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盐酸丁脒 | 3020-81-3

中文名称
盐酸丁脒
中文别名
盐酸丁
英文名称
butylamidine hydrochloride
英文别名
butyramidine hydrochloride;butanimidamide;hydrochloride
盐酸丁脒化学式
CAS
3020-81-3
化学式
C4H10N2*ClH
mdl
MFCD00054341
分子量
122.598
InChiKey
STYCVEYASXULRN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 熔点:
    107-108 °C
  • 溶解度:
    甲醇(微溶)、水(微溶)

计算性质

  • 辛醇/水分配系数(LogP):
    0.18
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    51.6
  • 氢给体数:
    2
  • 氢受体数:
    1

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S26
  • 危险类别码:
    R36
  • 海关编码:
    2942000000
  • 危险性防范说明:
    P264,P280,P305+P351+P338,P337+P313
  • 危险性描述:
    H319
  • 储存条件:
    应储存在室温、避光且充满惰性气体的环境中。

SDS

SDS:d2ca3dd547507096b537488a52011eef
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SECTION 1: Identification of the substance/mixture and of the company/undertaking
Product identifiers
Product name : Butanamidine Hydrochloride
REACH No. : A registration number is not available for this substance as the substance
or its uses are exempted from registration, the annual tonnage does not
require a registration or the registration is envisaged for a later
registration deadline.
Relevant identified uses of the substance or mixture and uses advised against
Identified uses : Laboratory chemicals, Manufacture of substances



SECTION 2: Hazards identification
Classification of the substance or mixture
Classification according to Regulation (EC) No 1272/2008
Eye irritation (Category 2), H319
For the full text of the H-Statements mentioned in this Section, see Section 16.
Classification according to EU Directives 67/548/EEC or 1999/45/EC
Xi Irritant R36
For the full text of the R-phrases mentioned in this Section, see Section 16.
Label elements
Labelling according Regulation (EC) No 1272/2008
Pictogram
Signal word Warning
Hazard statement(s)
H319 Causes serious eye irritation.
Precautionary statement(s)
P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove
contact lenses, if present and easy to do. Continue rinsing.
Supplemental Hazard none
Statements
Other hazards
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.

SECTION 3: Composition/information on ingredients
Substances
Molecular weight : 122,6 g/mol
Hazardous ingredients according to Regulation (EC) No 1272/2008
Component Classification Concentration
Butanamidine Hydrochloride
Eye Irrit. 2; H319 <= 100 %
Hazardous ingredients according to Directive 1999/45/EC
Component Classification Concentration
Butanamidine Hydrochloride
Xi, R36 <= 100 %
For the full text of the H-Statements and R-Phrases mentioned in this Section, see Section 16

SECTION 4: First aid measures
Description of first aid measures
General advice
Consult a physician. Show this safety data sheet to the doctor in attendance.
If inhaled
If breathed in, move person into fresh air. If not breathing, give artificial respiration. Consult a physician.
In case of skin contact
Wash off with soap and plenty of water. Consult a physician.
In case of eye contact
Rinse thoroughly with plenty of water for at least 15 minutes and consult a physician.
If swallowed
Never give anything by mouth to an unconscious person. Rinse mouth with water. Consult a physician.
Most important symptoms and effects, both acute and delayed
The most important known symptoms and effects are described in the labelling (see section 2.2) and/or in
section 11
Indication of any immediate medical attention and special treatment needed
No data available

SECTION 5: Firefighting measures
Extinguishing media
Suitable extinguishing media
Use water spray, alcohol-resistant foam, dry chemical or carbon dioxide.
Special hazards arising from the substance or mixture
Nature of decomposition products not known.
Advice for firefighters
Wear self-contained breathing apparatus for firefighting if necessary.
Further information
No data available

SECTION 6: Accidental release measures
Personal precautions, protective equipment and emergency procedures
Use personal protective equipment. Avoid dust formation. Avoid breathing vapours, mist or gas. Ensure
adequate ventilation. Avoid breathing dust.
For personal protection see section 8.
Environmental precautions
Do not let product enter drains.
Methods and materials for containment and cleaning up
Pick up and arrange disposal without creating dust. Sweep up and shovel. Keep in suitable, closed
containers for disposal.
Reference to other sections
For disposal see section 13.

SECTION 7: Handling and storage
Precautions for safe handling
Avoid contact with skin and eyes. Avoid formation of dust and aerosols.
Provide appropriate exhaust ventilation at places where dust is formed.
For precautions see section 2.2.
Conditions for safe storage, including any incompatibilities
Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
Storage class (TRGS 510): Non Combustible Solids
Specific end use(s)
Apart from the uses mentioned in section 1.2 no other specific uses are stipulated

SECTION 8: Exposure controls/personal protection
Control parameters
Components with workplace control parameters
Exposure controls
Appropriate engineering controls
Handle in accordance with good industrial hygiene and safety practice. Wash hands before breaks and
at the end of workday.
Personal protective equipment
Eye/face protection
Safety glasses with side-shields conforming to EN166 Use equipment for eye protection tested
and approved under appropriate government standards such as NIOSH (US) or EN 166(EU).
Skin protection
Handle with gloves. Gloves must be inspected prior to use. Use proper glove removal technique
(without touching glove's outer surface) to avoid skin contact with this product. Dispose of
contaminated gloves after use in accordance with applicable laws and good laboratory practices.
Wash and dry hands.
The selected protective gloves have to satisfy the specifications of EU Directive 89/686/EEC and
the standard EN 374 derived from it.
Body Protection
impervious clothing, The type of protective equipment must be selected according to the
concentration and amount of the dangerous substance at the specific workplace.
Respiratory protection
For nuisance exposures use type P95 (US) or type P1 (EU EN 143) particle respirator.For higher
level protection use type OV/AG/P99 (US) or type ABEK-P2 (EU EN 143) respirator cartridges.
Use respirators and components tested and approved under appropriate government standards
such as NIOSH (US) or CEN (EU).
Control of environmental exposure
Do not let product enter drains.

SECTION 9: Physical and chemical properties
Information on basic physical and chemical properties
a) Appearance Form: solid
b) Odour No data available
c) Odour Threshold No data available
d) pH No data available
e) Melting point/freezing No data available
point
f) Initial boiling point and No data available
boiling range
g) Flash point No data available
h) Evaporation rate No data available
i) Flammability (solid, gas) No data available
j) Upper/lower No data available
flammability or
explosive limits
k) Vapour pressure No data available
l) Vapour density No data available
m) Relative density No data available
n) Water solubility No data available
o) Partition coefficient: n- No data available
octanol/water
p) Auto-ignition No data available
temperature
q) Decomposition No data available
temperature
r) Viscosity No data available
s) Explosive properties No data available
t) Oxidizing properties No data available
Other safety information
No data available

SECTION 10: Stability and reactivity
Reactivity
No data available
Chemical stability
Stable under recommended storage conditions.
Possibility of hazardous reactions
No data available
Conditions to avoid
No data available
Incompatible materials
No data available
Hazardous decomposition products
In the event of fire: see section 5

SECTION 11: Toxicological information
Information on toxicological effects
Acute toxicity
No data available
Skin corrosion/irritation
No data available
Serious eye damage/eye irritation
No data available
Respiratory or skin sensitisation
No data available
Germ cell mutagenicity
No data available
Carcinogenicity
IARC: No component of this product present at levels greater than or equal to 0.1% is identified as
probable, possible or confirmed human carcinogen by IARC.
Reproductive toxicity
No data available
Specific target organ toxicity - single exposure
No data available
Specific target organ toxicity - repeated exposure
No data available
Aspiration hazard
No data available
Additional Information
RTECS: Not available

SECTION 12: Ecological information
Toxicity
No data available
Persistence and degradability
No data available
Bioaccumulative potential
No data available
Mobility in soil
No data available
Results of PBT and vPvB assessment
This substance/mixture contains no components considered to be either persistent, bioaccumulative and
toxic (PBT), or very persistent and very bioaccumulative (vPvB) at levels of 0.1% or higher.
Other adverse effects
No data available

SECTION 13: Disposal considerations
Waste treatment methods
Product
Offer surplus and non-recyclable solutions to a licensed disposal company. Dissolve or mix the material
with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber.
Contaminated packaging
Dispose of as unused product.

SECTION 14: Transport information
UN number
ADR/RID: - IMDG: - IATA: -
UN proper shipping name
ADR/RID: Not dangerous goods
IMDG: Not dangerous goods
IATA: Not dangerous goods
Transport hazard class(es)
ADR/RID: - IMDG: - IATA: -
Packaging group
ADR/RID: - IMDG: - IATA: -
Environmental hazards
ADR/RID: no IMDG Marine pollutant: no IATA: no
Special precautions for user
No data available

SECTION 15: Regulatory information
This safety datasheet complies with the requirements of Regulation (EC) No. 1907/2006.
Safety, health and environmental regulations/legislation specific for the substance or mixture
No data available
Chemical Safety Assessment
For this product a chemical safety assessment was not carried out

SECTION 16: Other information
Full text of H-Statements referred to under sections 2 and 3.
Eye Irrit. Eye irritation
H319 Causes serious eye irritation.
Full text of R-phrases referred to under sections 2 and 3
Xi Irritant
R36 Irritating to eyes.
Further information
Copyright 2014 Co. LLC. License granted to make unlimited paper copies for internal use
only.
The above information is believed to be correct but does not purport to be all inclusive and shall be
used only as a guide. The information in this document is based on the present state of our knowledge
and is applicable to the product with regard to appropriate safety precautions. It does not represent any
guarantee of the properties of the product. Corporation and its Affiliates shall not be held
liable for any damage resulting from handling or from contact with the above product. See
and/or the reverse side of invoice or packing slip for additional terms and conditions of sale.

制备方法与用途

化学性质:

  • 该物质为白色或类白色的粉末状固体,略显酸性。
  • 它易溶于水和甲醇,而不溶于丙酮等溶剂,并且极易吸潮。

用途: 它是生产抗球虫药安普罗林的重要中间体。

反应信息

  • 作为反应物:
    描述:
    盐酸丁脒 在 potassium chloride 、 fluorine 作用下, 生成 N,N,N'-Trichlor-butyramidin
    参考文献:
    名称:
    Synthesis of N,N,N′-trichloroamidines by a novel oxidative chlorination reaction
    摘要:
    DOI:
    10.1016/s0040-4039(01)82824-0
  • 作为产物:
    描述:
    丁腈盐酸 作用下, 以 甲醇 为溶剂, 生成 盐酸丁脒
    参考文献:
    名称:
    嘧啶4(3 H)-one衍生物作为氯沙坦类似物的合成及其对新型血管紧张素II受体1(AT 1)拮抗剂的降压活性
    摘要:
    提出了高效AT 1拮抗剂12a(BR-A-657,Fimasartan)拮抗剂的发现,体内和体外研究。合成了一系列作为氯沙坦类似物的嘧啶4-4(3 H)-one衍生物,并对其进行了一类新型的AT 1受体拮抗剂的评价。其中,含有硫酰胺基部分的12a表现出较高的体外功能拮抗作用和结合亲和力[分别为IC 50  = 0.42和0.13 nM],并在具有ED 50的成髓大鼠中强烈抑制了AngII诱导的升压反应。0.018 mg / kg。此外,在速尿治疗的大鼠和清醒的肾性高血压大鼠模型中进行的体内评估以及药代动力学研究表明,12a是一种高效且口服活性的AT 1选择性拮抗剂,具有比氯沙坦更强的体内效力。
    DOI:
    10.1016/j.bmcl.2011.12.116
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文献信息

  • Direct Preparation of Heteroaromatic Compounds from Alkenes
    作者:Timothy Donohoe、Mikhail Kabeshov、Akshat Rathi、Ian Smith
    DOI:10.1055/s-0030-1259034
    日期:2010.12
    A series of aromatic heterocycles, thiazoles, imidazoles, and dimethoxyindoles, can be synthesised directly from alkenes via a ketoiodination-cyclisation protocol. The alkene starting materials are themselves easily accessible by many different and well-established approaches, and allow access to various aromatic heterocycles with excellent yields and regioselectivity.
    一系列芳香杂环、噻唑、咪唑和二甲氧基吲哚,可以通过酮碘化-环化方案直接从烯烃合成。烯烃原料本身很容易通过许多不同的和完善的方法获得,并允许以优异的产率和区域选择性获得各种芳族杂环。
  • Intercepted Retro-Nazarov Reaction: Syntheses of Amidino-Rocaglate Derivatives and Their Biological Evaluation as eIF4A Inhibitors
    作者:Wenhan Zhang、Jennifer Chu、Andrew M. Cyr、Han Yueh、Lauren E. Brown、Tony T. Wang、Jerry Pelletier、John A. Porco
    DOI:10.1021/jacs.9b06446
    日期:2019.8.14
    rocaglate skeleton. Trapping of the oxyallyl cation with a diverse range of nucleophiles has been used to generate over fifty novel amidino-rocaglate (ADR) and amino-rocaglate derivatives. Subsequently, these derivatives were evaluated for their ability to inhibit cap-dependent protein synthesis where they were found to outperform previous lead compounds including the rocaglate hydroxamate CR-1-31-B.
    Rocaglates 是从米兰属中分离出来的一类天然产物,具有高度取代的环戊[b]苯并呋喃骨架,可抑制帽子依赖性蛋白质合成。Rocaglalate 是一种颇具吸引力的化合物,因为它们具有通过特异性靶向真核起始因子 4A (eIF4A) 并干扰核糖体募集至 mRNA 来抑制体内肿瘤细胞维持的潜力。在本文中,我们描述了一种截获的逆纳扎罗夫反应,利用分子内甲苯磺酰迁移在罗卡格特骨架上生成反应性氧化烯丙基阳离子。用多种亲核试剂捕获氧烯丙基阳离子已被用来生成五十多种新型脒基罗卡酸盐 (ADR) 和氨基罗卡酸盐衍生物。随后,对这些衍生物抑制帽子依赖性蛋白质合成的能力进行了评估,结果发现它们优于以前的先导化合物,包括罗卡格酯异羟肟酸 CR-1-31-B。
  • ‘Green' Synthesis of 2-Substituted 6-Hydroxy-[3H]-pyrimidin-4-ones and 4,6-Dichloropyrimidines: Improved Strategies and Mechanistic Study
    作者:Andreas Opitz、Werner Sulger、Ewald Daltrozzo、Rainer Koch
    DOI:10.1071/ch14073
    日期:——
    An improved route to 2-substituted 6-hydroxy-[3H]-pyrimidin-4-ones 4 and to 2-substituted 4,6-dichloropyrimidines 5 is reported. Without using highly toxic reactants, compounds 4 can be prepared conveniently in a one pot synthesis on a one mol scale with average yields up to 80 %. 4,6-Dichloropyrimidines 5, which are usually prepared in small quantities, are synthesized with average yields of 80 %
    一种改进的路线2-取代的6-羟基- [3 H ^ ] -嘧啶-4-酮4和2-取代的4,6-二氯嘧啶5报道。不使用剧毒反应物,就可以方便地在一锅合成中以1摩尔规模制备化合物4,平均收率可达80%。通常使用少量原料制备的4,6-二氯嘧啶5的平均收率为80%,最多可使用80 g起始原料。4氯化的机理是第一次进行计算研究。结果表明,磷酰氯的氯化反应以交替的磷酸化-氯化方式(途径1)进行,这比以两次磷酸化开始的顺序更可取。本文所述的研究的4,6-二氯嘧啶与二氯磷酸形成强络合物,但与盐酸形成弱络合物(在后处理期间生成)。后面这些配合物解释了在后处理过程中使用碳酸钠水溶液的必要性。为了防止在中间体或最终的二氯嘧啶和未反应的羟基嘧啶之间形成嘧啶鎓盐,可以用强酸(例如二氯磷酸)使后者失活,从而进行氯化反应,但阻止形成盐。
  • Direct preparation of thiazoles, imidazoles, imidazopyridines and thiazolidines from alkenes
    作者:Timothy J. Donohoe、Mikhail A Kabeshov、Akshat H. Rathi、Ian E. D. Smith
    DOI:10.1039/c1ob06587d
    日期:——
    A range of heterocycles, namely thiazoles, imidazoles, imidazopyridines, thiazolidines and dimethoxyindoles, have been synthesised directly from alkenesvia a two-step ketoidoination/cyclisation protocol. The alkene starting materials are themselves readily accessible using many different and well-established approaches, and allow access to a variety of heterocycles with excellent yields and regioselectivity.
    通过两步酮亚胺化/环化方案,一系列杂环化合物,包括噻唑、咪唑、咪唑并吡啶、噻唑烷和二甲氧基吲哚,已直接从烯烃合成。烯烃起始原料可通过多种不同且成熟的途径轻松获得,并能以优异的产率和区域选择性制备多种杂环化合物。
  • Copper-Catalyzed Sequential N-Arylation and Aerobic Oxidation: Synthesis of Quinazoline Derivatives
    作者:Hua Fu、Changmei Cheng、Qing Liu、Yufen Zhao
    DOI:10.1055/s-0033-1339800
    日期:——
    novel and efficient copper-catalyzed cascade method for the synthesis of quinazoline derivatives has been developed. The protocol uses readily available substituted (2-bromophenyl)methylamines and amidine hydrochlorides as the starting materials, inexpensive CuBr as the catalyst, and economical and environment friendly air as the oxidant, and the corresponding quinazoline derivatives were obtained in
    开发了一种新型高效的铜催化级联合成喹唑啉衍生物的方法。该方案以易得的取代(2-溴苯基)甲胺和脒盐酸盐为起始原料,以廉价的CuBr为催化剂,以经济环保的空气为氧化剂,以中等至良好的收率获得了相应的喹唑啉衍生物。该过程经历了连续的分子间 N-芳基化、分子内亲核取代和有氧氧化。
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