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Merck

W213713

Sigma-Aldrich

苯甲醇

greener alternative

natural, ≥98%, FG

别名:

苯甲醇

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About This Item

线性分子式:
C6H5CH2OH
CAS号:
分子量:
108.14
FEMA號碼:
2137
Beilstein:
878307
EC號碼:
歐洲委員會號碼:
58
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
2.010
NACRES:
NA.21
感官的:
fruity; floral; balsamic; sweet
等級:
FG
Fragrance grade
Halal
Kosher
natural
agency:
follows IFRA guidelines
meets purity specifications of JECFA
食物過敏原:
no known allergens

等級

FG
Fragrance grade
Halal
Kosher
natural

品質等級

agency

follows IFRA guidelines
meets purity specifications of JECFA

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

蒸汽密度

3.7 (vs air)

蒸汽壓力

13.3 mmHg ( 100 °C)
3.75 mmHg ( 77 °C)

化驗

≥98%

形狀

liquid

自燃溫度

817 °F

儲存期限

5 yr

成份

contains IFRA restricted benzyl alcohol

環保替代產品特色

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

技術

UV/Vis spectroscopy: suitable

折射率

n20/D 1.539 (lit.)

bp

203-205 °C (lit.)

mp

−16-−13 °C (lit.)

密度

1.045 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

香料過敏原

benzyl alcohol

環保替代類別

感官的

fruity; floral; balsamic; sweet

SMILES 字串

OCc1ccccc1

InChI

1S/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H2

InChI 密鑰

WVDDGKGOMKODPV-UHFFFAOYSA-N

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一般說明

Benzyl alcohol is an aromatic alcohol that is used as a flavoring agent and fragrance ingredient.
We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.

應用


  • Ni-Co hexacyanoferrate hollow nanoprism with CN vacancy for electrocatalytic benzyl alcohol oxidation.: This study explores the catalytic potential of benzyl alcohol in electrochemical oxidation processes using novel nanoprism catalysts. The research highlights the efficient conversion of benzyl alcohol to benzaldehyde, providing insights into sustainable chemical synthesis and energy conversion technologies (Lv et al., 2024).

  • Combining anodic alcohol oxidative coupling for C-C bond formation with cathodic ammonia production.: This research utilizes benzyl alcohol in a dual electrocatalytic system that not only enhances C-C bond formation but also contributes to environmentally friendly ammonia production, showcasing the compound′s versatility in green chemistry applications (Xu et al., 2024).

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

213.8 °F - DIN 51758

閃點(°C)

101 °C - DIN 51758

個人防護裝備

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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分析证书(COA)

Lot/Batch Number

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其他客户在看

Slide 1 of 2

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Burdock GA
Encyclopedia of Food and Color Additives, 1, 261-262 (1997)
Fragrance material review on anisyl alcohol
Scognamiglio J, et al.
Food And Chemical Toxicology, 50, S140-S160 (2012)
C L Froebe et al.
Dermatologica, 181(4), 277-283 (1990-01-01)
The relationship between the in vivo irritation potential of sodium lauryl sulfate (SLS) and linear alkyl benzene sulfonate (LAS) and the ability of these two surfactants to remove lipid from the stratum corneum (SC) in vitro were investigated. Either surfactant
Béatrice Hechler et al.
The Journal of pharmacology and experimental therapeutics, 314(1), 232-243 (2005-03-29)
Our aim was to determine whether the newly described P2X1 antagonist NF449 [4,4',4'',4'''-(carbonylbis(imino-5,1,3-benzenetriylbis(carbonylimino)))tetrakis-benzene-1,3-disulfonic acid octasodium salt] could selectively antagonize the platelet P2X1 receptor and how it affected platelet function. NF449 inhibited alpha,beta-methyleneadenosine 5'-triphosphate-induced shape change (IC50 = 83 +/- 13
A P De Leenheer et al.
Clinical chemistry, 31(1), 142-146 (1985-01-01)
For this sensitive RIA for 1 alpha,25-dihydroxyvitamin D, we used antibodies to 1 alpha,25-dihydroxycholecalciferol-3-hemisuccinate conjugated to bovine serum albumin, raised in rabbits. These antibodies show a high affinity for 1 alpha,25-dihydroxyvitamin D3 but cross react with other vitamin D metabolites

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