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Tetramethylpyrazine

HCID 14296
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Basic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
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Basic information

CAS
1124-11-4
Standard SMILES
Cc1nc(C)c(C)nc1C
InChIKey
FINHMKGKINIASC-UHFFFAOYSA-N
Molecular formula
C8H12N2
Average molar mass
136.19 g/mol
Monoisotopic mass
136.10004838

Overview

Tetramethylpyrazine is a member of the class of pyrazines that is pyrazine in which all four hydrogens have been replaced by methyl groups. An alkaloid extracted from Chuanxiong (Ligusticum wallichii). It has a role as an antineoplastic agent, a vasodilator agent, a platelet aggregation inhibitor, a neuroprotective agent, an apoptosis inhibitor and a bacterial metabolite. It is an alkaloid and a member of pyrazines.

Names & identifiers

Preferred name
Tetramethylpyrazine
IUPAC
2,3,5,6-tetramethylpyrazine
English name
Tetramethylpyrazine
Molecular formula
C8H12N2
Molecular weight
136.19

Names & synonyms

2,3,5,6-TetramethylpyrazineTETRAMETHYLPYRAZINE1124-11-4LigustrazineChuanxiongzineTetrapyrazinechuanxingzineFEMA No. 3237CHUANXIONGQINTMPZ2,3,5,6,-Tetramethyl-1,4-pyrazineDTXSID6047070
Show more names
FEMA 3237Pyrazine,tetramethyl-Tetramethylpyrazin2,3,5,6-TetramethyLtetramethyl-pyrazinBS FactorLigustizine
V80F4IA5XGDTXCID4027070NSC-36080NSC-46451CHEBI:133246tetramethyl pyrazineRefChem:799162214-391-2

Database identifiers

CAS
1124-11-4
PubChem CID
14296
DTXSID
DTXSID6047070
ChEMBL
CHEMBL303697
ChEBI
CHEBI:133246
UNII
V80F4IA5XG
EC Number
214-391-2
Nikkaji
J39.647H

Properties

Computed structural propertiesFilling in

XLogP
1.3
Topological polar surface area
25.8 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
2
Rotatable bonds
0
Heavy atoms
10
Formal charge
0
Complexity
87.8

Experimental & physicochemical properties

SpringerMaterials PropertiesCrystal structure
FragrancesFragrance Ingredient (2,3,5,6-Tetramethylpyrazine) -> IFRA transparency List
LogP1.28
Food AdditivesFLAVORING AGENT OR ADJUVANT -> FDA Substance added to food
Flavoring AgentsEU Flavoring substances
Solubility · 3 items

slightly soluble in water; soluble in oils, propylene glycol, organic solvents

very soluble (in ethanol)

<0.1 [ug/mL] (The mean of the results at pH 7.4)

Boiling Point · 2 items

190.00 °C. @ 760.00 mm Hg

190 °C

Melting Point86 °C
Physical Description · 2 items

Solid

white crystals or powder with a musty, fermented, coffee odour

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 6 items

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P264, P270, P301+P317, P330, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 1685 reports by companies from 8 notifications to the ECHA C&L Inventory.

Warning

H302: Harmful if swallowed [Warning Acute toxicity, oral]

Hazard information

Regulatory Information · 3 items

Chemical: Pyrazine, tetramethyl-

Regulation (EC) No 1831/2003 (amended)

2,3,5,6-Tetramethylpyrazine: Does not have an individual approval but may be used under an appropriate group standard

Hazard Classes and Categories · 2 items

Acute Tox. 4 (100%)

Acute toxicity (Oral) - Category 4

Safety data

wgk
3
tsca
TSCA listed
rtecs
UQ3905000
hs_code
29339990
risk_code
22-37/38-41-36/37/38
Signal word
Warning
Symbol(GHS)
GHS07
hazard_code
Xn,Xi
safety_code
26-39-24/25-37/39-36
Storage Class
11 - Combustible Solids
target organs
Respiratory system

Chemistry & industry

Pharmacology

MeSH Pharmacological ClassificationDrugs used to cause dilation of the blood vessels.
Cellular LocationsCytoplasm

Uses & manufacturing

Use Classification · 3 items

Fragrance Ingredients

Flavouring Agent -> FLAVOURING_AGENT -> JECFA Functional Classes

Flavoring Agents -> JECFA Flavorings Index

General Manufacturing InformationPyrazine, 2,3,5,6-tetramethyl-: ACTIVE
Applications · 10 items

DescriptionTetramethylpyrazine (TMP) is a kind of alkaloids identified in Ligusticum wallichii FRANCH. It has various kinds of medical applications. It has long been used in China for the treatment of cardiovascular problems. It also has antiinflammatory and analgesic effect. It can be used for the treatment of diabetic peripheral neuropathy. Through effectively penetrating across the blood-brain barrier, it can exert its neuroprotection function which is useful for the treatment of ischemic brain injury. Moreover, it can eliminate superoxide anion and decreases nitric oxide production in human polymorphonuclear leukocytes.

UsesPermissible edible flavors, mainly used to prepare meat, cocoa, peanut, nut, coffee, chocolate flavor and so on; For medicine production; Used as flavoring agents, sweeteners for alcoholic beverages, flavor and enriching supplement for cigarettes.

DescriptionLigustrazine is an alkaloid derived from chuanxiong (Ligusticum chuanxiong Hort; L. wallichii). Ligusticum wallichii Franchat (or Ligusticum chuanxiong Hort; L. wallichii), a member of the Umbelliferaceae family, is a Chinese medicinal herb that is a common constituent in polypharmaceutical herbal drugs. It has been widely used in Asian countries to increase coronary blood flow and systemic circulation and to relieve stasis.Ligusticum walliichi has the effects of promoting Qi and nourishing blood. Ligusticum walliichi, angelica, and peony were used as medicinal herbs, and thecommonly used Yangxue Siwu decoction was proposed for clinical practice. The combination of gypsum and Ligusticum walliichi can clear lung heat and eliminate cough and asthma. It is a common drug for clearing away heat and toxic substances and purging fire. The compatibility of Ligusticum walliichi and Radix Linderae can regulate the blood and Qi and treat women’s headaches and colds and retrograde and other related pains.Ligusticum walliichi is warm, acrid, and bitter. It can regulate the blood and conduct Qi, which is commonly used in oral administration. Ligusticum walliichi is used to treat apoplexy, headache, cold pain, the upper reaches of the wind, tears clogging of nose by cold, and so on. At present, the study of Chuanxiong in China and abroad has occurred at the molecular level .

Related reactions

22 records
New reaction record
HRID 443329 reaction equation
HRID 443329As reactantuspto-grants-1981_04
HRID 443330 reaction equation
HRID 443330As reactantuspto-grants-1981_04
HRID 443331 reaction equation
HRID 443331As reactantuspto-grants-1981_04
HRID 443332 reaction equation
HRID 443332As reactantuspto-grants-1981_04
HRID 443334 reaction equation
HRID 443334As reactantuspto-grants-1981_04
HRID 633772 reaction equation
HRID 633772As reactantuspto-grants-2016_04
HRID 633773 reaction equation
HRID 633773As reactantuspto-grants-2016_04
HRID 633774 reaction equation
HRID 633774As reactantuspto-grants-2016_04
Page 1 of 3

Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes

Physicochemical properties

Melting point
77 · 77-80 °C(lit.)
Boiling point
190 °C · 190 °C(lit.)
Density
1.08 · 1.08
refractive index
1.588 · 1.5880 (estimate)
FEMA
3237 · 3237 | 2,3,5,6-TETRAMETHYLPYRAZINE
FLAVIS Number
14.018 · 14.018 | 2,3,5,6-Tetramethylpyrazine
Flash point
128 · 128-130°C/200mm
storage temp.
Sealed in dry,Room Temperature
solubility
4 g/l · 4g/l
pka
3.2 · 3.20±0.10(Predicted)
form
Solid
color
White to Off-White
Odor
10 % · at 10.00 % in dipropylene glycol. nutty musty chocolate coffee cocoa brown lard burnt
Odor Type
nutty
biological source
synthetic
Water Solubility
Soluble in water (4 g/L at 20°C).
JECFA Number
780 · 780
BRN
113100 · 113100
Stability
Stable. Incompatible with strong acids, strong oxidizing agents.
Cosmetics Ingredients Functions
PERFUMING
InChI
1S/C8H12N2/c1-5-6(2)10-8(4)7(3)9-5/h1-4H3
InChIKey
FINHMKGKINIASC-UHFFFAOYSA-N
SMILES
Cc1nc(C)c(C)nc1C
LogP
1.56 · 1.56
CAS DataBase Reference
1124 · 1124-11-4(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS)
2 · 2,3,5,6-TETRAMETHYLPYRAZINE
EWG's Food Scores
1 · 1
FDA UNII
80 F4IA5XG · V80F4IA5XG
NIST Chemistry Reference
Pyrazine, tetramethyl-(1124-11-4)
EPA Substance Registry System
Tetramethylpyrazine (1124-11-4)
UNSPSC Code
85151701 · 85151701
NACRES
24 · NA.24
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302-H315-H319-H335
Precautionary statements
261 · P261-P264-P270-P301+P312-P302+P352-P305+P351+P338
target organs
Respiratory system
Hazard Codes
Xn,Xi
Risk Statements
22 · 22-37/38-41-36/37/38
Safety Statements
26 · 26-39-24/25-37/39-36
WGK Germany
3 · 3
RTECS
3905000 · UQ3905000
TSCA
TSCA listed
HS Code
29339990 · 29339990
Storage Class
11 · 11 - Combustible Solids
Hazard Classifications
4 OralEye · Acute Tox. 4 OralEye Irrit. 2Skin Irrit. 2STOT SE 3
Hazard statements
H302-H315-H319-H335
Hazard Classifications
Acute Tox. 4 OralEye Irrit. 2Skin Irrit. 2STOT SE 3
Precautionary statements
P261-P264-P270-P301+P312-P302+P352-P305+P351+P338

Description2,3,5,6-Tetramethylpyrazine is an alkaloid that has been found in L. wallichii and has diverse biological activities. It reduces kainate-induced increases in production of reactive oxygen species (ROS) and cytotoxicity in primary rat hippocampal neurons when used at a concentration of 5 μM. 2,3,5,6-Tetramethylpyrazine (0.1 mM) induces vasodilation in precontracted isolated and endothelium-denuded rat tail artery strips and reduces blood pressure in anesthetized rats. It decreases infarct volume, caspase-3 activation, and hypoxia-inducible factor-1α (HIF-1α) levels in a rat model of focal cerebral ischemia induced by middle cerebral artery occlusion (MCAO) when administered at a dose of 20 mg/kg.

OccurrenceReported found in French fried potato, bell pepper, wheat bread, emmental cheese, Swiss cheese, Camembert cheese, Gruyere cheese, boiled and cooked beef, grilled and roasted beef, fried beef, cooked lamb and mutton, lamb and mutton liver, grilled and roasted uncured pork, beer, black tea, green tea. Also reported present in cocoa products, coffee, dairy products, oatmeal, galbanum oil, roasted peanuts, soybean, beans, mushroom, trassi, coriander seed, rice bran, trassi, sukiyaki, soy sauce, malt, licorice, dried bonito, wild rice, shrimp, crab, clam, scallop, filberts, rum, sake, wine, whiskey, burley tobacco and soy products.

HistoryLigusticum walliichi has a long medicinal history in China and is used in the treatment of headache, promoting blood and Qi circulation, curing chills and alleviating pain”. Clinically, it is mainly used for the treatment of cardiovascular and cerebrovascular diseases. Ligustrazine (2,3,5,6-tetramethylpyrazine) is the main active ingredient of Ligusticum walliich. It was first isolated in 1962 .In recent years, studies have found that ligustrazine can inhibit the activity of the cerebral cortex and medullary respiratory center, excite vasomotors, induce the expansion of peripheral blood vessels, promote the blood flow of the coronary artery and lower limbs, and reduce blood pressure. Ligustrazine can also paralyze the nerve center and has sedative and analgesic effects.Studies have suggested that ligustrazine has a variety of new effects, including improving leptomeningeal and peripheral microcirculation and increasing cerebral blood flow, and its effect is better than that of papaverine. Ligustrazine can also protect against experimental cerebral ischemia and alleviate brain edema and the deposition of fibrin in microvessels. Ligustrazine is also used in the treatment of pulmonary heart disease, heart failure, dilated heart disease, portal hypertension, type II diabetes mellitus, tumor and coronary heart disease, and restenosis after stent implantation .

Usesetramethylpyrazine is an anti-inflammatory compound isolated from the fermented food natto. Tetramethylpyrazine demonstrated in vivo nootropic activity in rats.

Uses2,3,5,6-Tetramethylpyrazine may be used as an analytical reference standard for the quantification of the analyte in Ephedrae herba and Ephedra sinica Stapf using different chromatography techniques.

UsesUsually used in research and treatment of multiple disorders.

General Description2,3,5,6-Tetramethylpyrazine has been isolated from Ephedra sinica. It is useful in the treatment of several disorders such as asthma, heart failure, rhinitis and urinary incontinence. It is a flavor ingredient of tobacco. It forms cocrystal with 4-hydroxybenzoic acid which exhibits supramolecular synthon polymorphism.

Preparation methods · 2 items

PreparationButanedione monoxime generated by butanone and ethyl nitrite condensation is reduced and cyclized to produce methylpyrazine. The cyclization reaction product is subjected to steam distillation and the distillate is cooled,crystallized and filtered to generate crude tetramethylpyrazine which is refined with water recrystallization and activated carbon to decolor. Ethanol solution with 15% to 20% hydrogen chloride can be added into acetone to prepare hydrochloride salt. Condensed by 2,3-butanedione and 2,3-butanediamine.

PreparationFrom2,5-dimethylpyrazine by ring alkylationwithMeLi; also by condensation of 2,3-butanedionewith 2,3-butanediamine.

Upstream & downstream products

Upstream raw materials

2-Methylpyrazine2,3-ButanedioneAcetylacetoneSodium nitriteEthanol solutionEthyl nitrite1,4-Diaminobutane

Downstream products

Trimethyl thiazole

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
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枣庄九星生物科技有限公司0632-3759569 13589608009
INTATRADE GmbH+49 3493/605464 · [email protected]
爱斯特(成都)生物制药股份有限公司+86-28-85122536 85324413 · [email protected]
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Ark Pharm, Inc.847-367-3680 · [email protected]
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安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
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吉良化学21-62165282 · [email protected]
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嘉兴市艾森化工有限公司0573-85285100 18627885956 · [email protected]
Pure Chemistry Scientific Inc.001-857-928-2050 or 1-888-588-9418 · [email protected]
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深圳虹彩祥根生物科技有限公司+86-0755-89668383 · [email protected]
上海隆盛化工有限公司58099637 13585536065 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
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立合生物(山东)有限公司13176691201 15588824841 · [email protected]
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上海思域化工科技有限公司86-21-34053660 · [email protected]
赛默飞世尔科技(中国)有限公司800-810-5118 · [email protected]
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Additional notes

DefinitionChEBI: A member of the class of pyrazines that is pyrazine in which all four hydrogens have been replaced by methyl groups. An alkaloid extracted from Chuanxiong (Ligusticum wallichii).