Archive for August, 2008

Indanthrene blue RS

Sunday, August 31st, 2008


Indanthrene blue RS

Indanthrene blue RS, C.I. vat blue 4, carbon paper blue, blue O, carbanthrene blue 2R, fenan blue RSN, graphtol blue RL, medium blue, monolite fast blue 3R, indanthrene, indanthrone, pigment blue 60, or C.I. 69800, is a synthetic anthraquinone dye. It has the appearance of blue needles with metallic lustre and melting point of 470-500 °C.

When used as a food dye, it has E number E130.

Indanthrene Blue RS was patented in 1901 by Rene Bohn as the first anthraquinone vat dye, one of the dyes with very good fastness to light and washing. It is used to dye unmordanted cotton and as a pigment in quality paints and enamels.

Its CAS number is and its SMILES structure is O=C(C(C(NC (C=CC(C(C7=C6 C=CC=C7)=O)=C5 C6=O)=C5N4)=C4 C=C3)=C3C2=O) C1=C2C=CC=C1.

Retrieved from “http://en.wikipedia.org/wiki/Indanthrene_blue_RS
Categories: Anthraquinone dyes | Food colorings | Pigments

1,2-Bis(diphenylphosphino)ethane

Sunday, August 31st, 2008

1,2-Bis(diphenylphosphino)ethane

IUPAC name
1,2-Bis(diphenylphosphino)ethane

CAS number

Properties

Molecular formula
(C6H5)2PCH2CH2P(C6H5)2

Molar mass
397.95 g/mol

Melting point

140-142 °C

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

1,2-Bis(diphenylphosphino)ethane (dppe) is a commonly used bidentate ligand in coordination chemistry. Dppe is almost invariably chelated, although there are examples of unidentate (e.g., W(CO)5(dppe)) and of bridging behavior.

Contents

//

Preparation

The preparation of dppe is conducted via the alkylation of NaPPh2 which is typically prepared from triphenylphosphine (P(C6H5)3) as follows:

1. P(C6H5)3 + 2 Na → NaP(C6H5)2 + NaC6H5

NaP(C6H5)2, which is readily air-oxidized, is treated with 1,2-dichloroethane (ClCH2CH2Cl) to give dppe:

2. NaP(C6H5)2 + ClCH2CH2Cl → (C6H5)2PCH2CH2P(C6H5)2 + 2 NaCl

Reactions of dppe

Reduction

The reduction of dppe by lithium to give PhHP(CH2)2PHPh has been reported.

1. Ph2P(CH2)2PPh2 + 4 Li → PhLiP(CH2)2PLiPh + 2 PhLi

Hydrolysis by water gives:

2. PhLiP(CH2)2PLiPh + 2 PhLi + 4H2O → PhHP(CH2)2PHPh + 4 LiOH + 2C6H6

Oxidation

Treatment of dppe with conventional oxidants such as hydrogen peroxide (H2O2), aqueous bromine (Br2), etc., always produces dppeO in low yield (e.g., 13%) as a result of non-selective oxidation leading to mixtures of the starting material, the monoxide, and dioxide. Selective mono-oxidation of dppe can be achieved by reaction with PhCH2Br to give dppeO.

3. Ph2P(CH2)2PPh2 + PhCH2Br → Ph2P(CH2)2PPh2(CH2Ph)+Br-

This is followed by purification and alkaline catalyzed hydrolysis of the mono-phosphonium salt.

4. Ph2P(CH2)2PPh2(CH2Ph)+Br- + NaOH + H2O → Ph2P(CH2)2P(O)Ph2

Coordination complexes of dppe


Ball-and-stick model of

Coordination complexes of dppe, and diphosphine ligands in general, are almost entirely used as homogeneous catalysts for a wide range of reactions. Chiral diphosphines are especially important to the pharmaceutical industry

References

  1. ^ Cotton, F.A.; Wilkinson, G. Advanced Inorganic Chemistry: A Comprehensive Text, 4th ed.; Wiley-Interscience Publications: New York, NY, 1980; p.246. ISBN 0-471-02775-8
  2. ^ W. Hewertson and H. R. Watson (1962). “283. The preparation of di- and tri-tertiary phosphines”. J. Chem. Soc.: 1490–1494. doi:10.1039/JR9620001490. 
  3. ^ Girolami, G.; Rauchfuss, T.; Angelici, R. Synthesis and Technique in Inorganic Chemistry, 3rd ed.; University Science Books: Sausalito, CA, 1999; pp. 85-92. ISBN 0-935702-48-2
  4. ^ Dogan, J.; Schulte, J.B.; Swiegers, G.F.; Wild, S.B. (2000). “Mechanism of Phosphorus-Carbon Bond Cleavage by Lithium in Tertiary Phosphines. An Optimized Synthesis of 1, 2-Bis (phenylphosphino) ethane”. J. Org. Chem. 65 (4): 951-957. doi:10.1021/jo9907336′). 
  5. ^ a b Encyclopedia of Reagents for Organic Synthesis 2001 John Wiley & Sons, Ltd
  6. ^ Stibbs, W. Technology & Services Business Briefing: Future Drug Discovery 2003.
  7. ^ Imamoto, Tsuneo (2001). “New P-chirogenic diphosphines and their use in catalytic asymmetric reactions”. Pure and Applied Chemistry 73: 373. doi:10.1351/pac200173020373. 

Retrieved from “http://en.wikipedia.org/wiki/1,2-Bis(diphenylphosphino)ethane
Categories: Aromatic compounds | Chelating agents | Tertiary phosphines

Neodymium aluminium borate

Sunday, August 31st, 2008

This article or section is in need of attention from an expert on the subject.

WikiProject Chemistry or the Chemistry Portal may be able to help recruit one.

If a more appropriate WikiProject or portal exists, please adjust this template accordingly.

Neodymium aluminium borate

IUPAC name
Neodymium aluminium borate

Other names
NAB

Properties

Molecular formula
NdAl3(BO3)4

Molar mass
460.42 g/mol

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Neodymium aluminium borate is a chemical compound with the chemical formula NdAl3(BO3)4.

It is used in optics.

References

  • Luo Z. D., Huang Y. D., Montes M., Jaque D. (2004). “Improving the performance of a neodymium aluminium borate microchip laser crystal by resonant pumping”. Applied Physics Letters 85 (5): 715. doi:10.1063/1.1775281. 
  • Bilak V. I., Kuratev I. I., Leonyuk N. I., Pashkov V. A., Pashkova A. V., Timchenko T. I., Shestakov A. V. (1978). “Luminescence and lasing characteristics of neodymium-aluminum borate crystals”. Soviet Physics Doklady 23: 299. 


 This inorganic compound-related article is a stub. You can help Wikipedia by expanding it.

Retrieved from “http://en.wikipedia.org/wiki/Neodymium_aluminium_borate
Categories: Inorganic compounds | Neodymium compounds | Borates | Aluminium compounds | Inorganic compound stubsHidden categories: Chemistry articles needing expert attention | Articles needing expert attention | Pages needing expert attention | Chemical pages needing a structure drawing

Resiniferatoxin

Sunday, August 31st, 2008

Resiniferatoxin

Identifiers

CAS number
57444-62-9

Properties

Molecular formula
C37H40O9

Molar mass
628.71 g/mol

Density
1.35 ± 0.1 g/cm³

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Resiniferatoxin (RTX) is a naturally occurring, ultrapotent capsaicin analog that activates the vanilloid receptor in a subpopulation of primary afferent sensory neurons involved in nociception (the transmission of physiological pain).

Research is being conducted at the National Institutes of Health to design a novel class of analgesics from the latex of resin spurge (Euphorbia resinifera), a cactus-like plant commonly found in Morocco that contains high concentrations of RTX.

A total synthesis of (+)-resiniferatoxin was completed by the Wender group at Stanford University in 1997.

See also

  • Capsaicin
  • Transient receptor potential

References

The references used in this article may be clearer with a different or consistent style of citation, footnoting, or external linking. (September 2007)

  1. ^ Szallasi A, Blumberg PM (1989) Resiniferatoxin, a phorbol-related diterpene, acts as an ultrapotent analog of capsaicin, the irritant constituent in red pepper. Neuroscience 30(2): 515-20.
  2. ^ Szallasi A, Blumberg PM (1990) Resiniferatoxin and its analogs provide novel insights into the pharmacology of the vanilloid (capsaicin) receptor. Life Sci. 47(16): 1399-408.
  3. ^ Szallasi A, Blumberg PM (1992) Vanilloid receptor loss in rat sensory ganglia associated with long term desensitization to resiniferatoxin. Neurosci Lett. 140(1): 51-4.
  4. ^ Olah Z et al. (2001) Ligand-induced dynamic membrane changes and cell deletion conferred by vanilloid receptor 1. J Biol Chem. 276(14): 11021-30.
  5. ^ Neubert JK et al. (2003) Peripherally induced resiniferatoxin analgesia. Pain 104(1-2): 219-28.
  6. ^ Karai L et al. (2004) Deletion of vanilloid receptor 1-expressing primary afferent neurons for pain control. J Clin Invest. 113(9): 1344-52.
  7. ^ Brown DC et al. (2005) Physiologic and antinociceptive effects of intrathecal resiniferatoxin in a canine bone cancer model. Anesthesiology 103(5): 1052-9.
  8. ^ J. Am. Chem. Soc. 1997, 119, 12976-12977.
  9. ^ http://www.scripps.edu/chem/baran/images/grpmtgpdf/Seiple_Mar_07.pdf
  • Christopher S. J. Walpole, et al (1996). “Similarities and Differences in the Structure-Activity Relationships of Capsaicin and Resiniferatoxin Analogues”. J. Med. Chem. 39: 2939–2952. doi:10.1021/jm960139d. 

External links

  • Fiery pepper may hold key to easing pain
  • PubChem 442082
  • MeSH resiniferatoxin


 This cell biology article is a stub. You can help Wikipedia by expanding it.

Retrieved from “http://en.wikipedia.org/wiki/Resiniferatoxin
Categories: Neurotoxins | Plant toxins | Analgesics | Cell biology stubsHidden category: Wikipedia references cleanup

Eyespot apparatus

Sunday, August 31st, 2008

For other uses, see Eyespot.


Schematic representation of a Euglena cell with red eyespot (9)


Schematic representation of a Chlamydomonas cell with chloroplast eyespot (4)

The eyespot apparatus (or stigma) is a photoreceptive organelle found in the flagellate (motile) cells of green algae and other unicellular photosynthetic organisms such as euglenids. It allows the cells to sense light direction and intensity and respond to it by swimming either towards the light (phototaxis) or away from the light (”photoshock” or photophobic response). This helps the cells in finding an environment with optimal light conditions for photosynthesis. Eyespots are the simplest and most common “eyes” found in nature, composed of photoreceptors and a signal transduction system generating a phototactic response.

Contents

//

Microscopic structure

Under the light microscope, eyespots appear as dark, often reddish, spots or stigmata. They get their color from the chromoproteins they contain, such as chlamyopsin, volvoxopsin or other photopigments.

The eyespot apparatus of Euglena comprises the paraflagellar body connecting the eyespot to the flagellum. In electron microscopy, the eyespot apparatus appears as a highly ordered lamellar structure formed by membranous rods in a helical arrangement.

In Chlamydomonas, the eyespot is part of the chloroplast and takes on the appearance of a membranous sandwich structure. It is assembled from chloroplast membranes (outer, inner, and thylakoid membranes) and carotenoid-filled granules overlaid by plasma membrane. It disassembles during cell division and reforms in the daughter cells in an asymmetric fashion in relation to the cytoskeleton.

Eyespot proteins

The predominant eyespot proteins are the photoreceptor proteins that sense light. The photoreceptors found in unicellular organisms fall into two main groups: flavoproteins and retinylidene proteins (rhodopsins). Flavoproteins are characterized by containing flavin molecules as chromophores, whereas retinylidene proteins contain retinal. The photoreceptor protein in Euglena is likely a flavoprotein.

Besides photoreceptor proteins, eyespots contain a large number of structural, metabolic and signaling proteins. The eyespot proteome of Chlamydomonas cells consists of roughly 200 different proteins.

Photoreception and signal transduction

The Euglena photoreceptor was identified as a blue-light-activated adenylyl cyclase. Excitation of this receptor protein results in the formation of cyclic adenosine monophosphate (cAMP) as a second messenger. Chemical signal transduction ultimately triggers changes in flagellar beat patterns and cell movement.

The archaeal-type rhodopsins of Chlamydomonas contain an all-trans retinylidene chromatophore which undergoes photoisomerization to a 13-cis isomer. This activates a photoreceptor channel, leading to a change in membrane potential and cellular calcium ion concentration.

References

  1. ^ a b Hegemann P (1997). “Vision in microalgae”. Planta 203 (3): 265–74. doi:10.1007/s004250050191. PMID 9431675. 
  2. ^ a b Wolken J (1977). “Euglena: the photoreceptor system for phototaxis”. J Protozool 24 (4): 518–22. PMID 413913. 
  3. ^ Dieckmann C (2003). “Eyespot placement and assembly in the green alga Chlamydomonas”. Bioessays 25 (4): 410–6. doi:10.1002/bies.10259. PMID 12655648. 
  4. ^ a b Suzuki T, Yamasaki K, Fujita S, Oda K, Iseki M, Yoshida K, Watanabe M, Daiyasu H, Toh H, Asamizu E, Tabata S, Miura K, Fukuzawa H, Nakamura S, Takahashi T (2003). “Archaeal-type rhodopsins in Chlamydomonas: model structure and intracellular localization”. Biochem Biophys Res Commun 301 (3): 711–7. doi:10.1016/S0006-291X(02)03079-6. PMID 12565839. 
  5. ^ Schmidt M, Gessner G, Luff M, Heiland I, Wagner V, Kaminski M, Geimer S, Eitzinger N, Reissenweber T, Voytsekh O, Fiedler M, Mittag M, Kreimer G (2006). “Proteomic analysis of the eyespot of Chlamydomonas reinhardtii provides novel insights into its components and tactic movements”. Plant Cell 18 (8): 1908–30. doi:10.1105/tpc.106.041749. PMID 16798888. 
  6. ^ Iseki M, Matsunaga S, Murakami A, Ohno K, Shiga K, Yoshida K, Sugai M, Takahashi T, Hori T, Watanabe M (2002). “A blue-light-activated adenylyl cyclase mediates photoavoidance in Euglena gracilis”. Nature 415 (6875): 1047–51. doi:10.1038/4151047a. PMID 11875575. 

Retrieved from “http://en.wikipedia.org/wiki/Eyespot_apparatus
Categories: Sensory receptors | Signal transduction | Pigments | Integral membrane proteins | Organelles | Molecular biology | Microbiology

Copper gluconate

Sunday, August 31st, 2008

Copper gluconate

Systematic (IUPAC) name

Copper(II) gluconate

Identifiers

CAS number
527-09-3

ATC code
V03AB20

PubChem
 ?

Chemical data

Formula
C12H22CuO14

Mol. mass
453.8

Pharmacokinetic data

Bioavailability
 ?

Metabolism
 ?

Half life
 ?

Excretion
 ?

Therapeutic considerations

Pregnancy cat.

?

Legal status

Routes
Oral

Copper gluconate is the copper salt of D-gluconic acid.

Uses

  • Dietary supplement — metabolizable copper to treat copper deficiency.
  • Used to treat acne vulgaris, common cold, hypertension, premature labor, Leishmaniasis, visceral postoperative complications.
  • Ingredient of Retsyn.

Side effects

Toxic in large amounts. Side effects from too much copper gluconate may include breathing problems, chest pain, stomach upset, and rash or hives.

External links

  • National Pollutant Inventory - Copper and compounds fact sheet


 This pharmacology-related article is a stub. You can help Wikipedia by expanding it.

v • d • e

Dietary supplements

Types

Amino acids • Bodybuilding supplement • Energy drink • Energy bar • Fatty acids • Herbal Supplements • Minerals • Prebiotics • Probiotics (Lactobacillus, Bifidobacterium)• Vitamins • Whole food supplements

Vitamins and minerals

Retinol (Vitamin A) • B vitamins: Thiamine (B1)Riboflavin (B2)Niacin (B3)Pantothenic acid (B5)Pyridoxine (B6)Biotin (B7)Folic acid (B9)Cyanocobalamin (B12) • Ascorbic acid (Vitamin C) • Ergocalciferol and Cholecalciferol (Vitamin D) • Tocopherol (Vitamin E) • Naphthoquinone (Vitamin K) • Calcium • Choline • Chlorine • Chromium • Cobalt • Copper • Fluorine • Iodine • Iron • Magnesium • Manganese • Molybdenum • Phosphorus • Potassium • Selenium • Sodium • Sulfur • Zinc

Other common ingredients

Carnitine • Chondroitin sulfate • Cod liver oil • Copper gluconate • Creatine/Creatine supplements • Dietary fiber • Elemental calcium • Ephedra • Fish oil • Folic acid • Ginseng • Glucosamine • Glutamine • Iron supplements • Japanese Honeysuckle • Krill oil • Lingzhi • Linseed oil • Melatonin • Red yeast rice • Royal jelly • Saw palmetto • Spirulina • Taurine • Wheatgrass • Wolfberry • Yohimbine • Zinc gluconate

Related articles

Codex Alimentarius • Enzyte • Metabolife • Hadacol • Nutraceutical • Multivitamin • Nutrition

Retrieved from “http://en.wikipedia.org/wiki/Copper_gluconate
Categories: Copper compounds | Dietary supplements | Coordination compounds | Pharmacology stubsHidden category: Drug pages needing formula fontification

Aconitum anthora

Saturday, August 30th, 2008

Yellow Monkshood

Scientific classification

Kingdom:
Plantae

Division:
Magnoliophyta

Class:
Magnoliopsida

Order:
Ranunculales

Family:
Ranunculaceae

Genus:
Aconitum

Species:
A. anthora

Binomial name

Aconitum anthora
L.

Aconitum anthora, variously known as Anthora, Yellow Monkshood, or Healing Wolfsbane, is a yellow flowering plant species of the genus Aconitum in the family Ranunculaceae.

It’s native range is widespread, but mainly in European mountains, such as the Alps and the Carpathians, and the northern parts of Asia. Like all Aconitum species, it has great variability, due to isolation and hybridisation. Because of this polymorphism, Aconitum anthora is included in the Aconitum vulparia-group. It flowers from July to September.

Historically, its root, which is tuberous, was reputed to be a good antidote, and counter-poision to poisons from ‘thora’ or Aconitum pardalianches, whence its naming anthora or “against thora”. This plant is extremely toxic to livestock and humans. Even small doses can be deadly.

The root contains a large amount of volatile salt and essential oil, while the foliage and stems contain diterpenoid alkaloids. It has been used externally against rheumatism and deep pain, but it can irritate the skin. Internally, it has been used for weak pulse, vegetable poisons (shoot), feverish colds, pneumonia, croup, heart conditions, and cardiac arrest.

It is considered a threatened plant in the Czech Republic.

Synonyms

  • Aconitum pseudanthora Blocki ex Pacz.
  • Aconitum eulophum Rchb.
  • Aconitum jacquinii Rchb.
  • Aconitum nemorosum M.Bieb.

References

  1. ^ Greater Thora (Panthers-Bane) Herb, Greater Thora (Panthers-Bane) Use, Greater Thora (Panthers-Bane) Supplement
  • “Aconitum anthora”. Herbal Harmony’s Directory. Retrieved on 2006-01-16.
  • This article incorporates content from the 1728 Cyclopaedia, a publication in the public domain.

External links

  • Aconitum anthora in Topwalks


 This Ranunculales article is a stub. Please help Wikipedia by expanding it.

Retrieved from “http://en.wikipedia.org/wiki/Aconitum_anthora
Categories: Poisonous plants | Neurotoxins | Ranunculaceae | Ranunculales stubsHidden categories: All articles with unsourced statements | Articles with unsourced statements since February 2007

Potassium ferrioxalate

Saturday, August 30th, 2008

Potassium ferrioxalate

IUPAC name
Potassium ferric(III) oxalate

Other names
Potassium ferrioxalate

Potassium trioxalatoferrate (III)

Identifiers

CAS number

Properties

Molecular formula
K3

K3.3H2O

Molar mass
437.20 g/mol

Appearance
emerald green hydrated crystals

Density
2.13 g/cm3, solid

Melting point

230 °C (493.15 K)

Solubility in water
 ?M (20 °C)

Structure

Coordination
geometry

octahedral

Dipole moment
0 D

Hazards

Main hazards
Corrosive. Eye, respiratory and skin irritant.

R-phrases
R20 R21 R22 R34 R36 R37 R38

Related compounds

Related compounds
Fe(C2O4)2

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Potassium ferrioxalate, is a chemical compound with the formula K33-, which appears fluorescent green in colour. Potassium ferrioxalate is often used in chemical actinometry.

Contents

//

Preparation

The complex can be synthesised from the reaction between iron(III) sulfate, barium oxalate and potassium oxalate:

Fe2(SO4)3 + 3 Ba(C2O4) + 3 K2(C2O4) → 2 K3 + 3 BaSO4

The reactants are dissolved in water and heated for around 1.5 hours. BaSO4 precipitates out leaving behind the newly formed complex in solution. The complex can then be obtained by filtering off the BaSO4 and cooling the solution so that it crystallises out.

Isomerism

The ferrioxalate complex demonstrates optical activity since there are two non-superimposable stereoisomers of the complex. In accordance with the IUPAC convention, the isomer with the left handed screw axis is assigned the Greek symbol Λ (lambda). Its mirror image with the right handed screw axis is given the Greek symbol Δ (delta).

Photoreduction

In solution the ferrioxalate complex is decomposed by light. The complex reacts with a photon of light to form Fe(C2O4)22- and CO2. Iron is reduced (gains an electron) from the +3 oxidation state to +2. This process is called photoreduction:

2 2- + C2O42- + 2 CO2

If a solution of green K3 is left in sunlight for a few hours it turns orange due to the formation of Fe(C2O4)22- ions.

References

  1. ^ Greenwood, N. N.; Earnshaw, A. (1997). Chemistry of the Elements, 2nd Edition, Oxford:Butterworth-Heinemann. ISBN 0-7506-3365-4

Retrieved from “http://en.wikipedia.org/wiki/Potassium_ferrioxalate
Categories: Coordination compounds | Iron compounds | Potassium compounds

Methane (data page)

Saturday, August 30th, 2008

This page provides supplementary chemical data on methane.

Contents

//

Material Safety Data Sheet

The handling of this chemical may incur notable safety precautions. It is highly recommend that you seek the Material Safety Datasheet (MSDS) for this chemical from a reliable source such as SIRI, and follow its directions.

Structure and properties

Structure and properties

Index of refraction, nD
 ?

Dielectric constant, εr
 ? ε0 at ? °C

Bond strength
 ?

Bond length
 ?

Bond angle
109.5

Magnetic susceptibility
 ?

Thermodynamic properties

Phase behavior

Triple point
90.67 K (−182.48 °C), 0.117 bar

Critical point
190.6 K (−82.6 °C), 46 bar

Std enthalpy change
of fusion
, ΔfusHo
1.1 kJ/mol

Std entropy change
of fusion
, ΔfusSo
 ? J/(mol·K)

Std enthalpy change
of vaporization
, ΔvapHo
8.17 kJ/mol

Std entropy change
of vaporization
, ΔvapSo
 ? J/(mol·K)

Solid properties

Std enthalpy change
of formation
, ΔfHosolid
 ? kJ/mol

Standard molar entropy,
Sosolid
 ? J/(mol K)

Heat capacity, cp
 ? J/(mol K)

Liquid properties

Std enthalpy change
of formation
, ΔfHoliquid
 ? kJ/mol

Standard molar entropy,
Soliquid
 ? J/(mol K)

Heat capacity, cp
 ? J/(mol K)

Gas properties

Std enthalpy change
of formation
, ΔfHogas
−74.87 kJ/mol

Standard molar entropy,
Sogas
188 J/(mol K)

Enthalpy of combustion ΔcHo
–882.0 kJ/mol

Heat capacity, cp
35.69 J/(mol K)

van der Waals’ constants
a = 228.29 L2 kPa/mol2
b = 0.04278 liter per mole

Vapor pressure of liquid

P in mm Hg
1
10
40
100
400
760
1520
3800
7600
15200
30400
45600

T in °C
–205.9(s)
–195.5(s)
–187.7(s)
–181.4
–168.8
–161.5
–152.3
–138.3
–124.8
–108.5
–86.3
  —

Table data obtained from CRC Handbook of Chemistry and Physics 44th ed. Annotation “(s)” indicates equilibrium temperature of vapor over solid. Otherwise temperature is equilibrium of vapor over liquid.


log10 of methane vapor pressure vs. temperature. Uses formula: given in Lange’s Handbook of Chemistry, 10th ed. Note that formula loses accuracy near Tcrit = −82.6°C

Spectral data


Methane infrared spectrum

UV-Vis

λmax
 ? nm

Extinction coefficient, ε
 ?

IR

Major absorption bands
~3300 cm−1

~1300

NMR

Proton NMR
 

Carbon-13 NMR
 

Other NMR data
 

MS

Masses of
main fragments
 

References

  1. ^ Lange’s Handbook of Chemistry, 10th ed, pp 1522-1524

Except where noted otherwise, data relate to standard ambient temperature and pressure.

Disclaimer applies.

Retrieved from “http://en.wikipedia.org/wiki/Methane_(data_page)
Categories: Chemical data pages | Methane

Indian yellow

Saturday, August 30th, 2008

Indian Yellow

— Color coordinates —

Hex triplet
#e3a857

B
(r, g, b)
(227, 168, 87)

HSV
(h, s, v)
(35°, 62%, 89%)

Source
The Mother of All HTML Colo(u)r Charts

B: Normalized to (byte)

Euxanthic acid

Identifiers

CAS number

SMILES

 

O
(OC2=CC(C(C(C(O)=CC=C3)=C3O4)=O)
=C4C=C2)O1C(O)=O

Properties

Molecular formula
C19H16O10

Molar mass
404.32 g/mol

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox references

Indian yellow, also called euxanthin or euxanthine, is a transparent yellow pigment used in oil painting. Chemically it is a magnesium euxanthate, the magnesium salt of euxanthic acid. It is a clear, deep and luminescent yellow pigment. Its color is deeper than gamboge but less pure than cadmium yellow.

Indian yellow is a glycoside, a conjugate of the aglycone euxanthone with glucuronic acid, making the chromophore euxanthone much more water-soluble.

Indian yellow was used by artist painters in both oil paints and watercolors. Due to its fluorescence, it is especially vivid and bright in sunlight. It was likely first used by Dutch artists, and before the end of the 18th century it was commonly used by artists across Europe. Its origin was unknown until an investigation in the year 1883; however, in 2004, Victoria Finlay called this into question.

Indian yellow pigment is claimed to have been originally manufactured in rural India from the urine of cattle fed only on mango leaves and water. The urine was collected and dried, producing foul-smelling hard dirty yellow balls of the raw pigment., as the cows were extremely undernourished, partly because the leaves contain the toxin urushiol which is also found in poison ivy.

In her 2004 book Color: A Natural History of the Palette, Victoria Finlay examined whether Indian yellow was really made from cow urine. The only printed source mentioning this practice is a single letter written by a Mr. T.N. Mukharji of Calcutta, who claimed to have seen the color being made. Aside from this letter, there appear to be no written sources from the time period mentioning the production of Indian yellow. Finlay searched for legal records concerning the supposed banning of Indian yellow production in both the India Library in London and the National Library in Calcutta, and found none. She visited the town in India mentioned in Mukharji’s letter as the only source of the color, but found no trace of evidence that the color had ever been produced there. None of the locals she spoke with had ever heard of the practice. It is possible that Indian yellow came from another source, and that the cow urine story was fabricated by Mukharji, but came to be accepted by later authors. As such, the viability of producing Indian yellow from the urine of mango-leaf-fed cows is unknown.

The replacement for the original pigment (which was not entirely lightfast), synthetic Indian yellow hue, is a mixture of nickel azo, hansa yellow and quinacridone burnt orange. It is also known as azo yellow light and deep, or nickel azo yellow.

References

  1. ^ History of Indian Yellow
  2. ^ Baer, N. S. et al. ‘Indian Yellow’, in Feller, Robert L (ed.) Artists’ Pigments, Oxford 1986 ISBN 089468086
  3. ^ Color: A Natural History of the Palette, Random House, 2004

Retrieved from “http://en.wikipedia.org/wiki/Indian_yellow
Categories: Pigments | Natural dyes | Fluorescent dyes | Fluorone dyes