. No.
11/634,474
Granted
Aug 24, 2010
Kind
B2
Abstract

Disclosed herein are compounds of the formula: (R) x —Sn—(R′) 4-x wherein: R is alkyl; R′ is a moiety selected from the group consisting of: w is 0 or 1; x is 1 or 2; y is 1, 2, 3, or 4; and Z is a linear, branched, cyclic, or aromatic hydrocarbon. These compounds are excellent stabilizers for halogen-containing resins, such as PVC.

Claims (33)

1. A composition comprising:

(A) a halogen-containing resin; and

(B) an amount effective to stabilize the halogen-containing resin against elevated temperatures, UV light, oxidation, and high shear forces of at least one compound of the formula:

(R) x —Sn—(R′) 4-x

wherein:

R is alkyl;

R′ is a moiety selected from the group consisting of:

w is 0 or 1;

x is 1 or 2;

y is 1, 2, 3, or 4; and

Z is a linear, branched, cyclic, or aromatic hydrocarbon.

2. The composition of claim 1 wherein R is alkyl of from 1 to 12 carbon atoms.

3. The composition of claim 2 wherein R is methyl, butyl, or octyl.

4. The composition of claim 1 wherein the compound is selected from the group consisting of dimethyltin bis[di(2-mercaptoethyl)succinate], monomethyltin tris[di(2-mercaptoethyl)succinate], monomethyltin tris[di(2-mercaptoethyl)carbonate], dimethyltin bis[di(2-mercaptoethyl)carbonate], and mixtures thereof.

5. The composition of claim 1 , wherein the halogen-containing resin is a member selected from the group consisting of PVC, polyvinyl bromide, and polyvinylidene chloride.

6. The composition of claim 1 , wherein the effective amount is within a range of from about 0.5 to about 1.50 parts of the compound of (B) per hundred parts the resin of (A).

7. The composition of claim 1 , further comprising at least one additive selected from the group consisting of lubricants, fillers, pigments, flame retardants, UV absorbers, impact modifiers, and processing aids.

8. A method for stabilizing a halogen-containing resin against elevated temperatures, UV light, oxidation, and high shear forces comprising adding to said halogen-containing resin a stabilizing amount of at least one compound of the formula:

(R) x —Sn—(R′) 4-x

wherein:

R is alkyl;

R′ is a moiety selected from the group consisting of:

w is 0 or 1;

x is 1 or 2;

y is 1, 2, 3, or 4; and

Z is a linear, branched, cyclic, or aromatic hydrocarbon.

9. The method of claim 8 wherein R is alkyl of from 1 to 12 carbon atoms.

10. The method of claim 9 wherein R is methyl, butyl, or octyl.

11. The method of claim 9 , wherein said compound is selected from the group consisting of dimethyltin bis[di(2-mercaptoethyl)succinate], monomethyltin tris[di(2-mercaptoethyl)succinate], monomethyltin tris[di(2-mercaptoethyl)carbonate], dimethyltin bis[di(2-mercaptoethyl)carbonate], and mixtures thereof.

12. The composition of claim 1 , wherein the compound is dimethyltin bis[di(2-mercaptoethyl)succinate].

13. The composition of claim 1 , wherein the compound is a mixture of dimethyltin bis[di(2-mercaptoethyl)succinate] and monomethyltin tris[di(2-mercaptoethyl)succinate].

14. The method of claim 8 , wherein the compound is dimethyltin bis[di(2-mercaptoethyl)succinate].

15. The method of claim 8 , wherein the compound is a mixture of dimethyltin bis[di(2-mercaptoethyl)succinate] and monomethyltin tris[di(2-mercaptoethyl)succinate].

Assignments (6)
INTELLECTUAL PROPERTY SECURITY RELEASE AGREEMENT Recorded Mar 21, 2011
From: CITIBANK, N.A.
To: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; ASCK, INC; BIOLAB COMPANY STORE, LLC; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIOLAB TEXTILES ADDITIVES, LLC; BIOLAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON MONOCHEM, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GT SEED TREATMENT, INC.; ISCI, INC; GREAT LAKES CHEMICAL GLOBAL, INC.; HOMECARE LABS, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; NAUGATUCK TREATMENT COMPANY; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); MONOCHEM, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC; WRL OF INDIANA, INC.; BIOLAB FRANCHISE COMPANY, LLC
Reel/Frame 026039/0142 →
RELEASE OF SECURITY INTEREST Recorded May 12, 2010
From: CITIBANK, N.A.
To: CHEMTURA CORPORATION (AND ALL GRANTORS IDENTIFIED IN THE IP SECURITY AGREEMENTS DATED 3/18/09 AND 2/12/10)
Reel/Frame 024369/0172 →
SECURITY AGREEMENT Recorded May 12, 2010
From: GALATA CHEMICALS HOLDING COMPANY, LLC; GALATA CHEMICALS, LLC
To: WACHOVIA CAPITAL FINANCE CORPORATION (NEW ENGLAND)
Reel/Frame 024369/0232 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2010
From: CHEMTURA CORPORATION
To: GALATA CHEMICALS, LLC
Reel/Frame 024342/0736 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 22, 2010
From: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; AQUA CLEAR INDUSTRIES, LLC; ASCK, INC.; ASEPSIS, INC.; BIOLAB COMPANY STORE, LLC; BIOLAB FRANCHISE COMPANY, LLC; BIOLAB TEXTILE ADDITIVES, LLC; BIO-LAB, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; CROMPTON MONOCHEM, INC.; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; ISCI, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; MONOCHEM, INC.; NAUGATUCK TREATMENT COMPANY; RECREATIONAL WATER PRODUCTS, INC.; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); WEBER CITY ROAD LLC; WRL OF INDIANA, INC.
To: CITIBANK, N.A.
Reel/Frame 023998/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2007
From: KRAINER, EDWARD; FRENKEL, PETER
To: CHEMTURA CORPORATION
Reel/Frame 018789/0648 →