<\/p>\n
Structural formula<\/p>\n
2,4,5-Trichlorophenol,<\/p>\n
2,4,5-Trichloro-1-hydroxy-benzene,<\/p>\n
Aromatic halogen derivatives<\/p>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n
CAS number:<\/b>95-95-4<\/p>\n
MDL number:<\/b>MFCD00002170<\/p>\n
EINECS number:<\/b>202-467-8<\/p>\n
RTECS number:<\/b>SN1400000<\/p>\n
BRN number:<\/b>607569<\/p>\n
PubChem number:<\/b>24889473<\/p>\nPhysical property data<\/h2>\n
1. Properties: colorless needle-like crystals or gray flakes with a strong phenol smell. <\/p>\n
2. Density (g\/mL, 25\u2103): 1.678<\/p>\n
3. Relative vapor density (g\/mL, air=1): 7.4<\/p>\n
4. Melting point (\u00baC): 68<\/p>\n
5. Boiling point (\u00baC, normal pressure): 246<\/p>\n
6. Boiling point (\u00baC, 18mmHg): Undetermined<\/p>\n
7. Refractive index: Undetermined<\/p>\n
8. Flash point (\u00baC): Undetermined<\/p>\n
9. Specific rotation (\u00ba): Undetermined<\/p>\n
10. Autoignition point or ignition temperature (\u00baC): Undetermined<\/p>\n
11. Vapor pressure (mmHg, \u00baC): Undetermined<\/p>\n
12. Saturated vapor pressure (kPa, 72\u00baC) : 0.133<\/p>\n
13. Heat of combustion (KJ\/mol): Undetermined<\/p>\n
14. Critical temperature (\u00baC): Undetermined<\/p>\n
15. Critical pressure ( KPa): Undetermined<\/p>\n
16. Log value of oil-water (octanol\/water) partition coefficient: Undetermined<\/p>\n
17. Explosion upper limit (%, V\/V): Undetermined <\/p>\n
18. Lower explosion limit (%, V\/V): Undetermined<\/p>\n
19. Solubility: Insoluble in water, soluble in carbon tetrachloride, alcohol, benzene, and ether. <\/p>\n<\/p>\n
1. Acute toxicity: Rat oral LD50: 820mg\/kg; Rat intraperitoneal LD50: 355mg\/kg; Rat subcutaneous LD50: 2260mg\/kg;<\/p>\n
Mouse oral LD50 : 600mg\/kg; mouse intravenous LD50: 56mg\/kg; guinea pig oral LD50: 1mg\/kg; mammal LD50: 150mg\/kg; <\/p>\n
2. Other multiple dose toxicity: rat oral TDLo: 98mg\/kg\/98D-C;<\/p>\n
3. Chronic toxicity\/carcinogenicity<\/p>\n
Mouse skin contact TDLo: 6700mg\/kg\/16W-I;<\/p>\n
4. Reproductive toxicity<\/p>\n
Oral TDLo in mice: 4mg\/kg (8-12 days after conception in female mice);<\/p>\n
5. Mutagenicity<\/p>\n
Microbiology Salmonella typhimurium mutation: 10\u03bcg\/plate;<\/p>\n
Cytogenetic analysis of hamster ovary: 150mg\/L;<\/p>\n<\/p>\n
\n This substance is harmful to the environment and it is recommended not to let it enter the environment.\n <\/p>\n
1. Molar refractive index: 42.81<\/p>\n
2. Molar volume (cm3<\/sup>\/mol): 123.7<\/p>\n3. Isotonic specific volume (90.2K): 329.8<\/p>\n4. Surface tension (dyne\/cm): 50.5<\/p>\n5. Polarizability (10 -24cm3): 16.97<\/p>\n<\/p>\nCompute chemical data<\/h2>\n1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n2. Number of hydrogen bond donors: 1<\/p>\n3. Number of hydrogen bond acceptors: 1<\/p>\n4. Number of rotatable chemical bonds: 0<\/p>\n5. Number of tautomers: 3<\/p>\n6. Topological molecule polar surface area 20.2<\/p>\n7. Number of heavy atoms: 10<\/p>\n8. Surface charge: 0<\/p>\n9. Complexity: 120<\/p>\n10. Number of isotope atoms: 0<\/p>\n11. Determine the number of atomic stereocenters: 0<\/p>\n12. Uncertain number of atomic stereocenters: 0<\/p>\n13. Determine the number of chemical bond stereocenters: 0 <\/p>\n14. Number of uncertain chemical bond stereocenters: 0<\/p>\n15. Number of covalent bond units: 1<\/p>\n<\/p>\nProperties and stability<\/h2>\n1. Avoid contact with oxidants, acid anhydrides, and acid chlorides. <\/p>\n2. It is highly toxic and highly irritating if swallowed or inhaled. Can be poisoned by absorption through the skin. The oral dose for rats is LD50820mg\/kg, and the oral dose for guinea pigs is LD501000mg\/kg. \u3000<\/span><\/p>\n<\/p>\nStorage method<\/h2>\n1. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. The packaging is sealed. They should be stored separately from oxidants, acid anhydrides and acid chlorides, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills. <\/p>\n2. The wooden box outside the glass bottle is lined with padding or an iron drum. Store in a cool, ventilated warehouse; load and unload with care when handling to prevent damage to the container. <\/p>\n<\/p>\nSynthesis method<\/h2>\nPut 2,3,5,6-tetrachlorobenzene, solid alkali, and methanol into the autoclave, control the temperature at 135-152\u00b0C, and the pressure at 0.5-1.4MPa, and keep it for 14 hours. The reaction solution is cooled to 60\u00b0C, methanol is recovered by distillation, the residual liquid is released, cooled for crystallization, and filtered. Dissolve the crystals in water, heat to 70\u00b0C, add insurance powder, adjust pH = 9.2-9.6, add activated carbon, and decolorize at 95\u00b0C for half an hour. Filter, cool the filtrate to below 15\u00b0C, add hydrochloric acid to pH=2-3, filter out 2,4,5-trichlorophenol, and dry at 45\u00b0C to obtain the finished product. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as fungicide and gas chromatography comparison sample. <\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/1031<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9102-tertiary-amine-catalyst-triisocrylate-butyl-tin-arkema-pmc\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/157<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44701<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44834<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/stannous-octoate-CAS-301-10-0–T-9.pdf<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/jeffcat-zf-10\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/6\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/drier-butyl-tin-oxide-fascat-4101\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/134-2.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02A8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48598,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,1054,15243],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48599"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48598"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48599"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
3. Isotonic specific volume (90.2K): 329.8<\/p>\n
4. Surface tension (dyne\/cm): 50.5<\/p>\n
5. Polarizability (10 -24cm3): 16.97<\/p>\n<\/p>\n
1. Reference value for hydrophobic parameter calculation (XlogP): None<\/P><\/p>\n
2. Number of hydrogen bond donors: 1<\/p>\n
3. Number of hydrogen bond acceptors: 1<\/p>\n
4. Number of rotatable chemical bonds: 0<\/p>\n
5. Number of tautomers: 3<\/p>\n
6. Topological molecule polar surface area 20.2<\/p>\n
7. Number of heavy atoms: 10<\/p>\n
8. Surface charge: 0<\/p>\n
9. Complexity: 120<\/p>\n
10. Number of isotope atoms: 0<\/p>\n
11. Determine the number of atomic stereocenters: 0<\/p>\n
12. Uncertain number of atomic stereocenters: 0<\/p>\n
13. Determine the number of chemical bond stereocenters: 0 <\/p>\n
14. Number of uncertain chemical bond stereocenters: 0<\/p>\n
15. Number of covalent bond units: 1<\/p>\n<\/p>\n
1. Avoid contact with oxidants, acid anhydrides, and acid chlorides. <\/p>\n
2. It is highly toxic and highly irritating if swallowed or inhaled. Can be poisoned by absorption through the skin. The oral dose for rats is LD50820mg\/kg, and the oral dose for guinea pigs is LD501000mg\/kg. \u3000<\/span><\/p>\n<\/p>\nStorage method<\/h2>\n1. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. The packaging is sealed. They should be stored separately from oxidants, acid anhydrides and acid chlorides, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills. <\/p>\n2. The wooden box outside the glass bottle is lined with padding or an iron drum. Store in a cool, ventilated warehouse; load and unload with care when handling to prevent damage to the container. <\/p>\n<\/p>\nSynthesis method<\/h2>\nPut 2,3,5,6-tetrachlorobenzene, solid alkali, and methanol into the autoclave, control the temperature at 135-152\u00b0C, and the pressure at 0.5-1.4MPa, and keep it for 14 hours. The reaction solution is cooled to 60\u00b0C, methanol is recovered by distillation, the residual liquid is released, cooled for crystallization, and filtered. Dissolve the crystals in water, heat to 70\u00b0C, add insurance powder, adjust pH = 9.2-9.6, add activated carbon, and decolorize at 95\u00b0C for half an hour. Filter, cool the filtrate to below 15\u00b0C, add hydrochloric acid to pH=2-3, filter out 2,4,5-trichlorophenol, and dry at 45\u00b0C to obtain the finished product. <\/p>\n<\/p>\nPurpose<\/h2>\nUsed as fungicide and gas chromatography comparison sample. <\/p>\n<\/p>\n extended-reading:https:\/\/www.newtopchem.com\/archives\/1031<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9102-tertiary-amine-catalyst-triisocrylate-butyl-tin-arkema-pmc\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/157<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44701<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44834<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/stannous-octoate-CAS-301-10-0–T-9.pdf<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/jeffcat-zf-10\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/6\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/drier-butyl-tin-oxide-fascat-4101\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/134-2.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02A8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48598,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,1054,15243],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48599"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48598"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48599"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
1. Store in a cool, ventilated warehouse. Keep away from fire and heat sources. Protect from direct sunlight. The packaging is sealed. They should be stored separately from oxidants, acid anhydrides and acid chlorides, and avoid mixed storage. Equipped with the appropriate variety and quantity of fire equipment. Suitable materials should be available in the storage area to contain spills. <\/p>\n
2. The wooden box outside the glass bottle is lined with padding or an iron drum. Store in a cool, ventilated warehouse; load and unload with care when handling to prevent damage to the container. <\/p>\n<\/p>\n
Put 2,3,5,6-tetrachlorobenzene, solid alkali, and methanol into the autoclave, control the temperature at 135-152\u00b0C, and the pressure at 0.5-1.4MPa, and keep it for 14 hours. The reaction solution is cooled to 60\u00b0C, methanol is recovered by distillation, the residual liquid is released, cooled for crystallization, and filtered. Dissolve the crystals in water, heat to 70\u00b0C, add insurance powder, adjust pH = 9.2-9.6, add activated carbon, and decolorize at 95\u00b0C for half an hour. Filter, cool the filtrate to below 15\u00b0C, add hydrochloric acid to pH=2-3, filter out 2,4,5-trichlorophenol, and dry at 45\u00b0C to obtain the finished product. <\/p>\n<\/p>\n
Used as fungicide and gas chromatography comparison sample. <\/p>\n<\/p>\n
extended-reading:https:\/\/www.newtopchem.com\/archives\/1031<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/fascat9102-tertiary-amine-catalyst-triisocrylate-butyl-tin-arkema-pmc\/<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/category\/products\/page\/157<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44701<\/a><\/br>extended-reading:https:\/\/www.newtopchem.com\/archives\/44834<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/stannous-octoate-CAS-301-10-0–T-9.pdf<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/jeffcat-zf-10\/<\/a><\/br>extended-reading:https:\/\/www.morpholine.org\/category\/morpholine\/page\/6\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/drier-butyl-tin-oxide-fascat-4101\/<\/a><\/br>extended-reading:https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/134-2.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02A8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48598,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,1054,15243],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48599"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48598"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48599"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
Structural formula Business number 02A8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48598,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,1054,15243],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48599"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48598"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48599"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}
![\"2,4,5-Trichlorophenol](\"http:\/\/www.newtopchem.com\/wp-content\/uploads\/2024\/05\/0e57e01ba19e4ba0b9b8ea8ba218e79a.gif\")
<\/p>\n<\/p>\n![https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/134-2.jpg<\/a><\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"excerpt":{"rendered":"Structural formula Business number 02A8 Molecular formu…<\/p>\n","protected":false,"gt_translate_keys":[{"key":"rendered","format":"html"}]},"author":1,"featured_media":48598,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[6],"tags":[24,1054,15243],"gt_translate_keys":[{"key":"link","format":"url"}],"_links":{"self":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599"}],"collection":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/comments?post=48599"}],"version-history":[{"count":0,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/posts\/48599\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media\/48598"}],"wp:attachment":[{"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/media?parent=48599"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/categories?post=48599"},{"taxonomy":"post_tag","embeddable":true,"href":"http:\/\/www.newtopchem.com\/wp-json\/wp\/v2\/tags?post=48599"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}](\"https:\/\/www.bdmaee.net\/wp-content\/uploads\/2022\/08\/134-2.jpg\"){kind=link}