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LAPACHOL

LAPACHOL Structure
CAS No.
84-79-7
Chemical Name:
LAPACHOL
Synonyms
Tecomin;CI 75490;LAPACHOL;NSC 11905;nsc-11905;taiguwood;Taigu Wood;Greenharten;Greenhartin;Groenhartin
CBNumber:
CB1339480
Molecular Formula:
C15H14O3
Molecular Weight:
242.27
MOL File:
84-79-7.mol
MSDS File:
SDS
Modify Date:
2023/6/8 9:03:01

LAPACHOL Properties

Melting point 141-143 °C(lit.)
Boiling point 325.09°C (rough estimate)
Density 1.2077 (rough estimate)
refractive index 1.5740 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility ethanol: soluble10mg/mL, clear, light yellow to yellow
pka 4.81±0.10(Predicted)
Colour Index 75490
form Solid
color Yellow to Dark Yellow
Merck 13,5382
InChIKey CIEYTVIYYGTCCI-UHFFFAOYSA-N
LogP 2.516 (est)
CAS DataBase Reference 84-79-7

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P301+P312+P330
Hazard Codes  Xn
Risk Statements  20/21/22-36/37/38
Safety Statements  26-36
WGK Germany  3
RTECS  QL8750000
Toxicity LD50 in male, female BALB/c mice (g/kg): 0.487; 0.792 orally (Morrison)
NFPA 704
0
3 0

LAPACHOL price More Price(1)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 142905 Lapachol 98% 84-79-7 250MG ₹8447.1 2022-06-14 Buy
Product number Packaging Price Buy
142905 250MG ₹8447.1 Buy

LAPACHOL Chemical Properties,Uses,Production

Description

Lapachol, a benzoquinone, is a secondary allergen in teak (Tectona grandis).

Occurrence

Lapacol (CI Natural Yellow 16; CI 75490) (lapachic acid, taiguie acid, tecomin) is a yellow pigment occurring in the wood of trees of the genus Tecoma, native to the West Indies and tropical South America. The shavings of the wood, treated with lime water, give an extract that dyes cotton yellow.

Uses

It was used in the synthesis of the lapachol metal complexes.

General Description

Lapachol is natural naphthoquinone compound derived from Bignoniaceae (Tabebuia sp.).

Contact allergens

Lapachol, a benzoquinone, is a secondary allergen in teak (Tectona grandis L., Verbenaceae family), a wood largely used for various indoor and outdoor applications (doors, windows, etc.) because of its strong durability. It has similar reactivity to deoxylapachol. Seealso Chap. 46

Purification Methods

Crystallise Lapachol from pet ether/EtOH, EtOH or Et2O. [Beilstein 8 H 326, 8 I 644, 8 II 365, 8 III 2720.]

LAPACHOL Preparation Products And Raw materials

Global( 139)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
Henan Tianfu Chemical Co.,Ltd. +86-0371-55170693 +86-19937530512 China 21669 55 Inquiry
career henan chemical co +86-0371-86658258 +8613203830695 China 29897 58 Inquiry
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Hefei TNJ Chemical Industry Co.,Ltd. 0551-65418671 China 34571 58 Inquiry
LAPACHOL CI 75490 NATURAL YELLOW 16 2-HYDROXY-3-(3-METHYL-2-BUTENYL)-1,4-NAPHTHOQUINONE 2-HYDROXY-3-(3-METHYLBUT-2-ENYL)-1,4-NAPHTHOQUINONE 1,4-Naphthoquinone, 2-hydroxy-3-(3-methyl-2-butenyl)- 2-Hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthalenedione 2-hydroxy-3-(3-methyl-2-butenyl)-4-naphthoquinone 2-Hydroxy-3-(3-methyl-2-butenyl)naphthoquinone Bethabarra Wood bethabarrawood C.I. Natural Yellow 16 c.i.naturalyellow16 Greenharten Greenhartin Ipe-Tobacco Wood ipe-tobaccowood Lapachic acid lapachicacid Lapachol Wood Lapachol,CI 75490 lapacholwood NSC 11905 nsc-11905 Surinam Greenheart Wood surinamgreenheartwood Groenhartin Lapachoic acid 2-hydroxy-3-(3-Methylbut-2-en-1-yl)naphthalene-1,4-dione 2-hydroxy-3-(3-methylbut-2-enyl)naphthalene-1,4-dione Lapachol 98% Lapachol, >=99% Taigu Wood Taiguic acid taiguicacid taiguwood Tecomin Zlut prirodni 16 2-Hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone, Natural Yellow16 Taiquic acid 4-hydroxy-3-(3-methylbut-2-enyl)-1,2-naphthoquinone 4-hydroxy-3-(3-methylbut-2-enyl)naphthalene-1,2-dione LAPACHOL ISO 9001:2015 REACH 1,4-Naphthalenedione,2-hydroxy-3-(3-methyl-2-buten-1-yl)- 84-79-7 Ketones Organic Building Blocks C15 to C38 Carbonyl Compounds Building Blocks Building Blocks C15 to C38 Carbonyl Compounds Chemical Synthesis Ketones Organic Building Blocks Anthraquinones, Hydroquinones and Quinones