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448729

9-溴-1-壬醇

95%

别名:

伸壬基溴茚烷醇

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关于此项目

线性分子式:
Br(CH2)9OH
化学文摘社编号:
55362-80-6
分子量:
223.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24868427
MDL number:
MFCD00063348
Beilstein/REAXYS Number:
1737525
Assay:
95%
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Quality Level

100

assay

95%

bp

125-126 °C/2 mmHg (lit.)

mp

33-35 °C (lit.)

functional group

bromo, hydroxyl

SMILES string

OCCCCCCCCCBr

InChI

1S/C9H19BrO/c10-8-6-4-2-1-3-5-7-9-11/h11H,1-9H2

InChI key

USJDOLXCPFASNV-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKCM8787
MKCH1739
MKBZ3428V
MKBQ4154V
MKBL7743V

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Synthesis of the diacetylenic phospholipids 1, 2-(10', 12'-heptadecadiynoyl)-sn-glycero-3-phophatidylcholine and 1, 2-(4', 6'-tricosadiynoyl)-sn-glycero-3-phophatidylcholine.
Hennies PT, et al.
Journal of the Brazilian Chemical Society, 12(1), 64-72 (2001)
In vitro enzymatic oxidation of a fluorine-tagged sulfido substrate analogue: a 19F NMR investigation.
Tremblay AE, et al.
Magnetic Resonance in Chemistry, 44(6), 629-632 (2006)
Néstor M Carballeira et al.
Chemistry and physics of lipids, 145(1), 37-44 (2006-11-28)
The first total syntheses for the (Z)-15-methyl-10-hexadecenoic acid and the (Z)-13-methyl-8-tetradecenoic acid were accomplished in seven steps and in 31-32% overall yields. The (trimethylsilyl)acetylene was the key reagent in both syntheses. It is proposed that the best synthetic strategy towards
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全球贸易项目编号

货号GTIN
448729-25G04061832280103
448729-5G04061832312729