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Cocarboxylase

CAS No.
154-87-0
Chemical Name:
Cocarboxylase
Synonyms
Vitamin B1;THIAMINE PYROPHOSPHATE;thiamin diphosphate;Cocarboxylase hydrochloride;THIAMINE PYROPHOSPHATE CHLORIDE;COCARBOXYLASE CHLORIDE;co-bi;biosyth;nutrase;berolase
CBNumber:
CB6326133
Molecular Formula:
C12H19N4O7P2S.Cl
Molecular Weight:
460.77
MDL Number:
MFCD00038740
MOL File:
154-87-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-04-21 17:10:26
Product description Number Pack Size Price
Thiamine pyrophosphate ≥95% C8754 1g $62.1
Thiamine pyrophosphate ≥95% C8754 5g $81.6
Thiamine Pyrophosphate Chloride >98.0%(T) T0183 5g $138
Thiamine Pyrophosphate (chloride) ≥95% 20254 500mg $25
Thiamine Pyrophosphate (chloride) ≥95% 20254 1g $38
More product size

Cocarboxylase Properties

Melting point 240~241℃
bulk density 500kg/m3
storage temp. -20°C
solubility H2O: soluble50mg/mL, clear to very slightly hazy, colorless
pka 5.82
form Solid
color White to Off-White
PH 1.0-1.4 (20°C, 100g/L in H2O)
Water Solubility It is soluble in water.
BRN 3875902
Stability Hygroscopic
Cosmetics Ingredients Functions SKIN CONDITIONING
InChI InChI=1S/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
InChIKey YXVCLPJQTZXJLH-UHFFFAOYSA-N
SMILES [Cl-].S1C([H])=[N+](C([H])([H])C2=C([H])N=C(C([H])([H])[H])N=C2N([H])[H])C(C([H])([H])[H])=C1C([H])([H])C([H])([H])OP(=O)(O[H])OP(=O)(O[H])O[H]
CAS DataBase Reference 154-87-0(CAS DataBase Reference)
FDA UNII XMK8K8EVIU
EPA Substance Registry System Thiazolium, 3-[(4-amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-(4,6,6-trihydroxy-4,6-dioxido-3,5-dioxa-4,6-diphosphahex-1-yl)-, chloride (154-87-0)
UNSPSC Code 41116107
NACRES NA.54

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H317
Precautionary statements  P261-P272-P280-P302+P352-P333+P313-P362+P364
PPE Eyeshields, Gloves, type N95 (US)
Safety Statements  22-24/25
RIDADR  1759
WGK Germany  3
RTECS  XI7552000
3-8-10
TSCA  TSCA listed
HazardClass  8
PackingGroup  III
HS Code  29362200
Storage Class 11 - Combustible Solids
Hazard Classifications Skin Sens. 1
Toxicity LD50 intramuscular in mouse: > 1gm/kg

Cocarboxylase price More Price(25)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich C8754 Thiamine pyrophosphate ≥95% 154-87-0 1g $62.1 2026-03-19 Buy
Sigma-Aldrich C8754 Thiamine pyrophosphate ≥95% 154-87-0 5g $81.6 2026-03-19 Buy
TCI Chemical T0183 Thiamine Pyrophosphate Chloride >98.0%(T) 154-87-0 5g $138 2026-03-19 Buy
Cayman Chemical 20254 Thiamine Pyrophosphate (chloride) ≥95% 154-87-0 500mg $25 2024-03-01 Buy
Cayman Chemical 20254 Thiamine Pyrophosphate (chloride) ≥95% 154-87-0 1g $38 2024-03-01 Buy
Product number Packaging Price Buy
C8754 1g $62.1 Buy
C8754 5g $81.6 Buy
T0183 5g $138 Buy
20254 500mg $25 Buy
20254 1g $38 Buy

Cocarboxylase Chemical Properties,Uses,Production

Originator

Actimide,Tobishi

History

Best known as the anti-beriberi factor and called at first simply vitamin B by McCollum, thiamine was shown to be involved in the decarboxylation of pyruvate to acetaldehyde in alcohol fermentation and was named ‘cocarboxylase’ in 1932. Confirmation of its structure as TPP came 5 years later. Its name is meant to signify a vitamin containing sulfur (thios in Greek).

Uses

Cocarboxylase can be used in decarboxylation mechanisms in biological systems,and to investigate radical reactions of thiamin pyrophosphate in 2-oxoacid oxidoreductases.

Uses

Thiamine Pyrophosphate (Cocarboxylase) is a thiamine (T344185) derivative produced by enzyme thiamine pyrophosphatase. Thiamine pyrophosphate is a cofactor used to catalyze various biochemical reactions.

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

Biological Functions

Thiamine pyrophosphate, or cocarboxylase, functions as a cofactor in intermediary carbohydrate metabolism. It serves as a coenzyme in the decarboxylation of α-keto acids, that is, α-ketoglutaric acid and pyruvate dehydrogenase; it also acts as a cofactor to the enzyme transketolase in the hexose monophosphate shunt. Deficiency of thiamine in animals results in the accumulation of lactic acid and reduction in oxygen uptake, especially in the brainstem, and depression of transketolase activity, again most strikingly in the brainstem.

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′.

136-09-4
154-87-0
Synthesis of Cocarboxylase from 2-[3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-4-methyl-1,3-thiazoniol-5-yl]ethyl dihydrogen diphosphate

Cocarboxylase Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 451)Suppliers
Supplier Tel Email Country ProdList Advantage
Sense Chemicals (Shanghai) Co., Ltd.
+86-21-52751036; +8613818977689 david.dai@sensechemicals.com China 225 58
Aurora Industry Co., Ltd.
+86-13591747876 +86-13591747876; alex1_auco@126.com China 300 58
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8738 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-81139210 +86-18192627656 1059@dideu.com China 3590 58
RongNa Biotechnology Co.,Ltd
+86-86-13583358881 +8618560316533 Brad@rongnabiotech.com China 3365 58
Wuhan Fortuna Chemical Co., Ltd
+86-27-59207850 info@fortunachem.com China 5975 58
Hebei Zhuanglai Chemical Trading Co Ltd
+86-16264648883 niki@zlchemi.com China 7245 58
Moxin Chemicals
+86-17320513646 +8617320513646 anna@molcoo.com China 10000 58
Sinoway Industrial co., ltd.
+86-0592-5800732 +86-13806035118 xie@china-sinoway.com China 1369 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21592 55

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View Lastest Price from Cocarboxylase manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Cocarboxylase pictures 2026-04-24 Cocarboxylase
154-87-0
US $10.00 / ASSAYS 1ASSAYS 99% 1 ton RongNa Biotechnology Co.,Ltd
Cocarboxylase pictures 2026-04-24 Cocarboxylase
154-87-0
US $0.00-0.00 / mg 1mg 99.1% 10g/month WUHAN FORTUNA CHEMICAL CO., LTD
Thiamine Pyrophosphate pictures 2026-04-23 Thiamine Pyrophosphate
154-87-0
US $0.00-0.00 / kg 1kg 98% up by HPLC 20TONS Sinoway Industrial co., ltd.
  • Cocarboxylase pictures
  • Cocarboxylase
    154-87-0
  • US $10.00 / ASSAYS
  • 99%
  • RongNa Biotechnology Co.,Ltd
  • Cocarboxylase pictures
  • Cocarboxylase
    154-87-0
  • US $0.00-0.00 / mg
  • 99.1%
  • WUHAN FORTUNA CHEMICAL CO., LTD
ANEURINEPYROPHOSPHORIC ACID COCARBOXYLASE Thiamine, pyrophosphoric acid ester [2-[3-[(4-Amino-2-methyl-pyrimidin-5-yl)methyl]-4-methyl-1,3-thiazol-5-yl]ethoxy-hydroxy-phosphoryl]oxyphosphonic acid chloride Thiamine diphosphate chloride Aneurinepyrophosphoric acid, Cocarboxylase, Thiamine pyrophosphate chloride Thiamin diphosphate chloride Vitamin B1 pyrophosphate chloride Thiamine pyrophosphate,Aneurinepyrophosphoric acid, Cocarboxylase, Thiamine pyrophosphate chloride Thiazolium, 3-(4-amino-2-methyl-5-pyrimidinyl)methyl-4-methyl-5-(4,6,6-trihydroxy-4,6-dioxido-3,5-dioxa-4,6-diphosphahex-1-yl)-, chloride [2-[3-[(4-amino-2-methyl-pyrimidin-5-yl)methyl]-4-methyl-1-thia-3-azoniacyclopenta-2,4-dien-5-yl]ethoxy-hydroxy-phosphoryl]oxyphosphonic acid Cocarboxylase Vitamin B1 Pyrophosphoric Acid Ester Chloride 3-((4-Amino-2-methylpyrimidin-5-yl) -4-methylthiazol-3-ium chloride -5-(2-((hydroxy(phosphonooxy) phosphoryl) THIAMINIUM DIPHOSPHORIC ACID ESTER CHLORIDE THIAMINIUM PYROPHOSPHATE CHLORIDE THIAMINIUM PYROPHOSPHORIC ACID ESTER CHLORIDE THIAMINEPYROPHOSPHORIC ACID THIAMINE PYROPHOSPHORIC ACID ESTER CHLORIDE VITAMIN B1 PYROPHOSPHORIC ACID ESTER CHLORIDE berolase biosyth bioxylasi bivitasi b-neurox co-bi cocarbina cocarboxil coenbione coxylase diphosphothiamin diphosphothiamine farmaneurina metabolase nutrase pyrolase pyruvodehydrase roxy-3,5-dioxa-4,6-diphosphahex-1-yl)-,chloride,p,p’-dioxide tdp(thiaminester) thiamine,trihydrogenpyrophosphate(ester) thiamine-pp thiaminepyrophosphoricester thiaminpyrophosphate thiazolium,3-[(4-amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-(4,6,6-trihyd Thiazolium,3-[(4-amino-2-methyl-5-pyrimidinyl)methyl]-4-methyl-5-(4,6,6-trihydroxy-3,5-dioxa-4,6-diphosphahex-1-yl)-,chloride,P,P’-dioxide tpp(coenzyme) ThiazoliuM,3-[(4-aMino-2-Methyl-5-pyriMidinyl)Methyl]-4-Methyl-5-(4,6,6-trihydroxy-4,6-dioxido-3,5-dioxa-4,6-diphosphahex-1-yl)-,chloride (1:1) thiamine(1+) diphosphate 3-((4-Amino-2-methylpyrimidin-5-yl)methyl)-5-(2-((hydroxy(phosphonooxy)phosphoryl)oxy)ethyl)-4-methylthiazol-3-ium chloride Thiaminepyrophosphatehydrochloride Thiamine Impurity 30(Thiamine Pyrophosphate) Cocarboxylase (TPP) Thiamine Pyrophosphate Chloride > Thiamine pyrophosphate (Vitamin B1 pyrophosphate) solution hiamine(1+)diphosphate Cocarboxylase USP/EP/BP