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1185-53-1

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  • TRIS-HCL/ anti-virus/ buffer / intermediate/ white powder with cas no.1185-53-1/ worldwide Top Pharma factory vendor with most competitive price

    Cas No: 1185-53-1

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  • TRIS HCL CAS No: 1185-53-1 Tris HCL buffer Tris(hydroxymethyl)aminomethane HCL low price with high quality

    Cas No: 1185-53-1

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1185-53-1 Usage

Chemical Properties

White crystalline powder. Tris HCl has a pKa of 8.08 at 25°C and pH range of 7.0 to 9.0 that coincides with the physiological pH of most living organisms because of which it is commonly used as a component of buffer solutions in biology, biochemistry and molecular biology applications. Tris salts are also used for crystallization of proteins at various pH values. Neither Tris base nor Tris hydrochloride by itself provide adequate buffering capacity. Generally the two need to be mixed together to provide a buffer with pH between 7 and 9 to provide adequate buffering.

Uses

TRIS hydrochloride is a high quality buffer component used in SDS-PAGE. For precise applications, use a carefully calibrated pH meter with a glass/calomel combination electrode. The pH values of all buffers are temperature and concentration dependent. For Tris buffers, pH increases about 0.03 unit per °C decrease in temperature, and decreases 0.03-0.05 unit per ten-fold dilution. It is also used in the robust generation of transgenic mice.

Application

TRIS hydrochloride is highly soluble in water and is useful in the pH range 7.0-9.0. It is used in the preparation of Laemmli buffer, one of the most common SDS-PAGE buffers. In addition, Tris can also be used for many custom running and loading buffers, most often with glycine and SDS. The use of single-junction pH electrodes that contain silver should be avoided when determining the pH of a solution containing Tris buffer.

Preparation

The preparation of TRIS hydrochloride is as follows:After reacting 2-amino-1,3-propanediol (2.50 g, 27.44 mmol) and formic acid (1.26 g, 27.44 mmol) in 50 ml of water at room temperature for 3 hours, water was distilled off under reduced pressure, A liquid was obtained. By washing the obtained liquid,An ammonium formate salt (3.76 g, 27.44 mmol) was obtained as a colorless transparent liquid.

General Description

Trizma? hydrochloride is mainly required for preparation of buffer at physiological range of 7.3 to 7.5. The prepared buffer is compatible with biological fluids. It is of importance to laboratories as a standard pH solution.

Purification Methods

Crystallise the salt from 50% EtOH, then from 70% EtOH. TRIS-hydrochloride is also available commercially in a highly pure state. Otherwise, recrystallise it from 50% EtOH, then 70% EtOH, and dry it below 40o to avoid risk of decomposition. [Beilstein 4 H 304.]

Check Digit Verification of cas no

The CAS Registry Mumber 1185-53-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1185-53:
(6*1)+(5*1)+(4*8)+(3*5)+(2*5)+(1*3)=71
71 % 10 = 1
So 1185-53-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H11NO3.ClH/c5-4(1-6,2-7)3-8;/h6-8H,1-3,5H2;1H/p-1

1185-53-1 Well-known Company Product Price

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  • TCI America

  • (T0740)  Tris(hydroxymethyl)aminomethane Hydrochloride  >98.0%(N)

  • 1185-53-1

  • 25g

  • 90.00CNY

  • Detail
  • TCI America

  • (T0740)  Tris(hydroxymethyl)aminomethane Hydrochloride  >98.0%(N)

  • 1185-53-1

  • 500g

  • 860.00CNY

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  • Alfa Aesar

  • (A11379)  Tris(hydroxymethyl)aminomethane hydrochloride, 99+%   

  • 1185-53-1

  • 50g

  • 257.0CNY

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  • Alfa Aesar

  • (A11379)  Tris(hydroxymethyl)aminomethane hydrochloride, 99+%   

  • 1185-53-1

  • 250g

  • 723.0CNY

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  • Alfa Aesar

  • (A11379)  Tris(hydroxymethyl)aminomethane hydrochloride, 99+%   

  • 1185-53-1

  • 1000g

  • 2004.0CNY

  • Detail

1185-53-1SDS

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 2-Amino-2-(hydroxymethyl)-1,3-propanediol hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Amino-2-(hydroxymethyl)-1,3-propanediol Hydrochloride

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:1185-53-1 SDS

1185-53-1Synthetic route

cis-2,8-diphenyl-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

cis-2,8-diphenyl-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

tris hydrochloride
1185-53-1

tris hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In methanol for 1h; Heating;80%
2-amino-2-hydroxymethyl-1,3-propanediol
77-86-1

2-amino-2-hydroxymethyl-1,3-propanediol

tris hydrochloride
1185-53-1

tris hydrochloride

Conditions
ConditionsYield
With hydrogenchloride In water at 20℃; for 3h;
1,4-dithiane-2,5-diol
40018-26-6

1,4-dithiane-2,5-diol

tris hydrochloride
1185-53-1

tris hydrochloride

2-(2,5-dithia-7-azabicyclo[2.2.1]heptan-7-yl)-2-(hydroxymethyl)propane-1,3-diol

2-(2,5-dithia-7-azabicyclo[2.2.1]heptan-7-yl)-2-(hydroxymethyl)propane-1,3-diol

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 3h; Reflux;97%
cycloxexanone dimethyl ketal
933-40-4

cycloxexanone dimethyl ketal

tris hydrochloride
1185-53-1

tris hydrochloride

C10H19NO3

C10H19NO3

Conditions
ConditionsYield
Stage #1: cycloxexanone dimethyl ketal; tris hydrochloride With toluene-4-sulfonic acid In N,N-dimethyl-formamide for 17h;
Stage #2: With triethylamine In ethyl acetate
94%
benzaldehyde dimethyl acetal
1125-88-8

benzaldehyde dimethyl acetal

tris hydrochloride
1185-53-1

tris hydrochloride

5-amino-5-hydroxymethyl-2-phenyl-1,3-dioxane
51430-74-1

5-amino-5-hydroxymethyl-2-phenyl-1,3-dioxane

Conditions
ConditionsYield
With toluene-4-sulfonic acid; triethylamine for 12h; Ambient temperature;90%
3H3N*3H(1+)*[CrMo6O18(OH)6](3-)

3H3N*3H(1+)*[CrMo6O18(OH)6](3-)

tris hydrochloride
1185-53-1

tris hydrochloride

2-amino-2-hydroxymethyl-1,3-propanediol
77-86-1

2-amino-2-hydroxymethyl-1,3-propanediol

2C4H11NO3*2H(1+)*[H3NC(CH2O)3]CrMo6O18(OH)3(2-)

2C4H11NO3*2H(1+)*[H3NC(CH2O)3]CrMo6O18(OH)3(2-)

Conditions
ConditionsYield
Stage #1: 3H3N*3H(1+)*[CrMo6O18(OH)6](3-); 2-amino-2-hydroxymethyl-1,3-propanediol In water at 130℃; for 13h;
Stage #2: tris hydrochloride In water at 20℃; for 0.166667h;
90%
tris hydrochloride
1185-53-1

tris hydrochloride

2,2-dimethoxy-propane
77-76-9

2,2-dimethoxy-propane

(5-amino-2,2-dimethyl-1,3-dioxan-5-yl)methanol
53104-32-8

(5-amino-2,2-dimethyl-1,3-dioxan-5-yl)methanol

Conditions
ConditionsYield
With toluene-4-sulfonic acid; N,N-dimethyl-formamide for 12h; Ambient temperature;86%
Stage #1: tris hydrochloride; 2,2-dimethoxy-propane With toluene-4-sulfonic acid In N,N-dimethyl-formamide at 20℃; for 60h;
Stage #2: With triethylamine In methanol; N,N-dimethyl-formamide Sonication;
Stage #3: With triethylamine In methanol; ethyl acetate; N,N-dimethyl-formamide at 20℃; for 0.166667h;
86%
Stage #1: tris hydrochloride; 2,2-dimethoxy-propane; toluene-4-sulfonic acid In N,N-dimethyl-formamide at 20℃; for 18h;
Stage #2: With triethylamine In ethyl acetate for 0.5h;
85%
tris hydrochloride
1185-53-1

tris hydrochloride

β-naphthaldehyde
66-99-9

β-naphthaldehyde

5-amino-5-hydroxymethyl-2-(2-naphthyl)-1,3-dioxane
253437-24-0

5-amino-5-hydroxymethyl-2-(2-naphthyl)-1,3-dioxane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In benzene for 12h; Condensation; Heating;85%
tris hydrochloride
1185-53-1

tris hydrochloride

1-naphthaldehyde
66-77-3

1-naphthaldehyde

5-amino-5-hydroxymethyl-2-(1-naphthyl)-1,3-dioxane
253437-27-3

5-amino-5-hydroxymethyl-2-(1-naphthyl)-1,3-dioxane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In benzene for 12h; Condensation; Heating;82%
propargyl chloroformate
35718-08-2

propargyl chloroformate

tris hydrochloride
1185-53-1

tris hydrochloride

C8H13NO5

C8H13NO5

Conditions
ConditionsYield
With sodium hydrogencarbonate In 1,4-dioxane; water at 20℃; for 19h;80%
tris hydrochloride
1185-53-1

tris hydrochloride

4-chlorobenzaldehyde
104-88-1

4-chlorobenzaldehyde

2,8-di-(p-chlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

2,8-di-(p-chlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de;77%
cycloxexanone dimethyl ketal
933-40-4

cycloxexanone dimethyl ketal

tris hydrochloride
1185-53-1

tris hydrochloride

3-amino-3-(hydroxymethyl)-1,5-dioxaspiro[5.5]undecane
5452-79-9

3-amino-3-(hydroxymethyl)-1,5-dioxaspiro[5.5]undecane

Conditions
ConditionsYield
Stage #1: cycloxexanone dimethyl ketal; tris hydrochloride With toluene-4-sulfonic acid In N,N-dimethyl-formamide at 21 - 23℃; for 18h; Inert atmosphere; Sealed tube;
Stage #2: With triethylamine In ethyl acetate for 12h;
74%
water
7732-18-5

water

CrH6Mo6O24(3-)*3H(1+)*3H3N

CrH6Mo6O24(3-)*3H(1+)*3H3N

tris hydrochloride
1185-53-1

tris hydrochloride

C4H11CrMo6NO24(3-)*3H(1+)*2H3N*5H2O

C4H11CrMo6NO24(3-)*3H(1+)*2H3N*5H2O

Conditions
ConditionsYield
at 140℃; for 30h;70%
tris hydrochloride
1185-53-1

tris hydrochloride

3'-tert-butyldimethylsilylthymidine 5'-carboxaldehyde
131118-61-1

3'-tert-butyldimethylsilylthymidine 5'-carboxaldehyde

1-[(2R,4S,5S)-5-((R)-4,4-Bis-hydroxymethyl-oxazolidin-2-yl)-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

1-[(2R,4S,5S)-5-((R)-4,4-Bis-hydroxymethyl-oxazolidin-2-yl)-4-(tert-butyl-dimethyl-silanyloxy)-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione

Conditions
ConditionsYield
With triethylammonium bicarbonate buffer In acetonitrile at 20℃; pH=8;67%
1-(3-(4-(diethylamino)-2-(4-(3-(trifluoromethyl)benzylcarbamoyl)pyridin-2-yl)phenylcarbamoyl)phenyl)-5,8,11,14-tetraoxa-2-thiaheptadecan-17-oic acid bis(trifluoroacetate)

1-(3-(4-(diethylamino)-2-(4-(3-(trifluoromethyl)benzylcarbamoyl)pyridin-2-yl)phenylcarbamoyl)phenyl)-5,8,11,14-tetraoxa-2-thiaheptadecan-17-oic acid bis(trifluoroacetate)

tris hydrochloride
1185-53-1

tris hydrochloride

2-(5-(diethylamino)-2-(3-(20-hydroxy-19,19-bis(hydroxymethyl)-17-oxo-5,8,11,14-tetraoxa-2-thia-18-azaicosyl)benzamido)phenyl)-N-(3-(trifluoromethyl)benzyl)isonicotinamide bis(trifluoroacetate)

2-(5-(diethylamino)-2-(3-(20-hydroxy-19,19-bis(hydroxymethyl)-17-oxo-5,8,11,14-tetraoxa-2-thia-18-azaicosyl)benzamido)phenyl)-N-(3-(trifluoromethyl)benzyl)isonicotinamide bis(trifluoroacetate)

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In N,N-dimethyl-formamide for 2h;67%
tris hydrochloride
1185-53-1

tris hydrochloride

2,2,2-Trichloroethyl chloroformate
17341-93-4

2,2,2-Trichloroethyl chloroformate

C7H12Cl3NO5

C7H12Cl3NO5

Conditions
ConditionsYield
In methanol; water at 60℃; for 1h;58%
carbon disulfide
75-15-0

carbon disulfide

tris hydrochloride
1185-53-1

tris hydrochloride

A

4,4-bis(hydroxymethyl)thiazolidine-2-thione
81731-80-8

4,4-bis(hydroxymethyl)thiazolidine-2-thione

B

4,4-bis(hydroxymethyl)oxazolidine-2-thione
89417-47-0

4,4-bis(hydroxymethyl)oxazolidine-2-thione

C

4-hydroxymethyl-4-thiomethyl-thiazolidine-2-thione
1311029-71-6

4-hydroxymethyl-4-thiomethyl-thiazolidine-2-thione

Conditions
ConditionsYield
With sodium hydroxide In water at 60℃; for 24h;A 45%
B 18%
C 11%
tris hydrochloride
1185-53-1

tris hydrochloride

3,4-dichlorobenzaldehyde
6287-38-3

3,4-dichlorobenzaldehyde

2,8-di-(3,4-dichlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

2,8-di-(3,4-dichlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

B

2,8-di-(3,4-dichlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane
1311029-73-8

2,8-di-(3,4-dichlorophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

{bis-(2,8-di-(m,p-dichlorophenyl)-1-aza-3,7-dioxabicyclo[3.3.0]-octane 5-methoxy)methyl}-3,4-dichlorobenzene

{bis-(2,8-di-(m,p-dichlorophenyl)-1-aza-3,7-dioxabicyclo[3.3.0]-octane 5-methoxy)methyl}-3,4-dichlorobenzene

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de;A n/a
B n/a
C 35%
tris hydrochloride
1185-53-1

tris hydrochloride

4-fluorobenzaldehyde
459-57-4

4-fluorobenzaldehyde

(3R,5S,7as)-(3,5-bis(4-fluorophenyl)tetrahydro-1H-oxazolo[3,4-c]oxazol-7a-yl)methanol

(3R,5S,7as)-(3,5-bis(4-fluorophenyl)tetrahydro-1H-oxazolo[3,4-c]oxazol-7a-yl)methanol

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de;34%
N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-isocyanatoheptanediamide
1571096-82-6

N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-isocyanatoheptanediamide

tris hydrochloride
1185-53-1

tris hydrochloride

trifluoroacetic acid
76-05-1

trifluoroacetic acid

N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-(3-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)ureido)heptanediamide

N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-(3-(1,3-dihydroxy-2-(hydroxymethyl)propan-2-yl)ureido)heptanediamide

Conditions
ConditionsYield
Stage #1: N1,N7-bis(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethyl)-4-(3-(2-(2-(2-(3-((S)-6,8-dichloro-2-methyl-1,2,3,4-tetrahydroisoquinolin-4-yl)phenylsulfonamido)ethoxy)ethoxy)ethylamino)-3-oxopropyl)-4-isocyanatoheptanediamide; tris hydrochloride With N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 2h;
Stage #2: trifluoroacetic acid In water; N,N-dimethyl-formamide
26%
tris hydrochloride
1185-53-1

tris hydrochloride

4-bromo-benzaldehyde
1122-91-4

4-bromo-benzaldehyde

2,8-di-(m-bromophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

2,8-di-(m-bromophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

B

2,8-di-(m-bromophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane
1311029-72-7

2,8-di-(m-bromophenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

C

{bis-(2,8-di-(m-bromophenyl)-1-aza-3,7-dioxabicyclo[3.3.0]-octane 5-methoxy)methyl}-3-bromobenzene
1311029-92-1

{bis-(2,8-di-(m-bromophenyl)-1-aza-3,7-dioxabicyclo[3.3.0]-octane 5-methoxy)methyl}-3-bromobenzene

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de;A n/a
B n/a
C 25%
4-Trifluoromethylbenzaldehyde
455-19-6

4-Trifluoromethylbenzaldehyde

tris hydrochloride
1185-53-1

tris hydrochloride

A

2,8-di-(p-trifluoromethylphenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

2,8-di-(p-trifluoromethylphenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

2,8-di-(p-trifluoromethylphenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

2,8-di-(p-trifluoromethylphenyl)-5-hydroxymethyl-1-aza-3,7-dioxabicyclo[3.3.0]octane

C

{bis(2,8-di-(p-trifluoromethylphenyl)-1-aza-3,7-dioxabicyclo-[3.3.0]octane 5-methoxy)methyl}-4-trifluoromethylbenzene
1311029-91-0

{bis(2,8-di-(p-trifluoromethylphenyl)-1-aza-3,7-dioxabicyclo-[3.3.0]octane 5-methoxy)methyl}-4-trifluoromethylbenzene

Conditions
ConditionsYield
With toluene-4-sulfonic acid In toluene for 12h; Reflux; optical yield given as %de;A n/a
B n/a
C 13%
tris hydrochloride
1185-53-1

tris hydrochloride

acetic anhydride
108-24-7

acetic anhydride

1,3-diacetoxy-2-acetoxymethyl-2-amino-propane
2353-29-9

1,3-diacetoxy-2-acetoxymethyl-2-amino-propane

2-benzoyloxyacetyl chloride
54150-57-1

2-benzoyloxyacetyl chloride

tris hydrochloride
1185-53-1

tris hydrochloride

Benzoic acid (2-hydroxy-1,1-bis-hydroxymethyl-ethylcarbamoyl)-methyl ester
115193-31-2

Benzoic acid (2-hydroxy-1,1-bis-hydroxymethyl-ethylcarbamoyl)-methyl ester

Conditions
ConditionsYield
In benzene Ambient temperature;
tris hydrochloride
1185-53-1

tris hydrochloride

N,N'-dimethyl-N'-(p-nitrophenyl)-N-nitrosourea
72586-69-7

N,N'-dimethyl-N'-(p-nitrophenyl)-N-nitrosourea

A

3-(2-Hydroxy-1,1-bis-hydroxymethyl-ethyl)-1-methyl-1-(4-nitro-phenyl)-urea

3-(2-Hydroxy-1,1-bis-hydroxymethyl-ethyl)-1-methyl-1-(4-nitro-phenyl)-urea

B

N-methyl(p-nitroaniline)
100-15-2

N-methyl(p-nitroaniline)

Conditions
ConditionsYield
With water; sodium chloride; cetyltrimethylammonim bromide at 24.8℃; Rate constant; micellar effect investigated at pH 8.05;
myo-inositol-1,2-cyclic phosphate
41158-67-2

myo-inositol-1,2-cyclic phosphate

tris hydrochloride
1185-53-1

tris hydrochloride

Phosphoric acid 2-amino-3-hydroxy-2-hydroxymethyl-propyl ester (1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxy-cyclohexyl ester

Phosphoric acid 2-amino-3-hydroxy-2-hydroxymethyl-propyl ester (1S,2R,3R,4S,5S,6R)-2,3,4,5,6-pentahydroxy-cyclohexyl ester

Conditions
ConditionsYield
With glycerol In water bacterial phosphatidylinositol-specific phospholipase C presence;
tris hydrochloride
1185-53-1

tris hydrochloride

duplex of: 5\-CAAAGCG-3\ (ODN I) and 3\-GTTTCGC-5\ (ODN II)

duplex of: 5\-CAAAGCG-3\ (ODN I) and 3\-GTTTCGC-5\ (ODN II)

A

C29H35N13O19P2

C29H35N13O19P2

B

C33H44N14O21P2

C33H44N14O21P2

C

C39H50N18O26P4

C39H50N18O26P4

D

3\-GTTTCGC-5\

3\-GTTTCGC-5\

Conditions
ConditionsYield
With mesotetrakis(4-N-methylpiridiniumyl)porphyrinatomanganeseIII; oxygen; tris hydrochloride; sodium sulfite at 4℃; for 5h; pH=9; Product distribution; Enzymatic reaction;
tris hydrochloride
1185-53-1

tris hydrochloride

aminooxyacetic acid
645-88-5

aminooxyacetic acid

duplex of: 5\-CAAAGCG-3\ (ODN I) and 3\-GTTTCGC-5\ (ODN II)

duplex of: 5\-CAAAGCG-3\ (ODN I) and 3\-GTTTCGC-5\ (ODN II)

A

C29H35N13O19P2

C29H35N13O19P2

B

C31H38N14O21P2

C31H38N14O21P2

C

C33H44N14O21P2

C33H44N14O21P2

D

C39H50N18O26P4

C39H50N18O26P4

Conditions
ConditionsYield
With mesotetrakis(4-N-methylpiridiniumyl)porphyrinatomanganeseIII; oxygen; tris hydrochloride; sodium sulfite at 20℃; for 1h; pH=9; Product distribution; Enzymatic reaction;
DL-N-benzoylhomocysteine thiolactone
39837-09-7

DL-N-benzoylhomocysteine thiolactone

tris hydrochloride
1185-53-1

tris hydrochloride

C15H21NO5S

C15H21NO5S

Conditions
ConditionsYield
With N-ethyl-N,N-diisopropylamine In tetrahydrofuran at 20℃; for 16h;

1185-53-1Relevant articles and documents

The hydrophilic ionic liquid at room temperature and its use (by machine translation)

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Paragraph 0099; 0100; 0237; 0254, (2018/10/24)

PROBLEM TO BE SOLVED: To provide a novel ionic liquid that has a cation structure apt to become liquid, and is highly hydrophilic, particularly highly water-soluble, and use thereof.SOLUTION: This invention provides a hydrophilic room-temperature ionic liquid including a cation and an anion, the cation being a quaternary ammonium cation of the formula (I), where Rs independently represent a 2-8C straight-chain or branched-chain polyhydroxyalkyl group having two or more hydroxy groups, Rs independently represent a hydrogen atom or a 1-5C straight-chain or branched-chain monohydroxyalkyl group, and n represents an integer of 1-4.

Phenoxybenzylamine derivatives as SSRls

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, (2008/06/13)

A compound of general formula (I) wherein R1 and R2 are H, C1-C6alkyl or (CH2)d(C3-C6cycloalkyl) wherein d=0, 1, 2 or 3; or R1 and R2 together with the nitrogen to which they are attached form an azetidine ring; Z or Y is —SR3 and the other Z or Y is halogen or —R3; wherein R3 is C1-C4 alkyl optionally substituted with fluorine; except that R3 is not CF3; or Z and Y are linked so that, together with the interconnecting atoms, Z and Y form a fused 5 to 7-membered carbocyclic or heterocyclic ring, and wherein when Z and Y form a heterocyclic ring, in addition to carbon atoms, the linkage contains one or two heteroatoms independently selected from oxygen, sulfur and nitrogen; R4 and R5, which may be the same or different, are: A—X, wherein A═—CH═CH— or —(CH2)p— where p is 0, 1 or 2; X is hydrogen, F, Cl, Br, I, CONR6R7, SO2NR6R7, SO2NHC(═O)R6, OH, C1-4alkoxy, NR8SO2R9, NO2, NR6R11, CN, CO2R10, CHO, SR10, S(O)R9 or SO2R10; or a 5- or 6-membered heterocyclic ring containing 1, 2 or 3 heteroatoms selected from N, S and O, optionally substituted independently by one or more R13; wherein R13 is hydroxy, C1-C4alkoxy, F, C1-C6alkyl, haloalkyl, haloalkoxy, —NH2, —NH(C1-C6alkyl) or —N(C1-C6alkyl)2.

Methods for protecting ZEA mays plants against pest damage

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, (2008/06/13)

According to the invention there is provided a method of controlling insect larvae comprising the steps of feeding said larvae an insecticidal amount of a transgenic Zea mays plant that expresses a polypeptide having the insect toxicity properties of Bacillus thuringiensis crystal protein.

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