#1 kg camphor price

[camphor2]

use of camphor

Use of camphor as an ingredient in many traditional remedies for cold, flu, and cough.

Use of camphor in the production of topical analgesic creams and ointments for pain relief.

Use of camphor is an effective natural insecticide that can be used to keep insects away from stored clothing and bedding.

Use of camphor is an important ingredient in many cosmetic products such as creams, lotions, and hair tonics.

Use of camphor can be added to hot water or humidifiers to provide relief from nasal and chest congestion.

Use of camphor in aromatherapy to promote relaxation and reduce stress.

Use of camphor as an ingredient in some mouthwashes due to its antibacterial properties.

Use of camphor as a natural cleaning agent for removing stubborn stains and odors.

Use of camphor is an important ingredient in some traditional balms and salves for wound healing and skin irritations.

Use of camphor in the production of some types of incense sticks for spiritual and religious purposes.

Use of camphor to treat fungal infections such as athlete's foot and ringworm.

Use of camphor in some types of pain-relieving patches for targeted pain relief.

Use of camphor as an important ingredient in the production of some types of explosives and fireworks.

Use of camphor as a natural insect repellent for pets and livestock.

Use of camphor is a versatile substance with many uses in traditional medicine, natural health, and industry.

[chemwhat]

Benzyl alcohol CAS#: 100-51-6

IdentificationPhysical DataSpectraRoute of Synthesis(ROS)Safety and HazardsOther Data

Identification

Product NameBenzyl alcoholIUPAC NamephenylmethanolMolecular Structure

CAS Registry Number 100-51-6MDL NumberMFCD00004599Beilstein/REAXYS Number878307EC Number202-859-9eCl@ss39023110Synonymsbenzyl alcohol, benzylic alcohol, BenzylalcoholMolecular FormulaC6H5CH2OHMolecular Weight108.14InChIInChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2InChI KeyWVDDGKGOMKODPV-UHFFFAOYSA-NCanonical SMILESC1=CC=C(C=C1)CO

Physical Data

AppearanceColorless transparent liquidWater Solubility33 g/l at 20 °CFlash Point96 °CSolubilitywater: soluble 33 g/L at 20 °C Melting Point, °C 203 - 205 204 - 205 -15 120 - 121 -15.4 -15.19 -15.3 - 0 -15.5 -15.3 Boiling Point, °C Pressure (Boiling Point), Torr 205.1 760 195 - 200 760 130 - 140 6.37564 92 - 94 10 47 - 48 2 94 - 97 12 80 - 85 5 78 - 792.5 50 - 60 0.5 Refractive Index Wavelength (Refractive Index), nm Temperature (Refractive Index), °C 1.5831 589 24.99 1.53421 589 34.99 1.5342 589 20 1.53847 589 25 1.4018 589 601.5396 58913.6 Density, g·cm-3 Measurement Temperature, °C 1.0421 24.99 1.02912 39.99 1.0225 49.991.04129 251.0401 - 1.0206 25 - 50 1.061 - 0.81 0 - 280 0.9918 - 1.0706 -15 - 95 1.214 -195 Description (Adsorption (MCS)) Solvent (Adsorption (MCS)) Temperature (Adsorption (MCS)), °C Partner (Adsorption (MCS)) Partner (Adsorption (MCS)) Adsorption isotherm heptane 24.85 cellulose Adsorption 45 - 55 quartz sand Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence 2-phenylethanol, 2-methyl-benzyl alcohol Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence C18-silica gel Desorption 26.9 - 626.9ZnO, clean (0001)-Zn surface Desorption hexane, diethyl ether Ratio of solvents: 1:1 graphitized carbon black

Spectra

Description (NMR Spectroscopy) Nucleus (NMR Spectroscopy) Solvents (NMR Spectroscopy) Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz Chemical shifts, Spectrum 1H chloroform-d1 25600 Chemical shifts, Spectrum 13C chloroform-d1 25151Chemical shifts 1H chloroform-d1 400Chemical shifts, Spectrum 1H chloroform-d125300Chemical shifts, Spectrum 13C chloroform-d1 2575Chemical shifts 1H chloroform-d1 -30300 Description (IR Spectroscopy) Solvent (IR Spectroscopy) Temperature (IR Spectroscopy), °C Comment (IR Spectroscopy) Spectrum various solvent(s) 80 pressure dependence Spectrum liquid carbon dioxide 80high pressure. Object(s) of Study: pressure dependence Bands neat (no solvent) 3333 - 1496 cm**(-1) Bands KBr 3300 - 1460 cm**(-1) Spectrum neat (no solvent) 4000 - 666 cm**(-1) Intensity of IR bandsIntensitaet von OH-Valenzschwingungsbanden bei 3636.3 cmE-1 und 3617.1 cmE-1 von nicht-assoziiertem Benzylalkohol (CCl4). Description (UV/VIS Spectroscopy) Solvent (UV/VIS Spectroscopy) Comment (UV/VIS Spectroscopy) Absorption Maxima (UV/VIS), nm Spectrum H2O 250 - 550 nm Spectrum cyclohexane 220 - 280 nm Spectrum methanol 220 - 290 nm Absorption maxima cyclohexane 254.7 Spectrum LiCl 230 - 280 nm, sowie unverduennt. Absorption maxima bei -180grad sowie bei +30grad. 260

Route of Synthesis (ROS)

Route of Synthesis (ROS) of-Benzyl-alcohol-CAS-100-51-6 Conditions Yield With C18H28Br2N4Ru; potassium tert-butylate; hydrogen In 1,4-dioxane at 105℃under 22502.3 Torrfor 8h; A n/a B 94% With C30H37ClN4ORu; hydrogen; sodium t-butanolate In toluene at 105℃under 4500.45 Torrfor 20hReagent/catalystGloveboxSealed tubeOverall yield = 98 percent; Experimental Procedure General procedure: To a mixture of catalyst (0.01 mmol), KOtBu (10 mol %), and 1,4-dioxane (4.0 mL) in a Parr high-pressure reactor was added the ester(1.0 mmol). The dark red solution was purged with H2 and stirred under 400 psi of H2 at 105 °C for 8 h. Products isolation were performed via column chromatography using silica gel as stationary phase and n-pentane/ethylacetate or n-pentane/isopropanol mixture as eluent. The products were confirmed by 1H NMR.A n/a B 92% With C42H38N4OPRu(1+)*Cl(1-); potassium tert-butylate; hydrogen In toluene at 100℃under 4104.28Torrfor 2h;

Safety and Hazards

Pictogram(s)

SignalWarningGHS Hazard StatementsH302: Harmful if swallowed H332: Harmful if inhaled Precautionary Statement CodesP261, P264, P270, P271, P301+P312, P304+P312, P304+P340, P312, P330, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goodUnder the room temperature and away from lightHS Code290621StorageUnder the room temperature and away from lightShelf Life2 yearsMarket Price USD 2.1/kg Use PatternBenzyl alcohol CAS#: 100-51-6 can be used in cosmetics/dental/toilet inhibiting bacteria a cosmetic or dermatological composition, in combination with 4-(3-ethoxy-4-hydroxyphenyl)butan-2-onenatural broad-spectrum preservative composition in combination with extract of citrus grandis, fruit, octanohydroxamic acid and polyol a sensate in a personal care composition, in combination with 2-isopropyl-N,2,3-trimethylbutyramide Benzyl alcohol CAS#: 100-51-6 is a sensate in a personal care composition, in combination with camphor sensate in afier shaves lotionspreservative in pharmaceutical compositions comprising kisspeptin or derivatives thereof, used in synchronization programs of production animal estrus Read the full article

[kakakarinhhh-blog]

Buy GECKO Kalimba 17 Keys Thumb Pinao Camphor wood with Instruction and Tune Hammer

MUSICAL INSTRUMENTScompatible model:

Solid Kalimba: Solid Camphorwood, Pure sound, Sufficient resonance, Low vibration loss with no noise. Camphorwood: Rich volatile oil and fat, Natural and beautiful wood grain, Strong special aroma. The camphorwood Kalimba makes us feel good and clear. Wonderful Sound: Without any music basis, you just move your thumb to get the wonderful music that delights your day long. Applicable: The best instrument for performance, recording, family, outdoor, school, party, and relaxation. Study Guidance: With our professionally produced kalimba learning booklet, it introduces the use and performance method of kalimba in detail.QR Code to watch our video to learn as we guide you and communicate with you.Material: WoodPackage weight: 0.605 kg Product size: 19.00 x 16.00 x 5.00 cm / 7.48 x 6.3 x 1.97 inches Package size: 21.00 x 20.00 x 6.00 cm / 8.27 x 7.87 x 2.36 inchesPackage Contents: 1 x Thumb Piano,1 x Song book,1 x Instructions,1 x Hammer,1 x tune sticker,1 x Flannelette bag,1 x Cleaning cloth

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[bf1-malaysia-blog]

Skincare, Cosmetic Product And Cosmetic Ingredients Malaysia

Skincare, Cosmetic Product And Cosmetic Ingredients Malaysia

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Best Formula Industries ( Incorporated Since : 27th Dec 2002 ) ( Company No : 002150621-D )

BF1 Office And Showroom Lot : 146, Jalan Segambut, 51200 Kuala Lumpur, Malaysia. Location Map : https://goo.gl/maps/bxC2BvaNVAy

BF1 Contact Tel : +603-6257 6048 Fax : +603-6241 0436 Operation Hours : Mon - Fri = 10am - 6.30pm Sat = 10am - 5pm

Mobile : ( SMS or Whatsapp ) English : +60192618000 Bahasa Malaysia : +60123590344 中文 * 普通话 : +60173872066 Email: bestform18@yahoo.com

Malaysia cosmetic ingredients manufacturer and supplier. We supply perfume raw materials, bee wax, palm wax, soy wax, camphor crystal, menthol crystal, denatured alcohol, soap making ingredients, perfume making ingredients, shampoo making ingredients and cream making ingredients.

Shipping Charges : All price are base on own collection at BF1 Office, if you purchase other items and add on little weight for cosmetic ingredients will be considered free. If you purchase in bulk, please email us to quote for shipping or you may order first and top up shipping fee later.

Cash On Delivery ( Minimum Order RM200.00 )- Within KL and Selangor ( Limited within 15KM from our office location )

Peninsular Malaysia by Courier : RM10.00 Per KG - More KG refer to courier fees or forwarding fees.

East Malaysia by Courier : RM20.00 Per KG - More KG refer to courier fees or forwarding fees ( Sea Shipping will take about 7 working days ).

Singapore by Courier : RM25.00 Per KG - More KG refer to courier fees or forwarding fees.

GMP Cosmetic Manufacturer Malaysia - BF1 Cosmetic Best Formula Industries ( BF1 ) are license GMP Cosmetic Manufacturer in Malaysia, conform to the requirement of Good Manufacturing Practices (GMP) in accordance with the ASEAN Guidelines for Cosmetic Good Manufacturing Practice. The GMP licensing enable Best Formula Industries ( BF1 ) to apply Cosmetic Notification Number ( NOT ) for major cosmetic products with Health Ministry Malaysia.

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[camphor2]

Nautral camphor

Nautral camphor is a waxy, white crystalline substance that is extracted from the wood of the camphor tree.

Nautral camphor  has a strong, distinctive fragrance and a cooling, soothing effect on the skin.

Nautral camphor  is commonly used in traditional medicine for its antiseptic, analgesic, and anti-inflammatory properties.

Nautral camphor  is a popular ingredient in many herbal remedies for coughs, colds, and respiratory ailments.

In India, Nautral camphor  is used in religious ceremonies as an offering to deities and for purification purposes.

Nautral camphor is also used as a natural insect repellent and as a moth deterrent.

Nautral camphor is a natural decongestant that helps to relieve nasal and chest congestion.

Nautral camphor  can be used in aromatherapy to promote relaxation and reduce stress.

Nautral camphor  is an effective natural remedy for muscle pain and soreness.

Nautral camphor  is used in the production of some types of plastics, including celluloid.

Nautral camphor  has been used in traditional Chinese medicine for thousands of years to treat a variety of ailments.

Nautral camphor is a powerful natural stimulant that can improve mental clarity and alertness.

Nautral camphor can be used to treat skin conditions such as acne, eczema, and psoriasis.

Nautral camphor  is a safe and effective natural alternative to chemical insecticides and mothballs.

Nautral camphor  is a versatile substance with many uses in traditional medicine, spirituality, and natural health.

[camphor2]

camphor

Camphor  is a white crystalline substance with a strong, fragrant odor.

Camphor is commonly used in traditional medicine and as an insect repellent.

Camphor has a cooling effect on the skin and can provide relief from itching and irritation.

In many cultures, Camphor is believed to have spiritual and healing properties.

Camphor is often used in aromatherapy to promote relaxation and reduce stress.

Camphor is a natural product obtained from the wood of the camphor tree.

Camphor can be synthesized from turpentine oil or obtained from other sources, such as eucalyptus leaves.

Camphor can be toxic if ingested in large quantities and should be used with caution.

Camphor  is also used in the production of celluloid, a type of plastic.

In some countries, Camphor is used in religious ceremonies and rituals.

Camphor is often included in ointments and balms for its analgesic and anti-inflammatory properties.

Camphor is an effective natural remedy for chest congestion and coughs.

Camphor has a long history of use in traditional Chinese medicine.

Camphor is used in the manufacture of fireworks and explosives.

Camphor is a versatile substance with many uses in medicine, industry, and culture.

[camphor2]

pure camphor

Pure camphor has been used for centuries in traditional medicine to treat a range of ailments, including coughs, colds, and headaches.

Pure camphor is derived from the wood of the camphor tree and is a white, crystalline substance with a strong, fragrant odor.

Pure camphor has also been used in religious rituals and is believed to have purifying and cleansing properties.

When burned,Pure camphorproduces a fragrant smoke that is said to ward off evil spirits and negative energies.

In aromatherapy, Pure camphor is used to promote relaxation, reduce stress, and improve mental clarity.

Pure camphor is often added to massage oils, diffusers, and bath salts to create a calming and soothing atmosphere.

Pure camphor is also used as an ingredient in many cosmetic and personal care products due to its cooling and soothing properties.

Pure camphor is commonly found in creams, lotions, and ointments designed to relieve sore muscles, joint pain, and inflammation.

Pure camphor is also a popular insect repellent and is used to protect clothing, linens, and stored items from moths and other pests.

However, Pure camphor is important to use pure camphor in moderation, as excessive use can be toxic and cause adverse effects.

Pure camphor is considered a natural remedy for respiratory conditions such as bronchitis and asthma.

Pure camphor is believed to have expectorant properties that help to loosen phlegm and clear airways.

In some cultures, Pure camphor is used as a traditional remedy for skin conditions such as eczema and psoriasis.

Pure camphor is said to have antimicrobial and antifungal properties that can help to soothe and heal irritated skin.

Overall, Pure camphor is a versatile and multi-purpose substance that has been used for centuries for its unique properties and benefits.

[gangotricamphor]

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[gangotricamphor]

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[chemwhat]

Benzyl alcohol CAS#: 100-51-6

IdentificationPhysical DataSpectraRoute of Synthesis(ROS)Safety and HazardsOther Data

Identification

Product NameBenzyl alcoholIUPAC NamephenylmethanolMolecular Structure

CAS Registry Number 100-51-6MDL NumberMFCD00004599Beilstein/REAXYS Number878307EC Number202-859-9eCl@ss39023110Synonymsbenzyl alcohol, benzylic alcohol, BenzylalcoholMolecular FormulaC6H5CH2OHMolecular Weight108.14InChIInChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2InChI KeyWVDDGKGOMKODPV-UHFFFAOYSA-NCanonical SMILESC1=CC=C(C=C1)CO

Physical Data

AppearanceColorless transparent liquidWater Solubility33 g/l at 20 °CFlash Point96 °CSolubilitywater: soluble 33 g/L at 20 °C Melting Point, °C 203 - 205 204 - 205 -15 120 - 121 -15.4 -15.19 -15.3 - 0 -15.5 -15.3 Boiling Point, °C Pressure (Boiling Point), Torr 205.1 760 195 - 200 760 130 - 140 6.37564 92 - 94 10 47 - 48 2 94 - 97 12 80 - 85 5 78 - 792.5 50 - 60 0.5 Refractive Index Wavelength (Refractive Index), nm Temperature (Refractive Index), °C 1.5831 589 24.99 1.53421 589 34.99 1.5342 589 20 1.53847 589 25 1.4018 589 601.5396 58913.6 Density, g·cm-3 Measurement Temperature, °C 1.0421 24.99 1.02912 39.99 1.0225 49.991.04129 251.0401 - 1.0206 25 - 50 1.061 - 0.81 0 - 280 0.9918 - 1.0706 -15 - 95 1.214 -195 Description (Adsorption (MCS)) Solvent (Adsorption (MCS)) Temperature (Adsorption (MCS)), °C Partner (Adsorption (MCS)) Partner (Adsorption (MCS)) Adsorption isotherm heptane 24.85 cellulose Adsorption 45 - 55 quartz sand Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence 2-phenylethanol, 2-methyl-benzyl alcohol Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence C18-silica gel Desorption 26.9 - 626.9ZnO, clean (0001)-Zn surface Desorption hexane, diethyl ether Ratio of solvents: 1:1 graphitized carbon black

Spectra

Description (NMR Spectroscopy) Nucleus (NMR Spectroscopy) Solvents (NMR Spectroscopy) Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz Chemical shifts, Spectrum 1H chloroform-d1 25600 Chemical shifts, Spectrum 13C chloroform-d1 25151Chemical shifts 1H chloroform-d1 400Chemical shifts, Spectrum 1H chloroform-d125300Chemical shifts, Spectrum 13C chloroform-d1 2575Chemical shifts 1H chloroform-d1 -30300 Description (IR Spectroscopy) Solvent (IR Spectroscopy) Temperature (IR Spectroscopy), °C Comment (IR Spectroscopy) Spectrum various solvent(s) 80 pressure dependence Spectrum liquid carbon dioxide 80high pressure. Object(s) of Study: pressure dependence Bands neat (no solvent) 3333 - 1496 cm**(-1) Bands KBr 3300 - 1460 cm**(-1) Spectrum neat (no solvent) 4000 - 666 cm**(-1) Intensity of IR bandsIntensitaet von OH-Valenzschwingungsbanden bei 3636.3 cmE-1 und 3617.1 cmE-1 von nicht-assoziiertem Benzylalkohol (CCl4). Description (UV/VIS Spectroscopy) Solvent (UV/VIS Spectroscopy) Comment (UV/VIS Spectroscopy) Absorption Maxima (UV/VIS), nm Spectrum H2O 250 - 550 nm Spectrum cyclohexane 220 - 280 nm Spectrum methanol 220 - 290 nm Absorption maxima cyclohexane 254.7 Spectrum LiCl 230 - 280 nm, sowie unverduennt. Absorption maxima bei -180grad sowie bei +30grad. 260

Route of Synthesis (ROS)

Route of Synthesis (ROS) of-Benzyl-alcohol-CAS-100-51-6 Conditions Yield With C18H28Br2N4Ru; potassium tert-butylate; hydrogen In 1,4-dioxane at 105℃under 22502.3 Torrfor 8h; A n/a B 94% With C30H37ClN4ORu; hydrogen; sodium t-butanolate In toluene at 105℃under 4500.45 Torrfor 20hReagent/catalystGloveboxSealed tubeOverall yield = 98 percent; Experimental Procedure General procedure: To a mixture of catalyst (0.01 mmol), KOtBu (10 mol %), and 1,4-dioxane (4.0 mL) in a Parr high-pressure reactor was added the ester(1.0 mmol). The dark red solution was purged with H2 and stirred under 400 psi of H2 at 105 °C for 8 h. Products isolation were performed via column chromatography using silica gel as stationary phase and n-pentane/ethylacetate or n-pentane/isopropanol mixture as eluent. The products were confirmed by 1H NMR.A n/a B 92% With C42H38N4OPRu(1+)*Cl(1-); potassium tert-butylate; hydrogen In toluene at 100℃under 4104.28Torrfor 2h;

Safety and Hazards

Pictogram(s)

SignalWarningGHS Hazard StatementsH302: Harmful if swallowed H332: Harmful if inhaled Precautionary Statement CodesP261, P264, P270, P271, P301+P312, P304+P312, P304+P340, P312, P330, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goodUnder the room temperature and away from lightHS Code290621StorageUnder the room temperature and away from lightShelf Life2 yearsMarket Price USD 2.1/kg Use PatternBenzyl alcohol CAS#: 100-51-6 can be used in cosmetics/dental/toilet inhibiting bacteria a cosmetic or dermatological composition, in combination with 4-(3-ethoxy-4-hydroxyphenyl)butan-2-onenatural broad-spectrum preservative composition in combination with extract of citrus grandis, fruit, octanohydroxamic acid and polyol a sensate in a personal care composition, in combination with 2-isopropyl-N,2,3-trimethylbutyramide Benzyl alcohol CAS#: 100-51-6 is a sensate in a personal care composition, in combination with camphor sensate in afier shaves lotionspreservative in pharmaceutical compositions comprising kisspeptin or derivatives thereof, used in synchronization programs of production animal estrus Read the full article

[chemwhat]

Benzyl alcohol CAS#: 100-51-6

IdentificationPhysical DataSpectraRoute of Synthesis(ROS)Safety and HazardsOther Data

Identification

Product NameBenzyl alcoholIUPAC NamephenylmethanolMolecular Structure

CAS Registry Number 100-51-6MDL NumberMFCD00004599Beilstein/REAXYS Number878307EC Number202-859-9eCl@ss39023110Synonymsbenzyl alcohol, benzylic alcohol, BenzylalcoholMolecular FormulaC6H5CH2OHMolecular Weight108.14InChIInChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2InChI KeyWVDDGKGOMKODPV-UHFFFAOYSA-NCanonical SMILESC1=CC=C(C=C1)CO

Physical Data

AppearanceColorless transparent liquidWater Solubility33 g/l at 20 °CFlash Point96 °CSolubilitywater: soluble 33 g/L at 20 °C Melting Point, °C 203 - 205 204 - 205 -15 120 - 121 -15.4 -15.19 -15.3 - 0 -15.5 -15.3 Boiling Point, °C Pressure (Boiling Point), Torr 205.1 760 195 - 200 760 130 - 140 6.37564 92 - 94 10 47 - 48 2 94 - 97 12 80 - 85 5 78 - 792.5 50 - 60 0.5 Refractive Index Wavelength (Refractive Index), nm Temperature (Refractive Index), °C 1.5831 589 24.99 1.53421 589 34.99 1.5342 589 20 1.53847 589 25 1.4018 589 601.5396 58913.6 Density, g·cm-3 Measurement Temperature, °C 1.0421 24.99 1.02912 39.99 1.0225 49.991.04129 251.0401 - 1.0206 25 - 50 1.061 - 0.81 0 - 280 0.9918 - 1.0706 -15 - 95 1.214 -195 Description (Adsorption (MCS)) Solvent (Adsorption (MCS)) Temperature (Adsorption (MCS)), °C Partner (Adsorption (MCS)) Partner (Adsorption (MCS)) Adsorption isotherm heptane 24.85 cellulose Adsorption 45 - 55 quartz sand Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence 2-phenylethanol, 2-methyl-benzyl alcohol Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence C18-silica gel Desorption 26.9 - 626.9ZnO, clean (0001)-Zn surface Desorption hexane, diethyl ether Ratio of solvents: 1:1 graphitized carbon black

Spectra

Description (NMR Spectroscopy) Nucleus (NMR Spectroscopy) Solvents (NMR Spectroscopy) Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz Chemical shifts, Spectrum 1H chloroform-d1 25600 Chemical shifts, Spectrum 13C chloroform-d1 25151Chemical shifts 1H chloroform-d1 400Chemical shifts, Spectrum 1H chloroform-d125300Chemical shifts, Spectrum 13C chloroform-d1 2575Chemical shifts 1H chloroform-d1 -30300 Description (IR Spectroscopy) Solvent (IR Spectroscopy) Temperature (IR Spectroscopy), °C Comment (IR Spectroscopy) Spectrum various solvent(s) 80 pressure dependence Spectrum liquid carbon dioxide 80high pressure. Object(s) of Study: pressure dependence Bands neat (no solvent) 3333 - 1496 cm**(-1) Bands KBr 3300 - 1460 cm**(-1) Spectrum neat (no solvent) 4000 - 666 cm**(-1) Intensity of IR bandsIntensitaet von OH-Valenzschwingungsbanden bei 3636.3 cmE-1 und 3617.1 cmE-1 von nicht-assoziiertem Benzylalkohol (CCl4). Description (UV/VIS Spectroscopy) Solvent (UV/VIS Spectroscopy) Comment (UV/VIS Spectroscopy) Absorption Maxima (UV/VIS), nm Spectrum H2O 250 - 550 nm Spectrum cyclohexane 220 - 280 nm Spectrum methanol 220 - 290 nm Absorption maxima cyclohexane 254.7 Spectrum LiCl 230 - 280 nm, sowie unverduennt. Absorption maxima bei -180grad sowie bei +30grad. 260

Route of Synthesis (ROS)

Route of Synthesis (ROS) of-Benzyl-alcohol-CAS-100-51-6 Conditions Yield With C18H28Br2N4Ru; potassium tert-butylate; hydrogen In 1,4-dioxane at 105℃under 22502.3 Torrfor 8h; A n/a B 94% With C30H37ClN4ORu; hydrogen; sodium t-butanolate In toluene at 105℃under 4500.45 Torrfor 20hReagent/catalystGloveboxSealed tubeOverall yield = 98 percent; Experimental Procedure General procedure: To a mixture of catalyst (0.01 mmol), KOtBu (10 mol %), and 1,4-dioxane (4.0 mL) in a Parr high-pressure reactor was added the ester(1.0 mmol). The dark red solution was purged with H2 and stirred under 400 psi of H2 at 105 °C for 8 h. Products isolation were performed via column chromatography using silica gel as stationary phase and n-pentane/ethylacetate or n-pentane/isopropanol mixture as eluent. The products were confirmed by 1H NMR.A n/a B 92% With C42H38N4OPRu(1+)*Cl(1-); potassium tert-butylate; hydrogen In toluene at 100℃under 4104.28Torrfor 2h;

Safety and Hazards

Pictogram(s)

SignalWarningGHS Hazard StatementsH302: Harmful if swallowed H332: Harmful if inhaled Precautionary Statement CodesP261, P264, P270, P271, P301+P312, P304+P312, P304+P340, P312, P330, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goodUnder the room temperature and away from lightHS Code290621StorageUnder the room temperature and away from lightShelf Life2 yearsMarket Price USD 2.1/kg Use PatternBenzyl alcohol CAS#: 100-51-6 can be used in cosmetics/dental/toilet inhibiting bacteria a cosmetic or dermatological composition, in combination with 4-(3-ethoxy-4-hydroxyphenyl)butan-2-onenatural broad-spectrum preservative composition in combination with extract of citrus grandis, fruit, octanohydroxamic acid and polyol a sensate in a personal care composition, in combination with 2-isopropyl-N,2,3-trimethylbutyramide Benzyl alcohol CAS#: 100-51-6 is a sensate in a personal care composition, in combination with camphor sensate in afier shaves lotionspreservative in pharmaceutical compositions comprising kisspeptin or derivatives thereof, used in synchronization programs of production animal estrus Read the full article

[chemwhat]

Benzyl alcohol CAS#: 100-51-6

IdentificationPhysical DataSpectraRoute of Synthesis(ROS)Safety and HazardsOther Data

Identification

Product NameBenzyl alcoholIUPAC NamephenylmethanolMolecular Structure

CAS Registry Number 100-51-6MDL NumberMFCD00004599Beilstein/REAXYS Number878307EC Number202-859-9eCl@ss39023110Synonymsbenzyl alcohol, benzylic alcohol, BenzylalcoholMolecular FormulaC6H5CH2OHMolecular Weight108.14InChIInChI=1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2InChI KeyWVDDGKGOMKODPV-UHFFFAOYSA-NCanonical SMILESC1=CC=C(C=C1)CO

Physical Data

AppearanceColorless transparent liquidWater Solubility33 g/l at 20 °CFlash Point96 °CSolubilitywater: soluble 33 g/L at 20 °C Melting Point, °C 203 - 205 204 - 205 -15 120 - 121 -15.4 -15.19 -15.3 - 0 -15.5 -15.3 Boiling Point, °C Pressure (Boiling Point), Torr 205.1 760 195 - 200 760 130 - 140 6.37564 92 - 94 10 47 - 48 2 94 - 97 12 80 - 85 5 78 - 792.5 50 - 60 0.5 Refractive Index Wavelength (Refractive Index), nm Temperature (Refractive Index), °C 1.5831 589 24.99 1.53421 589 34.99 1.5342 589 20 1.53847 589 25 1.4018 589 601.5396 58913.6 Density, g·cm-3 Measurement Temperature, °C 1.0421 24.99 1.02912 39.99 1.0225 49.991.04129 251.0401 - 1.0206 25 - 50 1.061 - 0.81 0 - 280 0.9918 - 1.0706 -15 - 95 1.214 -195 Description (Adsorption (MCS)) Solvent (Adsorption (MCS)) Temperature (Adsorption (MCS)), °C Partner (Adsorption (MCS)) Partner (Adsorption (MCS)) Adsorption isotherm heptane 24.85 cellulose Adsorption 45 - 55 quartz sand Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence 2-phenylethanol, 2-methyl-benzyl alcohol Adsorption methanol, H2O 27Ratio of solvents: 1:1 v/v, concentration dependence C18-silica gel Desorption 26.9 - 626.9ZnO, clean (0001)-Zn surface Desorption hexane, diethyl ether Ratio of solvents: 1:1 graphitized carbon black

Spectra

Description (NMR Spectroscopy) Nucleus (NMR Spectroscopy) Solvents (NMR Spectroscopy) Temperature (NMR Spectroscopy), °C Frequency (NMR Spectroscopy), MHz Chemical shifts, Spectrum 1H chloroform-d1 25600 Chemical shifts, Spectrum 13C chloroform-d1 25151Chemical shifts 1H chloroform-d1 400Chemical shifts, Spectrum 1H chloroform-d125300Chemical shifts, Spectrum 13C chloroform-d1 2575Chemical shifts 1H chloroform-d1 -30300 Description (IR Spectroscopy) Solvent (IR Spectroscopy) Temperature (IR Spectroscopy), °C Comment (IR Spectroscopy) Spectrum various solvent(s) 80 pressure dependence Spectrum liquid carbon dioxide 80high pressure. Object(s) of Study: pressure dependence Bands neat (no solvent) 3333 - 1496 cm**(-1) Bands KBr 3300 - 1460 cm**(-1) Spectrum neat (no solvent) 4000 - 666 cm**(-1) Intensity of IR bandsIntensitaet von OH-Valenzschwingungsbanden bei 3636.3 cmE-1 und 3617.1 cmE-1 von nicht-assoziiertem Benzylalkohol (CCl4). Description (UV/VIS Spectroscopy) Solvent (UV/VIS Spectroscopy) Comment (UV/VIS Spectroscopy) Absorption Maxima (UV/VIS), nm Spectrum H2O 250 - 550 nm Spectrum cyclohexane 220 - 280 nm Spectrum methanol 220 - 290 nm Absorption maxima cyclohexane 254.7 Spectrum LiCl 230 - 280 nm, sowie unverduennt. Absorption maxima bei -180grad sowie bei +30grad. 260

Route of Synthesis (ROS)

Route of Synthesis (ROS) of Benzyl alcohol CAS 100-51-6 Conditions Yield With C18H28Br2N4Ru; potassium tert-butylate; hydrogen In 1,4-dioxane at 105℃under 22502.3 Torrfor 8h; A n/a B 94% With C30H37ClN4ORu; hydrogen; sodium t-butanolate In toluene at 105℃under 4500.45 Torrfor 20hReagent/catalystGloveboxSealed tubeOverall yield = 98 percent; Experimental Procedure General procedure: To a mixture of catalyst (0.01 mmol), KOtBu (10 mol %), and 1,4-dioxane (4.0 mL) in a Parr high-pressure reactor was added the ester(1.0 mmol). The dark red solution was purged with H2 and stirred under 400 psi of H2 at 105 °C for 8 h. Products isolation were performed via column chromatography using silica gel as stationary phase and n-pentane/ethylacetate or n-pentane/isopropanol mixture as eluent. The products were confirmed by 1H NMR.A n/a B 92% With C42H38N4OPRu(1+)*Cl(1-); potassium tert-butylate; hydrogen In toluene at 100℃under 4104.28Torrfor 2h;

Safety and Hazards

Pictogram(s)

SignalWarningGHS Hazard StatementsH302: Harmful if swallowed H332: Harmful if inhaled Precautionary Statement CodesP261, P264, P270, P271, P301+P312, P304+P312, P304+P340, P312, P330, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

Other Data

TransportationNot dangerous goodUnder the room temperature and away from lightHS Code290621StorageUnder the room temperature and away from lightShelf Life2 yearsMarket Price USD 2.1/kg Use PatternBenzyl alcohol CAS#: 100-51-6 can be used in cosmetics/dental/toilet inhibiting bacteria a cosmetic or dermatological composition, in combination with 4-(3-ethoxy-4-hydroxyphenyl)butan-2-onenatural broad-spectrum preservative composition in combination with extract of citrus grandis, fruit, octanohydroxamic acid and polyol a sensate in a personal care composition, in combination with 2-isopropyl-N,2,3-trimethylbutyramide Benzyl alcohol CAS#: 100-51-6 is a sensate in a personal care composition, in combination with camphor sensate in afier shaves lotionspreservative in pharmaceutical compositions comprising kisspeptin or derivatives thereof, used in synchronization programs of production animal estrus Read the full article