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116-37-0

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116-37-0 Usage

Uses

Bisphenol A bis(2-hydroxypropyl) ether is an engineered material used as a coating for improved adhesion of aminoplasts to metals.

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 116-37-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 116-37:
(5*1)+(4*1)+(3*6)+(2*3)+(1*7)=40
40 % 10 = 0
So 116-37-0 is a valid CAS Registry Number.

116-37-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1'-[Isopropylidenebis(p-phenyleneoxy)]di-2-propanol

1.2 Other means of identification

Product number -
Other names 2,2'-(4,4'-(propane-2,2-diyl)bis(4,1-phenylene))-bis(oxy)dipropan-2-ol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:116-37-0 SDS

116-37-0Synthetic route

diphenylolpropane diglycidyl ether
1675-54-3

diphenylolpropane diglycidyl ether

Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

Conditions
ConditionsYield
With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); potassium tert-butylate; hydrogen In toluene at 75℃; under 37503.8 Torr; for 24h; regioselective reaction;99%
methyloxirane
75-56-9, 16033-71-9

methyloxirane

A

Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

B

4-(2-(4-(2-hydroxypropoxy)phenyl)propan-2-yl)phenol
57372-69-7

4-(2-(4-(2-hydroxypropoxy)phenyl)propan-2-yl)phenol

C

BPA-3PO
210979-67-2

BPA-3PO

Conditions
ConditionsYield
anion exchange resin A (OH-type) In 2-methoxy-ethanol at 100℃; for 6h;A 99 %Chromat.
B 0.1 %Chromat.
C 0.8 %Chromat.
propylene glycol
57-55-6

propylene glycol

hydroquinone
123-31-9

hydroquinone

A

Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

B

2-(4-(2-(4-(2-hydroxypropoxy)phenyl)propan-2-yl)phenoxy)propan-1-ol
1003045-91-7

2-(4-(2-(4-(2-hydroxypropoxy)phenyl)propan-2-yl)phenoxy)propan-1-ol

Conditions
ConditionsYield
With sodium carbonate; urea; zinc(II) oxide at 170 - 190℃;
methyloxirane
75-56-9, 16033-71-9

methyloxirane

Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

Conditions
ConditionsYield
Stage #1: BPA With sodium hydroxide In tetrahydrofuran at 20℃; for 3h; Inert atmosphere;
Stage #2: methyloxirane In tetrahydrofuran Inert atmosphere;
1,2-propylene cyclic carbonate
108-32-7

1,2-propylene cyclic carbonate

A

Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

B

2-(4-(2-(4-(2-hydroxypropoxy)phenyl)propan-2-yl)phenoxy)propan-1-ol
1003045-91-7

2-(4-(2-(4-(2-hydroxypropoxy)phenyl)propan-2-yl)phenoxy)propan-1-ol

Conditions
ConditionsYield
With potassium hydroxide Inert atmosphere; Heating;
Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

3-mercaptobutyric acid
26473-49-4

3-mercaptobutyric acid

2,2-bis[4-{2-(3-mercaptobutyloyloxy)-2-methylethoxy}phenyl]propane

2,2-bis[4-{2-(3-mercaptobutyloyloxy)-2-methylethoxy}phenyl]propane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene at 140℃; for 4h;95.1%
Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

sulfuric acid mono-[1-methyl-2-(4-{1-methyl-1-[4-(2-sulfooxy-propoxy)-phenyl]-ethyl}-phenoxy)-ethyl] ester; compound with ammonia

sulfuric acid mono-[1-methyl-2-(4-{1-methyl-1-[4-(2-sulfooxy-propoxy)-phenyl]-ethyl}-phenoxy)-ethyl] ester; compound with ammonia

Conditions
ConditionsYield
Stage #1: Bisphenol A propoxylate With pyridine; sulfuric acid; acetic anhydride at 50 - 55℃; for 0.5h;
Stage #2: With ammonium hydroxide at 0℃; for 0.25h;
Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

(E,E)-2-cyanohexa-2,4-dienoic acid
83697-84-1

(E,E)-2-cyanohexa-2,4-dienoic acid

2,2-Bis-[p-(2-(2-Cyano-2,4-hexadienoyl)-oxypropoxy)-phenyl]-propane
274695-40-8

2,2-Bis-[p-(2-(2-Cyano-2,4-hexadienoyl)-oxypropoxy)-phenyl]-propane

Conditions
ConditionsYield
With 2,6-di-tert-butyl-4-methyl-phenol In acetone
Bisphenol A propoxylate
116-37-0

Bisphenol A propoxylate

methyl (α-chloromethyl)acrylate
922-15-6

methyl (α-chloromethyl)acrylate

C31H40O8

C31H40O8

Conditions
ConditionsYield
Stage #1: Bisphenol A propoxylate With 2,6-di-tert-butyl-4-methyl-phenol; sodium hydride In tetrahydrofuran for 2h; Inert atmosphere;
Stage #2: methyl (α-chloromethyl)acrylate In tetrahydrofuran at 20℃; Inert atmosphere;

116-37-0Relevant articles and documents

Ruthenium-Catalyzed Selective Hydrogenation of Epoxides to Secondary Alcohols

Thiyagarajan, Subramanian,Gunanathan, Chidambaram

supporting information, p. 9774 - 9778 (2019/12/02)

A ruthenium(II)-catalyzed highly selective Markovnikov hydrogenation of terminal epoxides to secondary alcohols is reported. Diverse substitutions on the aryl ring of styrene oxides are tolerated. Benzylic, glycidyl, and aliphatic epoxides as well as diepoxides also underwent facile hydrogenation to provide secondary alcohols with exclusive selectivity. Metal-ligand cooperation-mediated ruthenium trans-dihydride formation and its reaction involving oxygen and the less substituted terminal carbon of the epoxide is envisaged for the origin of the observed selectivity.

Compositions And Methods For Bioactive Dental Composites

-

Paragraph 0111, (2016/05/24)

Described herein are compositions and methods which produce hydrolytically stable resin monomers, bioactive fillers, phosphorus coupling agent and surface coating method, which can be combined to produce new generation dental composites; compositions comprising the same, as well as methods of making and using the same are also described.

Aromatic ethers and process for producing aromatic ethers

-

Page 13-14, (2010/02/08)

According to a production process, aromatic ethers are producible by reacting phenols with an oxirane compound with use of an anion exchange resin as a catalyst. According to another production process, aromatic ethers having an alcoholic hydroxyl group are producible by a crystallization-purification step of using a solvent having a solubility parameter ranging from 7.5 to 12.5 for purification by crystallization. Further, according to still another production process, producible are aromatic ethers having an alcoholic hydroxyl group, wherein the content of a metal in the aromatic ethers is less than 100 ppm by mass, and the content of a halogen element in the aromatic ethers is less than 100 ppm by mass.

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