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10213-78-2

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10213-78-2 Usage

Flammability and Explosibility

Nonflammable

Check Digit Verification of cas no

The CAS Registry Mumber 10213-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,1 and 3 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10213-78:
(7*1)+(6*0)+(5*2)+(4*1)+(3*3)+(2*7)+(1*8)=52
52 % 10 = 2
So 10213-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H47NO2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23(21(2)24)22(3)25/h21-22,24-25H,4-20H2,1-3H3

10213-78-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Stearyldiethanolamine

1.2 Other means of identification

Product number -
Other names 2,2'-(Octadecylazanediyl)diethanol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Processing aids, not otherwise listed,Surface active agents
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:10213-78-2 SDS

10213-78-2Synthetic route

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

1-Bromooctadecane
112-89-0

1-Bromooctadecane

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

Conditions
ConditionsYield
In acetonitrile Heating;100%
With potassium carbonate; potassium iodide In acetonitrile100%
With potassium hydrogencarbonate; potassium iodide In acetonitrile for 3h; Heating / reflux;100%
With 2-pentanol das Hydrobromid ensteht;
oxirane
75-21-8

oxirane

1-aminooctadecane
124-30-1

1-aminooctadecane

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

1-chlorooctadecane
3386-33-2

1-chlorooctadecane

2,2'-iminobis[ethanol]
111-42-2

2,2'-iminobis[ethanol]

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

Conditions
ConditionsYield
With benzyl alcohol
at 80℃; for 5h;
triethanolamine
102-71-6

triethanolamine

sodium octadecyl sulfate

sodium octadecyl sulfate

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

Conditions
ConditionsYield
With water at 200℃;
2,5-Bis(2-hydroxypropylthio)-1,3,4-thiadiazole
107641-99-6

2,5-Bis(2-hydroxypropylthio)-1,3,4-thiadiazole

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

boric acid
11113-50-1

boric acid

C52H102B2N4O6S3

C52H102B2N4O6S3

Conditions
ConditionsYield
for 8h;100%
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

1,3-dibromo-propane
109-64-8

1,3-dibromo-propane

C47H100N2O4(2+)*2Br(1-)

C47H100N2O4(2+)*2Br(1-)

Conditions
ConditionsYield
In butan-1-ol at 70 - 140℃; for 8h; Temperature; Microwave irradiation; High pressure;92%
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

N,N-bis(2-chloroethyl)octadecylamine
102886-03-3

N,N-bis(2-chloroethyl)octadecylamine

Conditions
ConditionsYield
With thionyl chloride In chloroform for 3h; Heating;70%
With thionyl chloride In chloroform at 0℃; for 3h; Heating / reflux;70%
1 ,6-dibromohexane
629-03-8

1 ,6-dibromohexane

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

1,6-hexamethylenebis(N,N-dihydroxyethyl-N-octadecylammonium) dibromide

1,6-hexamethylenebis(N,N-dihydroxyethyl-N-octadecylammonium) dibromide

Conditions
ConditionsYield
In acetonitrile for 69h; Heating;65%
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

2,2',2''-Tris-allyloxy-3,3''-bis-bromomethyl-5,5',5''-trimethyl-[1,1';3',1'']terphenyl
155616-93-6

2,2',2''-Tris-allyloxy-3,3''-bis-bromomethyl-5,5',5''-trimethyl-[1,1';3',1'']terphenyl

C54H79NO5
155616-96-9

C54H79NO5

Conditions
ConditionsYield
With sodium hydride In tetrahydrofuran Heating;58%
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

sulfuric acid monomethyl ester; ammonium salt
19803-43-1

sulfuric acid monomethyl ester; ammonium salt

Methylbis(2-hydroxyethyl)octadecyl Ammonium Methyl Sulfate

Methylbis(2-hydroxyethyl)octadecyl Ammonium Methyl Sulfate

Conditions
ConditionsYield
With dimethyl sulfate In polyoxyethylene(5)glycol octadecanoate48%
methylene chloride
74-87-3

methylene chloride

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

bis-(2-hydroxy-ethyl)-methyl-octadecyl-ammonium; chloride
3010-24-0

bis-(2-hydroxy-ethyl)-methyl-octadecyl-ammonium; chloride

Conditions
ConditionsYield
at 150℃;
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

sodium monochloroacetic acid
3926-62-3

sodium monochloroacetic acid

carboxymethyl-bis-(2-hydroxy-ethyl)-octadecyl-ammonium betaine
24170-14-7

carboxymethyl-bis-(2-hydroxy-ethyl)-octadecyl-ammonium betaine

Conditions
ConditionsYield
With water
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

2-{2-[(2-hydroxy-ethyl)-octadecyl-amino]-ethoxy}-ethanesulfonic acid ; sodium-salt
117026-89-8

2-{2-[(2-hydroxy-ethyl)-octadecyl-amino]-ethoxy}-ethanesulfonic acid ; sodium-salt

Conditions
ConditionsYield
With sodium hydroxide anschliessend mit Natrium-<2-brom-aethansulfonat>;
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

2-chloro-ethanol
107-07-3

2-chloro-ethanol

tris-(2-hydroxy-ethyl)-octadecyl-ammonium; chloride
35239-12-4

tris-(2-hydroxy-ethyl)-octadecyl-ammonium; chloride

Conditions
ConditionsYield
at 170℃;
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

C45H67NO5
155616-99-2

C45H67NO5

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 58 percent / NaH / tetrahydrofuran / Heating
2: 86 percent / Pd(PPh3)2, Et3N*HCOOH, H2O / ethanol / Heating
View Scheme
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

(CH3C6H2CH2OCH2CH2)2(CH3C6H2)(OC(2)H2CO2H)3N(C18H37)
186250-05-5

(CH3C6H2CH2OCH2CH2)2(CH3C6H2)(OC(2)H2CO2H)3N(C18H37)

Conditions
ConditionsYield
Multi-step reaction with 4 steps
1: 58 percent / NaH / tetrahydrofuran / Heating
2: 86 percent / Pd(PPh3)2, Et3N*HCOOH, H2O / ethanol / Heating
3: K2CO3 / acetonitrile / Heating
4: H2O, NaOMe, D2O / CH3OD / Ambient temperature
View Scheme
N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

C54H73(2)H6NO11
186250-01-1

C54H73(2)H6NO11

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 58 percent / NaH / tetrahydrofuran / Heating
2: 86 percent / Pd(PPh3)2, Et3N*HCOOH, H2O / ethanol / Heating
3: K2CO3 / acetonitrile / Heating
View Scheme
1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

stearamidopropyl dimethylamine
7651-02-7

stearamidopropyl dimethylamine

A

18APDMA-3(OH)-18APDMA

18APDMA-3(OH)-18APDMA

B

18APDMA-3(OH)-18HE2

18APDMA-3(OH)-18HE2

C

18HE2-3(OH)-18HE2

18HE2-3(OH)-18HE2

Conditions
ConditionsYield
Product distribution / selectivity;
C7H7O3S(1-)*C26H54ClN2O2(1+)

C7H7O3S(1-)*C26H54ClN2O2(1+)

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

18APDMA-3(OH)-18HE2

18APDMA-3(OH)-18HE2

1,3-Dichloro-2-propanol
96-23-1

1,3-Dichloro-2-propanol

N,N-diethanolstearylamine
10213-78-2

N,N-diethanolstearylamine

C47H100N2O5(2+)

C47H100N2O5(2+)

Conditions
ConditionsYield
With sodium carbonate at 115 - 125℃; for 3h; pH=7.5-8.5;

10213-78-2Relevant articles and documents

Novel preorganized hemispherands to encapsulate rare earth ions: Shielding and ligand deuteration for prolonged lifetimes of excited Eu3+ ions

Oude Wolbers, Manon P.,Van Veggel, Frank C. J. M.,Snellink-Ru?l, Bianca H. M.,Hofstraat, Johannes W.,Geurts, Frank A. J.,Reinhoudt, David N.

, p. 138 - 144 (1997)

Quenching of the luminescent excited state of Eu3+ ions by C-H high-vibrational modes was studied by deuteration of the encapsulating ligand and the solvent. Novel polydentate hemispherands providing nine donor atoms, which form overall neutral complexes with rare earth ions, were synthesized in nine steps, allowing the easy incorporation of deuterium atoms (IIa-d·Eu3+). The introduction of tert-butyl groups at the aromatic rings of the ligand further increased the solubility of the complexes in organic solvents (29·Eu3+ and 34·Eu3+). Photophysical studies, viz., luminescence spectra and lifetime measurements, revealed that significant quenching of the Eu3+ excited state is induced by nearby C-H vibrational modes. Substitution of these quenching C-H modes for C-D bonds in the azacrown bridge leads to an enhancement of the luminescent lifetime by a factor of 1.5. C-H high-vibrational modes of the pendant arms which are at a larger distance to the Eu3+ ion than the azacrown bridge hydrogen atoms (determined from the MD calculations) are less efficient quenchers. The number of coordinating methanol molecules to 11a·Eu3+, 29·Eu3+, and 34·Eu3+ estimated by the 'Horrocks equation' is 0.9, 1.2, and 1.9, respectively, as was predicted by MD calculations. Moreover, the experimental data show that quenching of the excited state of well-shielded Eu3+ ions by the C-H modes of the ligand is of the e order of magnitude as quenching by one O-H mode.

Design of new potent and selective secretory phospholipase A2 inhibitors. Part 5: Synthesis and biological activity of 1-alkyl-4-[4,5-dihydro-1,2,4-[4H]-oxadiazol-5-one-3-ylmethylbenz-4′-yl(oyl)] piperazines

Boukli, Latifa,Touaibia, Mohamed,Meddad-Belhabich, Nadia,Djimde, Atime,Park, Chang-Ha,Kim, Jung-Joo,Yoon, Joo-Hyoung,Lamouri, Aazdine,Heymans, Francoise

, p. 1242 - 1253 (2008/09/17)

Among the different PLA2s identified to date, the group IIA secretory PLA2 (sPLA2 GIIA) is implied in diverse pathological conditions. In this work we describe the synthesis, inhibitory activities, and structure-activity relationships (SAR) of a new class of substituted piperazine derivatives. The in vitro fluorimetric assay using two groups of enzymes, GIB and GIIA, revealed several compounds as highly potent inhibitors (IC50 = 0.1 μM). The in vivo activity assessed by ip or per os administration in a carrageenan-induced edema test in rats showed that two compounds proved to be as potent as indomethacin (10 mg/kg).

Low pressure derived mixed phosphorous- and sulfur-containing reaction products useful in power transmitting compositions and process for preparing the same

-

, (2008/06/13)

A phosphorous- and sulfur-containing additive and its use to impart anti-wear and/or antioxidant properties to oleaginous compositions such as fuels and lubricating oils, particularly power transmission compositions, such as automatic transmission fluids, is disclosed. The additive comprises a mixture of products formed by simultaneously reacting (1) a beta-hydroxy thioether, such as thiobisethanol, and (2) a phosphorous-containing reactant, such as tributyl phosphite. The reaction is carried out under reduced pressure conditions (e.g., -40 KPa to -100 KPa) to limit the amount of thioether species in said additive to less than about 45 mole %.

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