Welcome to LookChem.com Sign In|Join Free

CAS

  • or

154-87-0

Post Buying Request

154-87-0 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

154-87-0 Usage

Originator

Actimide,Tobishi

Uses

Different sources of media describe the Uses of 154-87-0 differently. You can refer to the following data:
1. Thiamine Pyrophosphate is a thiamine (T344185) derivative produced by enzyme thiamine pyrophosphatase. Thiamine pyrophosphate is a cofactor used to catalyze various biochemical reactions.
2. Cocarboxylase is a thiamine (T344185) derivative produced by enzyme thiamine pyrophosphatase. Thiamine pyrophosphate is a cofactor used to catalyze various biochemical reactions.
3. Cocarboxylase can be used in decarboxylation mechanisms in biological systems,and to investigate radical reactions of thiamin pyrophosphate in 2-oxoacid oxidoreductases.

Definition

The active coenzyme form of vitamin B1 which functions in aldehyde transfer reactions.

Manufacturing Process

4.5 kg of aqueous 89% orthophosphoric acid are heated to 135°C, and kept at this temperature for about 3 h while being actively stirred. Then, the heating is discontinued and 3.5 kg of phosphorouspentoxide are added during a period of 2.5 to 3 h, while being actively stirred. During this period, the interior temperature rises to 165°-175°C. After completion of the addition of phosphorouspentoxide, the stirring is continued until all phosphorouspentoxide is dissolved. The phosphoric acid mixture thus produced is subsequently cooled down to 130°C. At this temperature 2.0 kg of thiamine chloride hydrochloride (vitamin B1) were added during 2 to 3 h while being well stirred. The stirring is continued at 130°C until the phosphorylated mixture no longer contains chlorine ions. A phosphorylated melt is thus obtained. The thus obtained phosphorylation melt is dissolved in 6-8 L of water (with ice) at a temperature below 10°C, while being vigorously stirred. The aqueous solution is stirred into 100 L of 96% alcohol and left standing overnight. The supernatant solvent is decanted from the separated syrup; the latter is taken up in 4 L of water. The solution thus obtained is fed, depending upon the volume of phosphoric acid contained therein, to an exchanger column filled with anion exchanger (weak basic, for instance Amberlite IRA 45, 20-30 L) (a polystyrene resin with primary, secondary and quaternary amino groups). The solution is caused to seep into the column from the top thereof and is then washed with water until the runoff at the bottom no longer shows any thiamine reaction. About 25 L of the solution are obtained, which are concentrated to 6 L at 30°C and 12 Torr. The concentrated residue is added to 20 to 30 L of a cationic exchanger (Amberlite IRC 50) in order to separate the thiamine-orthophosphoric acid ester from the thiamine-pyrophosphoric acid ester, and subsequently washed with water until the eluate is free of thiamine. 70-80 L of a solution are obtained which are concentrated to 1.5 L in a circulation evaporator at 30°C and 12 Torr. 7.5 L of 96% ethanol are slowly added to a concentrate while being stirred. The cocarboxylase-tetrahydrate separates in the form of fine needles. The yield is 530.0 g with a melting point of 220°-225°C (dec.). 10.0 g of cocarboxylase-tetrahydrate are dissolved in 25 ml of 5% aqueous hydrochloric acid, and 75 ml acetone are added dropwise while being stirred. The precipitated hydrochloride of the cocarboxylase, melting point 240°C is sucked off. The yield is 9.5 g.

Therapeutic Function

Coenzyme, Metabolic

General Description

Certified pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Thiamine pyrophosphate is a coenzyme of transketolase that catalyzes the cleavage of ribulose-5-phosphate; thereby forming D-glyceraldehyde-3-phosphate. This reaction requires the addition of an acceptor aldehyde such as ribose-5-phosphate, glyceraldehye or glycolaldehyde.

Biochem/physiol Actions

Thiamine pyrophosphate (TPP) is a coenzyme of transketolase, that catalyzes the cleavage of ribulose-5-phosphate. This reaction leads to the formation of D-glyceraldehyde-3-phosphate. It requires the addition of an acceptor aldehyde such as ribose-5-phosphate, glyceraldehye or glycolaldehyde. TPP is capable of decarboxylating hydroxypyruvate in the presence of an ′acceptor aldehyde′.

Check Digit Verification of cas no

The CAS Registry Mumber 154-87-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 154-87:
(5*1)+(4*5)+(3*4)+(2*8)+(1*7)=60
60 % 10 = 0
So 154-87-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H18N4O7P2S.ClH/c1-8-11(3-4-22-25(20,21)23-24(17,18)19)26-7-16(8)6-10-5-14-9(2)15-12(10)13;/h5,7H,3-4,6H2,1-2H3,(H4-,13,14,15,17,18,19,20,21);1H

154-87-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (T0183)  Thiamine Pyrophosphate Chloride  >98.0%(T)

  • 154-87-0

  • 5g

  • 480.00CNY

  • Detail
  • TCI America

  • (T0183)  Thiamine Pyrophosphate Chloride  >98.0%(T)

  • 154-87-0

  • 25g

  • 1,730.00CNY

  • Detail
  • Sigma-Aldrich

  • (PHR1369)  Thiamine pyrophosphate  pharmaceutical secondary standard; traceable to USP

  • 154-87-0

  • PHR1369-500MG

  • 1,024.57CNY

  • Detail

154-87-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name thiamine(1+) diphosphate

1.2 Other means of identification

Product number -
Other names Thiamine Pyrophosphate Chloride

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:154-87-0 SDS

154-87-0Synthetic route

thiamin triphosphate
50851-39-3

thiamin triphosphate

Thiamine hydrochloride
67-03-8

Thiamine hydrochloride

A

thiamine diphosphate
154-87-0

thiamine diphosphate

B

2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethyl dihydrogen phosphate
10023-48-0

2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethyl dihydrogen phosphate

Conditions
ConditionsYield
With meta-phosphoric acid
4-methyl-5-oxyethyl thiazol diphosphate
2606-90-8

4-methyl-5-oxyethyl thiazol diphosphate

4-amino-5-bromomethyl-2-methylpyrimidine hydrobromide
2908-71-6

4-amino-5-bromomethyl-2-methylpyrimidine hydrobromide

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
(i) , (ii) ion exchange resin (H+-form); Multistep reaction;
diphosphoric acid 1,1-dibenzyl ester 2-[2-(4-methyl-thiazol-5-yl)-ethyl] ester; cyclohexylamine salt
4066-53-9

diphosphoric acid 1,1-dibenzyl ester 2-[2-(4-methyl-thiazol-5-yl)-ethyl] ester; cyclohexylamine salt

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (i) ion exchange resin +-form>, (ii) H2, PdCl2, MeOH, (iii) ion exchange resin --form>
2: (i) , (ii) ion exchange resin (H+-form)
View Scheme
Thiamine hydrochloride
67-03-8

Thiamine hydrochloride

A

thiamine monophosphate chloride
532-40-1

thiamine monophosphate chloride

B

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
With sodium pyrophosphate at 120℃;
vitamin B1
59-43-8

vitamin B1

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
With thiamin pyrophosphokinase; ATP; magnesium chloride In aq. buffer at 37℃; for 2h; pH=8; Inert atmosphere; Enzymatic reaction;
5-(3-acetoxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran
594859-88-8

5-(3-acetoxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-acetoxyphenyl)-5-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane
594859-89-9

1-(3-acetoxyphenyl)-5-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate97.6%
5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate97.5%
5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,3-dihydrofuran

5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,6,7-trioxabicyclo[3.2.0]heptane

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate83.6%
5-(3-acetoxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

5-(3-acetoxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-acetoxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

1-(3-acetoxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate82.5%
5-(3-acetoxyphenyl)-4-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran
594859-90-2

5-(3-acetoxyphenyl)-4-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-acetoxyphenyl)-5-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane
594859-91-3

1-(3-acetoxyphenyl)-5-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate75%
bis(acetylacetonate)oxovanadium
3153-26-2

bis(acetylacetonate)oxovanadium

water
7732-18-5

water

thiamine diphosphate
154-87-0

thiamine diphosphate

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

PV14O42(9-)*3C2H7N*3H(1+)*2C12H17N4O4PS*6H3O(1+)

PV14O42(9-)*3C2H7N*3H(1+)*2C12H17N4O4PS*6H3O(1+)

Conditions
ConditionsYield
With nitric acid at 20 - 100℃; for 75h; pH=3; Sealed tube; High pressure;73%
octane-2,3-dione
585-25-1

octane-2,3-dione

thiamine diphosphate
154-87-0

thiamine diphosphate

A

(3S)-3-hydroxy-3-methylnonane-2,4-dione
1421833-45-5

(3S)-3-hydroxy-3-methylnonane-2,4-dione

B

3-hydroxy-3-pentylpentane-2,4-dione
1421833-43-3

3-hydroxy-3-pentylpentane-2,4-dione

Conditions
ConditionsYield
With ethylenediaminetetraacetic acid; acetylacetoin synthase; magnesium sulfate In aq. phosphate buffer at 30 - 80℃; for 20.3333h; pH=6.5; Enzymatic reaction;A 68%
B 30%
thiamine diphosphate
154-87-0

thiamine diphosphate

thiamine monophosphate chloride
532-40-1

thiamine monophosphate chloride

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; iodide

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; iodide

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; dihydrogenphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; dihydrogenphosphate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; fluoride-dihydro fluoride

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; fluoride-dihydro fluoride

Conditions
ConditionsYield
With sulfuric acid
thiamin triphosphate
50851-39-3

thiamin triphosphate

Thiamine hydrochloride
67-03-8

Thiamine hydrochloride

A

thiamine diphosphate
154-87-0

thiamine diphosphate

B

2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethyl dihydrogen phosphate
10023-48-0

2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-3-ium-5-yl]ethyl dihydrogen phosphate

Conditions
ConditionsYield
With meta-phosphoric acid
4-methyl-5-oxyethyl thiazol diphosphate
2606-90-8

4-methyl-5-oxyethyl thiazol diphosphate

4-amino-5-bromomethyl-2-methylpyrimidine hydrobromide
2908-71-6

4-amino-5-bromomethyl-2-methylpyrimidine hydrobromide

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
(i) , (ii) ion exchange resin (H+-form); Multistep reaction;
diphosphoric acid 1,1-dibenzyl ester 2-[2-(4-methyl-thiazol-5-yl)-ethyl] ester; cyclohexylamine salt
4066-53-9

diphosphoric acid 1,1-dibenzyl ester 2-[2-(4-methyl-thiazol-5-yl)-ethyl] ester; cyclohexylamine salt

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (i) ion exchange resin +-form>, (ii) H2, PdCl2, MeOH, (iii) ion exchange resin --form>
2: (i) , (ii) ion exchange resin (H+-form)
View Scheme
Thiamine hydrochloride
67-03-8

Thiamine hydrochloride

A

thiamine monophosphate chloride
532-40-1

thiamine monophosphate chloride

B

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
With sodium pyrophosphate at 120℃;
vitamin B1
59-43-8

vitamin B1

thiamine diphosphate
154-87-0

thiamine diphosphate

Conditions
ConditionsYield
With thiamin pyrophosphokinase; ATP; magnesium chloride In aq. buffer at 37℃; for 2h; pH=8; Inert atmosphere; Enzymatic reaction;
5-(3-acetoxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran
594859-88-8

5-(3-acetoxyphenyl)-4-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-acetoxyphenyl)-5-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane
594859-89-9

1-(3-acetoxyphenyl)-5-(13-carboxy-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate97.6%
5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate97.5%
5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,3-dihydrofuran

5-(3-t-butyldimethylsiloxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,6,7-trioxabicyclo[3.2.0]heptane

1-(3-t-butyldimethylsiloxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-7-succinimidoxycarbonyl-3-oxaheptyl)-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate83.6%
5-(3-acetoxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

5-(3-acetoxyphenyl)-3,3-dimethyl-4-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-acetoxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

1-(3-acetoxyphenyl)-4,4-dimethyl-5-(1,1-dimethyl-13-succinimidoxycarbonyl-3-oxatridecan-1-yl)-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate82.5%
5-(3-acetoxyphenyl)-4-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran
594859-90-2

5-(3-acetoxyphenyl)-4-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-3,3-dimethyl-2,3-dihydrofuran

thiamine diphosphate
154-87-0

thiamine diphosphate

1-(3-acetoxyphenyl)-5-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane
594859-91-3

1-(3-acetoxyphenyl)-5-(13-ethoxycarbonyl-1,1-dimethyl-3-oxatridecan-1-yl)-4,4-dimethyl-2,6,7-trioxabicyclo[3.2.0]heptane

Conditions
ConditionsYield
In hexane; dichloromethane; ethyl acetate75%
bis(acetylacetonate)oxovanadium
3153-26-2

bis(acetylacetonate)oxovanadium

water
7732-18-5

water

thiamine diphosphate
154-87-0

thiamine diphosphate

N,N-dimethyl-formamide
68-12-2, 33513-42-7

N,N-dimethyl-formamide

PV14O42(9-)*3C2H7N*3H(1+)*2C12H17N4O4PS*6H3O(1+)

PV14O42(9-)*3C2H7N*3H(1+)*2C12H17N4O4PS*6H3O(1+)

Conditions
ConditionsYield
With nitric acid at 20 - 100℃; for 75h; pH=3; Sealed tube; High pressure;73%
octane-2,3-dione
585-25-1

octane-2,3-dione

thiamine diphosphate
154-87-0

thiamine diphosphate

A

(3S)-3-hydroxy-3-methylnonane-2,4-dione
1421833-45-5

(3S)-3-hydroxy-3-methylnonane-2,4-dione

B

3-hydroxy-3-pentylpentane-2,4-dione
1421833-43-3

3-hydroxy-3-pentylpentane-2,4-dione

Conditions
ConditionsYield
With ethylenediaminetetraacetic acid; acetylacetoin synthase; magnesium sulfate In aq. phosphate buffer at 30 - 80℃; for 20.3333h; pH=6.5; Enzymatic reaction;A 68%
B 30%
thiamine diphosphate
154-87-0

thiamine diphosphate

thiamine monophosphate chloride
532-40-1

thiamine monophosphate chloride

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; iodide

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; iodide

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; dihydrogenphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; dihydrogenphosphate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; fluoride-dihydro fluoride

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; fluoride-dihydro fluoride

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; hydrochloride
129681-12-5

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; hydrochloride

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; bromide hydrobromide

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; bromide hydrobromide

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; nitrate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; nitrate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; perchlorate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; perchlorate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; hydrogen sulfate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; hydrogen sulfate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; naphthalene-2-sulfonate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; naphthalene-2-sulfonate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; bis phosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; bis phosphate

Conditions
ConditionsYield
With sulfuric acid
thiamine diphosphate
154-87-0

thiamine diphosphate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; disulfate

3-(4-amino-2-methyl-pyrimidin-5-ylmethyl)-4-methyl-5-(2-phosphonooxy-ethyl)-thiazolium; disulfate

Conditions
ConditionsYield
With sulfuric acid
t-butyl pyruvate
76849-54-2

t-butyl pyruvate

thiamine diphosphate
154-87-0

thiamine diphosphate

C19H31N4O10P2S(1+)*Cl(1-)
76849-52-0

C19H31N4O10P2S(1+)*Cl(1-)

Conditions
ConditionsYield
With tetra(n-butyl)ammonium hydroxide; sodium t-butanolate 1) water; 2) DMF, -5 deg C, 30 min; Multistep reaction;
formaldehyd
50-00-0

formaldehyd

thiamine diphosphate
154-87-0

thiamine diphosphate

2-Hydroxymethylthiamine diphosphate

2-Hydroxymethylthiamine diphosphate

Conditions
ConditionsYield
With sodium hydroxide In various solvent(s) at 20℃; for 24h; pH=5.6; Addition;

154-87-0Related news

Application of Microwave Irradiation for Concentrating of the Cocarboxylase (cas 154-87-0) Water Solutions09/30/2019

A process for concentrating of cocarboxylase water solutions under microwave irradiation is investigated. Perspectives of application of microwave technology for evaporating of the water solutions are showndetailed

Effects of Cocarboxylase (cas 154-87-0) in Amikacin-Induced Ototoxicity in Immature Animals09/29/2019

Possible otoprotective properties of cocarboxylase were studied on the model of amikacin-induced ototoxicity in immature rabbits. Auditory function was evaluated by the short-latency auditory brainstem response (ABR) and distortion product otoacoustic emission (DPOAE) tests. Administration of co...detailed

Influence of microwave technology on Cocarboxylase (cas 154-87-0) hydrochloride particle diversity and drying efficiency09/28/2019

Two possible ways of crystallite downsizing of cocarboxylase hydrochloride namely mechanical milling and precipitation under high supersaturation conditions were studied as well as their influence on the drying parameters of the produced powders. It was found that both methods allowed shortening...detailed

154-87-0Relevant articles and documents

Synthesis and characterization of catalytically active thiazolium gold(i)-carbenes

Dince, Clément C.,Meoded, Roy A.,Hilvert, Donald

, p. 7585 - 7587 (2017)

Thiamin analogs were used to synthesize mono gold(i)-carbene derivatives in a single step under aqueous conditions. The resulting thiazolium gold(i)-carbenes catalyze 5-endo-dig carbocyclization of an acetylenic dicarbonyl compound in organic solvents and hydroalkoxylation of an allene in aqueous buffer.

Preparation method of co-carboxylase and tetrahydrate or salt thereof

-

Paragraph 0043; 0049-0052; 0056-0058; 0062-0075, (2021/09/21)

The invention discloses a preparation method of co-carboxylase and tetrahydrate or salt thereof. The invention provides a preparation method of a co-carboxylase shown as a formula I. The method comprises the following steps: eluting a mixture containing the co-carboxylase as shown in the formula I by using weakly-alkaline anion exchange resin through water and a weakly-alkaline aqueous solution with the pH value of 10-12 as eluent in sequence, and collecting eluate to obtain an aqueous solution containing the co-carboxylase as shown in the formula I, wherein the mixture containing the co-carboxylase as shown in the formula I comprises thiamine monophosphate and the co-carboxylase as shown in the formula I.

Use of vitamin b1 as agents for controlling plant diseases

-

, (2008/06/13)

The present invention relates to an agent for controlling plant diseases containing vitamin B1, or salts or derivatives thereof as an active ingredient, which exhibits excellent disease controlling effects by rapid induction of defense-related genes in plants infected with pathogens.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 154-87-0